{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,22]],"date-time":"2026-01-22T21:18:09Z","timestamp":1769116689177,"version":"3.49.0"},"reference-count":321,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2020,8,1]],"date-time":"2020-08-01T00:00:00Z","timestamp":1596240000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2020,8,1]],"date-time":"2020-08-01T00:00:00Z","timestamp":1596240000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2020,5,13]],"date-time":"2020-05-13T00:00:00Z","timestamp":1589328000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"DOI":"10.13039\/100000049","name":"National Institute on Aging","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100000049","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["R01AG067426"],"award-info":[{"award-number":["R01AG067426"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Neurobiology of Disease"],"published-print":{"date-parts":[[2020,8]]},"DOI":"10.1016\/j.nbd.2020.104946","type":"journal-article","created":{"date-parts":[[2020,5,18]],"date-time":"2020-05-18T21:51:15Z","timestamp":1589838675000},"page":"104946","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":42,"special_numbering":"C","title":["Genetic architecture of common non-Alzheimer\u2019s disease dementias"],"prefix":"10.1016","volume":"142","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-5879-3486","authenticated-orcid":false,"given":"Rita","family":"Guerreiro","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Elizabeth","family":"Gibbons","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Miguel","family":"T\u00e1buas-Pereira","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Celia","family":"Kun-Rodrigues","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Gustavo C.","family":"Santo","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8186-0333","authenticated-orcid":false,"given":"Jose","family":"Bras","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.nbd.2020.104946_bb0005","doi-asserted-by":"crossref","first-page":"42","DOI":"10.3389\/fnins.2020.00042","article-title":"The overlapping genetics of amyotrophic lateral sclerosis and frontotemporal dementia","volume":"14","author":"Abramzon","year":"2020","journal-title":"Front. Neurosci."},{"key":"10.1016\/j.nbd.2020.104946_bb0010","doi-asserted-by":"crossref","first-page":"769","DOI":"10.1177\/1533317514539541","article-title":"Synergistic epistasis of paraoxonase 1 (rs662 and rs85460) and apolipoprotein E4 genes in pathogenesis of Alzheimer\u2019s disease and vascular dementia","volume":"29","author":"Alam","year":"2014","journal-title":"Am. J. Alzheimers Dis. Other Dement."},{"key":"10.1016\/j.nbd.2020.104946_bb0015","doi-asserted-by":"crossref","first-page":"864","DOI":"10.1542\/peds.97.6.864","article-title":"Cognitive functioning and brain magnetic resonance imaging in children with sickle Cell disease. Neuropsychology Committee of the Cooperative Study of Sickle Cell Disease","volume":"97","author":"Armstrong","year":"1996","journal-title":"Pediatrics"},{"key":"10.1016\/j.nbd.2020.104946_bb0020","doi-asserted-by":"crossref","first-page":"331","DOI":"10.1016\/j.ymgme.2007.10.001","article-title":"Urinary globotriaosylceramide excretion correlates with the genotype in children and adults with Fabry disease","volume":"93","author":"Auray-Blais","year":"2008","journal-title":"Mol. Genet. Metab."},{"key":"10.1016\/j.nbd.2020.104946_bb0025","doi-asserted-by":"crossref","first-page":"175","DOI":"10.1038\/nrneurol.2016.14","article-title":"Parkinsonism, movement disorders and genetics in frontotemporal dementia","volume":"12","author":"Baizabal-Carvallo","year":"2016","journal-title":"Nat. Rev. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0030","doi-asserted-by":"crossref","first-page":"916","DOI":"10.1038\/nature05016","article-title":"Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17","volume":"442","author":"Baker","year":"2006","journal-title":"Nature"},{"key":"10.1016\/j.nbd.2020.104946_bb0035","doi-asserted-by":"crossref","first-page":"544","DOI":"10.1038\/s41582-018-0047-2","article-title":"C9orf72-mediated ALS and FTD: multiple pathways to disease","volume":"14","author":"Balendra","year":"2018","journal-title":"Nat. Rev. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0040","doi-asserted-by":"crossref","first-page":"2329","DOI":"10.1093\/brain\/awu138","article-title":"A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement","volume":"137","author":"Bannwarth","year":"2014","journal-title":"Brain"},{"issue":"Suppl. 11","key":"10.1016\/j.nbd.2020.104946_bb0045","first-page":"16","article-title":"Lewy body dementia: the litmus test for neuroleptic sensitivity and extrapyramidal symptoms","volume":"65","author":"Baskys","year":"2004","journal-title":"J. Clin. Psychiatry"},{"key":"10.1016\/j.nbd.2020.104946_bb0050","doi-asserted-by":"crossref","first-page":"266","DOI":"10.1097\/NEN.0b013e31824b211b","article-title":"Accuracy of the clinical diagnosis of Alzheimer disease at national institute on aging Alzheimer disease centers, 2005\u20132010","volume":"71","author":"Beach","year":"2012","journal-title":"J. Neuropathol. Exp. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0055","doi-asserted-by":"crossref","first-page":"111","DOI":"10.5114\/fn.2013.35953","article-title":"Paraoxonase 1 (PON1) gene-108C>T and p.Q192R polymorphisms and arylesterase activity of the enzyme in patients with dementia","volume":"51","author":"Bednarska-Makaruk","year":"2013","journal-title":"Folia Neuropathol."},{"key":"10.1016\/j.nbd.2020.104946_bb0060","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pgen.1004606","article-title":"Genome-wide association meta-analysis of neuropathologic features of Alzheimer\u2019s disease and related dementias","volume":"10","author":"Beecham","year":"2014","journal-title":"PLoS Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0065","doi-asserted-by":"crossref","first-page":"331","DOI":"10.1111\/jnc.13570","article-title":"The contribution of alpha synuclein to neuronal survival and function \u2013 implications for Parkinson\u2019s disease","volume":"137","author":"Benskey","year":"2016","journal-title":"J. Neurochem."},{"key":"10.1016\/j.nbd.2020.104946_bb0070","doi-asserted-by":"crossref","first-page":"48","DOI":"10.1016\/j.neulet.2017.08.040","article-title":"The GBA variant E326K is associated with Parkinson\u2019s disease and explains a genome-wide association signal","volume":"658","author":"Berge-Seidl","year":"2017","journal-title":"Neurosci. Lett."},{"key":"10.1016\/j.nbd.2020.104946_bb0075","doi-asserted-by":"crossref","first-page":"245","DOI":"10.14283\/jpad.2018.35","article-title":"Clinical application of APOE in Alzheimer\u2019s prevention: a precision medicine approach","volume":"5","author":"Berkowitz","year":"2018","journal-title":"J Prev Alzheimers Dis"},{"key":"10.1016\/j.nbd.2020.104946_bb0080","doi-asserted-by":"crossref","first-page":"1390","DOI":"10.1172\/JCI114027","article-title":"Fabry disease: six gene rearrangements and an exonic point mutation in the alpha-galactosidase gene","volume":"83","author":"Bernstein","year":"1989","journal-title":"J. Clin. Invest."},{"key":"10.1016\/j.nbd.2020.104946_bb0085","first-page":"247","article-title":"Considerations on a mutation in the NOTCH3 gene sparing a cysteine residue: a rare polymorphism rather than a CADASIL variant","volume":"27","author":"Bersano","year":"2012","journal-title":"Funct. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0090","doi-asserted-by":"crossref","first-page":"898","DOI":"10.1212\/WNL.0000000000000202","article-title":"Two novel HTRA1 mutations in a European CARASIL patient","volume":"82","author":"Bianchi","year":"2014","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb0095","doi-asserted-by":"crossref","first-page":"234","DOI":"10.1093\/brain\/awz350","article-title":"Genetic modifiers of risk and age at onset in GBA associated Parkinson\u2019s disease and Lewy body dementia","volume":"143","author":"Blauwendraat","year":"2020","journal-title":"Brain"},{"key":"10.1016\/j.nbd.2020.104946_bb0100","doi-asserted-by":"crossref","first-page":"833","DOI":"10.1212\/WNL.0b013e3182a2cbd1","article-title":"Risk factors for dementia with Lewy bodies: a case-control study","volume":"81","author":"Boot","year":"2013","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb0105","doi-asserted-by":"crossref","first-page":"82","DOI":"10.1016\/j.parkreldis.2016.12.002","article-title":"Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene","volume":"35","author":"Bougea","year":"2017","journal-title":"Parkinsonism Relat. Disord."},{"key":"10.1016\/j.nbd.2020.104946_bb0110","doi-asserted-by":"crossref","first-page":"6139","DOI":"10.1093\/hmg\/ddu334","article-title":"Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies","volume":"23","author":"Bras","year":"2014","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0115","article-title":"Mutant ADA2 in vasculopathies","author":"Bras","year":"2014","journal-title":"N. Engl. J. Med."},{"key":"10.1016\/j.nbd.2020.104946_bb0120","doi-asserted-by":"crossref","first-page":"1656","DOI":"10.1056\/NEJMcpc0810839","article-title":"Case records of the Massachusetts General Hospital. Case 12-2009. A 46-year-old man with migraine, aphasia, and hemiparesis and similarly affected family members","volume":"360","author":"Brass","year":"2009","journal-title":"N. Engl. J. Med."},{"key":"10.1016\/j.nbd.2020.104946_bb0125","doi-asserted-by":"crossref","first-page":"7512","DOI":"10.1074\/jbc.M111.288720","article-title":"Cellular model of TAR DNA-binding protein 43 (TDP-43) aggregation based on its C-terminal Gln\/Asn-rich region","volume":"287","author":"Budini","year":"2012","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.nbd.2020.104946_bb0130","doi-asserted-by":"crossref","first-page":"1777","DOI":"10.1212\/WNL.0000000000003251","article-title":"Cathepsin A-related arteriopathy with strokes and leukoencephalopathy (CARASAL)","volume":"87","author":"Bugiani","year":"2016","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb0135","doi-asserted-by":"crossref","first-page":"1387","DOI":"10.1007\/s10072-015-2121-5","article-title":"A frameshift mutation in HTRA1 expands CARASIL syndrome and peripheral small arterial disease to the Chinese population","volume":"36","author":"Cai","year":"2015","journal-title":"Neurol. Sci."},{"key":"10.1016\/j.nbd.2020.104946_bb0140","doi-asserted-by":"crossref","first-page":"28","DOI":"10.1186\/s13024-015-0025-8","article-title":"Regulation of human MAPT gene expression","volume":"10","author":"Caillet-Boudin","year":"2015","journal-title":"Mol. Neurodegener."},{"key":"10.1016\/j.nbd.2020.104946_bb0145","doi-asserted-by":"crossref","first-page":"721","DOI":"10.1016\/S1474-4422(18)30232-1","article-title":"The role of TREM2 in Alzheimer\u2019s disease and other neurodegenerative disorders","volume":"17","author":"Carmona","year":"2018","journal-title":"Lancet Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0150","doi-asserted-by":"crossref","DOI":"10.1212\/NXG.0000000000000080","article-title":"Defining the spectrum of frontotemporal dementias associated with TARDBP mutations","volume":"2","author":"Caroppo","year":"2016","journal-title":"Neurol. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0155","doi-asserted-by":"crossref","first-page":"890","DOI":"10.1016\/j.ajhg.2010.11.002","article-title":"Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma","volume":"87","author":"Carrasquillo","year":"2010","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0160","doi-asserted-by":"crossref","first-page":"934","DOI":"10.1016\/S0140-6736(95)91557-5","article-title":"Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy","volume":"346","author":"Chabriat","year":"1995","journal-title":"Lancet"},{"key":"10.1016\/j.nbd.2020.104946_bb0165","doi-asserted-by":"crossref","first-page":"1401","DOI":"10.1161\/01.STR.29.7.1401","article-title":"ACE, MTHFR, factor V Leiden, and APOE polymorphisms in patients with vascular and Alzheimer\u2019s dementia","volume":"29","author":"Chapman","year":"1998","journal-title":"Stroke"},{"key":"10.1016\/j.nbd.2020.104946_bb0170","first-page":"e358","article-title":"APOE and cortical superficial siderosis in CAA: meta-analysis and potential mechanisms","volume":"93","author":"Charidimou","year":"2019","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb0175","doi-asserted-by":"crossref","first-page":"881","DOI":"10.1136\/jmg.2004.030171","article-title":"Pseudoxanthoma elasticum: a clinical, pathophysiological and genetic update including 11 novel ABCC6 mutations","volume":"42","author":"Chassaing","year":"2005","journal-title":"J. Med. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0180","doi-asserted-by":"crossref","first-page":"578","DOI":"10.1001\/archneurol.2009.54","article-title":"Association of glucocerebrosidase mutations with dementia with lewy bodies","volume":"66","author":"Clark","year":"2009","journal-title":"Arch. