{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,26]],"date-time":"2026-09-26T09:34:50Z","timestamp":1790415290852,"version":"4.1.0"},"reference-count":188,"publisher":"Elsevier","isbn-type":[{"value":"9780128096727","type":"print"}],"license":[{"start":{"date-parts":[[2016,1,1]],"date-time":"2016-01-01T00:00:00Z","timestamp":1451606400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2016,1,1]],"date-time":"2016-01-01T00:00:00Z","timestamp":1451606400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2016,1,1]],"date-time":"2016-01-01T00:00:00Z","timestamp":1451606400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2016,1,1]],"date-time":"2016-01-01T00:00:00Z","timestamp":1451606400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2016,1,1]],"date-time":"2016-01-01T00:00:00Z","timestamp":1451606400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2016,1,1]],"date-time":"2016-01-01T00:00:00Z","timestamp":1451606400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2016,1,1]],"date-time":"2016-01-01T00:00:00Z","timestamp":1451606400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2016]]},"DOI":"10.1016\/bs.adgen.2016.08.003","type":"book-chapter","created":{"date-parts":[[2016,10,9]],"date-time":"2016-10-09T11:54:11Z","timestamp":1476014051000},"page":"53-97","source":"Crossref","is-referenced-by-count":63,"title":["Advances in Dyslexia Genetics\u2014New Insights Into the Role of Brain Asymmetries"],"prefix":"10.1016","member":"78","reference":[{"issue":"5","key":"10.1016\/bs.adgen.2016.08.003_bib1","doi-asserted-by":"crossref","first-page":"e65179","DOI":"10.1371\/journal.pone.0065179","article-title":"Position of neocortical neurons transfected at different gestational ages with shRNA targeted against candidate dyslexia susceptibility genes","volume":"8","author":"Adler","year":"2013","journal-title":"PLoS One"},{"issue":"7","key":"10.1016\/bs.adgen.2016.08.003_bib2","doi-asserted-by":"crossref","first-page":"967","DOI":"10.1002\/ajmg.b.30926","article-title":"Association studies and gene expression analyses of the DISC1-interacting molecules, pericentrin 2 (PCNT2) and DISC1-binding zinc finger protein (DBZ), with schizophrenia and with bipolar disorder","volume":"150B","author":"Anitha","year":"2009","journal-title":"American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics"},{"key":"10.1016\/bs.adgen.2016.08.003_bib3","series-title":"Left, Right, Hand and Brain: The right Shift theory","author":"Annett","year":"1985"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib4","doi-asserted-by":"crossref","first-page":"509","DOI":"10.1007\/s10519-012-9532-3","article-title":"The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language","volume":"42","author":"Anthoni","year":"2012","journal-title":"Behavior Genetics"},{"issue":"6","key":"10.1016\/bs.adgen.2016.08.003_bib5","doi-asserted-by":"crossref","first-page":"667","DOI":"10.1093\/hmg\/ddm009","article-title":"A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia","volume":"16","author":"Anthoni","year":"2007","journal-title":"Human Molecular Genetics"},{"issue":"3","key":"10.1016\/bs.adgen.2016.08.003_bib6","doi-asserted-by":"crossref","first-page":"221","DOI":"10.1038\/hdy.2013.93","article-title":"Genome-wide association study of handedness excludes simple genetic models","volume":"112","author":"Armour","year":"2014","journal-title":"Heredity"},{"issue":"6","key":"10.1016\/bs.adgen.2016.08.003_bib7","doi-asserted-by":"crossref","first-page":"e67251","DOI":"10.1371\/journal.pone.0067251","article-title":"VNTR polymorphism is associated with degree of handedness but not direction of handedness","volume":"8","author":"Arning","year":"2013","journal-title":"PLoS One"},{"key":"10.1016\/bs.adgen.2016.08.003_bib8","series-title":"G is for genes: The impact of genetics on education and achievement","author":"Asbury","year":"2013"},{"issue":"11","key":"10.1016\/bs.adgen.2016.08.003_bib9","doi-asserted-by":"crossref","first-page":"2699","DOI":"10.1093\/cercor\/bhp024","article-title":"Reading and subcortical auditory function","volume":"19","author":"Banai","year":"2009","journal-title":"Cerebral Cortex"},{"issue":"6","key":"10.1016\/bs.adgen.2016.08.003_bib10","doi-asserted-by":"crossref","first-page":"1108","DOI":"10.1016\/j.neuron.2012.10.027","article-title":"Tangentially migrating neurons assemble a primary cilium that promotes their reorientation to the cortical plate","volume":"76","author":"Baudoin","year":"2012","journal-title":"Neuron"},{"issue":"5","key":"10.1016\/bs.adgen.2016.08.003_bib11","doi-asserted-by":"crossref","first-page":"675","DOI":"10.1038\/ejhg.2013.199","article-title":"Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort","volume":"22","author":"Becker","year":"2014","journal-title":"European Journal of Human Genetics"},{"issue":"7414","key":"10.1016\/bs.adgen.2016.08.003_bib12","doi-asserted-by":"crossref","first-page":"57","DOI":"10.1038\/nature11247","article-title":"An integrated encyclopedia of DNA elements in the human genome","volume":"489","author":"Bernstein","year":"2012","journal-title":"Nature"},{"issue":"6138","key":"10.1016\/bs.adgen.2016.08.003_bib13","doi-asserted-by":"crossref","first-page":"1230531","DOI":"10.1126\/science.1230531","article-title":"Cerebral asymmetry and language development: cause, correlate, or consequence?","volume":"340","author":"Bishop","year":"2013","journal-title":"Science"},{"issue":"1806","key":"10.1016\/bs.adgen.2016.08.003_bib14","first-page":"20143139","article-title":"The interface between genetics and psychology: lessons from developmental dyslexia","volume":"282","author":"Bishop","year":"2015","journal-title":"Proceedings. Biological Sciences"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib15","doi-asserted-by":"crossref","first-page":"111","DOI":"10.1093\/ije\/dys064","article-title":"Cohort profile: the \u2018children of the 90s\u2019\u2013the index offspring of the Avon longitudinal study of parents and children","volume":"42","author":"Boyd","year":"2013","journal-title":"International Journal of Epidemiology"},{"issue":"9","key":"10.1016\/bs.adgen.2016.08.003_bib16","doi-asserted-by":"crossref","first-page":"e1003751","DOI":"10.1371\/journal.pgen.1003751","article-title":"Common variants in left\/right asymmetry genes and pathways are associated with relative hand skill","volume":"9","author":"Brandler","year":"2013","journal-title":"PLoS Genetics"},{"issue":"2","key":"10.1016\/bs.adgen.2016.08.003_bib17","doi-asserted-by":"crossref","first-page":"83","DOI":"10.1016\/j.molmed.2013.10.008","article-title":"The genetic relationship between handedness and neurodevelopmental disorders","volume":"20","author":"Brandler","year":"2014","journal-title":"Trends in Molecular Medicine"},{"issue":"7","key":"10.1016\/bs.adgen.2016.08.003_bib18","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0069986","article-title":"Cep63 and Cep152 cooperate to ensure centriole duplication","volume":"8","author":"Brown","year":"2013","journal-title":"PLoS One"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib19","doi-asserted-by":"crossref","first-page":"63","DOI":"10.1016\/0896-6273(95)90065-9","article-title":"T-Brain-1 A homolog of Brachyury whose expression defines molecularly distinct domains within the cerebral cortex","volume":"15","author":"Bulfone","year":"1995","journal-title":"Neuron"},{"issue":"22","key":"10.1016\/bs.adgen.2016.08.003_bib20","doi-asserted-by":"crossref","first-page":"9130","DOI":"10.1073\/pnas.1300454110","article-title":"Perineuronal nets protect fast-spiking interneurons against oxidative stress","volume":"110","author":"Cabungcal","year":"2013","journal-title":"Proceedings of the National Academy of Sciences of the United States of America"},{"issue":"5183","key":"10.1016\/bs.adgen.2016.08.003_bib21","doi-asserted-by":"crossref","first-page":"276","DOI":"10.1126\/science.7939663","article-title":"Quantitative