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Nature Genetics|August 31, 2012
Incomplete methylation reprogramming in SCNT embryosJulian R Peat, Wolf ReikNature Genetics|September 25, 2012
Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer riskNick Orr, Alina Lemnrau, Rosie Cooke, et al.Nature Genetics|July 10, 2012
FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repairWeibin Zhou, Edgar A Otto, Andrew Cluckey, et al.Nature Genetics|July 10, 2012
Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosisMary J Emond, Tin Louie, Julia Emerson, et al.Nature Genetics|July 4, 2012
Activation of the AXL kinase causes resistance to EGFR-targeted therapy in lung cancerZhenfeng Zhang, Jae Cheol Lee, Luping Lin, et al.Nature Genetics|July 4, 2012
Structural diversity and African origin of the 17q21.31 inversion polymorphismKaryn Meltz Steinberg, Francesca Antonacci, Peter H Sudmant, et al.Nature Genetics|June 19, 2012
Genome-wide efficient mixed-model analysis for association studiesXiang Zhou, Matthew StephensNature Genetics|June 19, 2012
An efficient multi-locus mixed-model approach for genome-wide association studies in structured populationsVincent Segura, Bjarni J Vilhjálmsson, Alexander Platt, et al.Nature Genetics|September 10, 1998
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2BR Bashir, S Britton, T Strachan, et al.Pageof 745