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Molecular Autism|October 9, 2020
De novo missense variants disrupting protein-protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell typesSiwei Chen, Jiebiao Wang, Ercument Cicek, et al.
Genetic Epidemiology|January 8, 2005
Characterization of multilocus linkage disequilibriumAlessandro Rinaldo, Silviu-Alin Bacanu, B Devlin, et al.
Biorxiv : the Preprint Server for Biology|October 4, 2023
Evaluating and Improving Health Equity and Fairness of Polygenic ScoresTianyu Zhang, Lambertus Klei, Peng Liu, et al.
Nucleic Acids Research|June 14, 2021
Cell type hierarchy reconstruction via reconciliation of multi-resolution cluster treeMinshi Peng, Brie Wamsley, Andrew G Elkins, et al.
American Journal of Human Genetics|April 19, 2016
A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control StudiesCorneliu A Bodea, Benjamin M Neale, Stephan Ripke, et al.
Human Genetics|April 17, 2007
Genetic liability to schizophrenia in Oceanic Palau: a search in the affected and maternal generationBernie Devlin, Lambertus Klei, Marina Myles-Worsley, et al.
Neuron|December 25, 2012
The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disordersJoseph D Buxbaum, Mark J Daly, Bernie Devlin, et al.
Statistics in Medicine|September 24, 2010
Using ancestry matching to combine family-based and unrelated samples for genome-wide association studiesAndrew Crossett, Brian P Kent, Lambertus Klei, et al.
European Heart Journal. Case Reports|December 4, 2023
Case series: cardiac sarcomaMichael Killian, Timothy Barry, Carolyn Larsen, et al.
Plos One|April 23, 2025
Exploring turn demands of an English Premier League team across league and knockout competitions over a full seasonErin Griffiths, Thomas Dos'Santos, Christopher Gaffney, et al.
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