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Medrxiv : the Preprint Server for Health Sciences|February 13, 2023
Population analyses of mosaic X chromosome loss identify genetic drivers and widespread signatures of cellular selectionAoxing Liu, Giulio Genovese, Yajie Zhao, et al.American Journal of Human Genetics|September 2, 2022
Genetic structure correlates with ethnolinguistic diversity in eastern and southern AfricaElizabeth G Atkinson, Shareefa Dalvie, Yakov Pichkar, et al.Nature|June 12, 2024
Genetic drivers and cellular selection of female mosaic X chromosome lossAoxing Liu, Giulio Genovese, Yajie Zhao, et al.Science (New York, N.Y.)|May 9, 2015
Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptomeManuel A Rivas, Matti Pirinen, Donald F Conrad, et al.Molecular Psychiatry|March 5, 2008
Whole-genome association study of bipolar disorderP Sklar, J W Smoller, J Fan, et al.Neuron|January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disordersElaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.American Journal of Human Genetics|March 26, 2021
Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populationsAlicia R Martin, Elizabeth G Atkinson, Sinéad B Chapman, et al.Gut|September 25, 2014
Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohortsWeronica E Ek, Anna Reznichenko, Stephan Ripke, et al.Nature|June 15, 2018
Author Correction: Discovery of stimulation-responsive immune enhancers with CRISPR activationDimitre R Simeonov, Benjamin G Gowen, Mandy Boontanrart, et al.Circulation. Cardiovascular Genetics|January 30, 2015
Exome sequencing in suspected monogenic dyslipidemiasNathan O Stitziel, Gina M Peloso, Marianne Abifadel, et al.Pageof 163