trait locus for reading disability on chromosome 6","volume":"266","author":"Cardon","year":"1994","journal-title":"Science"},{"issue":"7","key":"10.1016\/bs.adgen.2016.08.003_bib22","doi-asserted-by":"crossref","first-page":"1753","DOI":"10.1093\/cercor\/bht028","article-title":"Knockdown of the dyslexia-associated gene Kiaa0319 impairs temporal responses to speech stimuli in rat primary auditory cortex","volume":"24","author":"Centanni","year":"2014","journal-title":"Cerebral Cortex"},{"issue":"10","key":"10.1016\/bs.adgen.2016.08.003_bib23","doi-asserted-by":"crossref","first-page":"1165","DOI":"10.1038\/ejhg.2014.4","article-title":"Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment","volume":"22","author":"Ceroni","year":"2014","journal-title":"European Journal of Human Genetics"},{"issue":"5","key":"10.1016\/bs.adgen.2016.08.003_bib24","doi-asserted-by":"crossref","first-page":"e63123","DOI":"10.1371\/journal.pone.0063123","article-title":"The zebrafish orthologue of the dyslexia candidate gene DYX1C1 is essential for cilia growth and function","volume":"8","author":"Chandrasekar","year":"2013","journal-title":"PLoS One"},{"issue":"7","key":"10.1016\/bs.adgen.2016.08.003_bib25","doi-asserted-by":"crossref","first-page":"1427","DOI":"10.1242\/dev.074666","article-title":"Switching on cilia: transcriptional networks regulating ciliogenesis","volume":"141","author":"Choksi","year":"2014","journal-title":"Development"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib26","doi-asserted-by":"crossref","first-page":"412","DOI":"10.1002\/aur.1456","article-title":"T-Brain-1\u2013A potential master regulator in autism spectrum disorders","volume":"8","author":"Chuang","year":"2015","journal-title":"Autism Research"},{"key":"10.1016\/bs.adgen.2016.08.003_bib27","doi-asserted-by":"crossref","first-page":"1063","DOI":"10.1038\/ng.3092","article-title":"Refining analyses of copy number variation identifies specific genes associated with developmental delay","volume":"46","author":"Coe","year":"2014","journal-title":"Nature Genetics"},{"issue":"9","key":"10.1016\/bs.adgen.2016.08.003_bib28","doi-asserted-by":"crossref","first-page":"1146","DOI":"10.1101\/gad.14.9.1146","article-title":"SPC4\/PACE4 regulates a TGFbeta signaling network during axis formation","volume":"14","author":"Constam","year":"2000","journal-title":"Genes Development"},{"issue":"9","key":"10.1016\/bs.adgen.2016.08.003_bib29","doi-asserted-by":"crossref","first-page":"838","DOI":"10.1038\/ng.909","article-title":"A copy number variation morbidity map of developmental delay","volume":"43","author":"Cooper","year":"2011","journal-title":"Nature Genetics"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib30","doi-asserted-by":"crossref","first-page":"581","DOI":"10.1086\/429131","article-title":"Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia","volume":"76","author":"Cope","year":"2005","journal-title":"American Journal of Human Genetics"},{"issue":"1519","key":"10.1016\/bs.adgen.2016.08.003_bib31","doi-asserted-by":"crossref","first-page":"867","DOI":"10.1098\/rstb.2008.0232","article-title":"The evolution and genetics of cerebral asymmetry","volume":"364","author":"Corballis","year":"2009","journal-title":"Philosophical Transactions of the Royal Society London Series B Biological Sciences"},{"issue":"3","key":"10.1016\/bs.adgen.2016.08.003_bib32","doi-asserted-by":"crossref","first-page":"505","DOI":"10.1016\/S0896-6273(00)80562-0","article-title":"Regulation of class I MHC gene expression in the developing and mature CNS by neural activity","volume":"21","author":"Corriveau","year":"1998","journal-title":"Neuron"},{"key":"10.1016\/bs.adgen.2016.08.003_bib33","doi-asserted-by":"crossref","first-page":"4204","DOI":"10.1038\/ncomms5204","article-title":"The correlation between reading and mathematics ability at age twelve has a substantial genetic component","volume":"5","author":"Davis","year":"2014","journal-title":"Nature Communications"},{"issue":"9419","key":"10.1016\/bs.adgen.2016.08.003_bib34","doi-asserted-by":"crossref","first-page":"1451","DOI":"10.1016\/S0140-6736(04)16106-0","article-title":"Developmental dyslexia","volume":"363","author":"Demonet","year":"2004","journal-title":"Lancet"},{"issue":"3","key":"10.1016\/bs.adgen.2016.08.003_bib35","doi-asserted-by":"crossref","first-page":"e1000436","DOI":"10.1371\/journal.pgen.1000436","article-title":"A common variant associated with dyslexia reduces expression of the KIAA0319 gene","volume":"5","author":"Dennis","year":"2009","journal-title":"PLoS Genetics"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib36","doi-asserted-by":"crossref","first-page":"32","DOI":"10.2174\/187152410790780118","article-title":"The doublecortin gene family and disorders of neuronal structure","volume":"10","author":"Dijkmans","year":"2010","journal-title":"Central Nervous System Agents in Medicinal Chemistry"},{"key":"10.1016\/bs.adgen.2016.08.003_bib37","doi-asserted-by":"crossref","first-page":"647","DOI":"10.1146\/annurev-genet-112414-055322","article-title":"Asymmetry of the brain: development and implications","volume":"49","author":"Duboc","year":"2015","journal-title":"Annual Review of Genetics"},{"issue":"04","key":"10.1016\/bs.adgen.2016.08.003_bib38","doi-asserted-by":"crossref","first-page":"681","DOI":"10.1017\/S0140525X00032325","article-title":"Coevolution of neocortical size, group size and language in humans","volume":"16","author":"Dunbar","year":"1993","journal-title":"Behavioral and Brain Sciences"},{"key":"10.1016\/bs.adgen.2016.08.003_bib39","doi-asserted-by":"crossref","DOI":"10.1111\/gbb.12085","article-title":"Genome-wide association study of shared components of reading disability and language impairment","volume":"12","author":"Eicher","year":"2013","journal-title":"Genes Brain and Behavior"},{"issue":"11\u201312","key":"10.1016\/bs.adgen.2016.08.003_bib40","doi-asserted-by":"crossref","first-page":"1239","DOI":"10.1007\/s00439-015-1602-1","article-title":"Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family","volume":"134","author":"Einarsdottir","year":"2015","journal-title":"Human Genetics"},{"issue":"3\u20134","key":"10.1016\/bs.adgen.2016.08.003_bib41","first-page":"475","article-title":"Does dyslexia exist?","volume":"42","author":"Elliott","year":"2009","journal-title":"Journal of Philosophy of Education"},{"issue":"9","key":"10.1016\/bs.adgen.2016.08.003_bib42","first-page":"664","article-title":"A new gene (DYX3) for dyslexia is located on chromosome 2","volume":"36","author":"Fagerheim","year":"1999","journal-title":"Journal of Medical Genetics"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib43","doi-asserted-by":"crossref","first-page":"56","DOI":"10.1111\/gbb.12003","article-title":"Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36","volume":"12","author":"Field","year":"2013","journal-title":"Genes Brain and Behavior"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib44","doi-asserted-by":"crossref","first-page":"86","DOI":"10.1038\/ng792","article-title":"Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia","volume":"30","author":"Fisher","year":"2002","journal-title":"Nature Genetics"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib45","doi-asserted-by":"crossref","first-page":"146","DOI":"10.1086\/302190","article-title":"A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia","volume":"64","author":"Fisher","year":"1999","journal-title":"American Journal of Human Genetics"},{"issue":"3","key":"10.1016\/bs.adgen.2016.08.003_bib46","doi-asserted-by":"crossref","first-page":"800","DOI":"10.1086\/339249","article-title":"A genomewide linkage screen for relative hand skill in sibling pairs","volume":"70","author":"Francks","year":"2002","journal-title":"American