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Nature Genetics|September 5, 2007
Methods and strategies for analyzing copy number variation using DNA microarraysNigel P CarterNature Genetics|September 5, 2007
Copy-number variation and association studies of human diseaseSteven A McCarroll, David M AltshulerNature Genetics|July 3, 2007
Germline gain-of-function mutations in RAF1 cause Noonan syndromeM Abdur Razzaque, Tsutomu Nishizawa, Yuta Komoike, et al.Nature Genetics|July 3, 2007
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathyBhaswati Pandit, Anna Sarkozy, Len A Pennacchio, et al.Nature Genetics|July 31, 2007
Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosusMin Ae Lee-Kirsch, Maolian Gong, Dipanjan Chowdhury, et al.Nature Genetics|May 15, 2007
Variation in FTO contributes to childhood obesity and severe adult obesityChristian Dina, David Meyre, Sophie Gallina, et al.Nature Genetics|May 29, 2007
A conserved molecular pathway mediates myoblast fusion in insects and vertebratesBhylahalli P Srinivas, Jennifer Woo, Wan Ying Leong, et al.Nature Genetics|April 24, 2007
Modifiers of epigenetic reprogramming show paternal effects in the mouseSuyinn Chong, Nicola Vickaryous, Alyson Ashe, et al.Nature Genetics|April 17, 2007
Direct quantitative trait locus mapping of mammalian metabolic phenotypes in diabetic and normoglycemic rat modelsMarc-Emmanuel Dumas, Steven P Wilder, Marie-Thérèse Bihoreau, et al.Nature Genetics|June 6, 2006
Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle diseaseMark I Rees, Kirsten Harvey, Brian R Pearce, et al.Pageof 745