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Nature Genetics|May 13, 2014
An atlas of genetic influences on human blood metabolitesSo-Youn Shin, Eric B Fauman, Ann-Kristin Petersen, et al.Nature Genetics|May 13, 2014
The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader-Willi syndromeYonatan Stelzer, Ido Sagi, Ofra Yanuka, et al.Nature Genetics|October 4, 2016
Reference-based phasing using the Haplotype Reference Consortium panelPo-Ru Loh, Petr Danecek, Pier Francesco Palamara, et al.Nature Genetics|October 4, 2016
Mutations in the HECT domain of NEDD4L lead to AKT-mTOR pathway deregulation and cause periventricular nodular heterotopiaLoïc Broix, Hélène Jagline, Ekaterina Ivanova, et al.Nature Genetics|April 8, 2014
Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytomaAdam M Fontebasso, Simon Papillon-Cavanagh, Jeremy Schwartzentruber, et al.Nature Genetics|April 30, 2014
Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancerLars A Forsberg, Chiara Rasi, Niklas Malmqvist, et al.Nature Genetics|June 12, 2012
Genome-wide association analysis identifies susceptibility loci for migraine without auraTobias Freilinger, Verneri Anttila, Boukje de Vries, et al.Nature Genetics|June 12, 2012
Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafnessSaskia B Wortmann, Frédéric M Vaz, Thatjana Gardeitchik, et al.Nature Genetics|April 24, 2012
Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycanTony Roscioli, Erik-Jan Kamsteeg, Karen Buysse, et al.Nature Genetics|September 29, 2014
Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphomaJames R Cerhan, Sonja I Berndt, Joseph Vijai, et al.Pageof 745