Journal of Human Genetics"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib47","doi-asserted-by":"crossref","first-page":"35","DOI":"10.1097\/00041444-200203000-00005","article-title":"Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1","volume":"12","author":"Francks","year":"2002","journal-title":"Psychiatric Genetics"},{"issue":"12","key":"10.1016\/bs.adgen.2016.08.003_bib48","doi-asserted-by":"crossref","first-page":"1129","DOI":"10.1038\/sj.mp.4002053","article-title":"LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia","volume":"12","author":"Francks","year":"2007","journal-title":"Molecular Psychiatry"},{"issue":"6","key":"10.1016\/bs.adgen.2016.08.003_bib49","doi-asserted-by":"crossref","first-page":"1046","DOI":"10.1086\/426404","article-title":"A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States","volume":"75","author":"Francks","year":"2004","journal-title":"American Journal of Human Genetics"},{"issue":"11","key":"10.1016\/bs.adgen.2016.08.003_bib50","doi-asserted-by":"crossref","first-page":"1124","DOI":"10.1111\/j.1467-9280.2008.02213.x","article-title":"Parental education moderates genetic influences on reading disability","volume":"19","author":"Friend","year":"2008","journal-title":"Psychological Science"},{"issue":"10","key":"10.1016\/bs.adgen.2016.08.003_bib51","doi-asserted-by":"crossref","first-page":"1213","DOI":"10.1038\/nn1772","article-title":"From genes to behavior in developmental dyslexia","volume":"9","author":"Galaburda","year":"2006","journal-title":"Nature Neuroscience"},{"issue":"2","key":"10.1016\/bs.adgen.2016.08.003_bib52","doi-asserted-by":"crossref","first-page":"222","DOI":"10.1002\/ana.410180210","article-title":"Developmental dyslexia: four consecutive patients with cortical anomalies","volume":"18","author":"Galaburda","year":"1985","journal-title":"Annals of Neurology"},{"issue":"Suppl. 3","key":"10.1016\/bs.adgen.2016.08.003_bib53","doi-asserted-by":"crossref","first-page":"52","DOI":"10.1007\/PL00010695","article-title":"Reading disability: evidence for a genetic etiology","volume":"8","author":"Gayan","year":"1999","journal-title":"European Child & Adolescent Psychiatry"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib54","doi-asserted-by":"crossref","first-page":"32","DOI":"10.1016\/j.cell.2009.03.023","article-title":"The vertebrate primary cilium in development, homeostasis, and disease","volume":"137","author":"Gerdes","year":"2009","journal-title":"Cell"},{"issue":"7","key":"10.1016\/bs.adgen.2016.08.003_bib55","doi-asserted-by":"crossref","first-page":"686","DOI":"10.1111\/gbb.12158","article-title":"Genome-wide screening for DNA variants associated with reading and language traits","volume":"13","author":"Gialluisi","year":"2014","journal-title":"Genes Brain and Behavior"},{"issue":"11","key":"10.1016\/bs.adgen.2016.08.003_bib56","doi-asserted-by":"crossref","first-page":"e1002334","DOI":"10.1371\/journal.pgen.1002334","article-title":"Relative burden of large CNVs on a range of neurodevelopmental phenotypes","volume":"7","author":"Girirajan","year":"2011","journal-title":"PLoS Genetics"},{"issue":"14","key":"10.1016\/bs.adgen.2016.08.003_bib57","doi-asserted-by":"crossref","first-page":"1321","DOI":"10.1056\/NEJMoa1200395","article-title":"Phenotypic heterogeneity of genomic disorders and rare copy-number variants","volume":"367","author":"Girirajan","year":"2012","journal-title":"The New England Journal of Medicine"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib58","doi-asserted-by":"crossref","first-page":"43","DOI":"10.1016\/j.conb.2012.11.006","article-title":"Decoding the genetics of speech and language","volume":"23","author":"Graham","year":"2013","journal-title":"Current Opinion in Neurobiology"},{"issue":"9","key":"10.1016\/bs.adgen.2016.08.003_bib59","doi-asserted-by":"crossref","first-page":"2482","DOI":"10.1093\/hmg\/ddv009","article-title":"A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation","volume":"24","author":"Grati","year":"2015","journal-title":"Human Molecular Genetics"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib60","first-page":"27","article-title":"Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15","volume":"60","author":"Grigorenko","year":"1997","journal-title":"American Journal of Human Genetics"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib61","doi-asserted-by":"crossref","first-page":"120","DOI":"10.1002\/1096-8628(20010108)105:1<120::AID-AJMG1075>3.0.CO;2-T","article-title":"Linkage studies suggest a possible locus for developmental dyslexia on chromosome 1p","volume":"105","author":"Grigorenko","year":"2001","journal-title":"American Journal of Medical Genetics"},{"issue":"3","key":"10.1016\/bs.adgen.2016.08.003_bib62","doi-asserted-by":"crossref","first-page":"511","DOI":"10.1016\/j.neuron.2014.04.024","article-title":"Primary cilia in the developing and mature brain","volume":"82","author":"Guemez-Gamboa","year":"2014","journal-title":"Neuron"},{"issue":"5","key":"10.1016\/bs.adgen.2016.08.003_bib63","doi-asserted-by":"crossref","first-page":"391","DOI":"10.1177\/0022219409345005","article-title":"Newborn event-related potentials predict poorer pre-reading skills in children at risk for dyslexia","volume":"43","author":"Guttorm","year":"2010","journal-title":"Journal of Learning Disabilities"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib64","doi-asserted-by":"crossref","first-page":"e50","DOI":"10.1371\/journal.pgen.0010050","article-title":"The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia","volume":"1","author":"Hannula-Jouppi","year":"2005","journal-title":"PLoS Genetics"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib65","doi-asserted-by":"crossref","first-page":"373","DOI":"10.1111\/j.1469-7610.2004.00358.x","article-title":"Genetic influences on early word recognition abilities and disabilities: a study of 7-year-old twins","volume":"46","author":"Harlaar","year":"2005","journal-title":"Journal of Child Psychology and Psychiatry"},{"issue":"2","key":"10.1016\/bs.adgen.2016.08.003_bib66","doi-asserted-by":"crossref","first-page":"69","DOI":"10.1016\/j.tics.2012.12.004","article-title":"Revisiting human hemispheric specialization with neuroimaging","volume":"17","author":"Herve","year":"2013","journal-title":"Trends in Cognitive Sciences"},{"issue":"5","key":"10.1016\/bs.adgen.2016.08.003_bib67","doi-asserted-by":"crossref","first-page":"925","DOI":"10.1016\/j.devcel.2012.09.019","article-title":"Arl13b in primary cilia regulates the migration and placement of interneurons in the developing cerebral cortex","volume":"23","author":"Higginbotham","year":"2012","journal-title":"Developmental Cell"},{"issue":"16","key":"10.1016\/bs.adgen.2016.08.003_bib68","doi-asserted-by":"crossref","first-page":"1533","DOI":"10.1056\/NEJMra1010172","article-title":"Ciliopathies","volume":"364","author":"Hildebrandt","year":"2011","journal-title":"The New England Journal of Medicine"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib69","doi-asserted-by":"crossref","first-page":"31","DOI":"10.1016\/j.ceb.2012.01.002","article-title":"Cilia, KIF3 molecular motor and nodal flow","volume":"24","author":"Hirokawa","year":"2012","journal-title":"Current Opinion in Cell Biology"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib70","doi-asserted-by":"crossref","first-page":"33","DOI":"10.1016\/j.cell.2006.03.002","article-title":"Nodal flow and the generation of left-right asymmetry","volume":"125","author":"Hirokawa","year":"2006","journal-title":"Cell"},{"issue":"3","key":"10.1016\/bs.adgen.2016.08.003_bib71","doi-asserted-by":"crossref","first-page":"320","DOI":"10.1002\/cne.903000305","article-title":"Monoclonal antibody Cat-301 identifies Y-cells in the dorsal lateral geniculate nucleus of the