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Nature|May 27, 2026
Mechanism of age-related accumulation of mtDNA mutations in human bloodRahul Gupta, Timothy J Durham, Grant Chau, et al.
Nature|August 16, 2023
Nuclear genetic control of mtDNA copy number and heteroplasmy in humansRahul Gupta, Masahiro Kanai, Timothy J Durham, et al.
European Journal of Human Genetics : EJHG|November 24, 2016
A framework for the detection of de novo mutations in family-based sequencing dataLaurent C Francioli, Mircea Cretu-Stancu, Kiran V Garimella, et al.
Psychiatric Genetics|October 28, 2010
No NRG1 V266L in Chinese patients with schizophreniaMaria-Mercè Garcia-Barceló, Xiaoping Miao, Clara S Tang, et al.
BMC Cancer|November 11, 2011
Clinicopathologic and gene expression parameters predict liver cancer prognosisKe Hao, John Lamb, Chunsheng Zhang, et al.
Circulation|September 29, 2016
Amelioration of X-Linked Related Autophagy Failure in Danon Disease With DNA Methylation InhibitorKwong-Man Ng, Pamela Y Mok, Amy W Butler, et al.
The New England Journal of Medicine|June 30, 2021
Problems with Using Polygenic Scores to Select EmbryosPatrick Turley, Michelle N Meyer, Nancy Wang, et al.
American Journal of Human Genetics|September 13, 2024
Semi-supervised machine learning method for predicting homogeneous ancestry groups to assess Hardy-Weinberg equilibrium in diverse whole-genome sequencing studiesDerek Shyr, Rounak Dey, Xihao Li, et al.
Cell Genomics|November 17, 2022
Proteome-wide Mendelian randomization in global biobank meta-analysis reveals multi-ancestry drug targets for common diseasesHuiling Zhao, Humaria Rasheed, Therese Haugdahl Nøst, et al.
Translational Psychiatry|January 26, 2019
Disentangling polygenic associations between attention-deficit/hyperactivity disorder, educational attainment, literacy and languageEllen Verhoef, Ditte Demontis, Stephen Burgess, et al.
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