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Nature Genetics|July 6, 2021
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analysesAlison R Barton, Maxwell A Sherman, Ronen E Mukamel, et al.
Nature Genetics|May 13, 2022
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translationAnubha Mahajan, Cassandra N Spracklen, Weihua Zhang, et al.
Nature Genetics|May 9, 2022
The disordered N-terminal domain of DNMT3A recognizes H2AK119ub and is required for postnatal developmentTianpeng Gu, Dapeng Hao, Junsung Woo, et al.
Nature Genetics|May 9, 2022
Meningioma DNA methylation groups identify biological drivers and therapeutic vulnerabilitiesAbrar Choudhury, Stephen T Magill, Charlotte D Eaton, et al.
Nature Genetics|October 10, 2017
The draft genome of tropical fruit durian (Durio zibethinus)Bin Tean Teh, Kevin Lim, Chern Han Yong, et al.
Nature Genetics|October 10, 2017
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probandsSheng Chih Jin, Jason Homsy, Samir Zaidi, et al.
Nature Genetics|November 29, 2017
Mutant-IDH1-dependent chromatin state reprogramming, reversibility, and persistenceSevin Turcan, Vladimir Makarov, Julian Taranda, et al.
Nature Genetics|April 13, 2021
Minor intron retention drives clonal hematopoietic disorders and diverse cancer predispositionDaichi Inoue, Jacob T Polaski, Justin Taylor, et al.
Nature Genetics|April 13, 2021
Chromothripsis as an on-target consequence of CRISPR-Cas9 genome editingMitchell L Leibowitz, Stamatis Papathanasiou, Phillip A Doerfler, et al.
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