cat","volume":"300","author":"Hockfield","year":"1990","journal-title":"Journal of Comparative Neurology"},{"issue":"12","key":"10.1016\/bs.adgen.2016.08.003_bib72","doi-asserted-by":"crossref","first-page":"e52166","DOI":"10.1371\/journal.pone.0052166","article-title":"Transcriptional program of ciliated epithelial cells reveals new cilium and centrosome components and links to human disease","volume":"7","author":"Hoh","year":"2012","journal-title":"PLoS One"},{"issue":"3","key":"10.1016\/bs.adgen.2016.08.003_bib73","doi-asserted-by":"crossref","first-page":"419","DOI":"10.1016\/j.ajhg.2015.07.016","article-title":"Increased power for detection of parent-of-origin effects via the use of haplotype estimation","volume":"97","author":"Howey","year":"2015","journal-title":"American Journal of Human Genetics"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib74","doi-asserted-by":"crossref","first-page":"112","DOI":"10.1002\/ajmg.b.20082","article-title":"A dyslexia susceptibility locus (DYX7) linked to dopamine D4 receptor (DRD4) region on chromosome 11p15.5","volume":"125B","author":"Hsiung","year":"2004","journal-title":"American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics: the Official Publication of the International Society of Psychiatric Genetics"},{"issue":"7","key":"10.1016\/bs.adgen.2016.08.003_bib75","doi-asserted-by":"crossref","first-page":"673","DOI":"10.1016\/0028-3932(90)90122-5","article-title":"Immune and autoimmune diseases in dyslexic children","volume":"28","author":"Hugdahl","year":"1990","journal-title":"Neuropsychologia"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib76","doi-asserted-by":"crossref","first-page":"e35618","DOI":"10.1371\/journal.pone.0035618","article-title":"Exploring the transcriptome of ciliated cells using in silico dissection of human tissues","volume":"7","author":"Ivliev","year":"2012","journal-title":"PLoS One"},{"issue":"5","key":"10.1016\/bs.adgen.2016.08.003_bib77","doi-asserted-by":"crossref","first-page":"1287","DOI":"10.1086\/340449","article-title":"Evidence for linkage and association with reading disability on 6p21.3-22","volume":"70","author":"Kaplan","year":"2002","journal-title":"American Journal of Human Genetics"},{"issue":"8","key":"10.1016\/bs.adgen.2016.08.003_bib78","doi-asserted-by":"crossref","first-page":"2755","DOI":"10.1073\/pnas.83.8.2755","article-title":"The primate retina contains two types of ganglion cells, with high and low contrast sensitivity","volume":"83","author":"Kaplan","year":"1986","journal-title":"Proceedings of the National Academy of Sciences of the United States of America"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib79","doi-asserted-by":"crossref","first-page":"368","DOI":"10.1016\/j.lindif.2011.04.008","article-title":"A twin and adoption study of reading achievement: exploration of shared-environmental and gene-environment-interaction effects","volume":"21","author":"Kirkpatrick","year":"2011","journal-title":"Learning and Individual Differences"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib80","doi-asserted-by":"crossref","first-page":"55","DOI":"10.1046\/j.1440-169x.2002.00624.x","article-title":"Xenopus Brachyury regulates mesodermal expression of Zic3, a gene controlling left-right asymmetry","volume":"44","author":"Kitaguchi","year":"2002","journal-title":"Development, Growth & Differentiation"},{"issue":"6","key":"10.1016\/bs.adgen.2016.08.003_bib81","doi-asserted-by":"crossref","first-page":"639","DOI":"10.1038\/ng.2262","article-title":"Mutations in the chromatin modifier gene\u00a0KANSL1 cause the 17q21.31 microdeletion syndrome","volume":"44","author":"Koolen","year":"2012","journal-title":"Nature Genetics"},{"issue":"9","key":"10.1016\/bs.adgen.2016.08.003_bib82","doi-asserted-by":"crossref","first-page":"652","DOI":"10.1136\/jmg.2003.012294","article-title":"Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family","volume":"41","author":"de Kovel","year":"2004","journal-title":"Journal of Medical Genetics"},{"issue":"Spec No 2","key":"10.1016\/bs.adgen.2016.08.003_bib83","doi-asserted-by":"crossref","first-page":"R262","DOI":"10.1093\/hmg\/ddl205","article-title":"Usher syndrome: molecular links of pathogenesis, proteins and pathways","volume":"15","author":"Kremer","year":"2006","journal-title":"Human Molecular Genetics"},{"issue":"Suppl. 1","key":"10.1016\/bs.adgen.2016.08.003_bib84","doi-asserted-by":"crossref","first-page":"P56","DOI":"10.1186\/2046-2530-4-S1-P56","article-title":"X-box promoter motif searches: from C. elegans to humans to novel candidate ciliopathies","volume":"4","author":"Lauter","year":"2015","journal-title":"Cilia"},{"issue":"6","key":"10.1016\/bs.adgen.2016.08.003_bib85","doi-asserted-by":"crossref","first-page":"2129","DOI":"10.1158\/0008-5472.CAN-10-2684","article-title":"Cep63 recruits Cdk1 to the centrosome: implications for regulation of mitotic entry, centrosome amplification, and genome maintenance","volume":"71","author":"Loffler","year":"2011","journal-title":"Cancer Research"},{"issue":"2","key":"10.1016\/bs.adgen.2016.08.003_bib86","doi-asserted-by":"crossref","first-page":"149","DOI":"10.1038\/gim.2014.83","article-title":"Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature","volume":"17","author":"Lowther","year":"2014","journal-title":"Genetics in Medicine"},{"issue":"6","key":"10.1016\/bs.adgen.2016.08.003_bib87","doi-asserted-by":"crossref","first-page":"645","DOI":"10.1111\/gbb.12053","article-title":"A genome-wide association study for reading and language abilities in two population cohorts","volume":"12","author":"Luciano","year":"2013","journal-title":"Genes Brain and Behavior"},{"issue":"8","key":"10.1016\/bs.adgen.2016.08.003_bib88","doi-asserted-by":"crossref","first-page":"743","DOI":"10.1038\/mp.2009.28","article-title":"Supporting evidence for LRRTM1 imprinting effects in schizophrenia","volume":"14","author":"Ludwig","year":"2009","journal-title":"Molecular Psychiatry"},{"key":"10.1016\/bs.adgen.2016.08.003_bib89","doi-asserted-by":"crossref","first-page":"e229","DOI":"10.1038\/tp.2012.148","article-title":"A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults","volume":"3","author":"Ludwig","year":"2013","journal-title":"Translational Psychiatry"},{"issue":"6","key":"10.1016\/bs.adgen.2016.08.003_bib90","doi-asserted-by":"crossref","first-page":"577","DOI":"10.1002\/dev.21114","article-title":"Vertebrate whole-body-action asymmetries and the evolution of right handedness: a comparison between humans and marine mammals","volume":"55","author":"MacNeilage","year":"2013","journal-title":"Developmental Psychobiology"},{"key":"10.1016\/bs.adgen.2016.08.003_bib91","doi-asserted-by":"crossref","first-page":"1223","DOI":"10.1016\/j.cell.2012.02.039","article-title":"CNVs: harbingers of a rare variant revolution in psychiatric genetics","volume":"148","author":"Malhotra","year":"2012","journal-title":"Cell"},{"issue":"6","key":"10.1016\/bs.adgen.2016.08.003_bib92","doi-asserted-by":"crossref","first-page":"e20580","DOI":"10.1371\/journal.pone.0020580","article-title":"Increased expression of the dyslexia candidate gene DCDC2 affects length and signaling of primary cilia in neurons","volume":"6","author":"Massinen","year":"2011","journal-title":"PLoS One"},{"issue":"1373","key":"10.1016\/bs.adgen.2016.08.003_bib93","doi-asserted-by":"crossref","first-page":"961","DOI":"10.1098\/rspb.1996.0142","article-title":"Auditory temporal coding in dyslexia","volume":"263","author":"McAnally","year":"1996","journal-title":"Proceedings Biological Sciences"},{"issue":"7","key":"10.1016\/bs.adgen.2016.08.003_bib94","doi-asserted-by":"crossref","first-page":"729","DOI":"10.1038\/sj.mp.4002063","article-title":"Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children","volume":"13","author":"Meaburn","year":"2008","journal-title":"Molecular