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653 results

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Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights.
Gusev A, Mancuso N, Won H, Kousi M, Finucane HK, Reshef Y, Song L, Safi A; Schizophrenia Working Group of the Psychiatric Genomics Consortium; McCarroll S, Neale BM, Ophoff RA, O'Donovan MC, Crawford GE, Geschwind DH, Katsanis N, Sullivan PF, Pasaniuc B, Price AL. Gusev A, et al. Among authors: sullivan pf. Nat Genet. 2018 Apr;50(4):538-548. doi: 10.1038/s41588-018-0092-1. Epub 2018 Apr 9. Nat Genet. 2018. PMID: 29632383 Free PMC article.
A genome scan of neuroticism in nicotine dependent smokers.
Neale BM, Sullivan PF, Kendler KS. Neale BM, et al. Among authors: sullivan pf. Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):65-9. doi: 10.1002/ajmg.b.30095. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15389754
The genetics of schizophrenia.
Sullivan PF. Sullivan PF. PLoS Med. 2005 Jul;2(7):e212. doi: 10.1371/journal.pmed.0020212. Epub 2005 Jul 26. PLoS Med. 2005. PMID: 16033310 Free PMC article. Review.
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.
International Schizophrenia Consortium; Purcell SM, Wray NR, Stone JL, Visscher PM, O'Donovan MC, Sullivan PF, Sklar P. International Schizophrenia Consortium, et al. Among authors: sullivan pf. Nature. 2009 Aug 6;460(7256):748-52. doi: 10.1038/nature08185. Epub 2009 Jul 1. Nature. 2009. PMID: 19571811 Free PMC article.
Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children.
Hancock DB, Romieu I, Shi M, Sienra-Monge JJ, Wu H, Chiu GY, Li H, del Rio-Navarro BE, Willis-Owen SA, Weiss ST, Raby BA, Gao H, Eng C, Chapela R, Burchard EG, Tang H, Sullivan PF, London SJ. Hancock DB, et al. Among authors: sullivan pf. PLoS Genet. 2009 Aug;5(8):e1000623. doi: 10.1371/journal.pgen.1000623. Epub 2009 Aug 28. PLoS Genet. 2009. PMID: 19714205 Free PMC article.
Microduplications of 16p11.2 are associated with schizophrenia.
McCarthy SE, Makarov V, Kirov G, Addington AM, McClellan J, Yoon S, Perkins DO, Dickel DE, Kusenda M, Krastoshevsky O, Krause V, Kumar RA, Grozeva D, Malhotra D, Walsh T, Zackai EH, Kaplan P, Ganesh J, Krantz ID, Spinner NB, Roccanova P, Bhandari A, Pavon K, Lakshmi B, Leotta A, Kendall J, Lee YH, Vacic V, Gary S, Iakoucheva LM, Crow TJ, Christian SL, Lieberman JA, Stroup TS, Lehtimäki T, Puura K, Haldeman-Englert C, Pearl J, Goodell M, Willour VL, Derosse P, Steele J, Kassem L, Wolff J, Chitkara N, McMahon FJ, Malhotra AK, Potash JB, Schulze TG, Nöthen MM, Cichon S, Rietschel M, Leibenluft E, Kustanovich V, Lajonchere CM, Sutcliffe JS, Skuse D, Gill M, Gallagher L, Mendell NR; Wellcome Trust Case Control Consortium; Craddock N, Owen MJ, O'Donovan MC, Shaikh TH, Susser E, Delisi LE, Sullivan PF, Deutsch CK, Rapoport J, Levy DL, King MC, Sebat J. McCarthy SE, et al. Among authors: sullivan pf. Nat Genet. 2009 Nov;41(11):1223-7. doi: 10.1038/ng.474. Epub 2009 Oct 25. Nat Genet. 2009. PMID: 19855392 Free PMC article.
653 results