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Year Number of Results
1965 2
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2008 1
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2011 3
2012 1
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2015 7
2016 1
2017 3
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100 results

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Page 1
The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaboration.
Palmer DS, Hill B, Hodgson S, Jõeloo M, Kalantzis G, Kousathanas A, Koyama S, Lu W, Namba S, Rodriguez ZB, Shortt JA, Sonehara K, Vartanian N, Vy HMT, Wade IA, White SL, Baya NA, Chami N, Do R, Estrada K, Finer S, Genovese G, Guez J, Itan Y, Kanai M, Lassen FH, Matsuda K, Moutsianas L, Peloso GM, Palta P, Rader DJ, Rendon A, Rocheleau G, Sadeghi-Alavijeh O, Selvaraj MS, Smit RA, Wang D, Wigdor EM, Yu Z; Colorado Center for Personalized Medicine; Estonian Biobank Research Team; Genes & Health Industry Consortium1; Genes & Health Research Team; Penn Medicine BioBank; BioBank Japan Project; Gignoux CR, Heyne H, Loos RJ, Martin HC, Milani L, Natarajan P, Okada Y, Pozdeyev N, van Heel DA, Verma A, Zhou W, Karczewski KJ, Lindgren CM, Neale BM. Palmer DS, et al. Among authors: finer s. medRxiv [Preprint]. 2026 May 24:2026.05.21.26353759. doi: 10.64898/2026.05.21.26353759. medRxiv. 2026. PMID: 42238450 Free PMC article. Preprint.
An ancestry-enriched HNF4A variant and GP2 reveal distinct mechanisms of type 2 diabetes in exome-wide study of 13,674 cases and 41,024 controls.
Hodgson S, Bui V, Hu S, Maroteau C, Bigossi M, Huerta-Chagoya A, Nguyen T, Dawed AY, Koesterer R, Vora M, Stow D, Williamson A, Blee AM, Carrasco-Zanini Sanchez J, Baskar V, Jebarani S, Jacobs BM, Kalantzis G, Rison S, Walter K, Pennarun E, Taylor K, Hsu S; Genes & Health Research Team; MDRF Research Team; Manning A, Udler M, Martin HC, Barroso I, Flannick J, Fumagalli M, Radha V, Pradeepa R, Langenberg C, Mohan V, Anjana RM, van Heel DA, Mercader JM, Jamshidi Y, Finer S, Majithia AR, Siddiqui MK. Hodgson S, et al. Among authors: finer s. medRxiv [Preprint]. 2026 May 19:2025.09.24.25336527. doi: 10.1101/2025.09.24.25336527. medRxiv. 2026. PMID: 42238389 Free PMC article. Preprint.
Multi-ancestry, trans-generational GWAS meta-analysis of gestational diabetes and glycaemic traits during pregnancy reveals limited evidence of pregnancy-specific genetic effects.
Brito Nunes C, Rukins V, Cisse AH, White F, McBride N, Kuang A, Allard C, Ronkainen J, Hughes A, Elliott A, Thorleifsson G, Vaudel M, Laisk T, Gu Y, Lamri A, Chen L, Tuhkanen J, Lahti J, Calas L, Muntaner M, Karhunen V, Choi J, Heiskala A, Hatem G, Fragoso-Bargas N, Rifas-Shiman SL, Paz-Lopez G, Stinson SE, Bhowmik B, Ahlqvist E; Estonian Biobank Research Team; Genes & Health Research Team; Deleuze JF, Eriksson JG, Park J, Teo K, Räikkönen K, Stefansson K, Molina-Vega M, Subbarao P, Beaumont RN, Johansson S, Tuomi T, Hansen T, Engelbrechtsen L, Morcillo S, Oken E, Quigstad E, Birkeland KI, Vääräsmäki M, Hattersley AT, Sebert S, Hitman GA, Kwak SH, Järvelin MR, Prasad RB, Heude B, Meirhaeghe A, Bouchard L, Jacques PÉ, Laivuori H, Tan KH, Anand SS, van Heel DA, Liu S, Njølstad PR, Steinthorsdottir V, Widén E, Keikkala E, Scholtens DM, Lowe WL, Finer S, Morris AP, Mägi R, Zöllner J, Borges MC, Lawlor DA, Hivert MF, Freathy RM, Evans DM, Moen GH. Brito Nunes C, et al. Among authors: finer s. Nat Commun. 2026 Jun 1;17(1):4726. doi: 10.1038/s41467-026-73509-y. Nat Commun. 2026. PMID: 42225636 Free PMC article.
