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Nature Genetics|July 21, 2014
Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune diseaseSarah E Flanagan, Emma Haapaniemi, Mark A Russell, et al.Nature Genetics|July 21, 2014
Most genetic risk for autism resides with common variationTrent Gaugler, Lambertus Klei, Stephan J Sanders, et al.Nature Genetics|June 26, 2013
Integrated molecular analysis of clear-cell renal cell carcinomaYusuke Sato, Tetsuichi Yoshizato, Yuichi Shiraishi, et al.Nature Genetics|August 11, 2014
A common missense variant in NUDT15 confers susceptibility to thiopurine-induced leukopeniaSuk-Kyun Yang, Myunghee Hong, Jiwon Baek, et al.Nature Genetics|December 3, 2013
A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemiaHelen E Speedy, Maria Chiara Di Bernardo, Georgina P Sava, et al.Nature Genetics|December 14, 2011
Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromesTimothy A Graubert, Dong Shen, Li Ding, et al.Nature Genetics|December 20, 2011
A chromatin-modifying function of JNK during stem cell differentiationVijay K Tiwari, Michael B Stadler, Christiane Wirbelauer, et al.Nature Genetics|December 20, 2011
Whole-genome sequencing of rifampicin-resistant Mycobacterium tuberculosis strains identifies compensatory mutations in RNA polymerase genesIñaki Comas, Sonia Borrell, Andreas Roetzer, et al.Nature Genetics|December 18, 2012
Whole-genome sequencing of giant pandas provides insights into demographic history and local adaptationShancen Zhao, Pingping Zheng, Shanshan Dong, et al.Nature Genetics|December 25, 2012
Chromatin marks identify critical cell types for fine mapping complex trait variantsGosia Trynka, Cynthia Sandor, Buhm Han, et al.Pageof 745