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Nature Genetics|August 19, 2007
RNA interference and inhibition of MEK-ERK signaling prevent abnormal skeletal phenotypes in a mouse model of craniosynostosisVivek Shukla, Xavier Coumoul, Rui-Hong Wang, et al.Nature Genetics|April 3, 2012
Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repairYuka Nakazawa, Kensaku Sasaki, Norisato Mitsutake, et al.Nature Genetics|February 28, 2012
Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophyJaakko Sarparanta, Per Harald Jonson, Christelle Golzio, et al.Nature Genetics|February 28, 2012
On not reinventing the wheelNature Genetics|February 28, 2012
Self-fertilization sweeps up variation in the worm genomePatrick C PhillipsNature Genetics|April 10, 2012
A genome-wide association meta-analysis identifies new childhood obesity lociJonathan P Bradfield, H Rob Taal, Nicholas J Timpson, et al.Nature Genetics|April 10, 2012
Exome sequencing of gastric adenocarcinoma identifies recurrent somatic mutations in cell adhesion and chromatin remodeling genesZhi Jiang Zang, Ioana Cutcutache, Song Ling Poon, et al.Nature Genetics|November 22, 2011
Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesiaWan-Jin Chen, Yu Lin, Zhi-Qi Xiong, et al.Nature Genetics|April 28, 2012
Photosensitivity syndrome brings to light a new transcription-coupled DNA repair cofactorJames E CleaverPageof 745