{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,13]],"date-time":"2026-01-13T04:14:22Z","timestamp":1768277662405,"version":"3.49.0"},"reference-count":49,"publisher":"Springer Science and Business Media LLC","issue":"5","license":[{"start":{"date-parts":[[2013,9,11]],"date-time":"2013-09-11T00:00:00Z","timestamp":1378857600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Eur J Hum Genet"],"published-print":{"date-parts":[[2014,5]]},"DOI":"10.1038\/ejhg.2013.199","type":"journal-article","created":{"date-parts":[[2013,9,11]],"date-time":"2013-09-11T10:19:27Z","timestamp":1378894767000},"page":"675-680","source":"Crossref","is-referenced-by-count":57,"title":["Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort"],"prefix":"10.1038","volume":"22","author":[{"given":"Jessica","family":"Becker","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Darina","family":"Czamara","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tom S","family":"Scerri","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Franck","family":"Ramus","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Val\u00e9ria","family":"Cs\u00e9pe","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Joel B","family":"Talcott","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"John","family":"Stein","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Andrew","family":"Morris","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kerstin U","family":"Ludwig","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-6573-983X","authenticated-orcid":false,"given":"Per","family":"Hoffmann","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ferenc","family":"Honbolyg\u00f3","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D\u00e9nes","family":"T\u00f3th","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fabien","family":"Fauchereau","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Caroline","family":"Bogliotti","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"St\u00e9phanie","family":"Iannuzzi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yves","family":"Chaix","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sylviane","family":"Valdois","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Catherine","family":"Billard","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Florence","family":"George","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Isabelle","family":"Soares-Boucaud","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Christophe-Lo\u00efc","family":"G\u00e9rard","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sanne","family":"van der Mark","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Enrico","family":"Schulz","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anniek","family":"Vaessen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Urs","family":"Maurer","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kaisa","family":"Lohvansuu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Heikki","family":"Lyytinen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Marco","family":"Zucchelli","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Daniel","family":"Brandeis","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Leo","family":"Blomert","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Paavo HT","family":"Lepp\u00e4nen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jennifer","family":"Bruder","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anthony P","family":"Monaco","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Bertram","family":"M\u00fcller-Myhsok","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Juha","family":"Kere","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Karin","family":"Landerl","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Markus M","family":"N\u00f6then","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Gerd","family":"Schulte-K\u00f6rne","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Silvia","family":"Paracchini","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Myriam","family":"Peyrard-Janvid","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Johannes","family":"Schumacher","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2013,9,11]]},"reference":[{"key":"BFejhg2013199_CR1","doi-asserted-by":"publisher","first-page":"1081","DOI":"10.4065\/76.11.1081","volume":"76","author":"SK