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Nature Genetics|September 18, 2012
Exome sequencing identifies MVK mutations in disseminated superficial actinic porokeratosisSheng-Quan Zhang, Tao Jiang, Min Li, et al.Nature Genetics|September 25, 2012
Breast cancer risk-associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expressionRichard Cowper-Sal lari, Xiaoyang Zhang, Jason B Wright, et al.Nature Genetics|September 25, 2012
Estimating the human mutation rate using autozygosity in a founder populationCatarina D Campbell, Jessica X Chong, Maika Malig, et al.Nature Genetics|July 31, 2012
Mutations in NMNAT1 cause Leber congenital amaurosis with early-onset severe macular and optic atrophyIsabelle Perrault, Sylvain Hanein, Xavier Zanlonghi, et al.Nature Genetics|July 31, 2012
Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degenerationRobert K Koenekoop, Hui Wang, Jacek Majewski, et al.Nature Genetics|August 7, 2012
Shigella sonnei genome sequencing and phylogenetic analysis indicate recent global dissemination from EuropeKathryn E Holt, Stephen Baker, François-Xavier Weill, et al.Nature Genetics|August 7, 2012
Plasmodium cynomolgi genome sequences provide insight into Plasmodium vivax and the monkey malaria cladeShin-Ichiro Tachibana, Steven A Sullivan, Satoru Kawai, et al.Nature Genetics|August 28, 2012
A low-frequency variant at 8q24.21 is strongly associated with risk of oligodendroglial tumors and astrocytomas with IDH1 or IDH2 mutationRobert B Jenkins, Yuanyuan Xiao, Hugues Sicotte, et al.Nature Genetics|September 4, 2012
Common variants at 6p21.1 are associated with large artery atherosclerotic strokeElizabeth G Holliday, Jane M Maguire, Tiffany-Jane Evans, et al.Nature Genetics|August 31, 2012
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