{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,14]],"date-time":"2026-01-14T14:05:45Z","timestamp":1768399545034,"version":"3.49.0"},"reference-count":56,"publisher":"Springer Science and Business Media LLC","issue":"7","license":[{"start":{"date-parts":[[2007,8,7]],"date-time":"2007-08-07T00:00:00Z","timestamp":1186444800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.springer.com\/tdm"},{"start":{"date-parts":[[2007,8,7]],"date-time":"2007-08-07T00:00:00Z","timestamp":1186444800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Mol Psychiatry"],"published-print":{"date-parts":[[2008,7]]},"DOI":"10.1038\/sj.mp.4002063","type":"journal-article","created":{"date-parts":[[2007,8,7]],"date-time":"2007-08-07T15:24:41Z","timestamp":1186500281000},"page":"729-740","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":93,"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"],"prefix":"10.1038","volume":"13","author":[{"given":"E L","family":"Meaburn","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"N","family":"Harlaar","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I W","family":"Craig","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L C","family":"Schalkwyk","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R","family":"Plomin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2007,8,7]]},"reference":[{"key":"BF4002063_CR1","doi-asserted-by":"publisher","first-page":"307","DOI":"10.1056\/NEJM199801293380507","volume":"338","author":"SE Shaywitz","year":"1998","unstructured":"Shaywitz SE . Dyslexia. New Engl J Med 1998; 338: 307\u2013312.","journal-title":"New Engl J Med"},{"key":"BF4002063_CR2","volume-title":"Dyslexia","author":"M Snowling","year":"2000","unstructured":"Snowling M . Dyslexia, 2nd edn. Blackwell: Oxford, 2000."},{"key":"BF4002063_CR3","doi-asserted-by":"publisher","first-page":"78","DOI":"10.1002\/(SICI)1099-0909(199906)5:2<78::AID-DYS127>3.0.CO;2-8","volume":"5","author":"C Jacobson","year":"1999","unstructured":"Jacobson C . How persistent is reading disability? Individual growth curves in reading. Dyslexia 1999; 5: 78\u201393.","journal-title":"Dyslexia"},{"key":"BF4002063_CR4","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, Shneider AE, Marchione KE, Stuebing KK et al. Persistence of dyslexia: the Connecticut Longitudinal Study at adolescence. Pediatrics 1999; 104: 1351\u20131359.","journal-title":"Pediatrics"},{"key":"BF4002063_CR5","first-page":"17","volume-title":"Reading and Attention Disorders: Neurobiological Correlates","author":"JC DeFries","year":"1999","unstructured":"DeFries JC, Knopik VS, Wadsworth SJ . Colorado Twin Study of reading disability. In: Duane DD (ed). Reading and Attention Disorders: Neurobiological Correlates. York Press: Baltimore Maryland, 1999, pp 17\u201341."},{"key":"BF4002063_CR6","doi-asserted-by":"publisher","first-page":"373","DOI":"10.1111\/j.1469-7610.2004.00358.x","volume":"46","author":"N Harlaar","year":"2005","unstructured":"Harlaar N, Spinath FM, Dale PS, Plomin R . Genetic influences on early word recognition abilities and disabilities: a study of 7-year-old twins. J Child Psychol Psychiatry 2005; 46: 373\u2013384.","journal-title":"J Child Psychol Psychiatry"},{"key":"BF4002063_CR7","doi-asserted-by":"publisher","first-page":"592","DOI":"10.1037\/0033-2909.131.4.592","volume":"131","author":"R Plomin","year":"2005","unstructured":"Plomin R, Kovas Y . Generalist genes and learning disabilities. Psychol Bull 2005; 131: 592\u2013617.","journal-title":"Psychol Bull"},{"key":"BF4002063_CR8","doi-asserted-by":"publisher","first-page":"1733","DOI":"10.1126\/science.8209254","volume":"264","author":"R