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Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum.
Ganna A, Satterstrom FK, Zekavat SM, Das I, Kurki MI, Churchhouse C, Alfoldi J, Martin AR, Havulinna AS, Byrnes A, Thompson WK, Nielsen PR, Karczewski KJ, Saarentaus E, Rivas MA, Gupta N, Pietiläinen O, Emdin CA, Lescai F, Bybjerg-Grauholm J, Flannick J; GoT2D/T2D-GENES Consortium; Mercader JM, Udler M; SIGMA Consortium Helmsley IBD Exome Sequencing Project; FinMetSeq Consortium; iPSYCH-Broad Consortium; Laakso M, Salomaa V, Hultman C, Ripatti S, Hämäläinen E, Moilanen JS, Körkkö J, Kuismin O, Nordentoft M, Hougaard DM, Mors O, Werge T, Mortensen PB, MacArthur D, Daly MJ, Sullivan PF, Locke AE, Palotie A, Børglum AD, Kathiresan S, Neale BM. Ganna A, et al. Among authors: sullivan pf. Am J Hum Genet. 2018 Jun 7;102(6):1204-1211. doi: 10.1016/j.ajhg.2018.05.002. Epub 2018 May 31. Am J Hum Genet. 2018. PMID: 29861106 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
Recurrence risks for schizophrenia in a Swedish national cohort.
Lichtenstein P, Björk C, Hultman CM, Scolnick E, Sklar P, Sullivan PF. Lichtenstein P, et al. Among authors: sullivan pf. Psychol Med. 2006 Oct;36(10):1417-25. doi: 10.1017/S0033291706008385. Epub 2006 Jul 25. Psychol Med. 2006. PMID: 16863597
A searchable database of genetic evidence for psychiatric disorders.
Konneker T, Barnes T, Furberg H, Losh M, Bulik CM, Sullivan PF. Konneker T, et al. Among authors: sullivan pf. Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):671-5. doi: 10.1002/ajmg.b.30802. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18548508 Free PMC article.
656 results