Psychiatry"},{"issue":"2","key":"10.1016\/bs.adgen.2016.08.003_bib95","doi-asserted-by":"crossref","first-page":"330","DOI":"10.1016\/j.neuropsychologia.2008.09.005","article-title":"Genetic influences on handedness: data from 25,732 Australian and Dutch twin families","volume":"47","author":"Medland","year":"2009","journal-title":"Neuropsychologia"},{"issue":"6","key":"10.1016\/bs.adgen.2016.08.003_bib96","doi-asserted-by":"crossref","first-page":"637","DOI":"10.1002\/dev.21150","article-title":"On the origins of human handedness and language: a comparative review of hand preferences for bimanual coordinated actions and gestural communication in nonhuman primates","volume":"55","author":"Meguerditchian","year":"2013","journal-title":"Developmental Psychobiology"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib97","doi-asserted-by":"crossref","first-page":"58","DOI":"10.1007\/s10519-010-9408-3","article-title":"A dyslexia-associated variant in DCDC2 changes gene expression","volume":"41","author":"Meng","year":"2011","journal-title":"Behavior Genetics"},{"issue":"47","key":"10.1016\/bs.adgen.2016.08.003_bib98","doi-asserted-by":"crossref","first-page":"17053","DOI":"10.1073\/pnas.0508591102","article-title":"DCDC2 is associated with reading disability and modulates neuronal development in the brain","volume":"102","author":"Meng","year":"2005","journal-title":"Proceedings of the National Academy of Sciences of the United States of America"},{"issue":"13","key":"10.1016\/bs.adgen.2016.08.003_bib99","doi-asserted-by":"crossref","first-page":"2497","DOI":"10.1242\/dev.02413","article-title":"Nodal specifies embryonic visceral endoderm and sustains pluripotent cells in the epiblast before overt axial patterning","volume":"133","author":"Mesnard","year":"2006","journal-title":"Development"},{"issue":"5","key":"10.1016\/bs.adgen.2016.08.003_bib100","doi-asserted-by":"crossref","first-page":"468","DOI":"10.1177\/1073858414543151","article-title":"Cilia: traffic directors along the road of cortical development","volume":"20","author":"Metin","year":"2014","journal-title":"Neuroscientist"},{"key":"10.1016\/bs.adgen.2016.08.003_bib101","doi-asserted-by":"crossref","first-page":"7889","DOI":"10.1038\/ncomms8889","article-title":"An epigenetic regulator emerges as microtubule minus-end binding and stabilizing factor in mitosis","volume":"6","author":"Meunier","year":"2015","journal-title":"Nature Communications"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib102","doi-asserted-by":"crossref","first-page":"69","DOI":"10.1006\/geno.2000.6239","article-title":"Chromosomal location and genomic structure of the human translin-associated factor X gene (TRAX; TSNAX) revealed by intergenic splicing to DISC1, a gene disrupted by a translocation segregating with schizophrenia","volume":"67","author":"Millar","year":"2000","journal-title":"Genomics"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib103","doi-asserted-by":"crossref","first-page":"1195","DOI":"10.1016\/j.bbrc.2004.03.163","article-title":"DISC1 localizes to the centrosome by binding to kendrin","volume":"317","author":"Miyoshi","year":"2004","journal-title":"Biochemical and Biophysical Research Communications"},{"issue":"8","key":"10.1016\/bs.adgen.2016.08.003_bib104","doi-asserted-by":"crossref","first-page":"1955","DOI":"10.1002\/dvdy.21493","article-title":"The primary cilium as a gravitational force transducer and a regulator of transcriptional noise","volume":"237","author":"Moorman","year":"2008","journal-title":"Developmental Dynamics"},{"issue":"1\u20132","key":"10.1016\/bs.adgen.2016.08.003_bib105","doi-asserted-by":"crossref","first-page":"332","DOI":"10.1016\/j.cell.2013.11.043","article-title":"The architecture of parent-of-origin effects in mice","volume":"156","author":"Mott","year":"2014","journal-title":"Cell"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib106","doi-asserted-by":"crossref","first-page":"379","DOI":"10.1016\/j.devcel.2015.08.008","article-title":"A phosphoinositide code for primary cilia","volume":"34","author":"Nakatsu","year":"2015","journal-title":"Developmental Cell"},{"issue":"7397","key":"10.1016\/bs.adgen.2016.08.003_bib107","doi-asserted-by":"crossref","first-page":"242","DOI":"10.1038\/nature11011","article-title":"Patterns and rates of exonic de novo mutations in autism spectrum disorders","volume":"485","author":"Neale","year":"2012","journal-title":"Nature"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib108","doi-asserted-by":"crossref","first-page":"361","DOI":"10.1038\/ejhg.2012.166","article-title":"Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder","volume":"21","author":"Newbury","year":"2013","journal-title":"European Journal of Human Genetics"},{"issue":"2","key":"10.1016\/bs.adgen.2016.08.003_bib109","doi-asserted-by":"crossref","first-page":"285","DOI":"10.3390\/genes5020285","article-title":"Reading and language disorders: the importance of both quantity and quality","volume":"5","author":"Newbury","year":"2014","journal-title":"Genes"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib110","doi-asserted-by":"crossref","first-page":"90","DOI":"10.1007\/s10519-010-9424-3","article-title":"Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects","volume":"41","author":"Newbury","year":"2011","journal-title":"Behavior Genetics"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib111","doi-asserted-by":"crossref","first-page":"e1000888","DOI":"10.1371\/journal.pgen.1000888","article-title":"Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS","volume":"6","author":"Nicolae","year":"2010","journal-title":"PLoS Genetics"},{"issue":"10","key":"10.1016\/bs.adgen.2016.08.003_bib112","doi-asserted-by":"crossref","first-page":"658","DOI":"10.1136\/jmg.38.10.658","article-title":"A dominant gene for developmental dyslexia on chromosome 3","volume":"38","author":"Nopola-Hemmi","year":"2001","journal-title":"Journal of Medical Genetics"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib113","doi-asserted-by":"crossref","first-page":"418","DOI":"10.1111\/gbb.12127","article-title":"Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment","volume":"13","author":"Nudel","year":"2014","journal-title":"Genes Brain and Behavior"},{"issue":"6","key":"10.1016\/bs.adgen.2016.08.003_bib114","doi-asserted-by":"crossref","first-page":"585","DOI":"10.1038\/ng.835","article-title":"Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations","volume":"43","author":"O'Roak","year":"2011","journal-title":"Nature Genetics"},{"issue":"7397","key":"10.1016\/bs.adgen.2016.08.003_bib115","doi-asserted-by":"crossref","first-page":"246","DOI":"10.1038\/nature10989","article-title":"Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations","volume":"485","author":"O'Roak","year":"2012","journal-title":"Nature"},{"issue":"1\u20132","key":"10.1016\/bs.adgen.2016.08.003_bib116","doi-asserted-by":"crossref","first-page":"55","DOI":"10.1016\/S0925-4773(00)00331-2","article-title":"Involvement of fibroblast growth factor (FGF)18-FGF8 signaling in specification of left-right asymmetry and\u00a0brain and limb development of the chick embryo","volume":"95","author":"Ohuchi","year":"2000","journal-title":"Mechanisms of Development"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib117","doi-asserted-by":"crossref","first-page":"97","DOI":"10.1016\/0028-3932(71)90067-4","article-title":"The assessment and analysis of handedness: the Edinburgh inventory","volume":"9","author":"Oldfield","year":"1971","journal-title":"Neuropsychologia"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib118","doi-asserted-by":"crossref","first-page":"320","DOI":"10.1016\/j.biopsych.2010.02.002","article-title":"Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia","volume":"68","author":"Pagnamenta","year":"2010","journal-title":"Biological