Nature Genetics
Journal Abbreviation: NAT GENET
ISSN: 1061-4036
eISSN: 1546-1718
Publisher: Nature Publishing Group
Publications (53)
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci (2017)
Aung T, Ozaki M, Lee MC, Schlötzer-Schrehardt U, Thorleifsson G, Mizoguchi T, Igo RP, et al.
Journal article
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 (2016)
Dunning AM, Michailidou K, Kuchenbaecker KB, Thompson D, French JD, Beesley J, Healey CS, et al.
Journal article
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma (2016)
Khor CC, Do T, Jia H, Nakano M, George R, Abu-Amero K, Duvesh R, et al.
Journal article
Genome-wide association meta-analysis in Chinese and European individuals identifies ten new loci associated with systemic lupus erythematosus (2016)
Morris DL, Sheng Y, Zhang Y, Wang YF, Zhu Z, Tombleson P, Chen L, et al.
Journal article
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing (2016)
Sifrim A, Hitz MP, Wilsdon A, Breckpot J, Al Turki SH, Thienpont B, Mcrae J, et al.
Journal article
Five endometrial cancer risk loci identified through genome-wide association analysis (2016)
Cheng THT, Thompson DJ, O'Mara TA, Painter JN, Glubb DM, Flach S, Lewis A, et al.
Journal article
Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia (2016)
Meyer E, Carss KJ, Rankin J, Nichols JME, Grozeva D, Joseph AP, Mencacci NE, et al.
Journal article
Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants (2016)
Jin Y, Andersen G, Yorgov D, Ferrara TM, Ben S, Brownson KM, Holland PJ, et al.
Journal article
A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis (2015)
Buch S, Stickel F, Trepo E, Way M, Herrmann A, Nischalke HD, Brosch M, et al.
Journal article
Mutations in the deubiquitinase gene USP8 cause Cushing's disease (2015)
Reincke M, Sbiera S, Hayakawa A, Theodoropoulou M, Osswald A, Beuschlein F, Meitinger T, et al.
Journal article