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0185","doi-asserted-by":"crossref","first-page":"3428","DOI":"10.1093\/brain\/awy284","article-title":"Frontotemporal dementia causative CHMP2B impairs neuronal endolysosomal traffic-rescue by TMEM106B knockdown","volume":"141","author":"Clayton","year":"2018","journal-title":"Brain"},{"key":"10.1016\/j.nbd.2020.104946_bb0190","doi-asserted-by":"crossref","first-page":"628","DOI":"10.1002\/ajmg.b.32080","article-title":"Genetics of dementia: update and guidelines for the clinician","volume":"159","author":"Cohn-Hokke","year":"2012","journal-title":"Am. J. Med. Genet. B Neuropsychiatr. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0200","doi-asserted-by":"crossref","first-page":"92","DOI":"10.1002\/ana.21397","article-title":"Gene expression study on peripheral blood identifies progranulin mutations","volume":"64","author":"Coppola","year":"2008","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0205","doi-asserted-by":"crossref","first-page":"3500","DOI":"10.1093\/hmg\/dds161","article-title":"Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer\u2019s diseases","volume":"21","author":"Coppola","year":"2012","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0210","doi-asserted-by":"crossref","first-page":"996","DOI":"10.1016\/j.metabol.2011.11.010","article-title":"Apolipoprotein E predicts incident cardiovascular disease risk in women but not in men with concurrently high levels of high-density lipoprotein cholesterol and C-reactive protein","volume":"61","author":"Corsetti","year":"2012","journal-title":"Metabolism"},{"key":"10.1016\/j.nbd.2020.104946_bb0215","doi-asserted-by":"crossref","first-page":"1311","DOI":"10.1038\/ng.3926","article-title":"Bayesian analysis of genetic association across tree-structured routine healthcare data in the UK Biobank","volume":"49","author":"Cortes","year":"2017","journal-title":"Nat. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0220","doi-asserted-by":"crossref","first-page":"126","DOI":"10.1038\/s41588-019-0550-4","article-title":"Identifying cross-disease components of genetic risk across hospital data in the UK Biobank","volume":"52","author":"Cortes","year":"2020","journal-title":"Nat. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0225","doi-asserted-by":"crossref","first-page":"628","DOI":"10.1111\/j.1468-1331.2006.01337.x","article-title":"A new de novo Notch3 mutation causing CADASIL","volume":"13","author":"Coto","year":"2006","journal-title":"Eur. J. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0230","doi-asserted-by":"crossref","first-page":"581","DOI":"10.1001\/archneurol.2010.350","article-title":"Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels","volume":"68","author":"Cruchaga","year":"2011","journal-title":"Arch. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0235","doi-asserted-by":"crossref","first-page":"186","DOI":"10.1016\/j.tig.2008.01.004","article-title":"Loss of progranulin function in frontotemporal lobar degeneration","volume":"24","author":"Cruts","year":"2008","journal-title":"Trends Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0240","doi-asserted-by":"crossref","first-page":"920","DOI":"10.1038\/nature05017","article-title":"Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21","volume":"442","author":"Cruts","year":"2006","journal-title":"Nature"},{"key":"10.1016\/j.nbd.2020.104946_bb0245","doi-asserted-by":"crossref","DOI":"10.1016\/j.neurobiolaging.2013.09.009","article-title":"Investigating the role of rare heterozygous TREM2 variants in Alzheimer\u2019s disease and frontotemporal dementia","volume":"35","author":"Cuyvers","year":"2014","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.nbd.2020.104946_bb0250","doi-asserted-by":"crossref","DOI":"10.1016\/j.neurobiolaging.2015.02.014","article-title":"Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study","volume":"36","author":"Cuyvers","year":"2015","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.nbd.2020.104946_bb0255","doi-asserted-by":"crossref","first-page":"2063","DOI":"10.1212\/WNL.0000000000000497","article-title":"Novel (ovario) leukodystrophy related to AARS2 mutations","volume":"82","author":"Dallabona","year":"2014","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb0260","doi-asserted-by":"crossref","first-page":"96","DOI":"10.1111\/j.1749-6632.2002.tb04802.x","article-title":"Paraoxonase 1 activity: a new vascular marker of dementia?","volume":"977","author":"Dantoine","year":"2002","journal-title":"Ann. N. Y. Acad. Sci."},{"key":"10.1016\/j.nbd.2020.104946_bb0265","doi-asserted-by":"crossref","DOI":"10.1126\/scitranslmed.aay3069","article-title":"APOE genotype regulates pathology and disease progression in synucleinopathy","volume":"12","author":"Davis","year":"2020","journal-title":"Sci. Transl. Med."},{"key":"10.1016\/j.nbd.2020.104946_bb0270","doi-asserted-by":"crossref","first-page":"898","DOI":"10.1016\/0888-7543(92)90182-R","article-title":"Familial amyloidosis, Finnish type: G654 \u2013 a mutation of the gelsolin gene in Finnish families and an unrelated American family","volume":"13","author":"de la Chapelle","year":"1992","journal-title":"Genomics"},{"key":"10.1016\/j.nbd.2020.104946_bb0275","doi-asserted-by":"crossref","first-page":"211","DOI":"10.1038\/nature10353","article-title":"Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS\/dementia","volume":"477","author":"Deng","year":"2011","journal-title":"Nature"},{"key":"10.1016\/j.nbd.2020.104946_bb0280","doi-asserted-by":"crossref","first-page":"337","DOI":"10.1038\/nrneurol.2014.78","article-title":"The role of FUS gene variants in neurodegenerative diseases","volume":"10","author":"Deng","year":"2014","journal-title":"Nat. Rev. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0285","doi-asserted-by":"crossref","first-page":"2383","DOI":"10.1093\/brain\/124.12.2383","article-title":"Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer\u2019s disease due to a novel presenilin 1 mutation","volume":"124","author":"Dermaut","year":"2001","journal-title":"Brain"},{"key":"10.1016\/j.nbd.2020.104946_bb0290","doi-asserted-by":"crossref","first-page":"617","DOI":"10.1002\/ana.20083","article-title":"A novel presenilin 1 mutation associated with Pick\u2019s disease but not beta-amyloid plaques","volume":"55","author":"Dermaut","year":"2004","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0295","doi-asserted-by":"crossref","first-page":"1588","DOI":"10.1038\/mp.2015.6","article-title":"Genetic overlap between Alzheimer\u2019s disease and Parkinson's disease at the MAPT locus","volume":"20","author":"Desikan","year":"2015","journal-title":"Mol. Psychiatry"},{"key":"10.1016\/j.nbd.2020.104946_bb0300","doi-asserted-by":"crossref","first-page":"1714","DOI":"10.1212\/WNL.57.9.1714","article-title":"NOTCH3 mutation involving three cysteine residues in a family with typical CADASIL","volume":"57","author":"Dichgans","year":"2001","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb0305","doi-asserted-by":"crossref","first-page":"112","DOI":"10.1007\/s10519-005-9001-3","article-title":"Endophenotypes successfully lead to gene identification: results from the collaborative study on the genetics of alcoholism","volume":"36","author":"Dick","year":"2006","journal-title":"Behav. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0310","doi-asserted-by":"crossref","DOI":"10.1212\/WNL.0000000000006212","article-title":"APOE \u03b54 is associated with severity of Lewy body pathology independent of Alzheimer pathology","author":"Dickson","year":"2018","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb0315","doi-asserted-by":"crossref","first-page":"120","DOI":"10.1002\/ana.24198","article-title":"C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis","volume":"76","author":"Diekstra","year":"2014","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0320","doi-asserted-by":"crossref","DOI":"10.1093\/brain\/awaa039","article-title":"CYLD is a causative gene for frontotemporal dementia \u2013 amyotrophic lateral sclerosis","author":"Dobson-Stone","year":"2020","journal-title":"Brain"},{"key":"10.1016\/j.nbd.2020.104946_bb0325","doi-asserted-by":"crossref","first-page":"97","DOI":"10.1186\/s12883-019-1326-2","article-title":"Cerebral amyloid angiopathy-related inflammation: a case report presenting with a rare variant in SORL1 gene","volume":"19","author":"Du","year":"2019","journal-title":"BMC Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0330","doi-asserted-by":"crossref","first-page":"12","DOI":"10.1186\/s40478-019-0662-1","article-title":"Apolipoprotein E and clusterin inhibit the early phase of amyloid-\u03b2 aggregation in an in vitro model of cerebral amyloid angiopathy","volume":"7","author":"Endo","year":"2019","journal-title":"Acta Neuropathol. Commun."},{"key":"10.1016\/j.nbd.2020.104946_bb0335","doi-asserted-by":"crossref","first-page":"1148","DOI":"10.1136\/jnnp.74.8.1148","article-title":"Prospective Belgian study of neurodegenerative and vascular dementia: APOE genotype effects","volume":"74","author":"Engelborghs","year":"2003","journal-title":"J. Neurol. Neurosurg. Psychiatry"},{"key":"10.1016\/j.nbd.2020.104946_bb0340","doi-asserted-by":"crossref","DOI":"10.1101\/cshperspect.a033118","article-title":"Clinical neurology and epidemiology of the major neurodegenerative diseases","volume":"10","author":"Erkkinen","year":"2018","journal-title":"Cold Spring Harb. Perspect. Biol."},{"key":"10.1016\/j.nbd.2020.104946_bb0345","doi-asserted-by":"crossref","first-page":"16","DOI":"10.3389\/fncel.2015.00016","article-title":"Mitochondrial function in neuronal cells depends on p97\/VCP\/Cdc48-mediated quality control","volume":"9","author":"Fang","year":"2015","journal-title":"Front. Cell. Neurosci."},{"key":"10.1016\/j.nbd.2020.104946_bb0350","doi-asserted-by":"crossref","first-page":"1440","DOI":"10.1001\/archneurol.2011.250","article-title":"SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis","volume":"68","author":"Fecto","year":"2011","journal-title":"Arch. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0355","doi-asserted-by":"crossref","first-page":"686","DOI":"10.1016\/S1474-4422(14)70065-1","article-title":"Frontotemporal dementia and its subtypes: a genome-wide association study","volume":"13","author":"Ferrari","year":"2014","journal-title":"Lancet Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0360","doi-asserted-by":"crossref","first-page":"152","DOI":"10.1136\/jnnp-2016-314411","article-title":"Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer\u2019s and Parkinson's diseases","volume":"88","author":"Ferrari","year":"2017","journal-title":"J. Neurol. Neurosurg. Psychiatry"},{"key":"10.1016\/j.nbd.2020.104946_bb0365","doi-asserted-by":"crossref","first-page":"98","DOI":"10.1016\/j.neurobiolaging.2019.02.006","article-title":"Genetics and molecular mechanisms of frontotemporal lobar degeneration: an update and future avenues","volume":"78","author":"Ferrari","year":"2019","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.nbd.2020.104946_bb0370","doi-asserted-by":"crossref","first-page":"928","DOI":"10.1002\/ana.22403","article-title":"Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium","volume":"69","author":"Fornage","year":"2011","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0375","doi-asserted-by":"crossref","first-page":"173","DOI":"10.1016\/S0022-510X(02)00286-1","article-title":"APOE genotype in cerebrovascular disease and vascular dementia","volume":"203-204","author":"Frank","year":"2002","journal-title":"J. Neurol. Sci."},{"key":"10.1016\/j.nbd.2020.104946_bb0380","doi-asserted-by":"crossref","first-page":"777","DOI":"10.1038\/ng.2307","article-title":"Genome-wide association analysis identifies susceptibility loci for migraine without aura","volume":"44","author":"Freilinger","year":"2012","journal-title":"Nat. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0385","doi-asserted-by":"crossref","first-page":"631","DOI":"10.1038\/nn.4000","article-title":"Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia","volume":"18","author":"Freischmidt","year":"2015","journal-title":"Nat. Neurosci."},{"key":"10.1016\/j.nbd.2020.104946_bb0390","doi-asserted-by":"crossref","first-page":"110","DOI":"10.1001\/jamaneurol.2016.3712","article-title":"Association of mutations in TBK1 with sporadic and familial amyotrophic lateral sclerosis and frontotemporal dementia","volume":"74","author":"Freischmidt","year":"2017","journal-title":"JAMA Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0395","doi-asserted-by":"crossref","first-page":"930","DOI":"10.1038\/embor.2008.136","article-title":"The tumour suppressor CYLD is a negative regulator of RIG-I-mediated antiviral response","volume":"9","author":"Friedman","year":"2008","journal-title":"EMBO Rep."