Katusic","year":"2001","unstructured":"Katusic SK, Colligan RC, Barbaresi WJ, Schaid DJ, Jacobsen SJ : Incidence of reading disability in a population-based birth cohort, 1976-1982, Rochester, Minn. Mayo Clin Proc 2001; 76: 1081\u20131092.","journal-title":"Mayo Clin Proc"},{"key":"BFejhg2013199_CR2","doi-asserted-by":"publisher","first-page":"998","DOI":"10.1001\/jama.1990.03450080084036","volume":"264","author":"SE Shaywitz","year":"1990","unstructured":"Shaywitz SE, Shaywitz BA, Fletcher JM, Escobar MD : Prevalence of reading disability in boys and girls. Results of the Connecticut Longitudinal Study. JAMA 1990; 264: 998\u20131002.","journal-title":"JAMA"},{"key":"BFejhg2013199_CR3","doi-asserted-by":"publisher","first-page":"1351","DOI":"10.1542\/peds.104.6.1351","volume":"104","author":"SE Shaywitz","year":"1999","unstructured":"Shaywitz SE, Fletcher JM, Holahan JM et al: Persistence of dyslexia: the Connecticut Longitudinal Study at adolescence. Pediatrics 1999; 104: 1351\u20131359.","journal-title":"Pediatrics"},{"key":"BFejhg2013199_CR4","unstructured":"ICD-10-GM Version 2008: Internationale statistische Klassifikation der Krankheiten und verwandter Gesundheitsprobleme, 10; Revision - German Modification -; Kapitel V: 192."},{"key":"BFejhg2013199_CR5","unstructured":"American Psychiatric Association: Diagnostic and Statistical Manual of Mental Disorders. Washington, DC: American Psychiatric Association, 2000 4th edn. Text Revision, pp 51-52."},{"key":"BFejhg2013199_CR6","doi-asserted-by":"publisher","first-page":"767","DOI":"10.1038\/nrn936","volume":"3","author":"SE Fisher","year":"2002","unstructured":"Fisher SE, DeFries JC : Developmental dyslexia: genetic dissection of a complex cognitive trait. Nat Rev Neurosci 2002; 3: 767\u2013780.","journal-title":"Nat Rev Neurosci"},{"key":"BFejhg2013199_CR7","doi-asserted-by":"publisher","first-page":"66","DOI":"10.1111\/j.1601-183X.2006.00232.x","volume":"6","author":"JG Barry","year":"2007","unstructured":"Barry JG, Yasin I, Bishop DV : Heritable risk factors associated with language impairments. Genes Brain Behav 2007; 6: 66\u201376.","journal-title":"Genes Brain Behav"},{"key":"BFejhg2013199_CR8","doi-asserted-by":"publisher","first-page":"681","DOI":"10.1038\/sj.ejhg.5201575","volume":"14","author":"J Williams","year":"2006","unstructured":"Williams J, O'Donovan MC : The genetics of developmental dyslexia. Eur J Hum Genet 2006; 14: 681\u2013689.","journal-title":"Eur J Hum Genet"},{"key":"BFejhg2013199_CR9","doi-asserted-by":"publisher","first-page":"289","DOI":"10.1136\/jmg.2006.046516","volume":"44","author":"J Schumacher","year":"2007","unstructured":"Schumacher J, Hoffmann P, Schmal C, Schulte-K\u00f6rne G, N\u00f6then MM : Genetics of dyslexia: the evolving landscape. J Med Genet 2007; 44: 289\u2013297.","journal-title":"J Med Genet"},{"key":"BFejhg2013199_CR10","doi-asserted-by":"publisher","first-page":"179","DOI":"10.1007\/s00787-009-0081-0","volume":"19","author":"TS Scerri","year":"2009","unstructured":"Scerri TS, Schulte-K\u00f6rne G : Genetics of developmental dyslexia. Eur Child Adolesc Psychiatry 2009; 19: 179\u2013197.","journal-title":"Eur Child Adolesc Psychiatry"},{"key":"BFejhg2013199_CR11","doi-asserted-by":"publisher","first-page":"11553","DOI":"10.1073\/pnas.1833911100","volume":"100","author":"M Taipale","year":"2003","unstructured":"Taipale M, Kaminen N, Nopola-Hemmi J et al: A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain. Proc Natl Acad Sci USA 2003; 100: 11553\u201311558.","journal-title":"Proc Natl Acad Sci USA"},{"key":"BFejhg2013199_CR12","doi-asserted-by":"publisher","first-page":"640","DOI":"10.1111\/j.1601-183X.2006.00291.x","volume":"6","author":"C Marino","year":"2007","unstructured":"Marino C, Citterio A, Giorda R et al: Association of short-term memory with a variant within DYX1C1 in developmental dyslexia. Genes Brain Behav 2007; 6: 640\u2013646.","journal-title":"Genes Brain Behav"},{"key":"BFejhg2013199_CR13","doi-asserted-by":"publisher","first-page":"853","DOI":"10.1136\/jmg.2004.018341","volume":"41","author":"TS Scerri","year":"2004","unstructured":"Scerri TS, Fisher SE, Francks C et al: Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK. J Med Genet 2004; 41: 853\u2013857.","journal-title":"J Med