Psychiatry"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib119","doi-asserted-by":"crossref","first-page":"365","DOI":"10.1007\/s11689-011-9091-6","article-title":"Dissection of genetic associations with language-related traits in population-based cohorts","volume":"3","author":"Paracchini","year":"2011","journal-title":"Journal of Neurodevelopmental Disorders"},{"key":"10.1016\/bs.adgen.2016.08.003_bib120","doi-asserted-by":"crossref","first-page":"57","DOI":"10.1146\/annurev.genom.8.080706.092312","article-title":"The genetic lexicon of dyslexia","volume":"8","author":"Paracchini","year":"2007","journal-title":"Annual Review of Genomics and Human Genetics"},{"issue":"12","key":"10.1016\/bs.adgen.2016.08.003_bib121","doi-asserted-by":"crossref","first-page":"1576","DOI":"10.1176\/appi.ajp.2008.07121872","article-title":"Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population","volume":"165","author":"Paracchini","year":"2008","journal-title":"The American Journal of Psychiatry"},{"issue":"10","key":"10.1016\/bs.adgen.2016.08.003_bib122","doi-asserted-by":"crossref","first-page":"1659","DOI":"10.1093\/hmg\/ddl089","article-title":"The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration","volume":"15","author":"Paracchini","year":"2006","journal-title":"Human Molecular Genetics"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib123","doi-asserted-by":"crossref","first-page":"189","DOI":"10.1016\/j.clch.2005.09.007","article-title":"Comorbidity of dyslexia, dyspraxia, attention deficit disorder (ADD), attention deficit hyperactive disorder (ADHD), obsessive compulsive disorder (OCD) and Tourette\u2019s syndrome in children: a prospective epidemiological study","volume":"8","author":"Pauc","year":"2005","journal-title":"Clinical Chiropractic"},{"issue":"7520","key":"10.1016\/bs.adgen.2016.08.003_bib124","doi-asserted-by":"crossref","first-page":"92","DOI":"10.1038\/nature13545","article-title":"Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche","volume":"514","author":"Perry","year":"2014","journal-title":"Nature"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib125","doi-asserted-by":"crossref","first-page":"369","DOI":"10.1111\/gbb.12213","article-title":"Lack of replication for the myosin-18B association with mathematical ability in independent cohorts","volume":"14","author":"Pettigrew","year":"2015","journal-title":"Genes Brain and Behavior"},{"key":"10.1016\/bs.adgen.2016.08.003_bib126","doi-asserted-by":"crossref","DOI":"10.1186\/s11689-016-9157-6","article-title":"Replication analysis for a parent-of-origin effect on language-related phenotypes at the NOP9 locus","author":"Pettigrew","year":"2016","journal-title":"Journal of Neurodevelopmental Disorders, 8, 24"},{"issue":"8","key":"10.1016\/bs.adgen.2016.08.003_bib127","doi-asserted-by":"crossref","first-page":"e0134997","DOI":"10.1371\/journal.pone.0134997","article-title":"Copy number variation screen identifies a rare de novo deletion at chromosome 15q13.1-13.3 in a child with language impairment","volume":"10","author":"Pettigrew","year":"2015","journal-title":"PLoS One"},{"key":"10.1016\/bs.adgen.2016.08.003_bib128","doi-asserted-by":"crossref","first-page":"368","DOI":"10.1038\/nature09146","article-title":"Functional impact of global rare copy number variation in autism spectrum disorders","volume":"466","author":"Pinto","year":"2010","journal-title":"Nature"},{"key":"10.1016\/bs.adgen.2016.08.003_bib129","doi-asserted-by":"crossref","first-page":"137","DOI":"10.1016\/S0091-679X(08)94007-3","volume":"94","author":"Plotnikova","year":"2009","journal-title":"Primary Cilia and the Cell Cycle"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib130","doi-asserted-by":"crossref","first-page":"365","DOI":"10.1038\/mp.2010.105","article-title":"A theoretical molecular network for dyslexia: integrating available genetic findings","volume":"16","author":"Poelmans","year":"2011","journal-title":"Molecular Psychiatry"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib131","doi-asserted-by":"crossref","first-page":"140","DOI":"10.1002\/ajmg.b.30787","article-title":"Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion","volume":"150B","author":"Poelmans","year":"2009","journal-title":"American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics"},{"issue":"8864","key":"10.1016\/bs.adgen.2016.08.003_bib132","doi-asserted-by":"crossref","first-page":"178","DOI":"10.1016\/0140-6736(93)91384-X","article-title":"Suggestive linkage of developmental dyslexia to chromosome 1p34-p36","volume":"342","author":"Rabin","year":"1993","journal-title":"Lancet"},{"issue":"Pt 4","key":"10.1016\/bs.adgen.2016.08.003_bib133","doi-asserted-by":"crossref","first-page":"841","DOI":"10.1093\/brain\/awg076","article-title":"Theories of developmental dyslexia: insights from a multiple case study of dyslexic adults","volume":"126","author":"Ramus","year":"2003","journal-title":"Brain"},{"key":"10.1016\/bs.adgen.2016.08.003_bib134","doi-asserted-by":"crossref","DOI":"10.7554\/eLife.02104","article-title":"Mof-associated complexes have overlapping and unique roles in regulating pluripotency in embryonic stem cells and during differentiation","volume":"3","author":"Ravens","year":"2014","journal-title":"eLife"},{"key":"10.1016\/bs.adgen.2016.08.003_bib135","doi-asserted-by":"crossref","first-page":"283","DOI":"10.1196\/annals.1325.027","article-title":"Yellow filters can improve magnocellular function: motion sensitivity, convergence, accommodation, and reading","volume":"1039","author":"Ray","year":"2005","journal-title":"Annals of the New York Academy of Sciences"},{"issue":"9","key":"10.1016\/bs.adgen.2016.08.003_bib136","doi-asserted-by":"crossref","first-page":"502","DOI":"10.1016\/S0168-9525(01)02410-6","article-title":"On the allelic spectrum of human disease","volume":"17","author":"Reich","year":"2001","journal-title":"Trends in Genetics"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib137","doi-asserted-by":"crossref","first-page":"264","DOI":"10.1007\/s11689-009-9031-x","article-title":"Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment","volume":"1","author":"Rice","year":"2009","journal-title":"Journal of Neurodevelopmental Disorders"},{"issue":"5281","key":"10.1016\/bs.adgen.2016.08.003_bib138","doi-asserted-by":"crossref","first-page":"1516","DOI":"10.1126\/science.273.5281.1516","article-title":"The future of genetic studies of complex human diseases","volume":"273","author":"Risch","year":"1996","journal-title":"Science"},{"key":"10.1016\/bs.adgen.2016.08.003_bib139","doi-asserted-by":"crossref","first-page":"205","DOI":"10.1016\/j.neuropsychologia.2016.02.020","article-title":"The PCSK6 gene is associated with handedness, the autism spectrum, and magical ideation in a non-clinical population","volume":"84","author":"Robinson","year":"2016","journal-title":"Neuropsychologia"},{"issue":"2","key":"10.1016\/bs.adgen.2016.08.003_bib140","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1038\/ejhg.2013.100","article-title":"Shining a light on CNTNAP2: complex functions to complex disorders","volume":"22","author":"Rodenas-Cuadrado","year":"2014","journal-title":"European Journal of Human Genetics"},{"issue":"6","key":"10.1016\/bs.adgen.2016.08.003_bib141","doi-asserted-by":"crossref","first-page":"555","DOI":"10.1002\/dvg.22741","article-title":"Asymmetry of brain and behavior in animals: its development, function, and human relevance","volume":"52","author":"Rogers","year":"2014","journal-title":"Genesis"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib142","doi-asserted-by":"crossref","first-page":"541","DOI":"10.1016\/j.ceb.2010.03.010","article-title":"The ciliary membrane","volume":"22","author":"Rohatgi","year":"2010","journal-title":"Current Opinion in Cell