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Nature Genetics|March 4, 2014
Loss-of-function mutations in SLC30A8 protect against type 2 diabetesJason Flannick, Gudmar Thorleifsson, Nicola L Beer, et al.Nature Genetics|March 4, 2014
An epigenetic mechanism of resistance to targeted therapy in T cell acute lymphoblastic leukemiaBirgit Knoechel, Justine E Roderick, Kaylyn E Williamson, et al.Nature Genetics|July 24, 2019
Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping diseaseHiroyuki Ishiura, Shota Shibata, Jun Yoshimura, et al.Nature Genetics|September 26, 2022
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroupsManuel Mattheisen, Jakob Grove, Thomas D Als, et al.Nature Genetics|September 26, 2022
Population-level variation in enhancer expression identifies disease mechanisms in the human brainPengfei Dong, Gabriel E Hoffman, Pasha Apontes, et al.Nature Genetics|July 24, 2012
Fast and accurate genotype imputation in genome-wide association studies through pre-phasingBryan Howie, Christian Fuchsberger, Matthew Stephens, et al.Nature Genetics|August 11, 1998
Pten is essential for embryonic development and tumour suppressionA Di Cristofano, B Pesce, C Cordon-Cardo, et al.Nature Genetics|August 11, 1998
Alpha-2 macroglobulin is genetically associated with Alzheimer diseaseD Blacker, M A Wilcox, N M Laird, et al.Nature Genetics|August 11, 1998
Mutations in a plasma membrane Ca2+-ATPase gene cause deafness in deafwaddler miceV A Street, J W McKee-Johnson, R C Fonseca, et al.Nature Genetics|August 11, 1998
Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresiaR J Clifton-Bligh, J M Wentworth, P Heinz, et al.Pageof 744