},{"key":"10.1016\/j.nbd.2020.104946_bb0400","doi-asserted-by":"crossref","first-page":"425","DOI":"10.1007\/s00401-012-1059-4","article-title":"Sequence variants in eukaryotic translation initiation factor 4-gamma (eIF4G1) are associated with Lewy body dementia","volume":"125","author":"Fujioka","year":"2013","journal-title":"Acta Neuropathol."},{"key":"10.1016\/j.nbd.2020.104946_bb0405","doi-asserted-by":"crossref","first-page":"296","DOI":"10.1016\/0006-291X(90)91273-U","article-title":"Partial deletion of human alpha-galactosidase A gene in Fabry disease: direct repeat sequences as a possible cause of slipped mispairing","volume":"170","author":"Fukuhara","year":"1990","journal-title":"Biochem. Biophys. Res. Commun."},{"key":"10.1016\/j.nbd.2020.104946_bb0410","doi-asserted-by":"crossref","first-page":"1066","DOI":"10.1002\/mds.26593","article-title":"GBA mutations are associated with earlier onset and male sex in dementia with lewy bodies","volume":"31","author":"G\u00e1mez-Valero","year":"2016","journal-title":"Mov. Disord."},{"key":"10.1016\/j.nbd.2020.104946_bb0415","doi-asserted-by":"crossref","first-page":"168","DOI":"10.1001\/archpsyc.63.2.168","article-title":"Role of genes and environments for explaining Alzheimer disease","volume":"63","author":"Gatz","year":"2006","journal-title":"Arch. Gen. Psychiatry"},{"key":"10.1016\/j.nbd.2020.104946_bb0420","doi-asserted-by":"crossref","first-page":"137","DOI":"10.1186\/1471-2318-13-137","article-title":"Characteristics of patients misdiagnosed with Alzheimer\u2019s disease and their medication use: an analysis of the NACC-UDS database","volume":"13","author":"Gaugler","year":"2013","journal-title":"BMC Geriatr."},{"key":"10.1016\/j.nbd.2020.104946_bb0425","doi-asserted-by":"crossref","first-page":"55","DOI":"10.1016\/j.nbd.2016.06.004","article-title":"Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodies","volume":"94","author":"Geiger","year":"2016","journal-title":"Neurobiol. Dis."},{"key":"10.1016\/j.nbd.2020.104946_bb0430","doi-asserted-by":"crossref","first-page":"162","DOI":"10.1016\/j.parkreldis.2019.02.011","article-title":"Neuropathological and genetic characteristics of a post-mortem series of cases with dementia with Lewy bodies clinically suspected of Creutzfeldt-Jakob\u2019s disease","volume":"63","author":"Geut","year":"2019","journal-title":"Parkinsonism Relat. Disord."},{"key":"10.1016\/j.nbd.2020.104946_bb0435","doi-asserted-by":"crossref","first-page":"442","DOI":"10.1097\/NEN.0b013e3181d88e63","article-title":"Inverse relationship between cerebrovascular lesions and severity of lewy body pathology in patients with lewy body diseases","volume":"69","author":"Ghebremedhin","year":"2010","journal-title":"J. Neuropathol. Exp. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0440","doi-asserted-by":"crossref","first-page":"744","DOI":"10.1073\/pnas.93.2.744","article-title":"Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP","volume":"93","author":"Ghetti","year":"1996","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"key":"10.1016\/j.nbd.2020.104946_bb0445","doi-asserted-by":"crossref","first-page":"24","DOI":"10.1111\/nan.12213","article-title":"Invited review: frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging","volume":"41","author":"Ghetti","year":"2015","journal-title":"Neuropathol. Appl. Neurobiol."},{"key":"10.1016\/j.nbd.2020.104946_bb0450","doi-asserted-by":"crossref","first-page":"2974","DOI":"10.1073\/pnas.83.9.2974","article-title":"Amyloid fibrils in hereditary cerebral hemorrhage with amyloidosis of Icelandic type is a variant of gamma-trace basic protein (cystatin C)","volume":"83","author":"Ghiso","year":"1986","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"key":"10.1016\/j.nbd.2020.104946_bb0455","doi-asserted-by":"crossref","first-page":"827","DOI":"10.1042\/bj2720827","article-title":"Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type","volume":"272","author":"Ghiso","year":"1990","journal-title":"Biochem. J."},{"key":"10.1016\/j.nbd.2020.104946_bb0460","doi-asserted-by":"crossref","first-page":"908","DOI":"10.1212\/01.wnl.0000230215.41296.18","article-title":"Glucocerebrosidase mutations are an important risk factor for Lewy body disorders","volume":"67","author":"Goker-Alpan","year":"2006","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb0465","doi-asserted-by":"crossref","first-page":"2672","DOI":"10.1161\/STR.0b013e3182299496","article-title":"Vascular contributions to cognitive impairment and dementia: a statement for healthcare professionals from the american heart association\/american stroke association","volume":"42","author":"Gorelick","year":"2011","journal-title":"Stroke"},{"key":"10.1016\/j.nbd.2020.104946_bb0470","doi-asserted-by":"crossref","first-page":"856","DOI":"10.1038\/ng.3598","article-title":"Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine","volume":"48","author":"Gormley","year":"2016","journal-title":"Nat. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0475","doi-asserted-by":"crossref","first-page":"1333","DOI":"10.1161\/01.STR.27.8.1333","article-title":"Apolipoprotein E epsilon 4 is associated with the presence and earlier onset of hemorrhage in cerebral amyloid angiopathy","volume":"27","author":"Greenberg","year":"1996","journal-title":"Stroke"},{"key":"10.1016\/j.nbd.2020.104946_bb0480","doi-asserted-by":"crossref","first-page":"78","DOI":"10.1001\/jamaneurol.2013.579","article-title":"Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement","volume":"70","author":"Guerreiro","year":"2013","journal-title":"JAMA Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0485","doi-asserted-by":"crossref","first-page":"117","DOI":"10.1056\/NEJMoa1211851","article-title":"TREM2 variants in Alzheimer\u2019s disease","volume":"368","author":"Guerreiro","year":"2013","journal-title":"N. Engl. J. Med."},{"key":"10.1016\/j.nbd.2020.104946_bb0490","doi-asserted-by":"crossref","first-page":"R47","DOI":"10.1093\/hmg\/ddu203","article-title":"Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associations","volume":"23","author":"Guerreiro","year":"2014","journal-title":"Hum. Mol. Genet."},{"issue":"Suppl. 1","key":"10.1016\/j.nbd.2020.104946_bb0495","first-page":"103","article-title":"Direct genotyping of the APOE E2, E3 and E4 haplotypes in a large international cohort of neuropathologically diagnosed dementia with Lewy bodies cases","volume":"4","author":"Guerreiro","year":"2015","journal-title":"Am. J. Neurodegener. Dis."},{"key":"10.1016\/j.nbd.2020.104946_bb0500","doi-asserted-by":"crossref","first-page":"64","DOI":"10.1016\/S1474-4422(17)30400-3","article-title":"Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study","volume":"17","author":"Guerreiro","year":"2018","journal-title":"Lancet Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0505","doi-asserted-by":"crossref","first-page":"492","DOI":"10.1016\/j.nbd.2019.04.004","article-title":"Heritability and genetic variance of dementia with Lewy bodies","volume":"127","author":"Guerreiro","year":"2019","journal-title":"Neurobiol. Dis."},{"key":"10.1016\/j.nbd.2020.104946_bb0510","doi-asserted-by":"crossref","DOI":"10.1136\/jmg.40.4.e38","article-title":"Clinical presentation in female patients with Fabry disease","author":"Guffon","year":"2003","journal-title":"J. Med. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0515","doi-asserted-by":"crossref","first-page":"1585","DOI":"10.1212\/01.WNL.0000034763.54161.1F","article-title":"Chromosome 3 linked frontotemporal dementia (FTD-3)","volume":"59","author":"Gydesen","year":"2002","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb0520","doi-asserted-by":"crossref","first-page":"735","DOI":"10.1016\/j.ajhg.2016.06.026","article-title":"Absence of the autophagy adaptor SQSTM1\/p62 causes childhood-onset neurodegeneration with ataxia, dystonia, and gaze palsy","volume":"99","author":"Haack","year":"2016","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0525","doi-asserted-by":"crossref","first-page":"544","DOI":"10.1016\/j.bbrc.2012.04.041","article-title":"The functional analysis of the CHMP2B missense mutation associated with neurodegenerative diseases in the endo-lysosomal pathway","volume":"421","author":"Han","year":"2012","journal-title":"Biochem. Biophys. Res. Commun."},{"key":"10.1016\/j.nbd.2020.104946_bb0530","doi-asserted-by":"crossref","first-page":"1729","DOI":"10.1056\/NEJMoa0801560","article-title":"Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease","volume":"360","author":"Hara","year":"2009","journal-title":"N. Engl. J. Med."},{"issue":"Pt B","key":"10.1016\/j.nbd.2020.104946_bb0535","doi-asserted-by":"crossref","first-page":"75","DOI":"10.1016\/j.expneurol.2013.11.006","article-title":"Motor neuron disease and frontotemporal dementia: sometimes related, sometimes not","volume":"262","author":"Hardy","year":"2014","journal-title":"Exp. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0540","doi-asserted-by":"crossref","first-page":"1230","DOI":"10.1016\/j.febslet.2013.01.059","article-title":"Recent insights into the complexity of Tank-binding kinase 1 signaling networks: the emerging role of cellular localization in the activation and substrate specificity of TBK1","volume":"587","author":"Helgason","year":"2013","journal-title":"FEBS Lett."},{"key":"10.1016\/j.nbd.2020.104946_bb0545","doi-asserted-by":"crossref","first-page":"292","DOI":"10.1212\/WNL.0000000000000061","article-title":"C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies","volume":"82","author":"Hensman Moss","year":"2014","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb0550","doi-asserted-by":"crossref","first-page":"347","DOI":"10.1001\/archneur.57.3.347","article-title":"Diagnostic accuracy of dementia with Lewy bodies","volume":"57","author":"Hohl","year":"2000","journal-title":"Arch. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0555","doi-asserted-by":"crossref","first-page":"364","DOI":"10.1111\/bpa.12773","article-title":"Putative risk alleles for LATE-NC with hippocampal sclerosis in population-representative autopsy cohorts","volume":"30","author":"Hokkanen","year":"2020","journal-title":"Brain Pathol."},{"key":"10.1016\/j.nbd.2020.104946_bb0560","doi-asserted-by":"crossref","DOI":"10.1523\/ENEURO.0100-17.2017","article-title":"Intracellular proteolysis of progranulin generates stable, lysosomal granulins that are haploinsufficient in patients with frontotemporal dementia caused by GRN mutations","volume":"4","author":"Holler","year":"2017","journal-title":"eNeuro"},{"key":"10.1016\/j.nbd.2020.104946_bb0565","doi-asserted-by":"crossref","first-page":"485","DOI":"10.1136\/jmg.2004.025734","article-title":"VEGF polymorphisms and severity of atherosclerosis","volume":"42","author":"Howell","year":"2005","journal-title":"J. Med. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0570","doi-asserted-by":"crossref","first-page":"654","DOI":"10.1016\/j.neuron.2010.09.034","article-title":"Sortilin-mediated endocytosis determines levels of the frontotemporal dementia protein, progranulin","volume":"68","author":"Hu","year":"2010","journal-title":"Neuron"},{"key":"10.1016\/j.nbd.2020.104946_bb0575","doi-asserted-by":"crossref","first-page":"39","DOI":"10.1007\/s10048-019-00592-3","article-title":"A novel cysteine-sparing G73A mutation of NOTCH3 in a Chinese CADASIL family","volume":"21","author":"Huang","year":"2020","journal-title":"Neurogenetics"},{"key":"10.1016\/j.nbd.2020.104946_bb0580","doi-asserted-by":"crossref","first-page":"48","DOI":"10.1186\/s12916-017-0813-9","article-title":"Genetics of vascular dementia - review from the ICVD working group","volume":"15","author":"Ikram","year":"2017","journal-title":"BMC Med."},{"key":"10.1016\/j.nbd.2020.104946_bb0585","doi-asserted-by":"crossref","first-page":"4","DOI":"10.1186\/s13039-019-0418-4","article-title":"Pathway-based classification of genetic diseases","volume":"12","author":"Iourov","year":"2019","journal-title":"Mol. Cytogenet."},{"key":"10.1016\/j.nbd.2020.104946_bb0590","doi-asserted-by":"crossref","first-page":"502","DOI":"10.1212\/WNL.0000000000000668","article-title":"Myelin oligodendrocyte basic protein and prognosis in behavioral-variant frontotemporal dementia","volume":"83","author":"Irwin","year":"2014","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb0595","doi-asserted-by":"crossref","first-page":"55","DOI":"10.1016\/S1474-4422(16)30291-5","article-title":"Neuropathological and genetic correlates of survival and dementia onset in synucleinopathies: a retrospective analysis","volume":"16","author":"Irwin","year":"2017","journal-title":"Lancet Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0600","doi-asserted-by":"crossref","first-page":"994","DOI":"10.1086\/339431","article-title":"Alternative splicing in the alpha-galactosidase A gene: increased exon inclusion results in the Fabry cardiac phenotype","volume":"70","author":"Ishii","year":"2002","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0605","doi-asserted-by":"crossref","first-page":"771","DOI":"10.1007\/s00702-003-0824-x","article-title":"Prevalence of vascular lesions in dementia with Lewy bodies. A postmortem study","volume":"110","author":"Jellinger","year":"2003","journal-title":"J. Neural Transm."