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18 results

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Page 1
Genetic Liabilities Differentiating Bipolar Disorder, Schizophrenia, and Major Depressive Disorder, and Phenotypic Heterogeneity in Bipolar Disorder.
Richards AL, Cardno A, Harold G, Craddock NJ, Di Florio A, Jones L, Gordon-Smith K, Jones I, Sellers R, Walters JTR, Holmans PA, Owen MJ, O'Donovan MC. Richards AL, et al. Among authors: craddock nj. JAMA Psychiatry. 2022 Oct 1;79(10):1032-1039. doi: 10.1001/jamapsychiatry.2022.2594. JAMA Psychiatry. 2022. PMID: 36044200 Free PMC article.
Specificity of polygenic signatures across symptom dimensions in bipolar disorder: an analysis of UK Bipolar Disorder Research Network data.
Allardyce J, Cardno AG, Gordon-Smith K, Jones L, Di Florio A, Walters JTR, Holmans PA, Craddock NJ, Jones I, Owen MJ, Escott-Price V, O'Donovan MC. Allardyce J, et al. Among authors: craddock nj. Lancet Psychiatry. 2023 Aug;10(8):623-631. doi: 10.1016/S2215-0366(23)00186-4. Epub 2023 Jul 9. Lancet Psychiatry. 2023. PMID: 37437579 Free article.
Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene.
Buxbaum JD, Georgieva L, Young JJ, Plescia C, Kajiwara Y, Jiang Y, Moskvina V, Norton N, Peirce T, Williams H, Craddock NJ, Carroll L, Corfas G, Davis KL, Owen MJ, Harroch S, Sakurai T, O'Donovan MC. Buxbaum JD, et al. Among authors: craddock nj. Mol Psychiatry. 2008 Feb;13(2):162-72. doi: 10.1038/sj.mp.4001991. Epub 2007 Apr 17. Mol Psychiatry. 2008. PMID: 17579610 Free PMC article.
Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women.
Shifman S, Johannesson M, Bronstein M, Chen SX, Collier DA, Craddock NJ, Kendler KS, Li T, O'Donovan M, O'Neill FA, Owen MJ, Walsh D, Weinberger DR, Sun C, Flint J, Darvasi A. Shifman S, et al. Among authors: craddock nj. PLoS Genet. 2008 Feb;4(2):e28. doi: 10.1371/journal.pgen.0040028. PLoS Genet. 2008. PMID: 18282107 Free PMC article.
GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia.
Chen X, Lee G, Maher BS, Fanous AH, Chen J, Zhao Z, Guo A, van den Oord E, Sullivan PF, Shi J, Levinson DF, Gejman PV, Sanders A, Duan J, Owen MJ, Craddock NJ, O'Donovan MC, Blackman J, Lewis D, Kirov GK, Qin W, Schwab S, Wildenauer D, Chowdari K, Nimgaonkar V, Straub RE, Weinberger DR, O'Neill FA, Walsh D, Bronstein M, Darvasi A, Lencz T, Malhotra AK, Rujescu D, Giegling I, Werge T, Hansen T, Ingason A, Nöethen MM, Rietschel M, Cichon S, Djurovic S, Andreassen OA, Cantor RM, Ophoff R, Corvin A, Morris DW, Gill M, Pato CN, Pato MT, Macedo A, Gurling HM, McQuillin A, Pimm J, Hultman C, Lichtenstein P, Sklar P, Purcell SM, Scolnick E, St Clair D, Blackwood DH, Kendler KS; GROUP investigators; International Schizophrenia Consortium. Chen X, et al. Among authors: craddock nj. Mol Psychiatry. 2011 Nov;16(11):1117-29. doi: 10.1038/mp.2010.96. Epub 2010 Sep 14. Mol Psychiatry. 2011. PMID: 20838396 Free PMC article.
18 results