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Nature Genetics|January 31, 2007
Human Genome Variation 2006: emerging views on structural variation and large-scale SNP analysisGonçalo Abecasis, Paul Kwong-Hang Tam, Carlos D Bustamante, et al.Nature Genetics|March 22, 2006
In vivo RNA interference demonstrates a role for Nramp1 in modifying susceptibility to type 1 diabetesStephan Kissler, Patrick Stern, Kazue Takahashi, et al.Nature Genetics|March 22, 2006
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndromePaul J Coucke, Andy Willaert, Marja W Wessels, et al.Nature Genetics|March 22, 2006
Distribution of fitness effects among beneficial mutations before selection in experimental populations of bacteriaRees Kassen, Thomas BataillonNature Genetics|April 4, 2006
BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locusCorinne Stoetzel, Virginie Laurier, Erica E Davis, et al.Nature Genetics|April 4, 2006
MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletionAntonella Spinazzola, Carlo Viscomi, Erika Fernandez-Vizarra, et al.Nature Genetics|February 24, 2006
Ciliogenesis defects in embryos lacking inturned or fuzzy function are associated with failure of planar cell polarity and Hedgehog signalingTae Joo Park, Saori L Haigo, John B WallingfordNature Genetics|February 24, 2006
Automating sequence-based detection and genotyping of SNPs from diploid samplesMatthew Stephens, James S Sloan, P D Robertson, et al.Nature Genetics|April 11, 2006
Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neuronsYevgenya Kraytsberg, Elena Kudryavtseva, Ann C McKee, et al.Nature Genetics|April 11, 2006
High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson diseaseAndreas Bender, Kim J Krishnan, Christopher M Morris, et al.Pageof 744