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Nature Genetics|December 27, 2011
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroidsRosa Rademakers, Matt Baker, Alexandra M Nicholson, et al.Nature Genetics|March 20, 2012
Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndromeGijs W E Santen, Emmelien Aten, Yu Sun, et al.Nature Genetics|March 20, 2012
Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traitsJian Yang, Teresa Ferreira, Andrew P Morris, et al.Nature Genetics|March 6, 2012
Ascorbic acid prevents loss of Dlk1-Dio3 imprinting and facilitates generation of all-iPS cell mice from terminally differentiated B cellsMatthias Stadtfeld, Effie Apostolou, Francesco Ferrari, et al.Nature Genetics|March 6, 2012
Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integrationColby Chiang, Jessie C Jacobsen, Carl Ernst, et al.Nature Genetics|February 28, 2012
De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndromeJean-Baptiste Rivière, Bregje W M van Bon, Alexander Hoischen, et al.Nature Genetics|February 28, 2012
Common variants at 11q12, 10q26 and 3p11.2 are associated with prostate cancer susceptibility in JapaneseShusuke Akamatsu, Ryo Takata, Christopher A Haiman, et al.Nature Genetics|January 7, 2015
Transposon mutagenesis identifies genes and evolutionary forces driving gastrointestinal tract tumor progressionHaruna Takeda, Zhubo Wei, Hideto Koso, et al.Nature Genetics|January 7, 2015
High-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitisPhilippe Goyette, Gabrielle Boucher, Dermot Mallon, et al.Pageof 743