Fine-Mapping of Type 2 Diabetes Loci
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Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-01574-3_6
Reference71 articles.
1. 1000 Genomes Project Consortium, Abecasis GR, Altshuler D, Auton A, Brooks LD, Durbin RM, Gibbs RA, Hurles ME, McVean GA (2010) A map of human genome variation from population-scale sequencing. Nature 467(7319):1061–1073. doi: 10.1038/nature09534
2. Abbott A (2011) Europe to map the human epigenome. Nature 477(7366):518. doi: 10.1038/477518a
3. Agarwala V, Flannick J, Sunyaev S, GoT2D Consortium, Altshuler D (2013) Evaluating empirical bounds on complex disease genetic architecture. Nat Genet 45(12):1418–1427. doi: 10.1038/ng.2804
4. Anderson CA, Soranzo N, Zeggini E, Barrett JC (2011) Synthetic associations are unlikely to account for many common disease genome-wide association signals. PLoS Biol 9(1), e1000580. doi: 10.1371/journal.pbio.1000580
5. Albrechtsen A, Grarup N, Li Y, Sparso T, Tian G, Cao H, Jiang T, Kim SY, Korneliussen T, Li Q, Nie C, Wu R, Skotte L, Morris AP, Ladenvall C, Cauchi S, Stancakova A, Andersen G, Astrup A, Banasik K, Bennett AJ, Bolund L, Charpentier G, Chen Y, Dekker JM, Doney AS, Dorkhan M, Forsen T, Frayling TM, Groves CJ, Gui Y, Hallmans G, Hattersley AT, He K, Hitman GA, Holmkvist J, Huang S, Jiang H, Jin X, Justesen JM, Kristiansen K, Kuusisto J, Lajer M, Lantieri O, Li W, Liang H, Liao Q, Liu X, Ma T, Ma X, Manijak MP, Marre M, Mokrosinski J, Morris AD, Mu B, Nielsen AA, Nijpels G, Nilsson P, Palmer CN, Rayner NW, Renstrom F, Ribel-Madsen R, Robertson N, Rolandsson O, Rossing P, Schwartz TW, D.E.S.I.R. Study Group, Slagboom PE, Sterner M, the DIAGRAM Consortium, Tang M, Tarnow L, Tuomi T, Van’t Riet E, van Leeuwen N, Varga TV, Vestmar MA, Walker M, Wang B, Wang Y, Wu H, Xi F, Yengo L, Yu C, Zhang X, Zhang J, Zhang Q, Zhang W, Zheng H, Zhou Y, Altshuler D, t Hart LM, Franks PW, Balkau B, Froguel P, McCarthy MI, Laakso M, Groop L, Christensen C, Brandslund I, Lauritzen T, Witte DR, Linneberg A, Jorgensen T, Hansen T, Wang J, Nielsen R, Pedersen O (2013) Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes. Diabetologia 56(2):298–310. doi: 10.1007/s00125-012-2756-1
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