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Author Details

William P Bone
University of Pennsylvania - Perelman School of Medicine
2015
21
11
PMIDPaper TitleJournal TitlePublished Year
37165871Evaluating the Contribution of Cell Type-Specific Alternative Splicing to Variation in Lipid Levels.Circ Genom Precis Med2023
35186008Multi-Trait Genome-Wide Association Study of Atherosclerosis Detects Novel Pleiotropic Loci.Front Genet2022
35701404Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders.Nat Commun2022
35894642ColocQuiaL: a QTL-GWAS colocalization pipeline.Bioinformatics2022
36376295Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure.Nat Commun2022
35285134Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations.J Thromb Haemost2022
32958772Regulation of cellular sterol homeostasis by the oxygen responsive noncoding RNA lincNORS.Nat Commun2020
33159065Publisher Correction: Regulation of cellular sterol homeostasis by the oxygen responsive noncoding RNA lincNORS.Nat Commun2020
30864329Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE network.Pac Symp Biocomput2019
31659023Natural human genetic variation determines basal and inducible expression of PM20D1, an obesity-associated gene.Proc Natl Acad Sci U S A2019
28603714Defining Disease, Diagnosis, and Translational Medicine within a Homeostatic Perturbation Paradigm: The National Institutes of Health Undiagnosed Diseases Program Experience.Front Med (Lausanne)2017
27568008Explorations to improve the completeness of exome sequencing.BMC Med Genomics2016
28078312Biallelic <i>SCN10A</i> mutations in neuromuscular disease and epileptic encephalopathy.Ann Clin Transl Neurol2016
26562225Computational evaluation of exome sequence data using human and model organism phenotypes improves diagnostic efficiency.Genet Med2016
26668131Disruption of Golgi morphology and altered protein glycosylation in PLA2G6-associated neurodegeneration.J Med Genet2016
27785453Distributed Cognition and Process Management Enabling Individualized Translational Research: The NIH Undiagnosed Diseases Program Experience.Front Med (Lausanne)2016
25577287York platelet syndrome is a CRAC channelopathy due to gain-of-function mutations in STIM1.Mol Genet Metab2015
25888122Impaired osteoblast and osteoclast function characterize the osteoporosis of Snyder - Robinson syndrome.Orphanet J Rare Dis2015
25845469MED23-associated intellectual disability in a non-consanguineous family.Am J Med Genet A2015
26562621Next-generation diagnostics and disease-gene discovery with the Exomiser.Nat Protoc2015
26251998PhenomeCentral: a portal for phenotypic and genotypic matchmaking of patients with rare genetic diseases.Hum Mutat2015
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Collaborators

National Human Genome Research Institute, National Institutes of Health
Co-authored papers 10
University of British Columbia
Co-authored papers 8
National Institutes of Health
Co-authored papers 6
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 6
Perelman School of Medicine, University of Pennsylvania
Co-authored papers 6
American Medical Informatics Association, Oregon Health and Science University, Oregon State University, University of Colorado Anschutz Medical Campus, University of North Carolina at Chapel Hill, University of Wisconsin-Madison
Co-authored papers 5
Center for Systems Genomics, Pennsylvania State University, University Park
Co-authored papers 5
Co-authored papers 5
National Institutes of Health
Co-authored papers 5
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 4
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 4
National Institutes of Health
Co-authored papers 4
Renaissance Computing Institute, University of North Carolina
Co-authored papers 4
NIH and National Human Genome Research Institute
Co-authored papers 4
National Institutes of Health Undiagnosed Diseases Program
Co-authored papers 4
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 4
Perelman School of Medicine, University of Pennsylvania
Co-authored papers 3
The Hospital for Sick Children
Co-authored papers 3
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 3
Northwestern University, Center for Genetic Medicine
Co-authored papers 3
National Human Genome Research Institute
Co-authored papers 3
Maryland Inova Translational Medicine Institute, Inova Health System
Co-authored papers 3
Boston University School of Public Health
Co-authored papers 3
University of Toronto
Co-authored papers 3
DATA Team and Techna Institute, University Health Network
Co-authored papers 3
Mayo Clinic
Co-authored papers 3
National Institutes of Health
Co-authored papers 3
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Co-authored papers 2
University of Washington
Co-authored papers 2
Co-authored papers 2