Plomin","year":"1994","unstructured":"Plomin R, Owen MJ, McGuffin P . The genetic basis of complex human behaviors. Science 1994; 264: 1733\u20131739.","journal-title":"Science"},{"key":"BF4002063_CR9","doi-asserted-by":"crossref","unstructured":"Paracchini S, Scerri T, Monaco AP . The genetic lexicon of dyslexia. Annu Rev Genomics Hum Genet 2007 [E-pub ahead of print].","DOI":"10.1146\/annurev.genom.8.080706.092312"},{"key":"BF4002063_CR10","doi-asserted-by":"publisher","first-page":"250","DOI":"10.1016\/j.tics.2006.04.003","volume":"10","author":"SE Fisher","year":"2006","unstructured":"Fisher SE, Francks C . Genes, cognition and dyslexia: learning to read the genome. Trends Cogn Sci 2006; 10: 250\u2013257.","journal-title":"Trends Cogn Sci"},{"key":"BF4002063_CR11","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":"BF4002063_CR12","doi-asserted-by":"publisher","first-page":"333","DOI":"10.1016\/j.molmed.2006.05.007","volume":"12","author":"LM McGrath","year":"2006","unstructured":"McGrath LM, Smith SD, Pennington BF . Breakthroughs in the search for dyslexia candidate genes. Trends Mol Med 2006; 12: 333\u2013341.","journal-title":"Trends Mol Med"},{"key":"BF4002063_CR13","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, Schmael C, Schulte-Korne G, Nothen MM . Genetics of dyslexia: the evolving landscape. J Med Genet 2007; 44: 289\u2013297.","journal-title":"J Med Genet"},{"key":"BF4002063_CR14","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, Olson RK, Pennington BF, DeFries JC 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":"BF4002063_CR15","doi-asserted-by":"publisher","first-page":"847","DOI":"10.1038\/35015718","volume":"405","author":"NJ Risch","year":"2000","unstructured":"Risch NJ . Searching for genetic determinants in the new millennium. Nature 2000; 405: 847\u2013856.","journal-title":"Nature"},{"key":"BF4002063_CR16","doi-asserted-by":"publisher","first-page":"1616","DOI":"10.1086\/302891","volume":"66","author":"PC Sham","year":"2000","unstructured":"Sham PC, Cherny SS, Purcell S, Hewitt JK . Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data. Am J Hum Genet 2000; 66: 1616\u20131630.","journal-title":"Am J Hum Genet"},{"key":"BF4002063_CR17","doi-asserted-by":"publisher","first-page":"89","DOI":"10.1038\/nrg1270","volume":"5","author":"KT Zondervan","year":"2004","unstructured":"Zondervan KT, Cardon LR . The complex interplay among factors that influence allelic association. Nat Rev Genet 2004; 5: 89\u2013100.","journal-title":"Nat Rev Genet"},{"key":"BF4002063_CR18","doi-asserted-by":"publisher","first-page":"91","DOI":"10.1038\/35052543","volume":"2","author":"LR Cardon","year":"2001","unstructured":"Cardon LR, Bell JI . Association study designs for complex diseases. Nat Rev Genet 2001; 2: 91\u201399.","journal-title":"Nat Rev Genet"},{"key":"BF4002063_CR19","doi-asserted-by":"publisher","first-page":"609","DOI":"10.1093\/aje\/kwj259","volume":"164","author":"JP Ioannidis","year":"2006","unstructured":"Ioannidis JP, Trikalinos TA, Khoury MJ . Implications of small effect sizes of individual genetic variants on the design and interpretation of genetic association studies of complex diseases. Am J Epidemiol 2006; 164: 609\u2013614.","journal-title":"Am J Epidemiol"},{"issue":"Suppl","key":"BF4002063_CR20","doi-asserted-by":"publisher","first-page":"S5","DOI":"10.1038\/ng1558","volume":"37","author":"AC Syvanen","year":"2005","unstructured":"Syvanen AC . Toward genome-wide SNP genotyping. Nat Genet 2005; 37 (Suppl): S5\u2013S10.","journal-title":"Nat Genet"},{"key":"BF4002063_CR21","doi-asserted-by":"publisher","first-page":"95","DOI":"10.1038\/nrg1521","volume":"6","author":"JN