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Plos Pathogens|March 1, 2022
Identification of cell type specific ACE2 modifiers by CRISPR screeningEmily J Sherman, Carmen Mirabelli, Vi T Tang, et al.Communications Medicine|November 22, 2025
Integrating large scale genetic and clinical information to predict cases of heart failureKuan-Han H Wu, Brooke N Wolford, Jiacong Du, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|September 21, 2007
Multiple sclerosis susceptibility and the X chromosomeB M Herrera, M Z Cader, D A Dyment, et al.Plos One|August 23, 2017
Genomic correlates of glatiramer acetate adverse cardiovascular effects lead to a novel locus mediating coronary riskIngrid Brænne, Lingyao Zeng, Christina Willenborg, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 18, 2007
A first stage genome-wide screen for regions shared identical-by-descent in Hutterite families with multiple sclerosisDavid Alexandre Dyment, M Zameel Cader, Anita Datta, et al.Genetic Epidemiology|November 3, 2025
Variant Classification Using Proteomics-Informed Large Language Models Increases Power of Rare Variant Association Studies and Enhances Target DiscoveryChristopher E Gillies, Joelle Mbatchou, Lukas Habegger, et al.Journal of Cardiopulmonary Rehabilitation and Prevention|September 4, 2019
Cardiopulmonary Exercise Testing Following Open Repair for a Proximal Thoracic Aortic Aneurysm or DissectionWhitney E Hornsby, Elizabeth L Norton, Samantha Fink, et al.Nature Genetics|May 20, 2020
Scalable generalized linear mixed model for region-based association tests in large biobanks and cohortsWei Zhou, Zhangchen Zhao, Jonas B Nielsen, et al.The Journal of Clinical Investigation|September 15, 2015
Perhexiline activates KLF14 and reduces atherosclerosis by modulating ApoA-I productionYanhong Guo, Yanbo Fan, Jifeng Zhang, et al.American Journal of Medical Genetics. Part A|January 29, 2022
Spontaneous coronary artery dissection is infrequent in individuals with heritable thoracic aortic disease despite partially shared genetic susceptibilityAndrea M Murad, Hannah L Hill, Yu Wang, et al.Pageof 20