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Nature Genetics|May 22, 2012
Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancerChristopher E Barbieri, Sylvan C Baca, Michael S Lawrence, et al.Nature Genetics|May 15, 2012
Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1Carine Bonnard, Anna C Strobl, Mohammad Shboul, et al.Nature Genetics|December 4, 2012
Large-scale association analysis identifies new risk loci for coronary artery disease, Panos Deloukas, Stavroula Kanoni, et al.Nature Genetics|November 27, 2012
The draft genome of sweet orange (Citrus sinensis)Qiang Xu, Ling-Ling Chen, Xiaoan Ruan, et al.Nature Genetics|December 3, 2013
EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertensionMélanie Eyries, David Montani, Barbara Girerd, et al.Nature Genetics|December 10, 2013
Fusion of TTYH1 with the C19MC microRNA cluster drives expression of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMRClaudia L Kleinman, Noha Gerges, Simon Papillon-Cavanagh, et al.Nature Genetics|October 30, 2013
Taking pan-cancer analysis globalNature Genetics|December 17, 2013
Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signalingClare V Logan, György Szabadkai, Jenny A Sharpe, et al.Pageof 744