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The flashfm approach for fine-mapping multiple quantitative traits.
Hernández N, Soenksen J, Newcombe P, Sandhu M, Barroso I, Wallace C, Asimit JL. Hernández N, et al. Among authors: asimit jl. Nat Commun. 2021 Oct 22;12(1):6147. doi: 10.1038/s41467-021-26364-y. Nat Commun. 2021. PMID: 34686674 Free PMC article.
Multi-trait discovery and fine-mapping of lipid loci in 125,000 individuals of African ancestry.
Kamiza AB, Touré SM, Zhou F, Soremekun O, Cissé C, Wélé M, Touré AM, Nashiru O, Corpas M, Nyirenda M, Crampin A, Shaffer J, Doumbia S, Zeggini E, Morris AP, Asimit JL, Chikowore T, Fatumo S. Kamiza AB, et al. Among authors: asimit jl. Nat Commun. 2023 Sep 5;14(1):5403. doi: 10.1038/s41467-023-41271-0. Nat Commun. 2023. PMID: 37669986 Free PMC article.
Trans-ethnic study design approaches for fine-mapping.
Asimit JL, Hatzikotoulas K, McCarthy M, Morris AP, Zeggini E. Asimit JL, et al. Eur J Hum Genet. 2016 Aug;24(9):1330-6. doi: 10.1038/ejhg.2016.1. Epub 2016 Feb 3. Eur J Hum Genet. 2016. PMID: 26839038 Free PMC article.
A Bayesian Approach to the Overlap Analysis of Epidemiologically Linked Traits.
Asimit JL, Panoutsopoulou K, Wheeler E, Berndt SI; GIANT consortium, the arcOGEN consortium; Cordell HJ, Morris AP, Zeggini E, Barroso I. Asimit JL, et al. Genet Epidemiol. 2015 Dec;39(8):624-34. doi: 10.1002/gepi.21919. Epub 2015 Sep 28. Genet Epidemiol. 2015. PMID: 26411566 Free PMC article.
TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport.
Schmidts M, Hou Y, Cortés CR, Mans DA, Huber C, Boldt K, Patel M, van Reeuwijk J, Plaza JM, van Beersum SE, Yap ZM, Letteboer SJ, Taylor SP, Herridge W, Johnson CA, Scambler PJ, Ueffing M, Kayserili H, Krakow D, King SM; UK10K; Beales PL, Al-Gazali L, Wicking C, Cormier-Daire V, Roepman R, Mitchison HM, Witman GB. Schmidts M, et al. Nat Commun. 2015 Jun 5;6:7074. doi: 10.1038/ncomms8074. Nat Commun. 2015. PMID: 26044572 Free PMC article.
Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms.
Horikoshi M, Pasquali L, Wiltshire S, Huyghe JR, Mahajan A, Asimit JL, Ferreira T, Locke AE, Robertson NR, Wang X, Sim X, Fujita H, Hara K, Young R, Zhang W, Choi S, Chen H, Kaur I, Takeuchi F, Fontanillas P, Thuillier D, Yengo L, Below JE, Tam CH, Wu Y, Abecasis G, Altshuler D, Bell GI, Blangero J, Burtt NP, Duggirala R, Florez JC, Hanis CL, Seielstad M, Atzmon G, Chan JC, Ma RC, Froguel P, Wilson JG, Bharadwaj D, Dupuis J, Meigs JB, Cho YS, Park T, Kooner JS, Chambers JC, Saleheen D, Kadowaki T, Tai ES, Mohlke KL, Cox NJ, Ferrer J, Zeggini E, Kato N, Teo YY, Boehnke M, McCarthy MI, Morris AP; T2D-GENES Consortium. Horikoshi M, et al. Among authors: asimit jl. Hum Mol Genet. 2016 May 15;25(10):2070-2081. doi: 10.1093/hmg/ddw048. Epub 2016 Feb 23. Hum Mol Genet. 2016. PMID: 26911676 Free PMC article.
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