Genet"},{"key":"BFejhg2013199_CR14","doi-asserted-by":"publisher","first-page":"1111","DOI":"10.1038\/sj.mp.4001543","volume":"9","author":"KG Wigg","year":"2004","unstructured":"Wigg KG, Couto JM, Feng Y et al: Support for EKN1 as the susceptibility locus for dyslexia on 15q21. Mol Psychiatry 2004; 9: 1111\u20131121.","journal-title":"Mol Psychiatry"},{"key":"BFejhg2013199_CR15","doi-asserted-by":"publisher","first-page":"1190","DOI":"10.1038\/mp.2009.120","volume":"15","author":"TC Bates","year":"2009","unstructured":"Bates TC, Lind PA, Luciano M, Montgomery GW, Martin NG, Wright MJ : Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation. Mol Psychiatry 2009; 15: 1190\u20131196.","journal-title":"Mol Psychiatry"},{"key":"BFejhg2013199_CR16","doi-asserted-by":"publisher","first-page":"59","DOI":"10.1097\/YPG.0b013e32832080e1","volume":"19","author":"F Dahdouh","year":"2009","unstructured":"Dahdouh F, Anthoni H, Tapia-Paez I et al: Further evidence for DYX1C1 as a susceptibility factor for dyslexia. Psychiatr Genet 2009; 19: 59\u201363.","journal-title":"Psychiatr Genet"},{"key":"BFejhg2013199_CR17","doi-asserted-by":"publisher","first-page":"3001","DOI":"10.1096\/fj.07-104455","volume":"22","author":"I Tapia-P\u00e1ez","year":"2008","unstructured":"Tapia-P\u00e1ez I, Tammimies K, Massinen S, Roy AL, Kere J : The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia. FASEB J 2008; 22: 3001\u20133009.","journal-title":"FASEB J"},{"key":"BFejhg2013199_CR18","doi-asserted-by":"publisher","first-page":"17053","DOI":"10.1073\/pnas.0508591102","volume":"102","author":"H Meng","year":"2005","unstructured":"Meng H, Smith SD, Hager K et al: DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc Natl Acad Sci USA 2005; 102: 17053\u201317058.","journal-title":"Proc Natl Acad Sci USA"},{"key":"BFejhg2013199_CR19","doi-asserted-by":"publisher","first-page":"52","DOI":"10.1086\/498992","volume":"78","author":"J Schumacher","year":"2006","unstructured":"Schumacher J, Anthoni H, Dahdouh F et al: Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. Am J Hum Genet 2006; 78: 52\u201362.","journal-title":"Am J Hum Genet"},{"key":"BFejhg2013199_CR20","doi-asserted-by":"publisher","first-page":"128","DOI":"10.1007\/s00439-004-1126-6","volume":"115","author":"KE Deffenbacher","year":"2004","unstructured":"Deffenbacher KE, Kenyon JB, Hoover DM et al: Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses. Hum Genet 2004; 115: 128\u2013138.","journal-title":"Hum Genet"},{"key":"BFejhg2013199_CR21","doi-asserted-by":"publisher","first-page":"1046","DOI":"10.1086\/426404","volume":"75","author":"C Francks","year":"2004","unstructured":"Francks C, Paracchini S, Smith SD et al: A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. Am J Hum Genet 2004; 75: 1046\u20131058.","journal-title":"Am J Hum Genet"},{"key":"BFejhg2013199_CR22","doi-asserted-by":"publisher","first-page":"581","DOI":"10.1086\/429131","volume":"76","author":"N Cope","year":"2005","unstructured":"Cope N, Harold D, Hill G et al: Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. Am J Hum Genet 2005; 76: 581\u2013591.","journal-title":"Am J Hum Genet"},{"key":"BFejhg2013199_CR23","doi-asserted-by":"publisher","first-page":"668","DOI":"10.1038\/ejhg.2009.237","volume":"18","author":"PA Lind","year":"2010","unstructured":"Lind PA, Luciano M, Wright MJ, Montgomery GW, Martin NG, Bates TC : Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample. Eur J Hum Genet 2010; 18: 668\u2013673.","journal-title":"Eur J Hum Genet"},{"key":"BFejhg2013199_CR24","doi-asserted-by":"publisher","first-page":"90","DOI":"10.1007\/s10519-010-9424-3","volume":"41","author":"DF Newbury","year":"2011","unstructured":"Newbury DF, Paracchini S, Scerri TS et al: Investigation of dyslexia and SLI risk variants in reading and language-impaired subjects. Behav Genet 2011; 41: 90\u2013104.","journal-title":"Behav Genet"},{"key":"BFejhg2013199_CR25","doi-asserted-by":"publisher","first-page":"310","DOI":"10.1097\/YPG.0b013e3283063a78","volume":"18","author":"KU Ludwig","year":"2008","unstructured":"Ludwig KU, Schumacher J, Schulte-K\u00f6rne G et al: Investigation of the DCDC2 intron 2 deletion\/compound short tandem repeat polymorphism in a large German dyslexia sample. Psychiatr Genet 2008; 18: 310\u2013312.","journal-title":"Psychiatr Genet"},{"key":"BFejhg2013199_CR26","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1007\/s11881-008-0020-7","volume":"59","author":"A