MED12 exon 2 mutations are common in uterine leiomyomas from South African patients. par Mäkinen, N, Heinonen, H, Moore, S, Moore, S, Tomlinson, I, Tomlinson, I, van der Spuy, Z, van der Spuy, Z, Aaltonen, L, Aaltonen, L

Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis par Gallagher, CS, Mäkinen, N, Harris, HR, Rahmioglu, N, Uimari, O, Cook, JP, Shigesi, N, Ferreira, T, Velez-Edwards, DR, Edwards, TL, Mortlock, S, Ruhioglu, Z, Day, F, Becker, CM, Karhunen, V, Martikainen, H, Järvelin, M-R, Cantor, RM, Ridker, PM, Terry, KL, Buring, JE, Gordon, SD, Medland, SE, Montgomery, GW, Nyholt, DR

Genome-wide association analysis identifies 27 novel loci associated with uterine leiomyomata revealing common genetic origins with endometriosis par Gallagher, C, Makinen, N, Harris, H, Uimari, O, Cook, J, Shigesi, N, Rahmioglu, N, Ferreira, T, Velez-Edwards, D, Edwards, T, Ruhioglu, Z, Day, F, Becker, C, Karhunen, V, Martikainen, H, Jarvelin, M, Cantor, R, Ridker, P, Terry, K, Buring, J, Gordon, S, Medland, S, Montgomery, G, Nyholt, D, Hinds, D, Tung, J, Perry, J, Lind, P, Painter, J, Martin, N, Morris, A, Chasman, D, Missmer, S, Zondervan, K, Morton, C, 23andMe Research Team