Hirschhorn","year":"2005","unstructured":"Hirschhorn JN, Daly MJ . Genome-wide association studies for common diseases and complex traits. Nat Rev Genet 2005; 6: 95\u2013108.","journal-title":"Nat Rev Genet"},{"key":"BF4002063_CR22","doi-asserted-by":"publisher","first-page":"446","DOI":"10.1038\/nature02623","volume":"429","author":"CS Carlson","year":"2004","unstructured":"Carlson CS, Eberle MA, Kruglyak L, Nickerson DA . Mapping complex disease loci in whole-genome association studies. Nature 2004; 429: 446\u2013452.","journal-title":"Nature"},{"key":"BF4002063_CR23","doi-asserted-by":"publisher","first-page":"54","DOI":"10.1016\/j.mrfmmm.2005.01.006","volume":"573","author":"C Newton-Cheh","year":"2005","unstructured":"Newton-Cheh C, Hirschhorn JN . Genetic association studies of complex traits: design and analysis issues. Mutat Res 2005; 573: 54\u201369.","journal-title":"Mutat Res"},{"key":"BF4002063_CR24","doi-asserted-by":"publisher","first-page":"337","DOI":"10.1086\/432962","volume":"77","author":"DC Thomas","year":"2005","unstructured":"Thomas DC, Haile RW, Duggan D . Recent developments in genomewide association scans: a workshop summary and review. Am J Hum Genet 2005; 77: 337\u2013345.","journal-title":"Am J Hum Genet"},{"key":"BF4002063_CR25","doi-asserted-by":"publisher","first-page":"109","DOI":"10.1038\/nrg1522","volume":"6","author":"WY Wang","year":"2005","unstructured":"Wang WY, Barratt BJ, Clayton DG, Todd JA . Genome-wide association studies: theoretical and practical concerns. Nat Rev Genet 2005; 6: 109\u2013118.","journal-title":"Nat Rev Genet"},{"key":"BF4002063_CR26","doi-asserted-by":"publisher","first-page":"665","DOI":"10.1007\/s10519-005-9016-9","volume":"36","author":"J Knight","year":"2006","unstructured":"Knight J, Sham P . Design and analysis of association studies using pooled DNA from large twin samples. Behav Genet 2006; 36: 665\u2013677.","journal-title":"Behav Genet"},{"key":"BF4002063_CR27","doi-asserted-by":"crossref","first-page":"1365","DOI":"10.1093\/genetics\/138.4.1365","volume":"138","author":"A Darvasi","year":"1994","unstructured":"Darvasi A, Soller M . Selective DNA pooling for determination of linkage between a molecular marker and a quantitative trait locus. Genetics 1994; 138: 1365\u20131373.","journal-title":"Genetics"},{"key":"BF4002063_CR28","doi-asserted-by":"publisher","first-page":"146","DOI":"10.1080\/07853890310021724","volume":"36","author":"N Norton","year":"2004","unstructured":"Norton N, Williams NM, O'Donovan MC, Owen MJ . DNA pooling as a tool for large-scale association studies in complex traits. Ann Med 2004; 36: 146\u2013152.","journal-title":"Ann Med"},{"key":"BF4002063_CR29","doi-asserted-by":"publisher","first-page":"549","DOI":"10.1023\/B:BEGE.0000038493.26202.d3","volume":"34","author":"LM Butcher","year":"2004","unstructured":"Butcher LM, Meaburn E, Liu L, Fernandes C, Hill L, Al Chalabi A et al. Genotyping pooled DNA on microarrays: a systematic genome screen of thousands of SNPs in large samples to detect QTLs for complex traits. Behav Genet 2004; 34: 549\u2013555.","journal-title":"Behav Genet"},{"key":"BF4002063_CR30","doi-asserted-by":"publisher","first-page":"52","DOI":"10.1186\/1471-2164-6-52","volume":"6","author":"E Meaburn","year":"2005","unstructured":"Meaburn E, Butcher LM, Liu L, Fernandes C, Hansen V, Al Chalabi A et al. Genotyping DNA pools on microarrays: tackling the QTL problem of large samples and large numbers of SNPs. BMC Genomics 2005; 6: 52.","journal-title":"BMC Genomics"},{"key":"BF4002063_CR31","doi-asserted-by":"publisher","first-page":"e27","DOI":"10.1093\/nar\/gnj027","volume":"34","author":"E Meaburn","year":"2006","unstructured":"Meaburn E, Butcher LM, Schalkwyk LC, Plomin R . Genotyping pooled DNA using 100K SNP microarrays: a step towards genomewide association scans. Nucleic Acids Res 2006; 34: e27.","journal-title":"Nucleic Acids Res"},{"key":"BF4002063_CR32","doi-asserted-by":"publisher","first-page":"126","DOI":"10.1086\/510686","volume":"80","author":"JV Pearson","year":"2007","unstructured":"Pearson JV, Huentelman MJ, Halperin RF, Tembe WD, Melquist S, Homer N et al. Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies. Am J Hum Genet 2007; 80: 126\u2013139.","journal-title":"Am J Hum Genet"},{"key":"BF4002063_CR33","doi-asserted-by":"publisher","first-page":"27","DOI":"10.1186\/1471-2164-7-27","volume":"7","author":"G Kirov","year":"2006","unstructured":"Kirov G, Nikolov I, Georgieva L, Moskvina V, Owen MJ, O'Donovan MC . Pooled DNA genotyping on Affymetrix SNP genotyping arrays. BMC Genomics 2006; 7: 27.","journal-title":"BMC Genomics"},{"key":"BF4002063_CR34","doi-asserted-by":"publisher","first-page":"1315","DOI":"10.1093\/hmg\/ddi142","volume":"14","author":"LM Butcher","year":"2005","unstructured":"Butcher LM, Meaburn E, Knight J, Sham PC, Schalkwyk LC, Craig IW et al. SNPs, microarrays, and pooled DNA: identification of four loci associated with mild mental impairment in a sample of 6000 children. Hum Mol Genet 2005; 14: 1315\u20131325.","journal-title":"Hum Mol Genet"},{"key":"BF4002063_CR35","doi-asserted-by":"publisher","first-page":"375","DOI":"10.1002\/gepi.20045","volume":"27","author":"DM Evans","year":"2004","unstructured":"Evans DM, Cardon LR, Morris AP . Genotype prediction using a dense map of SNPs. Genet Epidemiol 2004; 27: 375\u2013384.","journal-title":"Genet Epidemiol"},{"key":"BF4002063_CR36","doi-asserted-by":"publisher","first-page":"577","DOI":"10.1093\/hmg\/ddh060","volume":"13","author":"X Ke","year":"2004","unstructured":"Ke X, Hunt S, Tapper W, Lawrence R, Stavrides G, Ghori J et al. The impact of SNP density on fine-scale patterns of linkage disequilibrium. Hum Mol Genet 2004; 13: 577\u2013588.","journal-title":"Hum Mol Genet"},{"key":"BF4002063_CR37","doi-asserted-by":"publisher","first-page":"96","DOI":"10.1375\/twin.10.1.96","volume":"10","author":"B Oliver","year":"2007","unstructured":"Oliver B, Plomin R . Twins' Early Development Study (TEDS): a multivariate, longitudinal genetic investigation of language, cognition and behavior problems from childhood through adolescence. Twin Res Hum Genet 2007; 10: 96\u2013105.","journal-title":"Twin Res Hum Genet"},{"key":"BF4002063_CR38","doi-asserted-by":"publisher","first-page":"862","DOI":"10.1038\/nrg930","volume":"3","author":"P Sham","year":"2002","unstructured":"Sham P, Bader JS, Craig I, O'Donovan M, Owen M . DNA Pooling: a tool for large-scale association studies. Nat Rev Genet 2002; 3: 862\u2013871.","journal-title":"Nat Rev Genet"},{"key":"BF4002063_CR39","volume-title":"Test of Word Reading Efficiency","author":"JK Torgesen","year":"1999","unstructured":"Torgesen JK, Wagner RK, Rashotte CA . Test of Word Reading Efficiency. Pro-Ed: Austin, TX, 1999."},{"key":"BF4002063_CR40","unstructured":"Qualifications and Curriculum Authority. QCA Key Stage 1: Assessment and reporting arrangements. Great Britain Qualifications and Curriculum Authority 1999."