Wilcke","year":"2009","unstructured":"Wilcke A, Weissfuss J, Kirsten H, Wolfram G, Boltze J, Ahnert P : The role of gene DCDC2 in German dyslexics. Ann Dyslexia 2009; 59: 1\u201311.","journal-title":"Ann Dyslexia"},{"key":"BFejhg2013199_CR27","doi-asserted-by":"publisher","first-page":"237","DOI":"10.1016\/j.biopsych.2011.02.005","volume":"70","author":"TS Scerri","year":"2011","unstructured":"Scerri TS, Morris AP, Buckingham LL et al: DCDC2, KIAA0319 and CMIP are associated with reading-related traits. Biol Psychiatry 2011; 70: 237\u2013245.","journal-title":"Biol Psychiatry"},{"key":"BFejhg2013199_CR28","doi-asserted-by":"publisher","first-page":"1576","DOI":"10.1176\/appi.ajp.2008.07121872","volume":"165","author":"S Paracchini","year":"2008","unstructured":"Paracchini S, Steer CD, Buckingham LL et al: Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. Am J Psychiatry 2008; 165: 1576\u20131584.","journal-title":"Am J Psychiatry"},{"key":"BFejhg2013199_CR29","doi-asserted-by":"publisher","first-page":"811","DOI":"10.1016\/j.biopsych.2007.03.007","volume":"62","author":"M Luciano","year":"2007","unstructured":"Luciano M, Lind PA, Duffy DL et al: A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability. Biol Psychiatry 2007; 62: 811\u2013817.","journal-title":"Biol Psychiatry"},{"key":"BFejhg2013199_CR30","doi-asserted-by":"publisher","first-page":"e1000436","DOI":"10.1371\/journal.pgen.1000436","volume":"5","author":"MY Dennis","year":"2009","unstructured":"Dennis MY, Paracchini S, Scerri TS et al: A common variant associated with dyslexia reduces expression of the KIAA0319 gene. PLoS Genet 2009; 5: e1000436.","journal-title":"PLoS Genet"},{"key":"BFejhg2013199_CR31","doi-asserted-by":"publisher","first-page":"1061","DOI":"10.1038\/sj.mp.4001930","volume":"11","author":"D Harold","year":"2006","unstructured":"Harold D, Paracchini S, Scerri T et al: Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. Mol Psychiatry 2006; 11: 1061.","journal-title":"Mol Psychiatry"},{"key":"BFejhg2013199_CR32","doi-asserted-by":"publisher","first-page":"1659","DOI":"10.1093\/hmg\/ddl089","volume":"15","author":"S Paracchini","year":"2006","unstructured":"Paracchini S, Thomas A, Castro S et al: The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. Hum Mol Genet 2006; 15: 1659\u20131666.","journal-title":"Hum Mol Genet"},{"key":"BFejhg2013199_CR33","doi-asserted-by":"publisher","first-page":"1587","DOI":"10.1007\/s00702-008-0124-6","volume":"115","author":"KU Ludwig","year":"2008","unstructured":"Ludwig KU, Roeske D, Schumacher J et al: Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample. J Neural Transm 2008; 115: 1587\u20131589.","journal-title":"J Neural Transm"},{"key":"BFejhg2013199_CR34","doi-asserted-by":"publisher","first-page":"671","DOI":"10.1016\/j.biopsych.2012.05.008","volume":"72","author":"F Darki","year":"2012","unstructured":"Darki F, Peyrard-Janvid M, Matsson H, Kere J, Klingberg T : Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure. Biol Psychiatry 2012; 72: 671\u2013676.","journal-title":"Biol Psychiatry"},{"key":"BFejhg2013199_CR35","doi-asserted-by":"publisher","first-page":"667","DOI":"10.1093\/hmg\/ddm009","volume":"16","author":"H Anthoni","year":"2007","unstructured":"Anthoni H, Zucchelli M, Matsson H et al: A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. Hum Mol Genet 2007; 16: 667\u2013677.","journal-title":"Hum Mol Genet"},{"key":"BFejhg2013199_CR36","doi-asserted-by":"publisher","first-page":"e50321","DOI":"10.1371\/journal.pone.0050321","volume":"7","author":"TS Scerri","year":"2012","unstructured":"Scerri TS, Darki F, Newbury DF et al: The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure. PLoS One 2012; 7: e50321.","journal-title":"PLoS One"},{"key":"BFejhg2013199_CR37","doi-asserted-by":"publisher","first-page":"57","DOI":"10.1146\/annurev.genom.8.080706.092312","volume":"8","author":"S Paracchini","year":"2007","unstructured":"Paracchini S, Scerri T, Monaco AP : The genetic lexicon of dyslexia. Annu Rev Genomics Hum Genet 2007; 8: 57\u201379.","journal-title":"Annu Rev Genomics Hum Genet"},{"key":"BFejhg2013199_CR38","doi-asserted-by":"publisher","first-page":"6","DOI":"10.1007\/s10519-011-9444-7","volume":"41","author":"T Skiba","year":"2011","unstructured":"Skiba T, Landi N, Wagner R, Grigorenko EL : In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes. Behav Genet 2011; 41: 6\u201330.","journal-title":"Behav Genet"},{"key":"BFejhg2013199_CR39","doi-asserted-by":"publisher","first-page":"686","DOI":"10.1111\/jcpp.12029","volume":"54","author":"K Landerl","year":"2013","unstructured":"Landerl K, Ramus F, Moll K et al: Predictors of developmental dyslexia in European orthographies with varying complexity. J Child Psychol Psychiatry 2013; 54: 686\u2013694.","journal-title":"J Child Psychol Psychiatry"},{"key":"BFejhg2013199_CR40","doi-asserted-by":"crossref","unstructured":"Wechsler D : Wechsler Intelligence Scale for Children 4th edn 2003.","DOI":"10.1037\/t15174-000"},{"key":"BFejhg2013199_CR41","doi-asserted-by":"crossref","unstructured":"Achenbach T Child Behavior Check-List 2001.","DOI":"10.1037\/10517-028"},{"key":"BFejhg2013199_CR42","first-page":"24","volume":"9","author":"CK Conners","year":"1973","unstructured":"Conners CK : Rating scales for use in drug studies with children. Psychopharmacol Bull 1973; 9: 24\u201384.","journal-title":"Psychopharmacol Bull"},{"key":"BFejhg2013199_CR43","doi-asserted-by":"publisher","first-page":"1241","DOI":"10.1016\/j.cub.2008.07.049","volume":"18","author":"O Lao","year":"2008","unstructured":"Lao O, Lu TT, Nothnagel M et al: Correlation between genetic and geographic structure in Europe. Curr Biol 2008; 18: 1241\u20131248.","journal-title":"Curr Biol"},{"key":"BFejhg2013199_CR44","doi-asserted-by":"publisher","first-page":"98","DOI":"10.1038\/nature07331","volume":"456","author":"J Novembre","year":"2008","unstructured":"Novembre J, Johnson T, Bryc K et al: Genes mirror geography within Europe. Nature 2008; 456: 98\u2013101.","journal-title":"Nature"},{"key":"BFejhg2013199_CR45","doi-asserted-by":"publisher","first-page":"e5472","DOI":"10.1371\/journal.pone.0005472","volume":"4","author":"M Nelis","year":"2009","unstructured":"Nelis M, Esko T, Magi R et al: Genetic structure of Europeans: a view from the North-East. PLoS One 2009; 4: e5472.","journal-title":"PLoS One"},{"key":"BFejhg2013199_CR46","doi-asserted-by":"publisher","first-page":"e3519","DOI":"10.1371\/journal.pone.0003519","volume":"3","author":"E Salmela","year":"2008","unstructured":"Salmela E, Lappalainen T, Fransson I et al: Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe. PLoS One 2008; 3: e3519.","journal-title":"PLoS One"},{"key":"BFejhg2013199_CR47","doi-asserted-by":"publisher","first-page":"160","DOI":"10.1111\/j.1469-1809.2006.00312.x","volume":"71","author":"G Schulte-K\u00f6rne","year":"2007","unstructured":"Schulte-K\u00f6rne G, Ziegler A, Deimel W et al: Interrelationship and familiality of dyslexia related quantitative measures. Ann Hum Genet 2007; 71: 160\u2013175.","journal-title":"Ann Hum Genet"},{"key":"BFejhg2013199_CR48","doi-asserted-by":"publisher","first-page":"969","DOI":"10.1038\/ng.940","volume":"43","author":"S Ripke","year":"2011","unstructured":"Ripke S, Sanders AR, Kendler KS et al: Genome-wide association study identifies five new schizophrenia loci. Nat Genet 2011; 43: 969\u2013976.","journal-title":"Nat Genet"},{"key":"BFejhg2013199_CR49","doi-asserted-by":"publisher","first-page":"339","DOI":"10.1038\/ng.782","volume":"43","author":"C4D Genetics Consortium","year":"2011","unstructured":"C4D Genetics Consortium: A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. Nat Genet 2011; 43: 339\u2013344.","journal-title":"Nat Genet"}],"container-title":["European Journal of Human Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/www.nature.com\/articles\/ejhg2013199.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/www.nature.com\/articles\/ejhg2013199","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/www.nature.com\/articles\/ejhg2013199.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,7,4]],"date-time":"2023-07-04T13:44:03Z","timestamp":1688478243000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.nature.com\/articles\/ejhg2013199"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2013,9,11]]},"references-count":49,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2014,5]]}},"alternative-id":["BFejhg2013199"],"URL":"https:\/\/doi.org\/10.1038\/ejhg.2013.199","relation":{},"ISSN":["1018-4813","1476-5438"],"issn-type":[{"value":"1018-4813","type":"print"},{"value":"1476-5438","type":"electronic"}],"subject":[],"published":{"date-parts":[[2013,9,11]]}}}