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Medrxiv : the Preprint Server for Health Sciences|September 4, 2023
Clinical consequences of a polygenic predisposition to benign lower white blood cell counts: Consequences of benign WBC count geneticsJonathan D Mosley, John P Shelley, Alyson L Dickson, et al.Nature|December 3, 2010
Integrative genomics identifies LMO1 as a neuroblastoma oncogeneKai Wang, Sharon J Diskin, Haitao Zhang, et al.Human Genetics|April 3, 2021
Pathogenic variants in CDH11 impair cell adhesion and cause Teebi hypertelorism syndromeDong Li, Michael E March, Paola Fortugno, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 17, 2018
Genetic correlations among psychiatric and immune-related phenotypes based on genome-wide association dataDaniel S Tylee, Jiayin Sun, Jonathan L Hess, et al.Nature Genetics|November 12, 2005
A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarctionAnna Helgadottir, Andrei Manolescu, Agnar Helgason, et al.Diabetes Care|December 18, 2019
Genetic Discrimination Between LADA and Childhood-Onset Type 1 Diabetes Within the MHCRajashree Mishra, Mikael Åkerlund, Diana L Cousminer, et al.Human Molecular Genetics|March 29, 2012
Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosisJulien Couthouis, Michael P Hart, Renske Erion, et al.American Journal of Medical Genetics. Part A|June 6, 2020
Activating variants in PDGFRB result in a spectrum of disorders responsive to imatinib monotherapyTara L Wenger, Randall A Bly, Natalie Wu, et al.Nature Genetics|September 2, 2008
Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel diseaseSubra Kugathasan, Robert N Baldassano, Jonathan P Bradfield, et al.Nature Communications|April 22, 2024
Clinical associations with a polygenic predisposition to benign lower white blood cell countsJonathan D Mosley, John P Shelley, Alyson L Dickson, et al.Pageof 91