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Page 1
Leveraging Base Pair Mammalian Constraint to Understand Genetic Variation and Human Disease.
Sullivan PF, Meadows JRS, Gazal S, Phan BN, Li X, Genereux DP, Dong MX, Bianchi M, Andrews G, Sakthikumar S, Nordin J, Roy A, Christmas MJ, Marinescu VD, Wallerman O, Xue JR, Li Y, Yao S, Sun Q, Szatkiewicz J, Wen J, Huckins LM, Lawler AJ, Keough KC, Zheng Z, Zeng J, Wray NR, Johnson J, Chen J; Zoonomia Consortium; Paten B, Reilly SK, Hughes GM, Weng Z, Pollard KS, Pfenning AR, Forsberg-Nilsson K, Karlsson EK, Lindblad-Toh K. Sullivan PF, et al. Among authors: wray nr. bioRxiv [Preprint]. 2023 Mar 10:2023.03.10.531987. doi: 10.1101/2023.03.10.531987. bioRxiv. 2023. Update in: Science. 2023 Apr 28;380(6643):eabn2937. doi: 10.1126/science.abn2937. PMID: 36945512 Free PMC article. Updated. Preprint.
Multi-ancestry polygenic risk scores for venous thromboembolism.
Jee YH, Thibord F, Dominguez A, Sept C, Boulier K, Venkateswaran V, Ding Y, Cherlin T, Verma SS, Faro VL, Bartz TM, Boland A, Brody JA, Deleuze JF, Emmerich J, Germain M, Johnson AD, Kooperberg C, Morange PE, Pankratz N, Psaty BM, Reiner AP, Smadja DM, Sitlani CM, Suchon P, Tang W, Trégouët DA, Zöllner S, Pasaniuc B, Damrauer SM, Sanna S, Snieder H; Lifelines Cohort Study; Kabrhel C, Smith NL, Kraft P; INVENT Consortium. Jee YH, et al. Hum Mol Genet. 2024 Sep 3;33(18):1584-1591. doi: 10.1093/hmg/ddae097. Hum Mol Genet. 2024. PMID: 38879759
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: wray nr. 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 meta-analysis of ascertainment and symptom structures of major depression in case-enriched and community cohorts.
Adams MJ, Thorp JG, Jermy BS, Kwong ASF, Kõiv K, Grotzinger AD, Nivard MG, Marshall S, Milaneschi Y, Baune BT, Müller-Myhsok B, Penninx BWJH, Boomsma DI, Levinson DF, Breen G, Pistis G, Grabe HJ, Tiemeier H, Berger K, Rietschel M, Magnusson PK, Uher R, Hamilton SP, Lucae S, Lehto K, Li QS, Byrne EM, Hickie IB, Martin NG, Medland SE, Wray NR, Tucker-Drob EM; Estonian Biobank Research Team; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium; Lewis CM, McIntosh AM, Derks EM. Adams MJ, et al. Among authors: wray nr. Psychol Med. 2024 Sep;54(12):3459-3468. doi: 10.1017/S0033291724001880. Epub 2024 Sep 26. Psychol Med. 2024. PMID: 39324397 Free PMC article.
Genome-wide fine-mapping improves identification of causal variants.
Wu Y, Zheng Z, Thibaut L, Goddard ME, Wray NR, Visscher PM, Zeng J. Wu Y, et al. Among authors: wray nr. Res Sq [Preprint]. 2024 Aug 7:rs.3.rs-4759390. doi: 10.21203/rs.3.rs-4759390/v1. Res Sq. 2024. PMID: 39149449 Free PMC article. Preprint.
An axis of genetic heterogeneity in autism is indexed by age at diagnosis and is associated with varying developmental and mental health profiles.
Zhang X, Grove J, Gu Y, Buus CK, Nielsen LK, Neufeld SAS, Koko M, Malawsky DS, Wade E, Verhoef E, Gui A, Hegemann L; APEX consortium; iPSYCH Autism Consortium; PGC-PTSD Consortium; Geschwind DH, Wray NR, Havdahl A, Ronald A, St Pourcain B, Robinson EB, Bourgeron T, Baron-Cohen S, Børglum AD, Martin HC, Warrier V. Zhang X, et al. Among authors: wray nr. medRxiv [Preprint]. 2024 Aug 2:2024.07.31.24311279. doi: 10.1101/2024.07.31.24311279. medRxiv. 2024. PMID: 39132493 Free PMC article. Preprint.
Genome-wide meta-analyses of non-response to antidepressants identify novel loci and potential drugs.
Koch E, Jurgenson T, Einarsson G, Mitchell B, Harder A, Garcia-Marin LM, Krebs K, Lin Y, Xiong Y, Research Team EB, Lu Y, Hagg S, Renteria ME, Medland SE, Wray NR, Martin NG, Huebel C, Breen G, Thorgeirsson T, Stefansson H, Stefansson K, Milani L, Andreassen OA, O'Connell KS. Koch E, et al. Among authors: wray nr. medRxiv [Preprint]. 2024 Jul 15:2024.07.13.24310361. doi: 10.1101/2024.07.13.24310361. medRxiv. 2024. PMID: 39072048 Free PMC article. Preprint.
Genome-wide fine-mapping improves identification of causal variants.
Wu Y, Zheng Z, Thibaut L, Goddard ME, Wray NR, Visscher PM, Zeng J. Wu Y, et al. Among authors: wray nr. medRxiv [Preprint]. 2024 Aug 5:2024.07.18.24310667. doi: 10.1101/2024.07.18.24310667. medRxiv. 2024. PMID: 39072021 Free PMC article. Preprint.
422 results