Showing 1 - 3 results of 3 for search 'Makinen, N', query time: 0.02s
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MED12 exon 2 mutations are common in uterine leiomyomas from South African patients. by Mäkinen, N, Heinonen, H, Moore, S, Moore, S, Tomlinson, I, Tomlinson, I, van der Spuy, Z, van der Spuy, Z, Aaltonen, L, Aaltonen, L
Published 2013Journal article -
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Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis by 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
Published 2019Journal article -
3
Genome-wide association analysis identifies 27 novel loci associated with uterine leiomyomata revealing common genetic origins with endometriosis by 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
Published 2018Journal article