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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.Nature Genetics|April 26, 2016
Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequencesG David Poznik, Yali Xue, Fernando L Mendez, et al.Nature|June 12, 2024
Genetic drivers and cellular selection of female mosaic X chromosome lossAoxing Liu, Giulio Genovese, Yajie Zhao, et al.Translational Psychiatry|September 19, 2019
NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosisNey Alliey-Rodriguez, Tamar A Grey, Rebecca Shafee, et al.Science (New York, N.Y.)|October 12, 2023
Comparative transcriptomics reveals human-specific cortical featuresNikolas L Jorstad, Janet H T Song, David Exposito-Alonso, et al.Nature|May 3, 2008
Mapping and sequencing of structural variation from eight human genomesJeffrey M Kidd, Gregory M Cooper, William F Donahue, et al.American Journal of Human Genetics|December 4, 2018
The Genetic Landscape of Diamond-Blackfan AnemiaJacob C Ulirsch, Jeffrey M Verboon, Shideh Kazerounian, et al.Schizophrenia Bulletin|November 10, 2020
Genome-Wide Association Studies of Schizophrenia and Bipolar Disorder in a Diverse Cohort of US VeteransTim B Bigdeli, Ayman H Fanous, Yuli Li, et al.Translational Psychiatry|January 11, 2017
Evidence for genetic heterogeneity between clinical subtypes of bipolar disorderA W Charney, D M Ruderfer, E A Stahl, et al.Nature Genetics|April 28, 2018
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorderDonna M Werling, Harrison Brand, Joon-Yong An, et al.Pageof 88