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423 results

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Page 1
Genome-wide copy number variation association study in anorexia nervosa.
Walker A, Karlsson R, Szatkiewicz JP, Thornton LM, Yilmaz Z, Leppä VM, Savva A, Lin T, Sidorenko J, McRae A, Kirov G, Davies HL, Fundín BT, Chawner SJRA, Song J, Borg S, Wen J, Watson HJ, Munn-Chernoff MA, Baker JH, Gordon S, Berrettini WH, Brandt H, Crawford S, Halmi KA, Kaplan AS, Kaye WH, Mitchell J, Strober M, Woodside DB, Pedersen NL, Parker R, Jordan J, Kennedy MA, Birgegård A, Landén M, Martin NG, Sullivan PF, Bulik CM, Wray NR. Walker A, et al. Among authors: wray nr. Mol Psychiatry. 2024 Nov 12. doi: 10.1038/s41380-024-02811-2. Online ahead of print. Mol Psychiatry. 2024. PMID: 39533101
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.
Genome-wide association study of major anxiety disorders in 122,341 European-ancestry cases identifies 58 loci and highlights GABAergic signaling.
Strom NI, Verhulst B, Bacanu SA, Cheesman R, Purves KL, Gedik H, Mitchell BL, Kwong AS, Faucon AB, Singh K, Medland S, Colodro-Conde L, Krebs K, Hoffmann P, Herms S, Gehlen J, Ripke S, Awasthi S, Palviainen T, Tasanko EM, Peterson RE, Adkins DE, Shabalin AA, Adams MJ, Iveson MH, Campbell A, Thomas LF, Winsvold BS, Drange OK, Børte S, Ter Kuile AR, Nguyen TH, Meier SM, Corfield EC, Hannigan L, Levey DF, Czamara D, Weber H, Choi KW, Pistis G, Couvy-Duchesne B, Van der Auwera S, Teumer A, Karlsson R, Garcia-Argibay M, Lee D, Wang R, Bjerkeset O, Stordal E, Bäckmann J, Salum GA, Zai CC, Kennedy JL, Zai G, Tiwari AK, Heilmann-Heimbach S, Schmidt B, Kaprio J, Kennedy MM, Boden J, Havdahl A, Middeldorp CM, Lopes FL, Akula N, McMahon FJ, Binder EB, Fehm L, Ströhle A, Castelao E, Tiemeier H, Stein DJ, Whiteman D, Olsen C, Fuller Z, Wang X, Wray NR, Byrne EM, Lewis G, Timpson NJ, Davis LK, Hickie IB, Gillespie NA, Milani L, Schumacher J, Woldbye DP, Forstner AJ, Nöthen MM, Hovatta I, Horwood J, Copeland WE, Maes HH, McIntosh AM, Andreassen OA, Zwart JA, Mors O, Børglum AD, Mortensen PB, Ask H, Reichborn-Kjennerud T, Najman JM, Stein MB, Gelernter J, Milaneschi Y, Penninx BW, Boomsma … See abstract for full author list ➔ Strom NI, et al. Among authors: wray nr. medRxiv [Preprint]. 2024 Jul 5:2024.07.03.24309466. doi: 10.1101/2024.07.03.24309466. medRxiv. 2024. PMID: 39006447 Free PMC article. Preprint.
Distinct genetic liability profiles define clinically relevant patient strata across common diseases.
Trastulla L, Dolgalev G, Moser S, Jiménez-Barrón LT, Andlauer TFM, von Scheidt M; Schizophrenia Working Group of the Psychiatric Genomics Consortium; Budde M, Heilbronner U, Papiol S, Teumer A, Homuth G, Völzke H, Dörr M, Falkai P, Schulze TG, Gagneur J, Iorio F, Müller-Myhsok B, Schunkert H, Ziller MJ. Trastulla L, et al. Nat Commun. 2024 Jul 1;15(1):5534. doi: 10.1038/s41467-024-49338-2. Nat Commun. 2024. PMID: 38951512 Free PMC article.
423 results