},{"key":"10.1016\/j.nbd.2020.104946_bb0610","doi-asserted-by":"crossref","first-page":"421","DOI":"10.1007\/s00401-010-0654-5","article-title":"Prevalence of dementia disorders in the oldest-old: an autopsy study","volume":"119","author":"Jellinger","year":"2010","journal-title":"Acta Neuropathol."},{"key":"10.1016\/j.nbd.2020.104946_bb0615","doi-asserted-by":"crossref","first-page":"1557","DOI":"10.1161\/STROKEAHA.117.017073","article-title":"Imaging endophenotypes of stroke as a target for genetic studies","volume":"49","author":"Jian","year":"2018","journal-title":"Stroke"},{"key":"10.1016\/j.nbd.2020.104946_bb0620","doi-asserted-by":"crossref","first-page":"1858","DOI":"10.1172\/JCI34257","article-title":"Deubiquitinating enzyme CYLD negatively regulates RANK signaling and osteoclastogenesis in mice","volume":"118","author":"Jin","year":"2008","journal-title":"J. Clin. Invest."},{"key":"10.1016\/j.nbd.2020.104946_bb0625","doi-asserted-by":"crossref","first-page":"857","DOI":"10.1016\/j.neuron.2010.11.036","article-title":"Exome sequencing reveals VCP mutations as a cause of familial ALS","volume":"68","author":"Johnson","year":"2010","journal-title":"Neuron"},{"key":"10.1016\/j.nbd.2020.104946_bb0630","doi-asserted-by":"crossref","first-page":"707","DOI":"10.1038\/383707a0","article-title":"Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia","volume":"383","author":"Joutel","year":"1996","journal-title":"Nature"},{"key":"10.1016\/j.nbd.2020.104946_bb0635","doi-asserted-by":"crossref","first-page":"1511","DOI":"10.1016\/S0140-6736(97)08083-5","article-title":"Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients","volume":"350","author":"Joutel","year":"1997","journal-title":"Lancet"},{"key":"10.1016\/j.nbd.2020.104946_bb0640","doi-asserted-by":"crossref","first-page":"388","DOI":"10.1002\/1531-8249(200003)47:3<388::AID-ANA19>3.0.CO;2-Q","article-title":"De novo mutation in the Notch3 gene causing CADASIL","volume":"47","author":"Joutel","year":"2000","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0645","doi-asserted-by":"crossref","first-page":"860","DOI":"10.1001\/jamaneurol.2018.0372","article-title":"Selective genetic overlap between amyotrophic lateral sclerosis and diseases of the frontotemporal dementia spectrum","volume":"75","author":"Karch","year":"2018","journal-title":"JAMA Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0650","doi-asserted-by":"crossref","first-page":"275","DOI":"10.1212\/01.WNL.0000042479.55406.B3","article-title":"Stroke in young patients with hyperhomocysteinemia due to cystathionine beta-synthase deficiency","volume":"60","author":"Kelly","year":"2003","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb0655","doi-asserted-by":"crossref","DOI":"10.1038\/tp.2015.220","article-title":"Exome sequencing in dementia with Lewy bodies","volume":"6","author":"Keogh","year":"2016","journal-title":"Transl. Psychiatry"},{"key":"10.1016\/j.nbd.2020.104946_bb0660","doi-asserted-by":"crossref","DOI":"10.1586\/ern.11.6","article-title":"Abhorring the vacuum: use of Alzheimer\u2019s disease medications in frontotemporal dementia","author":"Kerchner","year":"2011","journal-title":"Expert. Rev. Neurother."},{"key":"10.1016\/j.nbd.2020.104946_bb0665","doi-asserted-by":"crossref","first-page":"753","DOI":"10.1007\/s00401-013-1096-7","article-title":"\u03b1-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson\u2019s disease and multiple system atrophy?","volume":"125","author":"Kiely","year":"2013","journal-title":"Acta Neuropathol."},{"key":"10.1016\/j.nbd.2020.104946_bb0670","doi-asserted-by":"crossref","first-page":"2843","DOI":"10.1161\/01.STR.0000244782.76917.87","article-title":"The gene encoding transforming growth factor beta 1 confers risk of ischemic stroke and vascular dementia","volume":"37","author":"Kim","year":"2006","journal-title":"Stroke"},{"key":"10.1016\/j.nbd.2020.104946_bb0675","doi-asserted-by":"crossref","first-page":"276","DOI":"10.1016\/j.neulet.2006.03.035","article-title":"Sequence variants of ACE, AGT, AT1R, and PAI-1 as genetic risk factors for vascular dementia","volume":"401","author":"Kim","year":"2006","journal-title":"Neurosci. Lett."},{"key":"10.1016\/j.nbd.2020.104946_bb0680","doi-asserted-by":"crossref","first-page":"332","DOI":"10.1002\/ajmg.b.30317","article-title":"Haplotype analysis of single nucleotide polymorphisms in VEGF gene for vascular dementia","volume":"141B","author":"Kim","year":"2006","journal-title":"Am. J. Med. Genet. B Neuropsychiatr. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0685","doi-asserted-by":"crossref","first-page":"467","DOI":"10.1038\/nature11922","article-title":"Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS","volume":"495","author":"Kim","year":"2013","journal-title":"Nature"},{"key":"10.1016\/j.nbd.2020.104946_bb0690","doi-asserted-by":"crossref","first-page":"220","DOI":"10.3109\/15622975.2011.559272","article-title":"Association of intronic sequence variant in the gene encoding spleen tyrosine kinase with susceptibility to vascular dementia","volume":"14","author":"Kim","year":"2013","journal-title":"World J. Biol. Psychiatry"},{"key":"10.1016\/j.nbd.2020.104946_bb0695","doi-asserted-by":"crossref","DOI":"10.1016\/j.neurobiolaging.2018.06.031","article-title":"Analysis of frontotemporal dementia, amyotrophic lateral sclerosis, and other dementia-related genes in 107 Korean patients with frontotemporal dementia","volume":"72","author":"Kim","year":"2018","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.nbd.2020.104946_bb0700","doi-asserted-by":"crossref","DOI":"10.1016\/j.neurobiolaging.2015.12.014","article-title":"Reduced secretion and altered proteolytic processing caused by missense mutations in progranulin","volume":"39","author":"Kleinberger","year":"2016","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.nbd.2020.104946_bb0705","doi-asserted-by":"crossref","first-page":"569","DOI":"10.1001\/archneur.60.4.569","article-title":"Vascular dementia in a population-based autopsy study","volume":"60","author":"Knopman","year":"2003","journal-title":"Arch. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0710","doi-asserted-by":"crossref","first-page":"1619","DOI":"10.1212\/01.WNL.0000033796.33205.B4","article-title":"A patient with dementia with Lewy bodies and codon 232 mutation of PRNP","volume":"59","author":"Koide","year":"2002","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb0715","doi-asserted-by":"crossref","first-page":"14","DOI":"10.1016\/j.parkreldis.2017.06.004","article-title":"DCTN1-related neurodegeneration: Perry syndrome and beyond","volume":"41","author":"Konno","year":"2017","journal-title":"Parkinsonism Relat. Disord."},{"key":"10.1016\/j.nbd.2020.104946_bb0720","doi-asserted-by":"crossref","first-page":"613","DOI":"10.1002\/ajmg.a.32712","article-title":"Prosaposin deficiency and saposin B deficiency (activator-deficient metachromatic leukodystrophy): report on two patients detected by analysis of urinary sphingolipids and carrying novel PSAP gene mutations","volume":"149A","author":"Kuchar","year":"2009","journal-title":"Am. J. Med. Genet. A"},{"key":"10.1016\/j.nbd.2020.104946_bb0725","doi-asserted-by":"crossref","DOI":"10.1016\/j.neurobiolaging.2018.10.019","article-title":"A comprehensive screening of copy number variability in dementia with Lewy bodies","volume":"75","author":"Kun-Rodrigues","year":"2019","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.nbd.2020.104946_bb0730","doi-asserted-by":"crossref","first-page":"849","DOI":"10.1212\/WNL.0000000000008459","article-title":"APOE \u03b54 is associated with younger age at ischemic stroke onset but not with stroke outcome","volume":"93","author":"Lagging","year":"2019","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb0735","doi-asserted-by":"crossref","first-page":"476","DOI":"10.1034\/j.1399-0004.2003.00077.x","article-title":"Analysis of splice-site mutations of the alpha-galactosidase A gene in Fabry disease","volume":"63","author":"Lai","year":"2003","journal-title":"Clin. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0740","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0202044","article-title":"Relative survival in patients with dementia with Lewy bodies and Parkinson\u2019s disease dementia","volume":"13","author":"Larsson","year":"2018","journal-title":"PLoS One"},{"key":"10.1016\/j.nbd.2020.104946_bb0745","doi-asserted-by":"crossref","first-page":"990","DOI":"10.1212\/WNL.0000000000000778","article-title":"Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disorders","volume":"83","author":"Lattante","year":"2014","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb0750","doi-asserted-by":"crossref","DOI":"10.1016\/j.neurobiolaging.2017.11.011","article-title":"ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosis","volume":"64","author":"Lattante","year":"2018","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.nbd.2020.104946_bb0755","doi-asserted-by":"crossref","first-page":"1408","DOI":"10.1038\/cdd.2008.82","article-title":"HtrA1-dependent proteolysis of TGF-beta controls both neuronal maturation and developmental survival","volume":"15","author":"Launay","year":"2008","journal-title":"Cell Death Differ."},{"key":"10.1016\/j.nbd.2020.104946_bb0760","first-page":"1403","article-title":"SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosis","volume":"70","author":"Le Ber","year":"2013","journal-title":"JAMA Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0765","doi-asserted-by":"crossref","DOI":"10.1016\/j.neurobiolaging.2013.09.016","article-title":"hnRNPA2B1 and hnRNPA1 mutations are rare in patients with \u201cmultisystem proteinopathy\u201d and frontotemporal lobar degeneration phenotypes","volume":"35","author":"Le Ber","year":"2014","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.nbd.2020.104946_bb0770","doi-asserted-by":"crossref","first-page":"1124","DOI":"10.1126\/science.2111584","article-title":"Mutation of the Alzheimer\u2019s disease amyloid gene in hereditary cerebral hemorrhage, Dutch type","volume":"248","author":"Levy","year":"1990","journal-title":"Science"},{"key":"10.1016\/j.nbd.2020.104946_bb0775","doi-asserted-by":"crossref","first-page":"1978","DOI":"10.1007\/s00415-009-0036-x","article-title":"Homozygosity for a NOTCH3 mutation in a 65-year-old CADASIL patient with mild symptoms: a family report","volume":"255","author":"Liem","year":"2008","journal-title":"J. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0780","doi-asserted-by":"crossref","first-page":"564","DOI":"10.1111\/j.1532-5415.1999.tb02571.x","article-title":"Clinico-neuropathological correlation of Alzheimer\u2019s disease in a community-based case series","volume":"47","author":"Lim","year":"1999","journal-title":"J. Am. Geriatr. Soc."},{"key":"10.1016\/j.nbd.2020.104946_bb0785","doi-asserted-by":"crossref","first-page":"416","DOI":"10.1016\/j.neuron.2013.07.033","article-title":"Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis","volume":"79","author":"Ling","year":"2013","journal-title":"Neuron"},{"key":"10.1016\/j.nbd.2020.104946_bb0790","doi-asserted-by":"crossref","first-page":"74","DOI":"10.1016\/j.jns.2010.04.001","article-title":"The MTHFR C677T polymorphism contributes to an increased risk for vascular dementia: a meta-analysis","volume":"294","author":"Liu","year":"2010","journal-title":"J. Neurol. Sci."},{"key":"10.1016\/j.nbd.2020.104946_bb0795","doi-asserted-by":"crossref","first-page":"860","DOI":"10.1161\/CIRCRESAHA.110.218271","article-title":"Notch3 is critical for proper angiogenesis and mural cell investment","volume":"107","author":"Liu","year":"2010","journal-title":"Circ. Res."},{"key":"10.1016\/j.nbd.2020.104946_bb0800","doi-asserted-by":"crossref","first-page":"357","DOI":"10.1093\/brain\/awl360","article-title":"Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH3 causing CADASIL","volume":"130","author":"Low","year":"2007","journal-title":"Brain"},{"key":"10.1016\/j.nbd.2020.104946_bb0805","doi-asserted-by":"crossref","first-page":"828","DOI":"10.1016\/S0140-6736(13)60630-3","article-title":"Genetics of dementia","volume":"383","author":"Loy","year":"2014","journal-title":"Lancet"},{"key":"10.1016\/j.nbd.2020.104946_bb0810","doi-asserted-by":"crossref","DOI":"10.1111\/gbb.12607","article-title":"Behavioural impairments in mice of a novel FUS transgenic line recapitulate features of frontotemporal lobar degeneration","volume":"18","author":"Lysikova","year":"2019","journal-title":"Genes Brain Behav."},{"issue":"Suppl. 