Nature Genetics

Journal Abbreviation: NAT GENET
ISSN: 1061-4036
eISSN: 1546-1718
Publisher: Nature Publishing Group

Publications (57)

close-button

Types of publications

Journal article
Unpublished / Preprint

Publication year

From
To

Abstract

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease (2017) Sims R, Van Der Lee SJ, Naj AC, Bellenguez C, Badarinarayan N, Jakobsdottir J, Kunkle BW, et al. Journal article Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer (2017) Milne RL, Kuchenbaecker KB, Michailidou K, Beesley J, Kar S, Lindstrom S, Hui S, et al. Journal article Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer (2017) Phelan CM, Kuchenbaecker KB, Tyrer JP, Kar SP, Lawrenson K, Winham SJ, Dennis J, et al. Journal article 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
1 2 3 4 5 6