},{"key":"BF4002063_CR41","doi-asserted-by":"publisher","first-page":"385","DOI":"10.1007\/s11145-004-8130-z","volume":"18","author":"PS Dale","year":"2005","unstructured":"Dale PS, Harlaar N, Plomin R . Telephone testing and teacher assessment of reading skills in 7-year-olds: I. Substantial correspondence for a sample of 5808 Children And for extremes. Reading and Writing: An Interdisciplinary Journal 2005; 18: 385\u2013400.","journal-title":"Reading and Writing: An Interdisciplinary Journal"},{"key":"BF4002063_CR42","doi-asserted-by":"publisher","first-page":"401","DOI":"10.1007\/s11145-005-0271-1","volume":"18","author":"N Harlaar","year":"2005","unstructured":"Harlaar N, Dale PS, Plomin R . Correspondence between telephone testing and teacher assessments of reading skills in a sample of 7-year-old twins: II. Strong genetic overlap. Reading and writing: An interdisciplinary journal 2005; 18: 401\u2013423.","journal-title":"Reading and writing: An interdisciplinary journal"},{"key":"BF4002063_CR43","first-page":"259","volume-title":"Rethinking Learning Disabilities, Thomas B","author":"JR Lyon","year":"2001","unstructured":"Lyon JR, Fletcher JM, Shaywitz BA, Shaywitz SE, Torgesen JK, Wood FB et al. Rethinking special education for a new century. In: Finn CE, Rotherham RAJ, Hokanson CR (eds). Rethinking Learning Disabilities, Thomas B. Fordham Foundation and Progressive Policy Institute: Washington, DC, 2001, pp 259\u2013287."},{"key":"BF4002063_CR44","doi-asserted-by":"publisher","first-page":"67","DOI":"10.1023\/A:1021055617738","volume":"33","author":"B Freeman","year":"2003","unstructured":"Freeman B, Smith N, Curtis C, Huckett L, Mill J, Craig I . DNA from buccal swabs recruited by mail: evaluation of storage effects on long-term stability and suitability for multiplex polymerase chain reaction genotyping. Behav Genet 2003; 33: 67\u201372.","journal-title":"Behav Genet"},{"key":"BF4002063_CR45","doi-asserted-by":"publisher","first-page":"109","DOI":"10.1038\/nmeth718","volume":"1","author":"H Matsuzaki","year":"2004","unstructured":"Matsuzaki H, Dong S, Loi H, Di X, Liu G, Hubbell E et al. Genotyping over 100\u2009000 SNPs on a pair of oligonucleotide arrays. Nat Methods 2004; 1: 109\u2013111.","journal-title":"Nat Methods"},{"key":"BF4002063_CR46","first-page":"398","volume":"16","author":"AR Tobler","year":"2005","unstructured":"Tobler AR, Short S, Andersen MR, Paner TM, Briggs JC, Lambert SM et al. The SNPlex genotyping system: a flexible and scalable platform for SNP genotyping. J Biomol Tech 2005; 16: 398\u2013406.","journal-title":"J Biomol Tech"},{"key":"BF4002063_CR47","volume-title":"Statistical Power Analysis for the Behavioral Sciences","author":"J Cohen","year":"2004","unstructured":"Cohen J . Statistical Power Analysis for the Behavioral Sciences. Academic Press: New York, 2004."},{"key":"BF4002063_CR48","doi-asserted-by":"publisher","first-page":"517","DOI":"10.1093\/bioinformatics\/btl615","volume":"23","author":"W Lau","year":"2007","unstructured":"Lau W, Kuo TY, Tapper W, Cox S, Collins A . Exploiting large scale computing to construct high resolution linkage disequilibrium maps of the human genome. Bioinformatics 2007; 23: 517\u2013519.","journal-title":"Bioinformatics"},{"key":"BF4002063_CR49","doi-asserted-by":"publisher","first-page":"385","DOI":"10.1126\/science.1109557","volume":"308","author":"RJ Klein","year":"2005","unstructured":"Klein RJ, Zeiss C, Chew EY, Tsai JY, Sackler RS, Haynes C et al. Complement factor H polymorphism in age-related macular degeneration. Science 2005; 308: 385\u2013389.","journal-title":"Science"},{"key":"BF4002063_CR50","doi-asserted-by":"publisher","first-page":"1461","DOI":"10.1126\/science.1135245","volume":"314","author":"RH Duerr","year":"2006","unstructured":"Duerr RH, Taylor KD, Brant SR, Rioux JD, Silverberg MS, Daly MJ et al. A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. Science 2006; 314: 1461\u20131463.","journal-title":"Science"},{"key":"BF4002063_CR51","doi-asserted-by":"publisher","first-page":"3","DOI":"10.1037\/10480-001","volume-title":"Behavioral Genetics in the Postgenomic Era","author":"R Plomin","year":"2003","unstructured":"Plomin R, DeFries JC, Craig IW, McGuffin P . Behavioral genetics. In: Plomin R, DeFries JC, Craig IW, McGuffin P (eds). Behavioral Genetics in the Postgenomic Era. American Psychological Association: Washington, DC, 2003, pp 3\u201315."