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Pitfalls in performing genome-wide association studies on ratio traits.
McCaw ZR, Dey R, Somineni H, Amar D, Mukherjee S, Sandor K; insitro Research Team; Karaletsos T, Koller D, Aschard H, Smith GD, MacArthur D, O'Dushlaine C, Soare TW. McCaw ZR, et al. Among authors: macarthur d. HGG Adv. 2025 Jan 15:100406. doi: 10.1016/j.xhgg.2025.100406. Online ahead of print. HGG Adv. 2025. PMID: 39818621
Investigating misclassification of type 1 diabetes in a population-based cohort of British Pakistanis and Bangladeshis using polygenic risk scores.
Liu T, Sankareswaran A, Paterson G; Genes & Health Research Team; Fraser DP, Hodgson S, Huang QQ, Heng TH, Ladwa M, Thomas N, van Heel DA, Weedon MN, Yajnik CS, Oram RA, Chandak GR, Martin HC, Finer S. Liu T, et al. Sci Rep. 2025 Jan 13;15(1):1168. doi: 10.1038/s41598-024-80348-8. Sci Rep. 2025. PMID: 39805939 Free PMC article.
Genetic basis of early onset and progression of type 2 diabetes in South Asians.
Hodgson S, Williamson A, Bigossi M, Stow D, Jacobs BM, Samuel M, Gafton J, Zöllner J, Spreckley M; Genes & Health Research Team; Langenberg C, van Heel DA, Mathur R, Siddiqui MK, Finer S. Hodgson S, et al. Nat Med. 2024 Nov 26. doi: 10.1038/s41591-024-03317-8. Online ahead of print. Nat Med. 2024. PMID: 39592779
Altered IL-6 signalling and risk of tuberculosis: a multi-ancestry mendelian randomisation study.
Hamilton F, Schurz H, Yates TA, Gilchrist JJ, Möller M, Naranbhai V, Ghazal P, Timpson NJ; Genes & Health Research Team; International Tuberculosis Host Genetics Consortium; Parks T, Pollara G. Hamilton F, et al. Lancet Microbe. 2025 Jan;6(1):100922. doi: 10.1016/S2666-5247(24)00162-9. Epub 2024 Nov 21. Lancet Microbe. 2025. PMID: 39579785 Free article.
Neurodevelopmental Disorder Caused by Deletion of CHASERR, a lncRNA Gene.
Ganesh VS, Riquin K, Chatron N, Yoon E, Lamar KM, Aziz MC, Monin P, O'Leary MC, Goodrich JK, Garimella KV, England E, Weisburd B, Aguet F, Bacino CA, Murdock DR, Dai H, Rosenfeld JA, Emrick LT, Ketkar S, Sarusi Y, Sanlaville D, Kayani S, Broadbent B, Pengam A, Isidor B, Bezieau S, Cogné B, MacArthur DG, Ulitsky I, Carvill GL, O'Donnell-Luria A. Ganesh VS, et al. Among authors: macarthur dg. N Engl J Med. 2024 Oct 24;391(16):1511-1518. doi: 10.1056/NEJMoa2400718. N Engl J Med. 2024. PMID: 39442041
Genetic architecture of routinely acquired blood tests in a British South Asian cohort.
Jacobs BM, Stow D, Hodgson S, Zöllner J, Samuel M, Kanoni S, Bidi S; Genes & Health Research Team; Walter K, Langenberg C, Dobson R, Finer S, Morton C, Siddiqui MK, Martin HC, Pietzner M, Mathur R, van Heel DA. Jacobs BM, et al. Nat Commun. 2024 Oct 16;15(1):8929. doi: 10.1038/s41467-024-53091-x. Nat Commun. 2024. PMID: 39414775 Free PMC article.
A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disorders.
Lee AS, Ayers LJ, Kosicki M, Chan WM, Fozo LN, Pratt BM, Collins TE, Zhao B, Rose MF, Sanchis-Juan A, Fu JM, Wong I, Zhao X, Tenney AP, Lee C, Laricchia KM, Barry BJ, Bradford VR, Jurgens JA, England EM, Lek M, MacArthur DG, Lee EA, Talkowski ME, Brand H, Pennacchio LA, Engle EC. Lee AS, et al. Among authors: macarthur dg. Nat Commun. 2024 Sep 27;15(1):8268. doi: 10.1038/s41467-024-52463-7. Nat Commun. 2024. PMID: 39333082 Free PMC article.
378 results