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American Journal of Human Genetics|April 4, 2017
Human Demographic History Impacts Genetic Risk Prediction across Diverse PopulationsAlicia R Martin, Christopher R Gignoux, Raymond K Walters, et al.Biorxiv : the Preprint Server for Biology|July 10, 2023
CHARR efficiently estimates contamination from DNA sequencing dataWenhan Lu, Laura D Gauthier, Timothy Poterba, et al.The Journal of Infectious Diseases|May 14, 2010
Significance of the myxovirus resistance A (MxA) gene -123C>a single-nucleotide polymorphism in suppressed interferon beta induction of severe acute respiratory syndrome coronavirus infectionJohannes Chi-Yun Ching, Kelvin Yuen Kwong Chan, Eric Hing Leung Lee, et al.Plos Genetics|March 17, 2011
Testing for an unusual distribution of rare variantsBenjamin M Neale, Manuel A Rivas, Benjamin F Voight, et al.Medrxiv : the Preprint Server for Health Sciences|July 18, 2023
Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK BiobankFrederik H Lassen, Samvida S Venkatesh, Nikolas Baya, et al.Medrxiv : the Preprint Server for Health Sciences|December 4, 2023
Early-onset schizophrenia is associated with immune-related rare variants in a Chinese sampleYuanxin Zhong, Justin D Tubbs, Perry B M Leung, et al.Medrxiv : the Preprint Server for Health Sciences|October 4, 2023
Pathway-Specific Polygenic Scores Improve Cross-Ancestry Prediction of Psychosis and Clinical OutcomesJustin D Tubbs, Perry B M Leung, Yuanxin Zhong, et al.Asian Journal of Psychiatry|April 25, 2024
Whole-exome sequencing in a Chinese sample provides preliminary evidence for the link between rare/low-frequency immune-related variants and early-onset schizophreniaYuanxin Zhong, Justin D Tubbs, Perry B M Leung, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 30, 2008
Non-random error in genotype calling procedures: implications for family-based and case-control genome-wide association studiesRichard J L Anney, Elaine Kenny, Colm T O'Dushlaine, et al.American Journal of Human Genetics|March 11, 2014
An excess of risk-increasing low-frequency variants can be a signal of polygenic inheritance in complex diseasesYingleong Chan, Elaine T Lim, Niina Sandholm, et al.Pageof 50