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Nature Genetics|February 26, 2011
Towards a medical grade human genome sequenceNature Genetics|January 18, 2011
Mutations of the SLX4 gene in Fanconi anemiaYonghwan Kim, Francis P Lach, Rohini Desetty, et al.Nature Genetics|October 19, 2010
Genome-wide association analysis identifies three psoriasis susceptibility lociPhilip E Stuart, Rajan P Nair, Eva Ellinghaus, et al.Nature Genetics|October 19, 2010
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1, Amy Strange, Francesca Capon, et al.Nature Genetics|June 22, 2010
Common SNPs explain a large proportion of the heritability for human heightJian Yang, Beben Benyamin, Brian P McEvoy, et al.Nature Genetics|July 27, 2010
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemiaChristopher T Johansen, Jian Wang, Matthew B Lanktree, et al.Nature Genetics|June 21, 2011
A genetic interaction network of five genes for human polycystic kidney and liver diseases defines polycystin-1 as the central determinant of cyst formationSorin V Fedeles, Xin Tian, Anna-Rachel Gallagher, et al.Nature Genetics|June 21, 2011
Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytomaIñaki Comino-Méndez, Francisco J Gracia-Aznárez, Francesca Schiavi, et al.Nature Genetics|June 7, 2011
The nuclear deubiquitinase BAP1 is commonly inactivated by somatic mutations and 3p21.1 losses in malignant pleural mesotheliomaMatthew Bott, Marie Brevet, Barry S Taylor, et al.Nature Genetics|June 14, 2011
Genome-wide association study identifies two new susceptibility loci for atopic dermatitis in the Chinese Han populationLiang-Dan Sun, Feng-Li Xiao, Yang Li, et al.Pageof 745