Biology"},{"key":"10.1016\/bs.adgen.2016.08.003_bib143","doi-asserted-by":"crossref","first-page":"377","DOI":"10.1146\/annurev.physiol.69.040705.141236","article-title":"Overview of structure and function of mammalian cilia","volume":"69","author":"Satir","year":"2007","journal-title":"Annual Review of Physiology"},{"issue":"3","key":"10.1016\/bs.adgen.2016.08.003_bib144","doi-asserted-by":"crossref","first-page":"608","DOI":"10.1093\/hmg\/ddq475","article-title":"PCSK6 is associated with handedness in individuals with dyslexia","volume":"20","author":"Scerri","year":"2011","journal-title":"Human Molecular Genetics"},{"issue":"3","key":"10.1016\/bs.adgen.2016.08.003_bib145","doi-asserted-by":"crossref","first-page":"237","DOI":"10.1016\/j.biopsych.2011.02.005","article-title":"DCDC2, KIAA0319 and CMIP are associated with reading-related traits","volume":"70","author":"Scerri","year":"2011","journal-title":"Biological Psychiatry"},{"issue":"3","key":"10.1016\/bs.adgen.2016.08.003_bib146","doi-asserted-by":"crossref","first-page":"179","DOI":"10.1007\/s00787-009-0081-0","article-title":"Genetics of developmental dyslexia","volume":"19","author":"Scerri","year":"2010","journal-title":"European Child & Adolescent Psychiatry"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib147","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1016\/j.ajhg.2014.12.002","article-title":"DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling","volume":"96","author":"Schueler","year":"2015","journal-title":"American Journal of Human Genetics"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib148","doi-asserted-by":"crossref","first-page":"279","DOI":"10.1086\/301919","article-title":"Evidence for linkage of spelling disability to chromosome 15","volume":"63","author":"Schulte-Korne","year":"1998","journal-title":"American Journal of Human Genetics"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib149","doi-asserted-by":"crossref","first-page":"52","DOI":"10.1086\/498992","article-title":"Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia","volume":"78","author":"Schumacher","year":"2006","journal-title":"American Journal of Human Genetics"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib150","doi-asserted-by":"crossref","first-page":"1051","DOI":"10.1016\/j.bbrc.2008.10.100","article-title":"DISC1-kendrin interaction is involved in centrosomal microtubule network formation","volume":"377","author":"Shimizu","year":"2008","journal-title":"Biochemical and Biophysical Research Communications"},{"issue":"9","key":"10.1016\/bs.adgen.2016.08.003_bib151","doi-asserted-by":"crossref","first-page":"1771","DOI":"10.1093\/hmg\/ddw047","article-title":"The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts","volume":"25","author":"Shore","year":"2016","journal-title":"Human Molecular Genetics"},{"issue":"10","key":"10.1016\/bs.adgen.2016.08.003_bib152","doi-asserted-by":"crossref","first-page":"1370","DOI":"10.1038\/ejhg.2014.296","article-title":"Genome-wide analysis identifies a role for common copy number variants in specific language impairment","volume":"23","author":"Simpson","year":"2015","journal-title":"European Journal of Human Genetics"},{"issue":"11","key":"10.1016\/bs.adgen.2016.08.003_bib153","doi-asserted-by":"crossref","first-page":"1147","DOI":"10.1038\/ng.971","article-title":"A primary microcephaly protein complex forms a ring around parental centrioles","volume":"43","author":"Sir","year":"2011","journal-title":"Nature Genetics"},{"issue":"3","key":"10.1016\/bs.adgen.2016.08.003_bib154","doi-asserted-by":"crossref","first-page":"278","DOI":"10.1038\/ncb1835","article-title":"An ATM- and ATR-dependent checkpoint inactivates spindle assembly by targeting CEP63","volume":"11","author":"Smith","year":"2009","journal-title":"Nature Cell Biology"},{"issue":"3","key":"10.1016\/bs.adgen.2016.08.003_bib155","doi-asserted-by":"crossref","first-page":"119","DOI":"10.4161\/19490992.2014.956593","article-title":"Organized chaos in Kupffer's vesicle: how a heterogeneous structure achieves consistent left-right patterning","volume":"4","author":"Smith","year":"2014","journal-title":"Bioarchitecture"},{"issue":"2","key":"10.1016\/bs.adgen.2016.08.003_bib156","doi-asserted-by":"crossref","first-page":"219","DOI":"10.1007\/BF00309831","article-title":"Phonemic deficits in developmental dyslexia","volume":"43","author":"Snowling","year":"1981","journal-title":"Psychological Research"},{"issue":"6","key":"10.1016\/bs.adgen.2016.08.003_bib157","doi-asserted-by":"crossref","first-page":"609","DOI":"10.1111\/j.1469-7610.2006.01725.x","article-title":"Children at family risk of dyslexia: a follow-up in early adolescence","volume":"48","author":"Snowling","year":"2007","journal-title":"Journal of Child Psychology and Psychiatry"},{"key":"10.1016\/bs.adgen.2016.08.003_bib158","doi-asserted-by":"crossref","first-page":"4831","DOI":"10.1038\/ncomms5831","article-title":"Common variation near ROBO2 is associated with expressive vocabulary in infancy","volume":"5","author":"St Pourcain","year":"2014","journal-title":"Nature Communications"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib159","doi-asserted-by":"crossref","first-page":"579","DOI":"10.1111\/j.1469-7610.1994.tb01208.x","article-title":"Annotation: does dyslexia exist?","volume":"35","author":"Stanovich","year":"1994","journal-title":"Journal of Child Psychology and Psychiatry"},{"issue":"7483","key":"10.1016\/bs.adgen.2016.08.003_bib160","doi-asserted-by":"crossref","first-page":"361","DOI":"10.1038\/nature12818","article-title":"CNVs conferring risk of autism or schizophrenia affect cognition in controls","volume":"505","author":"Stefansson","year":"2014","journal-title":"Nature"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib161","doi-asserted-by":"crossref","first-page":"147","DOI":"10.1016\/S0166-2236(96)01005-3","article-title":"To see but not to read; the magnocellular theory of dyslexia","volume":"20","author":"Stein","year":"1997","journal-title":"Trends in Neurosciences"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib162","doi-asserted-by":"crossref","first-page":"293","DOI":"10.1016\/j.ijdevneu.2012.01.009","article-title":"Neocortical disruption and behavioral impairments in rats following in utero RNAi of candidate dyslexia risk gene Kiaa0319","volume":"30","author":"Szalkowski","year":"2012","journal-title":"International Journal of Developmental Neuroscience"},{"issue":"20","key":"10.1016\/bs.adgen.2016.08.003_bib163","doi-asserted-by":"crossref","first-page":"11553","DOI":"10.1073\/pnas.1833911100","article-title":"A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain","volume":"100","author":"Taipale","year":"2003","journal-title":"Proceedings of the National Academy of Sciences of the United States of America"},{"issue":"5390","key":"10.1016\/bs.adgen.2016.08.003_bib164","doi-asserted-by":"crossref","first-page":"468","DOI":"10.1038\/241468a0","article-title":"Defects of non-verbal auditory perception in children with developmental aphasia","volume":"241","author":"Tallal","year":"1973","journal-title":"Nature"},{"issue":"7","key":"10.1016\/bs.adgen.2016.08.003_bib165","doi-asserted-by":"crossref","first-page":"480","DOI":"10.1136\/jmg.2008.065391","article-title":"Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndrome","volume":"46","author":"Tan","year":"2009","journal-title":"Journal of Medical Genetics"},{"issue":"9","key":"10.1016\/bs.adgen.2016.08.003_bib166","doi-asserted-by":"crossref","first-page":"995","DOI":"10.1038\/ng.2707","article-title":"DYX1C1 is required for axonemal dynein assembly and ciliary motility","volume":"45","author":"Tarkar","year":"2013","journal-title":"Nature Genetics"},{"issue":"7","key":"10.1016\/bs.adgen.2016.08.003_bib167","doi-asserted-by":"crossref","first-page":"784","DOI":"10.1038\/mp.2013.106","article-title":"Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations","volume":"19","author":"Toma","year":"2014","journal-title":"Molecular