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Nature Genetics|April 8, 2015
Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shorteningBridget D Stuart, Jungmin Choi, Samir Zaidi, et al.Nature Genetics|April 8, 2015
Genetic conflict reflected in tissue-specific maps of genomic imprinting in human and mouseTomas Babak, Brian DeVeale, Emily K Tsang, et al.Nature Genetics|April 8, 2015
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunctionNaiara Akizu, Vincent Cantagrel, Maha S Zaki, et al.Nature Genetics|March 26, 2015
Letters from IcelandNature Genetics|March 26, 2015
Identification of a large set of rare complete human knockoutsPatrick Sulem, Hannes Helgason, Asmundur Oddson, et al.Nature Genetics|May 11, 2023
Mobile element variation contributes to population-specific genome diversification, gene regulation and disease riskShohei Kojima, Satoshi Koyama, Mirei Ka, et al.Nature Genetics|January 7, 2014
Antagonistic roles of ubiquitin ligase HEI10 and SUMO ligase RNF212 regulate meiotic recombinationHuanyu Qiao, H B D Prasada Rao, Ye Yang, et al.Nature Genetics|October 30, 2012
A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancerJulius Gudmundsson, Patrick Sulem, Daniel F Gudbjartsson, et al.Nature Genetics|October 30, 2012
Bayesian refinement of association signals for 14 loci in 3 common diseases, Julian B Maller, Gilean McVean, et al.Nature Genetics|October 30, 2012
Exome sequencing of serous endometrial tumors identifies recurrent somatic mutations in chromatin-remodeling and ubiquitin ligase complex genesMatthieu Le Gallo, Andrea J O'Hara, Meghan L Rudd, et al.Pageof 744