1","key":"10.1016\/j.nbd.2020.104946_bb0815","doi-asserted-by":"crossref","first-page":"54","DOI":"10.1111\/jnc.13588","article-title":"Molecular neuropathology of frontotemporal dementia: insights into disease mechanisms from postmortem studies","volume":"138","author":"Mackenzie","year":"2016","journal-title":"J. Neurochem."},{"key":"10.1016\/j.nbd.2020.104946_bb0820","doi-asserted-by":"crossref","first-page":"1217","DOI":"10.1212\/WNL.0000000000002528","article-title":"Low-frequency and common genetic variation in ischemic stroke: the METASTROKE collaboration","volume":"86","author":"Malik","year":"2016","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb0825","doi-asserted-by":"crossref","first-page":"524","DOI":"10.1038\/s41588-018-0058-3","article-title":"Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes","volume":"50","author":"Malik","year":"2018","journal-title":"Nat. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0830","doi-asserted-by":"crossref","first-page":"2165","DOI":"10.1016\/S0002-9440(10)64688-3","article-title":"Amyloid angiopathy and variability in amyloid beta deposition is determined by mutation position in presenilin-1-linked Alzheimer\u2019s disease","volume":"158","author":"Mann","year":"2001","journal-title":"Am. J. Pathol."},{"key":"10.1016\/j.nbd.2020.104946_bb0835","doi-asserted-by":"crossref","first-page":"509","DOI":"10.3233\/JAD-2009-0986","article-title":"A novel Italian presenilin 2 gene mutation with prevalent behavioral phenotype","volume":"16","author":"Marcon","year":"2009","journal-title":"J. Alzheimers Dis."},{"key":"10.1016\/j.nbd.2020.104946_bb0840","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1007\/s00401-008-0372-4","article-title":"Clinical, neuropathological and genotypic variability in SNCA A53T familial Parkinson\u2019s disease. Variability in familial Parkinson's disease","volume":"116","author":"Markopoulou","year":"2008","journal-title":"Acta Neuropathol."},{"key":"10.1016\/j.nbd.2020.104946_bb0845","doi-asserted-by":"crossref","first-page":"223","DOI":"10.1038\/nature08971","article-title":"Mutations of optineurin in amyotrophic lateral sclerosis","volume":"465","author":"Maruyama","year":"2010","journal-title":"Nature"},{"key":"10.1016\/j.nbd.2020.104946_bb0850","doi-asserted-by":"crossref","first-page":"39","DOI":"10.1016\/j.pediatrneurol.2010.12.011","article-title":"Intracranial artery dissection in an adolescent with Marfan syndrome","volume":"45","author":"Maski","year":"2011","journal-title":"Pediatr. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0855","doi-asserted-by":"crossref","first-page":"95","DOI":"10.1002\/mds.26359","article-title":"GBA Variants are associated with a distinct pattern of cognitive deficits in Parkinson\u2019s disease","volume":"31","author":"Mata","year":"2016","journal-title":"Mov. Disord."},{"key":"10.1016\/j.nbd.2020.104946_bb0860","doi-asserted-by":"crossref","first-page":"45","DOI":"10.1016\/S0304-3940(98)00286-9","article-title":"High frequency of apolipoprotein E epsilon 2 allele is specific for patients with cerebral amyloid angiopathy-related haemorrhage","volume":"247","author":"McCarron","year":"1998","journal-title":"Neurosci. Lett."},{"key":"10.1016\/j.nbd.2020.104946_bb0865","doi-asserted-by":"crossref","first-page":"176","DOI":"10.1111\/j.1749-6632.2000.tb06366.x","article-title":"Apolipoprotein E genotype and cerebral amyloid angiopathy-related hemorrhage","volume":"903","author":"McCarron","year":"2000","journal-title":"Ann. N. Y. Acad. Sci."},{"key":"10.1016\/j.nbd.2020.104946_bb0870","doi-asserted-by":"crossref","first-page":"88","DOI":"10.1212\/WNL.0000000000004058","article-title":"Diagnosis and management of dementia with Lewy bodies: fourth consensus report of the DLB Consortium","volume":"89","author":"McKeith","year":"2017","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb0875","doi-asserted-by":"crossref","DOI":"10.1016\/j.neurobiolaging.2011.10.014","article-title":"DLB and PDD: a role for mutations in dementia and Parkinson disease genes?","volume":"33","author":"Meeus","year":"2012","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.nbd.2020.104946_bb0880","doi-asserted-by":"crossref","first-page":"548","DOI":"10.1136\/jmg.2008.065904","article-title":"Natural course of Fabry disease: changing pattern of causes of death in FOS \u2013 Fabry Outcome Survey","volume":"46","author":"Mehta","year":"2009","journal-title":"J. Med. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0885","doi-asserted-by":"crossref","first-page":"2033","DOI":"10.1212\/WNL.0b013e3181ff96ac","article-title":"A missense HTRA1 mutation expands CARASIL syndrome to the Caucasian population","volume":"75","author":"Mendioroz","year":"2010","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb0890","doi-asserted-by":"crossref","first-page":"117","DOI":"10.1038\/ncb2407","article-title":"Emerging functions of the VCP\/p97 AAA-ATPase in the ubiquitin system","volume":"14","author":"Meyer","year":"2012","journal-title":"Nat. Cell Biol."},{"key":"10.1016\/j.nbd.2020.104946_bb0895","doi-asserted-by":"crossref","first-page":"1437","DOI":"10.1093\/brain\/awx066","article-title":"Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia","volume":"140","author":"Mishra","year":"2017","journal-title":"Brain"},{"key":"10.1016\/j.nbd.2020.104946_bb0900","doi-asserted-by":"crossref","first-page":"99","DOI":"10.1007\/s12017-015-8381-7","article-title":"ApoA1, ApoJ and ApoE plasma levels and genotype frequencies in cerebral amyloid angiopathy","volume":"18","author":"Monta\u00f1ola","year":"2016","journal-title":"Neuro Mol. Med."},{"key":"10.1016\/j.nbd.2020.104946_bb0905","doi-asserted-by":"crossref","first-page":"145","DOI":"10.1016\/S1474-4422(19)30394-1","article-title":"Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study","volume":"19","author":"Moore","year":"2020","journal-title":"Lancet Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0910","doi-asserted-by":"crossref","first-page":"1333","DOI":"10.1016\/j.jalz.2019.06.4950","article-title":"Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer\u2019s disease and three causality networks: the GR@ACE project","volume":"15","author":"Moreno-Grau","year":"2019","journal-title":"Alzheimers Dement."},{"key":"10.1016\/j.nbd.2020.104946_bb0915","doi-asserted-by":"crossref","first-page":"942","DOI":"10.1016\/j.jocn.2005.11.040","article-title":"Dementia with Lewy bodies in an elderly Greek male due to alpha-synuclein gene mutation","volume":"13","author":"Morfis","year":"2006","journal-title":"J. Clin. Neurosci."},{"key":"10.1016\/j.nbd.2020.104946_bb0920","doi-asserted-by":"crossref","DOI":"10.3390\/ijms18091964","article-title":"Systematic review of cysteine-sparing NOTCH3 missense mutations in patients with clinical suspicion of CADASIL","volume":"18","author":"Mui\u00f1o","year":"2017","journal-title":"Int. J. Mol. Sci."},{"key":"10.1016\/j.nbd.2020.104946_bb0925","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0017477","article-title":"Optineurin is required for CYLD-dependent inhibition of TNF\u03b1-induced NF-\u03baB activation","volume":"6","author":"Nagabhushana","year":"2011","journal-title":"PLoS One"},{"key":"10.1016\/j.nbd.2020.104946_bb0930","doi-asserted-by":"crossref","first-page":"727","DOI":"10.1001\/jamaneurol.2013.1925","article-title":"A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies","volume":"70","author":"Nalls","year":"2013","journal-title":"JAMA Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0935","doi-asserted-by":"crossref","first-page":"1333","DOI":"10.1212\/WNL.47.5.1333","article-title":"Adult-onset neurodegenerative disorder due to proteolipid protein gene mutation in the mother of a man with Pelizaeus-Merzbacher disease","volume":"47","author":"Nance","year":"1996","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb0940","doi-asserted-by":"crossref","first-page":"453","DOI":"10.1001\/archneur.63.3.453","article-title":"Later-onset Fabry disease: an adult variant presenting with the cramp-fasciculation syndrome","volume":"63","author":"Nance","year":"2006","journal-title":"Arch. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0945","doi-asserted-by":"crossref","first-page":"856","DOI":"10.1038\/ng.3314","article-title":"The support of human genetic evidence for approved drug indications","volume":"47","author":"Nelson","year":"2015","journal-title":"Nat. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb0950","doi-asserted-by":"crossref","first-page":"90","DOI":"10.1001\/archneurol.2010.319","article-title":"Familial aggregation of dementia with Lewy bodies","volume":"68","author":"Nervi","year":"2011","journal-title":"Arch. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0955","doi-asserted-by":"crossref","first-page":"695","DOI":"10.1016\/S1474-4422(16)00102-2","article-title":"Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies","volume":"15","author":"Neurology Working Group of the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, the Stroke Genetics Network (SiGN), and the International Stroke Genetics Consortium (ISGC)","year":"2016","journal-title":"Lancet Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0960","doi-asserted-by":"crossref","first-page":"11992","DOI":"10.1038\/ncomms11992","article-title":"Prosaposin is a regulator of progranulin levels and oligomerization","volume":"7","author":"Nicholson","year":"2016","journal-title":"Nat. Commun."},{"key":"10.1016\/j.nbd.2020.104946_bb0965","doi-asserted-by":"crossref","first-page":"92","DOI":"10.1038\/ejhg.2015.61","article-title":"Mutation in the 3\u2019untranslated region of APP as a genetic determinant of cerebral amyloid angiopathy","volume":"24","author":"Nicolas","year":"2016","journal-title":"Eur. J. Hum. Genet."},{"issue":"Suppl. 1","key":"10.1016\/j.nbd.2020.104946_bb0970","first-page":"51","article-title":"APOE gene polymorphism as a risk factor for cerebral amyloid angiopathy-related hemorrhage","volume":"8","author":"Nicoll","year":"2001","journal-title":"Amyloid"},{"key":"10.1016\/j.nbd.2020.104946_bb0975","doi-asserted-by":"crossref","DOI":"10.1002\/ana.410390521","article-title":"High frequency of apolipoprotein E epsilon 2 in patients with cerebral hemorrhage due to cerebral amyloid angiopathy","author":"Nicoll","year":"1996","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0980","doi-asserted-by":"crossref","first-page":"716","DOI":"10.1002\/ana.410410607","article-title":"High frequency of apolipoprotein E epsilon 2 allele in hemorrhage due to cerebral amyloid angiopathy","volume":"41","author":"Nicoll","year":"1997","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0985","doi-asserted-by":"crossref","first-page":"174","DOI":"10.1016\/S1474-4422(15)00338-5","article-title":"Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study","volume":"15","author":"NINDS Stroke Genetics Network (SiGN), International Stroke Genetics Consortium (ISGC)","year":"2016","journal-title":"Lancet Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb0990","doi-asserted-by":"crossref","first-page":"55","DOI":"10.1016\/j.parkreldis.2010.09.009","article-title":"Glucocerebrosidase mutations in diffuse Lewy body disease","volume":"17","author":"Nishioka","year":"2011","journal-title":"Parkinsonism Relat. Disord."},{"key":"10.1016\/j.nbd.2020.104946_bb0995","doi-asserted-by":"crossref","first-page":"131","DOI":"10.1002\/ana.410430124","article-title":"Amyloid angiopathy in a Volga German family with Alzheimer\u2019s disease and a presenilin-2 mutation (N141I)","volume":"43","author":"Nochlin","year":"1998","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb1000","doi-asserted-by":"crossref","first-page":"39","DOI":"10.1186\/s12916-018-1029-3","article-title":"Genetic variation in clusterin and risk of dementia and ischemic vascular disease in the general population: cohort studies and meta-analyses of 362,338 individuals","volume":"16","author":"Nordestgaard","year":"2018","journal-title":"BMC Med."},{"key":"10.1016\/j.nbd.2020.104946_bb1005","doi-asserted-by":"crossref","first-page":"805","DOI":"10.1212\/01.WNL.0000139870.14385.3C","article-title":"Beta-synuclein gene alterations in dementia with Lewy bodies","volume":"63","author":"Ohtake","year":"2004","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb1010","doi-asserted-by":"crossref","first-page":"654","DOI":"10.1007\/s12311-018-0998-2","article-title":"Autosomal dominant gene negative frontotemporal dementia-think of SCA17","volume":"18","author":"Olszewska","year":"2019","journal-title":"Cerebellum"},{"key":"10.1016\/j.nbd.2020.104946_bb1015","doi-asserted-by":"crossref","first-page":"968","DOI":"10.1161\/STROKEAHA.113.004461","article-title":"Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASIL","volume":"45","author":"Opherk","year":"2014","journal-title":"Stroke"},{"key":"10.1016\/j.nbd.2020.104946_bb1020","doi-asserted-by":"crossref","first-page":"67","DOI":"10.1007\/s11910-018-0874-y","article-title":"The genetics of dementia with Lewy bodies: current understanding and future directions","volume":"18","author":"Orme","year":"2018","journal-title":"Curr. Neurol. Neurosci. Rep."