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Nature Genetics|September 1, 1996
Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish familiesM M Mahtani, E Widén, M Lehto, et al.Nature Genetics|September 1, 1996
Leptin activation of Stat3 in the hypothalamus of wild-type and ob/ob mice but not db/db miceC Vaisse, J L Halaas, C M Horvath, et al.Nature Genetics|September 1, 1996
Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contracturesG J Jöbsis, H Keizers, J P Vreijling, et al.Nature Genetics|October 11, 2016
Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variantsYing Jin, Genevieve Andersen, Daniel Yorgov, et al.Nature Genetics|October 11, 2016
Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiencyPaola G Bronson, Diana Chang, Tushar Bhangale, et al.Nature Genetics|October 11, 2016
Chromatin structure-based prediction of recurrent noncoding mutations in cancerKwoneel Kim, Kiwon Jang, Woojin Yang, et al.Nature Genetics|November 8, 2016
Identification of genomic loci associated with resting heart rate and shared genetic predictors with all-cause mortalityRuben N Eppinga, Yanick Hagemeijer, Stephen Burgess, et al.Nature Genetics|November 8, 2016
Mycobacterium tuberculosis lineage 4 comprises globally distributed and geographically restricted sublineagesDavid Stucki, Daniela Brites, Leïla Jeljeli, et al.Nature Genetics|March 31, 2017
25 more yearsNature Genetics|January 30, 2014
Advantages and pitfalls in the application of mixed-model association methodsJian Yang, Noah A Zaitlen, Michael E Goddard, et al.Pageof 744