Psychiatry"},{"issue":"8","key":"10.1016\/bs.adgen.2016.08.003_bib168","doi-asserted-by":"crossref","first-page":"802","DOI":"10.1111\/gbb.12170","article-title":"Mutation of Dcdc2 in mice leads to impairments in auditory processing and memory ability","volume":"13","author":"Truong","year":"2014","journal-title":"Genes Brain and Behavior"},{"issue":"14","key":"10.1016\/bs.adgen.2016.08.003_bib169","doi-asserted-by":"crossref","first-page":"3052","DOI":"10.1002\/jnr.21763","article-title":"Dock4 regulates dendritic development in hippocampal neurons","volume":"86","author":"Ueda","year":"2008","journal-title":"Journal of Neuroscience Research"},{"key":"10.1016\/bs.adgen.2016.08.003_bib170","doi-asserted-by":"crossref","first-page":"15038","DOI":"10.1038\/hgv.2015.38","article-title":"A novel KCNQ4 mutation and a private IMMP2L-DOCK4 duplication segregating with nonsyndromic hearing loss in a Brazilian family","volume":"2","author":"Uehara","year":"2015","journal-title":"Human Genome Variation"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib171","doi-asserted-by":"crossref","first-page":"36","DOI":"10.1016\/j.ydbio.2012.02.004","article-title":"Multiple Slits regulate the development of midline glial populations and the corpus callosum","volume":"365","author":"Unni","year":"2012","journal-title":"Developmental Biology"},{"issue":"12","key":"10.1016\/bs.adgen.2016.08.003_bib172","doi-asserted-by":"crossref","first-page":"987","DOI":"10.1038\/sj.ejhg.5201264","article-title":"Phenotypic variability in Angelman syndrome: comparison among different deletion classes and between deletion and UPD subjects","volume":"12","author":"Varela","year":"2004","journal-title":"European Journal of Human Genetics"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib173","doi-asserted-by":"crossref","first-page":"47","DOI":"10.1111\/j.1399-0004.2005.00377.x","article-title":"Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patients","volume":"67","author":"Varela","year":"2005","journal-title":"Clinical Genetics"},{"issue":"8","key":"10.1016\/bs.adgen.2016.08.003_bib174","doi-asserted-by":"crossref","first-page":"539","DOI":"10.1038\/jhg.2013.47","article-title":"Family-based genome-wide copy number scan identifies five new genes of dyslexia involved in dendritic spinal plasticity","volume":"58","author":"Veerappa","year":"2013","journal-title":"Journal of Human Genetics"},{"issue":"8","key":"10.1016\/bs.adgen.2016.08.003_bib175","doi-asserted-by":"crossref","first-page":"889","DOI":"10.1002\/ajmg.b.32199","article-title":"Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexia","volume":"162B","author":"Veerappa","year":"2013","journal-title":"American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics"},{"issue":"7","key":"10.1016\/bs.adgen.2016.08.003_bib176","doi-asserted-by":"crossref","first-page":"572","DOI":"10.1002\/ajmg.b.32260","article-title":"Family based genome-wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics","volume":"165B","author":"Veerappa","year":"2014","journal-title":"American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics"},{"issue":"6","key":"10.1016\/bs.adgen.2016.08.003_bib177","doi-asserted-by":"crossref","first-page":"859","DOI":"10.1093\/hmg\/ddm358","article-title":"The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms","volume":"17","author":"Velayos-Baeza","year":"2008","journal-title":"Human Molecular Genetics"},{"issue":"11","key":"10.1016\/bs.adgen.2016.08.003_bib178","doi-asserted-by":"crossref","first-page":"2609","DOI":"10.1002\/ajmg.a.34325","article-title":"Whole-exome sequencing detects somatic mutations of IDH1 in metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria (MC-HGA)","volume":"155A","author":"Vissers","year":"2011","journal-title":"American Journal of Medicinal Genetics Part A"},{"issue":"2","key":"10.1016\/bs.adgen.2016.08.003_bib179","doi-asserted-by":"crossref","first-page":"515","DOI":"10.1016\/j.neuroscience.2006.08.022","article-title":"DYX1C1 functions in neuronal migration in developing neocortex","volume":"143","author":"Wang","year":"2006","journal-title":"Neuroscience"},{"issue":"7145","key":"10.1016\/bs.adgen.2016.08.003_bib180","doi-asserted-by":"crossref","first-page":"661","DOI":"10.1038\/nature05911","article-title":"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls","volume":"447","author":"Wellcome Trust Case Control","year":"2007","journal-title":"Nature"},{"issue":"48","key":"10.1016\/bs.adgen.2016.08.003_bib181","doi-asserted-by":"crossref","first-page":"12887","DOI":"10.1523\/JNEUROSCI.2084-08.2008","article-title":"A crucial role for primary cilia in cortical morphogenesis","volume":"28","author":"Willaredt","year":"2008","journal-title":"The Journal of Neuroscience"},{"issue":"3","key":"10.1016\/bs.adgen.2016.08.003_bib182","doi-asserted-by":"crossref","first-page":"e14772","DOI":"10.1371\/journal.pone.0014772","article-title":"Visual perceptual difficulties and under-achievement at school in a large community-based sample of children","volume":"6","author":"Williams","year":"2011","journal-title":"PLoS One"},{"issue":"4","key":"10.1016\/bs.adgen.2016.08.003_bib183","doi-asserted-by":"crossref","first-page":"322","DOI":"10.1177\/002221940003300404","article-title":"Naming-speed processes and developmental reading disabilities: an introduction to the special issue on the double-deficit hypothesis","volume":"33","author":"Wolf","year":"2000","journal-title":"Journal of Learning Disabilities"},{"issue":"1","key":"10.1016\/bs.adgen.2016.08.003_bib184","doi-asserted-by":"crossref","first-page":"29","DOI":"10.1186\/1866-1955-5-29","article-title":"Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech","volume":"5","author":"Worthey","year":"2013","journal-title":"Journal of Neurodevelopmental Disorder"},{"issue":"3","key":"10.1016\/bs.adgen.2016.08.003_bib185","doi-asserted-by":"crossref","first-page":"755","DOI":"10.1016\/j.jmb.2006.01.017","article-title":"An isoform of GTPase regulator DOCK4 localizes to the stereocilia in the inner ear and binds to harmonin (USH1C)","volume":"357","author":"Yan","year":"2006","journal-title":"Journal of Molecular Biology"},{"issue":"2","key":"10.1016\/bs.adgen.2016.08.003_bib186","doi-asserted-by":"crossref","first-page":"259","DOI":"10.1016\/j.neuron.2012.11.002","article-title":"Using whole-exome sequencing to identify inherited causes of autism","volume":"77","author":"Yu","year":"2013","journal-title":"Neuron"},{"issue":"3","key":"10.1016\/bs.adgen.2016.08.003_bib187","doi-asserted-by":"crossref","first-page":"717","DOI":"10.1086\/367774","article-title":"The genetic legacy of the Mongols","volume":"72","author":"Zerjal","year":"2003","journal-title":"American Journal of Human Genetics"},{"key":"10.1016\/bs.adgen.2016.08.003_bib188","doi-asserted-by":"crossref","first-page":"51","DOI":"10.1016\/j.cortex.2015.12.004","article-title":"Altered hemispheric lateralization of white matter pathways in developmental dyslexia: evidence from spherical deconvolution tractography","volume":"76","author":"Zhao","year":"2016","journal-title":"Cortex"}],"container-title":["Advances in Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0065266016300542?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0065266016300542?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,24]],"date-time":"2025-09-24T19:47:56Z","timestamp":1758743276000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0065266016300542"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016]]},"ISBN":["9780128096727"],"references-count":188,"URL":"https:\/\/doi.org\/10.1016\/bs.adgen.2016.08.003","relation":{},"ISSN":["0065-2660"],"issn-type":[{"value":"0065-2660","type":"print"}],"subject":[],"published":{"date-parts":[[2016]]}}}