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Nature Genetics|September 24, 2013
Arabidopsis meiotic crossover hot spots overlap with H2A.Z nucleosomes at gene promotersKyuha Choi, Xiaohui Zhao, Krystyna A Kelly, et al.Nature Genetics|August 6, 2013
Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertensionElena A B Azizan, Hanne Poulsen, Petronel Tuluc, et al.Nature Genetics|September 28, 2013
Germline PAX5 mutations and B cell leukemiaR Katherine Hyde, P Paul LiuNature Genetics|September 28, 2013
Genomics informs glioblastoma biologyDavid L Schonberg, Shideng Bao, Jeremy N RichNature Genetics|September 28, 2013
Emerging landscape of oncogenic signatures across human cancersGiovanni Ciriello, Martin L Miller, Bülent Arman Aksoy, et al.Nature Genetics|October 1, 2013
Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autismChristian P Schaaf, Manuel L Gonzalez-Garay, Fan Xia, et al.Nature Genetics|August 20, 2013
Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasmsAyana Kon, Lee-Yung Shih, Masashi Minamino, et al.Nature Genetics|December 23, 2015
Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horsesFreyja Imsland, Kelly McGowan, Carl-Johan Rubin, et al.Nature Genetics|December 8, 2015
A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiencyHaifa H Jabara, Steven E Boyden, Janet Chou, et al.Nature Genetics|December 8, 2015
Abundant contribution of short tandem repeats to gene expression variation in humansMelissa Gymrek, Thomas Willems, Audrey Guilmatre, et al.Pageof 745