},{"key":"BF4002063_CR52","doi-asserted-by":"publisher","first-page":"e25","DOI":"10.1093\/nar\/gni028","volume":"33","author":"CL Simpson","year":"2005","unstructured":"Simpson CL, Knight J, Butcher LM, Hansen VK, Meaburn E, Schalkwyk LC et al. A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays. Nucleic Acids Res 2005; 33: e25.","journal-title":"Nucleic Acids Res"},{"key":"BF4002063_CR53","doi-asserted-by":"publisher","first-page":"27","DOI":"10.1517\/14622416.1.1.27","volume":"1","author":"M Cargill","year":"2000","unstructured":"Cargill M, Daley GQ . Mining for SNPs: putting the common variants--common disease hypothesis to the test. Pharmacogenomics 2000; 1: 27\u201337.","journal-title":"Pharmacogenomics"},{"key":"BF4002063_CR54","doi-asserted-by":"publisher","first-page":"138","DOI":"10.1186\/1471-2164-6-138","volume":"6","author":"DW Craig","year":"2005","unstructured":"Craig DW, Huentelman MJ, Hu-Lince D, Zismann VL, Kruer MC, Lee AM et al. Identification of disease causing loci using an array-based genotyping approach on pooled DNA. BMC Genomics 2005; 6: 138.","journal-title":"BMC Genomics"},{"key":"BF4002063_CR55","doi-asserted-by":"publisher","first-page":"444","DOI":"10.1038\/nature05329","volume":"444","author":"R Redon","year":"2006","unstructured":"Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, Andrews TD et al. Global variation in copy number in the human genome. Nature 2006; 444: 444\u2013454.","journal-title":"Nature"},{"key":"BF4002063_CR56","doi-asserted-by":"publisher","first-page":"91","DOI":"10.1086\/510560","volume":"80","author":"KK Wong","year":"2007","unstructured":"Wong KK, deLeeuw RJ, Dosanjh NS, Kimm LR, Cheng Z, Horsman DE et al. A comprehensive analysis of common copy-number variations in the human genome. Am J Hum Genet 2007; 80: 91\u2013104.","journal-title":"Am J Hum Genet"}],"container-title":["Molecular Psychiatry"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.nature.com\/articles\/4002063.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/www.nature.com\/articles\/4002063","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/www.nature.com\/articles\/4002063.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2022,4,1]],"date-time":"2022-04-01T12:32:10Z","timestamp":1648816330000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.nature.com\/articles\/4002063"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2007,8,7]]},"references-count":56,"journal-issue":{"issue":"7","published-print":{"date-parts":[[2008,7]]}},"alternative-id":["BF4002063"],"URL":"https:\/\/doi.org\/10.1038\/sj.mp.4002063","relation":{},"ISSN":["1359-4184","1476-5578"],"issn-type":[{"value":"1359-4184","type":"print"},{"value":"1476-5578","type":"electronic"}],"subject":[],"published":{"date-parts":[[2007,8,7]]},"assertion":[{"value":"30 March 2007","order":1,"name":"received","label":"Received","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"14 June 2007","order":2,"name":"revised","label":"Revised","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"27 June 2007","order":3,"name":"accepted","label":"Accepted","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"7 August 2007","order":4,"name":"first_online","label":"First Online","group":{"name":"ArticleHistory","label":"Article History"}}]}}