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Nature Genetics|March 8, 2011
Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosisBertrand Isidor, Pierre Lindenbaum, Olivier Pichon, et al.Nature Genetics|April 12, 2011
High conservation of transcription factor binding and evidence for combinatorial regulation across six Drosophila speciesQiye He, Anaïs F Bardet, Brianne Patton, et al.Nature Genetics|May 31, 2011
Genome-wide association identifies three new susceptibility loci for Paget's disease of boneOmar M E Albagha, Sachin E Wani, Micaela R Visconti, et al.Nature Genetics|December 15, 2010
Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel diseaseYukihide Momozawa, Myriam Mni, Kayo Nakamura, et al.Nature Genetics|December 15, 2010
Genome-wide association study identifies a locus at 7p15.2 associated with endometriosisJodie N Painter, Carl A Anderson, Dale R Nyholt, et al.Nature Genetics|February 1, 2011
Common variants in ZNF365 are associated with both mammographic density and breast cancer riskSara Lindström, Celine M Vachon, Jingmei Li, et al.Nature Genetics|February 1, 2011
Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and fliesDaniele Ghezzi, Paola Arzuffi, Mauro Zordan, et al.Nature Genetics|February 22, 2011
Association of a functional variant downstream of TNFAIP3 with systemic lupus erythematosusIndra Adrianto, Feng Wen, Amanda Templeton, et al.Nature Genetics|February 15, 2011
SUMOylation promotes de novo targeting of HP1α to pericentric heterochromatinChristèle Maison, Delphine Bailly, Danièle Roche, et al.Nature Genetics|February 15, 2011
Discovery and genotyping of genome structural polymorphism by sequencing on a population scaleRobert E Handsaker, Joshua M Korn, James Nemesh, et al.Pageof 745