The contribution of apolipoprotein E genetic variation to dementia risk in British South Asians.
Jacobs BM, Chandra A, Foote IF, Durrani F, Waters S, Liu Y, Proitsi P; Genes & Health Research Team; Croft CL, Williams DM, Finer S, Rison S, Mandal A, Siddiqui M, van Heel DA, Marshall CR. Jacobs BM, et al. Among authors: finer s. Brain Commun. 2026 Apr 17;8(3):fcag141. doi: 10.1093/braincomms/fcag141. eCollection 2026. Brain Commun. 2026. PMID: 42205162 Free PMC article.
Meta-analysis across six global biobanks identifies recessive coding associations with complex traits and diseases.
Lassen FH, Kalantzis G, Eoli A, Hill B, Sonehara K, Namba S, Wade I, Hodgson S, Zhou W; BioBank Japan Project; Genes & Health Research Team; BRaVa Consortium; Neale BM, Karczewski KJ, Okada Y, van Heel DA, Finer S, Lindgren CM, Heyne HO, Martin HC, Palmer DS. Lassen FH, et al. Among authors: finer s. Am J Hum Genet. 2026 Jun 4;113(6):1330-1346. doi: 10.1016/j.ajhg.2026.04.005. Epub 2026 May 1. Am J Hum Genet. 2026. PMID: 42068978 Free article.
Data-driven prioritization of high-risk individuals for weight loss interventions.
Demircan K, Carrasco-Zanini J, Williamson A, Beuchel C, Jackson L, Römisch-Margl W, Hansen AL, Finer S, van Heel DA; Genes & Health Research Team; Kastenmüller G, Coghlan M, Moeller I, Wareham NJ, Pietzner M, Langenberg C. Demircan K, et al. Among authors: finer s. Nat Med. 2026 Apr 30. doi: 10.1038/s41591-026-04353-2. Online ahead of print. Nat Med. 2026. PMID: 42062622
Publisher Correction: Multi-ancestry genome-wide association study of severe pregnancy nausea and vomiting.
Fejzo M, Wang X, Tan Q, Zöllner J, Pujol-Gualdo N, Laisk T; Estonian Biobank Research Team; Finer S, van Heel DA; Genes & Health Research Team; Brumpton B, Bhatta L, Hveem K, Jasper EA, Velez Edwards DR, Hellwege JN, Edwards T, Jarvik GP, Luo Y, Khan A, MacGibbon K, Gao Y, Ge G, Averbukh I, Soon E, Angelo M, Magnus P, Johansson S, Njølstad PR, Kim A, Gazal S, Vaudel M, Shu CA, Mancuso N. Fejzo M, et al. Among authors: finer s. Nat Genet. 2026 May;58(5):1186. doi: 10.1038/s41588-026-02608-9. Nat Genet. 2026. PMID: 42050060 No abstract available.
Multi-ancestry genome-wide association study of severe pregnancy nausea and vomiting.
Fejzo M, Wang X, Tan Q, Zöllner J, Pujol-Gualdo N, Laisk T; Estonian Biobank Research Team; Finer S, van Heel DA; Genes & Health Research Team; Brumpton B, Bhatta L, Hveem K, Jasper EA, Velez Edwards DR, Hellwege JN, Edwards T, Jarvik GP, Luo Y, Khan A, MacGibbon K, Gao Y, Ge G, Averbukh I, Soon E, Angelo M, Magnus P, Johansson S, Njølstad PR, Kim A, Gazal S, Vaudel M, Shu CA, Mancuso N. Fejzo M, et al. Among authors: finer s. Nat Genet. 2026 Apr;58(4):810-820. doi: 10.1038/s41588-026-02564-4. Epub 2026 Apr 14. Nat Genet. 2026. PMID: 41981316
100 results