},{"key":"10.1016\/j.nbd.2020.104946_bb1025","doi-asserted-by":"crossref","first-page":"5","DOI":"10.1186\/s40478-020-0879-z","article-title":"Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies","volume":"8","author":"Orme","year":"2020","journal-title":"Acta Neuropathol. Commun."},{"key":"10.1016\/j.nbd.2020.104946_bb1030","doi-asserted-by":"crossref","first-page":"5","DOI":"10.1186\/s13024-019-0306-8","article-title":"Dementia with Lewy bodies: an update and outlook","volume":"14","author":"Outeiro","year":"2019","journal-title":"Mol. Neurodegener."},{"key":"10.1016\/j.nbd.2020.104946_bb2000","author":"Paloneva","year":"2002","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.nbd.2020.104946_bb1035","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1176\/jnp.18.1.113","article-title":"Family history of dementia: dementia with lewy bodies and dementia in Parkinson\u2019s disease","volume":"18","author":"Papapetropoulos","year":"2006","journal-title":"J. Neuropsychiatr. Clin. Neurosci."},{"key":"10.1016\/j.nbd.2020.104946_bb1040","first-page":"123","article-title":"Genome-wide DNA methylation profiling in a rat model with vascular dementia","volume":"18","author":"Park","year":"2018","journal-title":"Mol. Med. Rep."},{"key":"10.1016\/j.nbd.2020.104946_bb1045","doi-asserted-by":"crossref","first-page":"1074","DOI":"10.1212\/01.wnl.0000231510.89311.8b","article-title":"ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)","volume":"67","author":"Parkinson","year":"2006","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb1050","doi-asserted-by":"crossref","DOI":"10.1016\/j.neurobiolaging.2014.03.024","article-title":"Novel \u03b1-synuclein mutation A53E associated with atypical multiple system atrophy and Parkinson\u2019s disease-type pathology","volume":"35","author":"Pasanen","year":"2014","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.nbd.2020.104946_bb1055","doi-asserted-by":"crossref","first-page":"299","DOI":"10.1007\/s13760-012-0174-2","article-title":"A novel Notch3 Gly89Cys mutation in a Serbian CADASIL family","volume":"113","author":"Pavlovic","year":"2013","journal-title":"Acta Neurol. Belg."},{"key":"10.1016\/j.nbd.2020.104946_bb1060","doi-asserted-by":"crossref","first-page":"1367","DOI":"10.1016\/j.neurobiolaging.2006.06.004","article-title":"A TGF-beta1 polymorphism association with dementia and neuropathologies: the HAAS","volume":"28","author":"Peila","year":"2007","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.nbd.2020.104946_bb1065","doi-asserted-by":"crossref","DOI":"10.1016\/j.neurobiolaging.2016.12.008","article-title":"Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients","volume":"51","author":"Perrone","year":"2017","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.nbd.2020.104946_bb1070","doi-asserted-by":"crossref","first-page":"307","DOI":"10.1002\/ana.410410305","article-title":"Transthyretin amyloidosis: a new mutation associated with dementia","volume":"41","author":"Petersen","year":"1997","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb1075","doi-asserted-by":"crossref","first-page":"388","DOI":"10.1016\/j.tins.2014.04.003","article-title":"Progranulin in neurodegenerative disease","volume":"37","author":"Petkau","year":"2014","journal-title":"Trends Neurosci."},{"key":"10.1016\/j.nbd.2020.104946_bb1080","doi-asserted-by":"crossref","first-page":"190","DOI":"10.1016\/j.neurobiolaging.2018.09.031","article-title":"UNC13A polymorphism contributes to frontotemporal disease in sporadic amyotrophic lateral sclerosis","volume":"73","author":"Placek","year":"2019","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.nbd.2020.104946_bb1085","doi-asserted-by":"crossref","first-page":"949","DOI":"10.1016\/S0531-5565(02)00031-1","article-title":"174 G\/C interleukin-6 gene polymorphism and increased risk of multi-infarct dementia: a case-control study","volume":"37","author":"Pola","year":"2002","journal-title":"Exp. Gerontol."},{"key":"10.1016\/j.nbd.2020.104946_bb1090","doi-asserted-by":"crossref","first-page":"77","DOI":"10.1007\/s00401-015-1436-x","article-title":"Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease","volume":"130","author":"Pottier","year":"2015","journal-title":"Acta Neuropathol."},{"key":"10.1016\/j.nbd.2020.104946_bb1095","doi-asserted-by":"crossref","first-page":"548","DOI":"10.1016\/S1474-4422(18)30126-1","article-title":"Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study","volume":"17","author":"Pottier","year":"2018","journal-title":"Lancet Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb1100","doi-asserted-by":"crossref","first-page":"25","DOI":"10.3389\/fnmol.2019.00025","article-title":"Molecular mechanisms of TDP-43 misfolding and pathology in amyotrophic lateral sclerosis","volume":"12","author":"Prasad","year":"2019","journal-title":"Front. Mol. Neurosci."},{"key":"10.1016\/j.nbd.2020.104946_bb1105","first-page":"814","article-title":"Alzheimer\u2019s disease pathology explains association between dementia with Lewy bodies and APOE-\u03b54\/TOMM40 long poly-T repeat allele variants","volume":"5","author":"Prokopenko","year":"2019","journal-title":"Alzheimers Dement."},{"key":"10.1016\/j.nbd.2020.104946_bb1110","doi-asserted-by":"crossref","first-page":"1947","DOI":"10.1007\/s10072-013-1418-5","article-title":"\u201cCADASIL coma\u201d in an Italian homozygous CADASIL patient: comparison with clinical and MRI findings in age-matched heterozygous patients with the same G528C NOTCH3 mutation","volume":"34","author":"Ragno","year":"2013","journal-title":"Neurol. Sci."},{"key":"10.1016\/j.nbd.2020.104946_bb1115","doi-asserted-by":"crossref","first-page":"118","DOI":"10.1002\/alz.12011","article-title":"Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases","volume":"16","author":"Ramos","year":"2020","journal-title":"Alzheimers Dement."},{"key":"10.1016\/j.nbd.2020.104946_bb1120","doi-asserted-by":"crossref","first-page":"300","DOI":"10.1136\/jnnp-2013-306485","article-title":"APOE associations with severe CAA-associated vasculopathic changes: collaborative meta-analysis","volume":"85","author":"Rannikm\u00e4e","year":"2014","journal-title":"J. Neurol. Neurosurg. Psychiatry"},{"key":"10.1016\/j.nbd.2020.104946_bb1125","doi-asserted-by":"crossref","first-page":"923","DOI":"10.1016\/j.dib.2016.01.060","article-title":"Data on plasma levels of apolipoprotein E, correlations with lipids and lipoproteins stratified by APOE genotype, and risk of ischemic heart disease","volume":"6","author":"Rasmussen","year":"2016","journal-title":"Data Brief"},{"key":"10.1016\/j.nbd.2020.104946_bb1130","doi-asserted-by":"crossref","first-page":"103","DOI":"10.1186\/s40478-019-0758-7","article-title":"Key role of UBQLN2 in pathogenesis of amyotrophic lateral sclerosis and frontotemporal dementia","volume":"7","author":"Renaud","year":"2019","journal-title":"Acta Neuropathol. Commun."},{"key":"10.1016\/j.nbd.2020.104946_bb1135","doi-asserted-by":"crossref","first-page":"115","DOI":"10.1007\/s00401-009-0501-8","article-title":"Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies","volume":"118","author":"Revesz","year":"2009","journal-title":"Acta Neuropathol."},{"key":"10.1016\/j.nbd.2020.104946_bb1140","doi-asserted-by":"crossref","first-page":"1068","DOI":"10.1038\/ng2082","article-title":"C-terminal truncations in human 3\u2019-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy","volume":"39","author":"Richards","year":"2007","journal-title":"Nat. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb1145","doi-asserted-by":"crossref","first-page":"358","DOI":"10.1136\/jnnp-2017-316844","article-title":"Accuracy of clinical diagnosis of dementia with Lewy bodies: a systematic review and meta-analysis","volume":"89","author":"Rizzo","year":"2018","journal-title":"J. Neurol. Neurosurg. Psychiatry"},{"key":"10.1016\/j.nbd.2020.104946_bb1150","doi-asserted-by":"crossref","first-page":"2181","DOI":"10.1093\/brain\/awy146","article-title":"Neurodegenerative disease concomitant proteinopathies are prevalent, age-related and APOE4-associated","volume":"141","author":"Robinson","year":"2018","journal-title":"Brain"},{"key":"10.1016\/j.nbd.2020.104946_bb1155","doi-asserted-by":"crossref","first-page":"1451","DOI":"10.1212\/WNL.0b013e3181bf997a","article-title":"The heritability and genetics of frontotemporal lobar degeneration","volume":"73","author":"Rohrer","year":"2009","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb1160","doi-asserted-by":"crossref","first-page":"7013","DOI":"10.1038\/s41598-019-43458-2","article-title":"GBA and APOE \u03b54 associate with sporadic dementia with Lewy bodies in European genome wide association study","volume":"9","author":"Rongve","year":"2019","journal-title":"Sci. Rep."},{"key":"10.1016\/j.nbd.2020.104946_bb1165","doi-asserted-by":"crossref","first-page":"793","DOI":"10.1016\/S1474-4422(10)70159-9","article-title":"The diagnosis of young-onset dementia","volume":"9","author":"Rossor","year":"2010","journal-title":"Lancet Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb1170","doi-asserted-by":"crossref","first-page":"41","DOI":"10.1016\/j.nbd.2008.03.004","article-title":"Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease","volume":"31","author":"Rovelet-Lecrux","year":"2008","journal-title":"Neurobiol. Dis."},{"key":"10.1016\/j.nbd.2020.104946_bb1175","doi-asserted-by":"crossref","first-page":"1486","DOI":"10.1002\/humu.22432","article-title":"Hypomorphic NOTCH3 alleles do not cause CADASIL in humans","volume":"34","author":"Rutten","year":"2013","journal-title":"Hum. Mutat."},{"key":"10.1016\/j.nbd.2020.104946_bb1180","doi-asserted-by":"crossref","first-page":"83","DOI":"10.1007\/s40120-017-0069-5","article-title":"Increasing precision of clinical diagnosis of Alzheimer\u2019s disease using a combined algorithm incorporating clinical and novel biomarker data","volume":"6","author":"Sabbagh","year":"2017","journal-title":"Neurol Ther"},{"key":"10.1016\/j.nbd.2020.104946_bb1185","doi-asserted-by":"crossref","first-page":"71","DOI":"10.1177\/089198879801100205","article-title":"CADASIL syndrome: a genetic form of vascular dementia","volume":"11","author":"Salloway","year":"1998","journal-title":"J. Geriatr. Psychiatry Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb1190","doi-asserted-by":"crossref","first-page":"774","DOI":"10.1212\/01.wnl.0000324928.44694.f7","article-title":"Cysteine-sparing notch3 mutations: cadasil or cadasil variants?","volume":"71","author":"Scheid","year":"2008","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb1195","doi-asserted-by":"crossref","first-page":"315","DOI":"10.1161\/STROKEAHA.111.628768","article-title":"Genome-wide association study of vascular dementia","volume":"43","author":"Schrijvers","year":"2012","journal-title":"Stroke"},{"key":"10.1016\/j.nbd.2020.104946_bb1200","doi-asserted-by":"crossref","DOI":"10.1016\/j.neurobiolaging.2014.01.152","article-title":"No mutations in hnRNPA1 and hnRNPA2B1 in Dutch patients with amyotrophic lateral sclerosis, frontotemporal dementia, and inclusion body myopathy","volume":"35","author":"Seelen","year":"2014","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.nbd.2020.104946_bb1205","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/j.arr.2014.10.005","article-title":"Genetic factors associated with longevity: a review of recent findings","volume":"19","author":"Shadyab","year":"2015","journal-title":"Ageing Res. Rev."},{"key":"10.1016\/j.nbd.2020.104946_bb1210","doi-asserted-by":"crossref","first-page":"182","DOI":"10.1016\/j.ejpn.2009.04.010","article-title":"A dominantly inherited mutation in collagen IV A1 (COL4A1) causing childhood onset stroke without porencephaly","volume":"14","author":"Shah","year":"2010","journal-title":"Eur. J. Paediatr. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb1215","doi-asserted-by":"crossref","first-page":"17","DOI":"10.1080\/13554794.2019.1601230","article-title":"CSF1R mutation presenting as dementia with Lewy bodies","volume":"25","author":"Sharma","year":"2019","journal-title":"Neurocase"},{"key":"10.1016\/j.nbd.2020.104946_bb1220","doi-asserted-by":"crossref","first-page":"799","DOI":"10.3233\/JAD-121594","article-title":"Clinicopathologic study of Alzheimer\u2019s disease: Alzheimer mimics","volume":"35","author":"Shim","year":"2013","journal-title":"J. Alzheimers Dis."