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Nature Genetics|August 22, 2017
A mutational signature reveals alterations underlying deficient homologous recombination repair in breast cancerPaz Polak, Jaegil Kim, Lior Z Braunstein, et al.Nature Genetics|August 15, 2017
Transcriptional risk scores link GWAS to eQTLs and predict complications in Crohn's diseaseUrko M Marigorta, Lee A Denson, Jeffrey S Hyams, et al.Nature Genetics|August 15, 2017
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephalyDaniela A Braun, Jia Rao, Geraldine Mollet, et al.Nature Genetics|July 18, 2017
Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery diseaseDerek Klarin, Qiuyu Martin Zhu, Connor A Emdin, et al.Nature Genetics|August 8, 2017
TMPRSS2-ERG fusion co-opts master transcription factors and activates NOTCH signaling in primary prostate cancerKen J Kron, Alexander Murison, Stanley Zhou, et al.Nature Genetics|October 24, 2017
Predicting causal variants affecting expression by using whole-genome sequencing and RNA-seq from multiple human tissuesAndrew Anand Brown, Ana Viñuela, Olivier Delaneau, et al.Nature Genetics|October 31, 2017
Ancient hybridization and strong adaptation to viruses across African vervet monkey populationsHannes Svardal, Anna J Jasinska, Cristian Apetrei, et al.Nature Genetics|October 31, 2017
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biologyManuel A Ferreira, Judith M Vonk, Hansjörg Baurecht, et al.Nature Genetics|September 19, 2017
Germline mutations affecting the histone H4 core cause a developmental syndrome by altering DNA damage response and cell cycle controlFederico Tessadori, Jacques C Giltay, Jane A Hurst, et al.Nature Genetics|September 26, 2017
Graphtyper enables population-scale genotyping using pangenome graphsHannes P Eggertsson, Hakon Jonsson, Snaedis Kristmundsdottir, et al.Pageof 744