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Page 1
Copy number variation in schizophrenia in Sweden.
Szatkiewicz JP, O'Dushlaine C, Chen G, Chambert K, Moran JL, Neale BM, Fromer M, Ruderfer D, Akterin S, Bergen SE, Kähler A, Magnusson PK, Kim Y, Crowley JJ, Rees E, Kirov G, O'Donovan MC, Owen MJ, Walters J, Scolnick E, Sklar P, Purcell S, Hultman CM, McCarroll SA, Sullivan PF. Szatkiewicz JP, et al. Among authors: kim y. Mol Psychiatry. 2014 Jul;19(7):762-73. doi: 10.1038/mp.2014.40. Epub 2014 Apr 29. Mol Psychiatry. 2014. PMID: 24776740 Free PMC article.
Deep resequencing and association analysis of schizophrenia candidate genes.
Crowley JJ, Hilliard CE, Kim Y, Morgan MB, Lewis LR, Muzny DM, Hawes AC, Sabo A, Wheeler DA, Lieberman JA, Sullivan PF, Gibbs RA. Crowley JJ, et al. Among authors: kim y. Mol Psychiatry. 2013 Feb;18(2):138-40. doi: 10.1038/mp.2012.28. Epub 2012 Apr 3. Mol Psychiatry. 2013. PMID: 22472875 Free PMC article. No abstract available.
Identifying bipolar disorder susceptibility loci in a densely affected pedigree.
Collins AL, Kim Y, Szatkiewicz JP, Bloom RJ, Hilliard CE, Quackenbush CR, Meier S, Rivas F, Mayoral F, Cichon S, Nöthen MM, Rietschel M, Sullivan PF. Collins AL, et al. Among authors: kim y. Mol Psychiatry. 2013 Dec;18(12):1245-6. doi: 10.1038/mp.2012.176. Epub 2012 Dec 18. Mol Psychiatry. 2013. PMID: 23247078 Free PMC article. No abstract available.
Schizophrenia genetic variants are not associated with intelligence.
van Scheltinga AF, Bakker SC, van Haren NE, Derks EM, Buizer-Voskamp JE, Cahn W, Ripke S; Psychiatric Genome-Wide Association Study (GWAS) Consortium; Ophoff RA, Kahn RS. van Scheltinga AF, et al. Psychol Med. 2013 Dec;43(12):2563-70. doi: 10.1017/S0033291713000196. Epub 2013 Feb 15. Psychol Med. 2013. PMID: 23410598 Free PMC article.
Transcriptional targets of the schizophrenia risk gene MIR137.
Collins AL, Kim Y, Bloom RJ, Kelada SN, Sethupathy P, Sullivan PF. Collins AL, et al. Among authors: kim y. Transl Psychiatry. 2014 Jul 1;4(7):e404. doi: 10.1038/tp.2014.42. Transl Psychiatry. 2014. PMID: 24984191 Free PMC article.
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis.
Wang S, Mandell JD, Kumar Y, Sun N, Morris MT, Arbelaez J, Nasello C, Dong S, Duhn C, Zhao X, Yang Z, Padmanabhuni SS, Yu D, King RA, Dietrich A, Khalifa N, Dahl N, Huang AY, Neale BM, Coppola G, Mathews CA, Scharf JM; Tourette International Collaborative Genetics Study (TIC Genetics); Tourette Syndrome Genetics Southern and Eastern Europe Initiative (TSGENESEE); Tourette Association of America International Consortium for Genetics (TAAICG); Fernandez TV, Buxbaum JD, De Rubeis S, Grice DE, Xing J, Heiman GA, Tischfield JA, Paschou P, Willsey AJ, State MW. Wang S, et al. Cell Rep. 2018 Sep 25;24(13):3441-3454.e12. doi: 10.1016/j.celrep.2018.08.082. Cell Rep. 2018. PMID: 30257206 Free PMC article.
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