},{"key":"10.1016\/j.nbd.2020.104946_bb1225","doi-asserted-by":"crossref","first-page":"1448","DOI":"10.1001\/jamaneurol.2016.1593","article-title":"High frequency of GBA gene mutations in dementia with Lewy Bodies among Ashkenazi Jews","volume":"73","author":"Shiner","year":"2016","journal-title":"JAMA Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb1230","doi-asserted-by":"crossref","DOI":"10.1093\/brain\/awx062","article-title":"Multi-infarct dementia of Swedish type is caused by a 3\u2019UTR mutation of COL4A1","volume":"140","author":"Siitonen","year":"2017","journal-title":"Brain"},{"key":"10.1016\/j.nbd.2020.104946_bb1235","doi-asserted-by":"crossref","first-page":"3105","DOI":"10.1093\/brain\/awx314","article-title":"A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophy","volume":"140","author":"Simons","year":"2017","journal-title":"Brain"},{"key":"10.1016\/j.nbd.2020.104946_bb1240","doi-asserted-by":"crossref","first-page":"1373","DOI":"10.1038\/ng.3916","article-title":"Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer\u2019s disease","volume":"49","author":"Sims","year":"2017","journal-title":"Nat. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb1245","doi-asserted-by":"crossref","first-page":"167","DOI":"10.1159\/000066022","article-title":"Clinical and neuropathological correlates of apolipoprotein E genotype in dementia with Lewy bodies","volume":"14","author":"Singleton","year":"2002","journal-title":"Dement. Geriatr. Cogn. Disord."},{"key":"10.1016\/j.nbd.2020.104946_bb1250","doi-asserted-by":"crossref","DOI":"10.1126\/science.1090278","article-title":"alpha-Synuclein locus triplication causes Parkinson\u2019s disease","volume":"302","author":"Singleton","year":"2003","journal-title":"Science"},{"key":"10.1016\/j.nbd.2020.104946_bb1255","doi-asserted-by":"crossref","first-page":"981","DOI":"10.3233\/JAD-150862","article-title":"A Validation Study of Vascular Cognitive Impairment Genetics Meta-Analysis Findings in an Independent Collaborative Cohort","volume":"53","author":"Skrobot","year":"2016","journal-title":"J. Alzheimers Dis."},{"key":"10.1016\/j.nbd.2020.104946_bb1260","doi-asserted-by":"crossref","first-page":"1102","DOI":"10.1016\/j.ajhg.2012.04.021","article-title":"Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage","volume":"90","author":"Smith","year":"2012","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb1265","doi-asserted-by":"crossref","first-page":"324","DOI":"10.1016\/j.neuron.2014.09.027","article-title":"Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS","volume":"84","author":"Smith","year":"2014","journal-title":"Neuron"},{"key":"10.1016\/j.nbd.2020.104946_bb1270","doi-asserted-by":"crossref","first-page":"45","DOI":"10.1016\/j.clineuro.2017.02.015","article-title":"Hereditary cerebral small vessel disease and stroke","volume":"155","author":"S\u00f8ndergaard","year":"2017","journal-title":"Clin. Neurol. Neurosurg."},{"key":"10.1016\/j.nbd.2020.104946_bb1275","doi-asserted-by":"crossref","first-page":"319","DOI":"10.1016\/j.jcma.2013.03.002","article-title":"A homozygous NOTCH3 mutation p.R544C and a heterozygous TREX1 variant p.C99MfsX3 in a family with hereditary small vessel disease of the brain","volume":"76","author":"Soong","year":"2013","journal-title":"J. Chin. Med. Assoc."},{"key":"10.1016\/j.nbd.2020.104946_bb1280","first-page":"48","article-title":"De novo mutation in the NOTCH3 gene causing CADASIL","volume":"14","author":"Stojanov","year":"2014","journal-title":"Bosn. J. Basic Med. Sci."},{"key":"10.1016\/j.nbd.2020.104946_bb1285","doi-asserted-by":"crossref","first-page":"43721","DOI":"10.18632\/oncotarget.17341","article-title":"Updated meta-analysis of the role of APOE \u03b52\/\u03b53\/\u03b54 alleles in frontotemporal lobar degeneration","volume":"8","author":"Su","year":"2017","journal-title":"Oncotarget"},{"key":"10.1016\/j.nbd.2020.104946_bb1290","doi-asserted-by":"crossref","first-page":"177","DOI":"10.1111\/ahg.12241","article-title":"The rs75932628 and rs2234253 polymorphisms of the TREM2 gene were associated with susceptibility to frontotemporal lobar degeneration in Caucasian populations","volume":"82","author":"Su","year":"2018","journal-title":"Ann. Hum. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb1295","doi-asserted-by":"crossref","first-page":"364","DOI":"10.1161\/01.STR.0000199065.12908.62","article-title":"Does apolipoprotein E genotype influence the risk of ischemic stroke, intracerebral hemorrhage, or subarachnoid hemorrhage? Systematic review and meta-analyses of 31 studies among 5961 cases and 17,965 controls","volume":"37","author":"Sudlow","year":"2006","journal-title":"Stroke"},{"key":"10.1016\/j.nbd.2020.104946_bb1300","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1016\/j.nicl.2017.04.015","article-title":"White matter hyperintensities are seen only in GRN mutation carriers in the GENFI cohort","volume":"15","author":"Sudre","year":"2017","journal-title":"Neuroimage Clin"},{"key":"10.1016\/j.nbd.2020.104946_bb1305","doi-asserted-by":"crossref","first-page":"611","DOI":"10.3233\/JAD-143102","article-title":"Genetics of vascular dementia: systematic review and meta-analysis","volume":"46","author":"Sun","year":"2015","journal-title":"J. Alzheimers Dis."},{"key":"10.1016\/j.nbd.2020.104946_bb1310","doi-asserted-by":"crossref","first-page":"869","DOI":"10.1016\/j.parkreldis.2013.05.013","article-title":"Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutations","volume":"19","author":"Sundal","year":"2013","journal-title":"Parkinsonism Relat. Disord."},{"key":"10.1016\/j.nbd.2020.104946_bb1315","doi-asserted-by":"crossref","first-page":"6226","DOI":"10.1016\/S0021-9258(18)68776-9","article-title":"Ehlers-Danlos syndrome type IV: a multi-exon deletion in one of the two COL3A1 alleles affecting structure, stability, and processing of type III procollagen","volume":"263","author":"Superti-Furga","year":"1988","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.nbd.2020.104946_bb1320","doi-asserted-by":"crossref","first-page":"260","DOI":"10.1212\/01.wnl.0000339484.61490.a4","article-title":"Autosomal dominant subcortical gliosis presenting as frontotemporal dementia","volume":"72","author":"Swerdlow","year":"2009","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb1325","doi-asserted-by":"crossref","first-page":"45","DOI":"10.1016\/S0896-6273(01)00179-9","article-title":"Notch1 and Notch3 instructively restrict bFGF-responsive multipotent neural progenitor cells to an astroglial fate","volume":"29","author":"Tanigaki","year":"2001","journal-title":"Neuron"},{"key":"10.1016\/j.nbd.2020.104946_bb1330","doi-asserted-by":"crossref","first-page":"282","DOI":"10.1093\/jnen\/61.3.282","article-title":"Two types of sporadic cerebral amyloid angiopathy","volume":"61","author":"Thal","year":"2002","journal-title":"J. Neuropathol. Exp. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb1335","doi-asserted-by":"crossref","first-page":"1007","DOI":"10.1007\/s00702-014-1360-6","article-title":"Frontotemporal lobar degeneration FTLD-tau: preclinical lesions, vascular, and Alzheimer-related co-pathologies","volume":"122","author":"Thal","year":"2015","journal-title":"J. Neural Transm."},{"key":"10.1016\/j.nbd.2020.104946_bb1340","doi-asserted-by":"crossref","first-page":"2697","DOI":"10.1093\/brain\/awt188","article-title":"Contribution of cerebrovascular disease in autopsy confirmed neurodegenerative disease cases in the National Alzheimer\u2019s Coordinating Centre","volume":"136","author":"Toledo","year":"2013","journal-title":"Brain"},{"key":"10.1016\/j.nbd.2020.104946_bb1345","doi-asserted-by":"crossref","first-page":"116604","DOI":"10.1016\/j.jns.2019.116604","article-title":"Genetic Creutzfeldt-Jakob disease mimicking dementia with Lewy bodies: clinical and radiological findings","volume":"409","author":"Tomizawa","year":"2020","journal-title":"J. Neurol. Sci."},{"key":"10.1016\/j.nbd.2020.104946_bb1350","doi-asserted-by":"crossref","first-page":"1017","DOI":"10.3389\/fimmu.2018.01017","article-title":"Dysfunction of optineurin in amyotrophic lateral sclerosis and glaucoma","volume":"9","author":"Toth","year":"2018","journal-title":"Front. Immunol."},{"key":"10.1016\/j.nbd.2020.104946_bb1355","doi-asserted-by":"crossref","first-page":"146","DOI":"10.1212\/WNL.0000000000002263","article-title":"Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke","volume":"86","author":"Traylor","year":"2016","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb1360","doi-asserted-by":"crossref","first-page":"e749","DOI":"10.1212\/WNL.0000000000006952","article-title":"Genetic variation in PLEKHG1 is associated with white matter hyperintensities (n = 11,226)","volume":"92","author":"Traylor","year":"2019","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb1365","doi-asserted-by":"crossref","first-page":"801","DOI":"10.1002\/ana.25486","article-title":"TMEM106B Effect on cognition in Parkinson disease and frontotemporal dementia","volume":"85","author":"Tropea","year":"2019","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb1370","doi-asserted-by":"crossref","first-page":"1944","DOI":"10.1212\/WNL.0b013e3182735e9a","article-title":"GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathology","volume":"79","author":"Tsuang","year":"2012","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb1375","doi-asserted-by":"crossref","first-page":"223","DOI":"10.1001\/jamaneurol.2013.600","article-title":"APOE \u03b54 increases risk for dementia in pure synucleinopathies","volume":"70","author":"Tsuang","year":"2013","journal-title":"JAMA Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb1380","doi-asserted-by":"crossref","first-page":"1767","DOI":"10.1161\/01.STR.32.8.1767","article-title":"Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutation","volume":"32","author":"Tuominen","year":"2001","journal-title":"Stroke"},{"key":"10.1016\/j.nbd.2020.104946_bb1385","first-page":"303","article-title":"A case of frontal lobe syndrome followed by serial 123I-IMP SPECT","volume":"30","author":"Uchida","year":"1993","journal-title":"Kaku Igaku"},{"key":"10.1016\/j.nbd.2020.104946_bb1390","doi-asserted-by":"crossref","first-page":"38","DOI":"10.1186\/1750-1326-9-38","article-title":"Genetic modifiers in carriers of repeat expansions in the C9ORF72 gene","volume":"9","author":"van Blitterswijk","year":"2014","journal-title":"Mol. Neurodegener."},{"key":"10.1016\/j.nbd.2020.104946_bb1395","doi-asserted-by":"crossref","unstructured":"Van Deerlin, V.M., Sleiman, P.M.A., Martinez-Lage, M., Chen-Plotkin, A., Wang, L.-S., Graff-Radford, N.R., Dickson, D.W., Rademakers, R., Boeve, B.F., Grossman, M., Arnold, S.E., Mann, D.M.A., Pickering-Brown, S.M., Seelaar, H., Heutink, P., van Swieten, J.C., Murrell, J.R., Ghetti, B., Spina, S., Grafman, J., Hodges, J., Spillantini, M.G., Gilman, S., Lieberman, A.P., Kaye, J.A., Woltjer, R.L., Bigio, E.H., Mesulam, M., Al-Sarraj, S., Troakes, C., Rosenberg, R.N., White, C.L., 3rd, Ferrer, I., Llad\u00f3, A., Neumann, M., Kretzschmar, H.A., Hulette, C.M., Welsh-Bohmer, K.A., Miller, B.L., Alzualde, A., Lopez de Munain, A., McKee, A.C., Gearing, M., Levey, A.I., Lah, J.J., Hardy, J., Rohrer, J.D., Lashley, T., Mackenzie, I.R.A., Feldman, H.H., Hamilton, R.L., Dekosky, S.T., van der Zee, J., Kumar-Singh, S., Van Broeckhoven, C., Mayeux, R., Vonsattel, J.P.G., Troncoso, J.C., Kril, J.J., Kwok, J.B.J., Halliday, G.M., Bird, T.D., Ince, P.G., Shaw, P.J., Cairns, N.J., Morris, J.C., McLean, C.A., DeCarli, C., Ellis, W.G., Freeman, S.H., Frosch, M.P., Growdon, J.H., Perl, D.P., Sano, M., Bennett, D.A., Schneider, J.A., Beach, T.G., Reiman, E.M., Woodruff, B.K., Cummings, J., Vinters, H.V., Miller, C.A., Chui, H.C., Alafuzoff, I., Hartikainen, P., Seilhean, D., Galasko, D., Masliah, E., Cotman, C.W., Tu\u00f1\u00f3n, M.T., Mart\u00ednez, M.C.C., Munoz, D.G., Carroll, S.L., Marson, D., Riederer, P.F., Bogdanovic, N., Schellenberg, G.D., Hakonarson, H., Trojanowski, J.Q., Lee, V.M.-Y., 2010. Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. Nat. Genet. 42, 234\u2013239. doi:10.1038\/ng.536.","DOI":"10.1038\/ng.536"},{"key":"10.1016\/j.nbd.2020.104946_bb1400","doi-asserted-by":"crossref","first-page":"237","DOI":"10.1007\/s00401-019-02026-8","article-title":"A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer\u2019s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity","volume":"138","author":"van der Lee","year":"2019","journal-title":"Acta Neuropathol."},{"key":"10.1016\/j.nbd.2020.104946_bb1405","doi-asserted-by":"crossref","first-page":"313","DOI":"10.1093\/hmg\/ddm309","article-title":"CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro","volume":"17","author":"van der Zee","year":"2008","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb1410","doi-asserted-by":"crossref","first-page":"397","DOI":"10.1007\/s00401-014-1298-7","article-title":"Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration","volume":"128","author":"van der Zee","year":"2014","journal-title":"Acta Neuropathol."},{"key":"10.1016\/j.nbd.2020.104946_bb1415","doi-asserted-by":"crossref","first-page":"363","DOI":"10.1038\/s41582-018-0009-8","article-title":"Genotype-phenotype links in frontotemporal lobar degeneration","volume":"14","author":"Van Mossevelde","year":"2018","journal-title":"Nat. Rev. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb1420","doi-asserted-by":"crossref","first-page":"673","DOI":"10.1017\/S0033291713000494","article-title":"The prevalence and incidence of dementia with Lewy bodies: a systematic review of population and clinical studies","volume":"44","author":"Vann Jones","year":"2014","journal-title":"Psychol. Med."},{"key":"10.1016\/j.nbd.2020.104946_bb1425","doi-asserted-by":"crossref","first-page":"190","DOI":"10.1007\/s11910-010-0102-x","article-title":"The role of glucocerebrosidase mutations in Parkinson disease and Lewy body disorders","volume":"10","author":"Velayati","year":"2010","journal-title":"Curr. Neurol. Neurosci. Rep."},{"key":"10.1016\/j.nbd.2020.104946_bb1430","doi-asserted-by":"crossref","first-page":"844","DOI":"10.1038\/ejhg.2012.20","article-title":"COL4A2 mutation associated with familial porencephaly and small-vessel disease","volume":"20","author":"Verbeek","year":"2012","journal-title":"Eur. J. Hum. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb1435","doi-asserted-by":"crossref","first-page":"2347","DOI":"10.1093\/brain\/awv155","article-title":"Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel disease","volume":"138","author":"Verdura","year":"2015","journal-title":"Brain"},{"key":"10.1016\/j.nbd.2020.104946_bb1440","doi-asserted-by":"crossref","first-page":"741","DOI":"10.1002\/ana.24782","article-title":"Disruption of a miR-29 binding site leading to COL4A1 upregulation causes pontine autosomal dominant microangiopathy with leukoencephalopathy","volume":"80","author":"Verdura","year":"2016","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb1445","doi-asserted-by":"crossref","first-page":"399","DOI":"10.1038\/sj.ejhg.5200820","article-title":"Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis","volume":"10","author":"Verpillat","year":"2002","journal-title":"Eur. J. Hum. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb1450","doi-asserted-by":"crossref","first-page":"776","DOI":"10.1038\/21637","article-title":"A stop-codon mutation in the BRI gene associated with familial British dementia","volume":"399","author":"Vidal","year":"1999","journal-title":"Nature"},{"key":"10.1016\/j.nbd.2020.104946_bb1455","doi-asserted-by":"crossref","first-page":"4920","DOI":"10.1073\/pnas.080076097","article-title":"A decamer duplication in the 3\u2019 region of the BRI gene originates an amyloid peptide that is associated with dementia in a Danish kindred","volume":"97","author":"Vidal","year":"2000","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"key":"10.1016\/j.nbd.2020.104946_bb1460","doi-asserted-by":"crossref","first-page":"91","DOI":"10.1007\/s10072-013-1580-9","article-title":"Homozygosity and severity of phenotypic presentation in a CADASIL family","volume":"35","author":"Vinciguerra","year":"2014","journal-title":"Neurol. Sci."},{"key":"10.1016\/j.nbd.2020.104946_bb1465","doi-asserted-by":"crossref","first-page":"28","DOI":"10.1186\/s40035-019-0172-x","article-title":"Beyond the synucleinopathies: alpha synuclein as a driving force in neurodegenerative comorbidities","volume":"8","author":"Visanji","year":"2019","journal-title":"Transl. Neurodegener."},{"key":"10.1016\/j.nbd.2020.104946_bb1470","doi-asserted-by":"crossref","first-page":"852","DOI":"10.1016\/j.fob.2015.10.006","article-title":"Association between Apolipoprotein E polymorphism and myocardial infarction risk: a systematic review and meta-analysis","volume":"5","author":"Wang","year":"2015","journal-title":"FEBS Open Biol."},{"key":"10.1016\/j.nbd.2020.104946_bb1475","doi-asserted-by":"crossref","first-page":"377","DOI":"10.1038\/ng1332","article-title":"Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein","volume":"36","author":"Watts","year":"2004","journal-title":"Nat. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb1480","doi-asserted-by":"crossref","first-page":"2482","DOI":"10.1016\/j.jstrokecerebrovasdis.2017.05.048","article-title":"Polymorphisms of MTHFR, eNOS, ACE, AGT, ApoE, PON1, PDE4D, and ischemic stroke: meta-analysis","volume":"26","author":"Wei","year":"2017","journal-title":"J. Stroke Cerebrovasc. Dis."},{"key":"10.1016\/j.nbd.2020.104946_bb1485","doi-asserted-by":"crossref","first-page":"715","DOI":"10.1023\/A:1012993305223","article-title":"Anderson-Fabry disease: clinical manifestations of disease in female heterozygotes","volume":"24","author":"Whybra","year":"2001","journal-title":"J. Inherit. Metab. Dis."},{"key":"10.1016\/j.nbd.2020.104946_bb1490","doi-asserted-by":"crossref","first-page":"11253","DOI":"10.1038\/ncomms11253","article-title":"CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia","volume":"7","author":"Williams","year":"2016","journal-title":"Nat. Commun."},{"key":"10.1016\/j.nbd.2020.104946_bb1495","doi-asserted-by":"crossref","first-page":"351","DOI":"10.1212\/WNL.0000000000002319","article-title":"Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke","volume":"86","author":"Williams","year":"2016","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2020.104946_bb1500","doi-asserted-by":"crossref","first-page":"3208","DOI":"10.1128\/jb.172.6.3208-3213.1990","article-title":"Role of the purine repressor in the regulation of pyrimidine gene expression in Escherichia coli K-12","volume":"172","author":"Wilson","year":"1990","journal-title":"J. Bacteriol."},{"key":"10.1016\/j.nbd.2020.104946_bb1505","doi-asserted-by":"crossref","first-page":"1361","DOI":"10.1093\/brain\/awu067","article-title":"PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology","volume":"137","author":"Wong","year":"2014","journal-title":"Brain"},{"key":"10.1016\/j.nbd.2020.104946_bb1510","doi-asserted-by":"crossref","first-page":"160","DOI":"10.1016\/j.gene.2012.03.010","article-title":"Genetic association of the gene encoding RPGRIP1L with susceptibility to vascular dementia","volume":"499","author":"Woo","year":"2012","journal-title":"Gene"},{"key":"10.1016\/j.nbd.2020.104946_bb1515","doi-asserted-by":"crossref","first-page":"511","DOI":"10.1016\/j.ajhg.2014.02.012","article-title":"Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage","volume":"94","author":"Woo","year":"2014","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb1520","doi-asserted-by":"crossref","first-page":"981","DOI":"10.1016\/j.ajhg.2013.04.017","article-title":"Hypermethylation of the CpG island near the G4C2 repeat in ALS with a C9orf72 expansion","volume":"92","author":"Xi","year":"2013","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.nbd.2020.104946_bb1525","doi-asserted-by":"crossref","first-page":"715","DOI":"10.1007\/s00401-015-1401-8","article-title":"The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients","volume":"129","author":"Xi","year":"2015","journal-title":"Acta Neuropathol."},{"key":"10.1016\/j.nbd.2020.104946_bb1530","doi-asserted-by":"crossref","first-page":"2840","DOI":"10.1016\/j.jstrokecerebrovasdis.2018.06.017","article-title":"A Chinese CARASIL patient caused by novel compound heterozygous mutations in HTRA1","volume":"27","author":"Xie","year":"2018","journal-title":"J. Stroke Cerebrovasc. Dis."},{"key":"10.1016\/j.nbd.2020.104946_bb1535","doi-asserted-by":"crossref","first-page":"3912175","DOI":"10.1155\/2016\/3912175","article-title":"Apolipoprotein E gene variants and risk of coronary heart disease: a meta-analysis","volume":"2016","author":"Xu","year":"2016","journal-title":"Biomed. Res. Int."},{"key":"10.1016\/j.nbd.2020.104946_bb1540","doi-asserted-by":"crossref","DOI":"10.1002\/ana.410390523","article-title":"Lack of an association between apolipoprotein E epsilon 4 and cerebral amyloid angiopathy in elderly Japanese","author":"Yamada","year":"1996","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb1545","doi-asserted-by":"crossref","DOI":"10.1212\/NXG.0000000000000176","article-title":"UNC5C variants are associated with cerebral amyloid angiopathy","volume":"3","author":"Yang","year":"2017","journal-title":"Neurol Genet"},{"key":"10.1016\/j.nbd.2020.104946_bb1550","doi-asserted-by":"crossref","first-page":"406","DOI":"10.1007\/s00406-006-0702-2","article-title":"Serum BDNF, TNF- \u03b1 and IL-1\u03b2 levels in dementia patients","volume":"256","author":"Yasutake","year":"2006","journal-title":"Eur. Arch. Psychiatry Clin. Neurosci."},{"key":"10.1016\/j.nbd.2020.104946_bb1555","doi-asserted-by":"crossref","first-page":"691","DOI":"10.1001\/jamaneurol.2016.0150","article-title":"Association between genetic traits for immune-mediated diseases and Alzheimer disease","volume":"73","author":"Yokoyama","year":"2016","journal-title":"JAMA Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb1560","doi-asserted-by":"crossref","first-page":"211","DOI":"10.1016\/j.neurobiolaging.2005.01.013","article-title":"Association of interleukin-1 gene polymorphisms with dementia in a community-based sample: the Honolulu-Asia Aging Study","volume":"27","author":"Yucesoy","year":"2006","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.nbd.2020.104946_bb1565","doi-asserted-by":"crossref","first-page":"164","DOI":"10.1002\/ana.10795","article-title":"The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia","volume":"55","author":"Zarranz","year":"2004","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.nbd.2020.104946_bb1570","doi-asserted-by":"crossref","first-page":"1520","DOI":"10.1074\/jbc.M111.275990","article-title":"High temperature requirement factor A1 (HTRA1) gene regulates angiogenesis through transforming growth factor-\u03b2 family member growth differentiation factor 6","volume":"287","author":"Zhang","year":"2012","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.nbd.2020.104946_bb1575","doi-asserted-by":"crossref","first-page":"2895","DOI":"10.1093\/brain\/awy238","article-title":"A C6orf10\/LOC101929163 locus is associated with age of onset in C9orf72 carriers","volume":"141","author":"Zhang","year":"2018","journal-title":"Brain"},{"key":"10.1016\/j.nbd.2020.104946_bb1580","doi-asserted-by":"crossref","DOI":"10.1126\/scitranslmed.aay1809","article-title":"APOE4 exacerbates \u03b1-synuclein pathology and related toxicity independent of amyloid","volume":"12","author":"Zhao","year":"2020","journal-title":"Sci. Transl. Med."},{"key":"10.1016\/j.nbd.2020.104946_bb1585","doi-asserted-by":"crossref","DOI":"10.1038\/tp.2015.64","article-title":"Genome-wide copy-number variation study of psychosis in Alzheimer\u2019s disease","volume":"5","author":"Zheng","year":"2015","journal-title":"Transl. Psychiatry"},{"key":"10.1016\/j.nbd.2020.104946_bb1590","doi-asserted-by":"crossref","first-page":"911","DOI":"10.1056\/NEJMoa1307361","article-title":"Early-onset stroke and vasculopathy associated with mutations in ADA2","volume":"370","author":"Zhou","year":"2014","journal-title":"N. Engl. J. Med."},{"key":"10.1016\/j.nbd.2020.104946_bb1595","doi-asserted-by":"crossref","first-page":"5534","DOI":"10.1007\/s12035-016-0099-5","article-title":"Mitochondrial CHCHD-containing proteins: physiologic functions and link with neurodegenerative diseases","volume":"54","author":"Zhou","year":"2017","journal-title":"Mol. Neurobiol."},{"key":"10.1016\/j.nbd.2020.104946_bb1600","doi-asserted-by":"crossref","first-page":"304","DOI":"10.1034\/j.1600-0404.2001.103005304.x","article-title":"Genetic polymorphisms in older subjects with vascular or Alzheimer\u2019s dementia","volume":"103","author":"Zuliani","year":"2001","journal-title":"Acta Neurol. Scand."},{"key":"10.1016\/j.nbd.2020.104946_bb1605","doi-asserted-by":"crossref","first-page":"686","DOI":"10.1016\/j.jpsychires.2006.02.008","article-title":"Plasma cytokines profile in older subjects with late onset Alzheimer\u2019s disease or vascular dementia","volume":"41","author":"Zuliani","year":"2007","journal-title":"J. Psychiatr. Res."}],"container-title":["Neurobiology of Disease"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0969996120302217?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0969996120302217?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T05:19:14Z","timestamp":1760851154000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0969996120302217"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,8]]},"references-count":321,"alternative-id":["S0969996120302217"],"URL":"https:\/\/doi.org\/10.1016\/j.nbd.2020.104946","relation":{},"ISSN":["0969-9961"],"issn-type":[{"value":"0969-9961","type":"print"}],"subject":[],"published":{"date-parts":[[2020,8]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Genetic architecture of common non-Alzheimer\u2019s disease dementias","name":"articletitle","label":"Article Title"},{"value":"Neurobiology of Disease","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.nbd.2020.104946","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2020 The Authors. Published by Elsevier Inc.","name":"copyright","label":"Copyright"}],"article-number":"104946"}}