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Asimit, Jennifer L ORCID: 0000-0002-4857-2249, Hatzikotoulas, Konstantinos ORCID: 0000-0002-4699-3672, McCarthy, Mark, Morris, Andrew P and Zeggini, Eleftheria (2016) Trans-ethnic study design approaches for fine-mapping. EUROPEAN JOURNAL OF HUMAN GENETICS, 24 (9). 1330 - 1336.

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Horikoshi, Momoko, Pasquali, Lorenzo ORCID: 0000-0003-2423-1826, Wiltshire, Steven, Huyghe, Jeroen R, Mahajan, Anubha ORCID: 0000-0001-5585-3420, Asimit, Jennifer L ORCID: 0000-0002-4857-2249, Ferreira, Teresa, Locke, Adam E ORCID: 0000-0001-6227-198X, Robertson, Neil R, Wang, Xu et al (show 49 more authors) , Sim, Xueling, Fujita, Hayato, Hara, Kazuo, Young, Robin, Zhang, Weihua, Choi, Sungkyoung, Chen, Han ORCID: 0000-0002-9510-4923, Kaur, Ismeet, Takeuchi, Fumihiko, Fontanillas, Pierre, Thuillier, Dorothee, Yengo, Loic ORCID: 0000-0002-4272-9305, Below, Jennifer E ORCID: 0000-0002-6372-6402, Tam, Claudia HT, Wu, Ying, Abecasis, Goncalo, Altshuler, David, Bell, Graeme I, Blangero, John, Burtt, Noel P, Duggirala, Ravindranath, Florez, Jose C, Hanis, Craig L, Seielstad, Mark ORCID: 0000-0001-5783-1401, Atzmon, Gil, Chan, Juliana CN ORCID: 0000-0003-1325-1194, Ma, Ronald CW ORCID: 0000-0002-1227-803X, Froguel, Philippe ORCID: 0000-0003-2972-0784, Wilson, James G, Bharadwaj, Dwaipayan, Dupuis, Josee ORCID: 0000-0003-2871-3603, Meigs, James B, Cho, Yoon Shin, Park, Taesung, Kooner, Jaspal S, Chambers, John C, Saleheen, Danish, Kadowaki, Takashi, Tai, E Shyong ORCID: 0000-0003-2929-8966, Mohlke, Karen L, Cox, Nancy J, Ferrer, Jorge, Zeggini, Eleftheria, Kato, Norihiro, Teo, Yik Ying, Boehnke, Michael, McCarthy, Mark I, Morris, Andrew P and Consortium, T2D-GENES (2016) Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms. HUMAN MOLECULAR GENETICS, 25 (10). 2070 - 2081.

Asimit, Jennifer L, Payne, Felicity ORCID: 0000-0003-4228-581X, Morris, Andrew P, Cordell, Heather J and Barroso, Ines ORCID: 0000-0001-5800-4520 (2017) A two-stage inter-rater approach for enrichment testing of variants associated with multiple traits. EUROPEAN JOURNAL OF HUMAN GENETICS, 25 (3). 341 - 349.