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Author Details

Scott J Hebbring
Marshfield Clinic Research Institute
2003
91
33
PMIDPaper TitleJournal TitlePublished Year
36746961Author Correction: Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits.Nat Commun2023
38020121Estimating the efficacy of pharmacogenomics over a lifetime.Front Med (Lausanne)2023
37216007Genetic and clinical determinants of telomere length.HGG Adv2023
37071725Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results.Circ Genom Precis Med2023
34380996Genetic association of primary nonresponse to anti-TNFα therapy in patients with inflammatory bowel disease.Pharmacogenet Genomics2022
35701404Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders.Nat Commun2022
35446370Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases.JAMA Oncol2022
36372681Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics.Obesity (Silver Spring)2022
35915156Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.Nat Med2022
35112343Kidney failure in Bardet-Biedl syndrome.Clin Genet2022
34282949Associations of Genetically Predicted Lp(a) (Lipoprotein [a]) Levels With Cardiovascular Traits in Individuals of European and African Ancestry.Circ Genom Precis Med2021
36046768Returning negative results from large-scale genomic screening: Experiences from the eMERGE III network.Am J Med Genet A2021
34377931Penetrance of Breast Cancer Susceptibility Genes From the eMERGE III Network.JNCI Cancer Spectr2021
34620889An independently validated, portable algorithm for the rapid identification of COPD patients using electronic health records.Sci Rep2021
33941608Medical Records-Based Genetic Studies of the Complement System.J Am Soc Nephrol2021
34341450The genetic architecture of plasma kynurenine includes cardiometabolic disease mechanisms associated with the SH2B3 gene.Sci Rep2021
33977795Pleiotropy of systemic lupus erythematosus risk alleles and cardiometabolic disorders: A phenome-wide association study and inverse-variance weighted meta-analysis.Lupus2021
34086863E-Pedigrees: a large-scale automatic family pedigree prediction application.Bioinformatics2021
32413979Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network.J Pers Med2020
31959670Cardiac Anomalies in Liveborn and Stillborn Monochorionic Twins.Clin Med Res2020
32307929Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis: A Phenome-Wide Association Study and Inverse Variance-Weighted Meta-Analysis.Arthritis Rheumatol2020
30342790Genomic and Phenomic Research in the 21st Century.Trends Genet2019
31342140Ancestry-specific polygenic scores and SNP heritability of 25(OH)D in African- and European-ancestry populations.Hum Genet2019
31279534Targeted Treatment of Individuals With Psychosis Carrying a Copy Number Variant Containing a Genomic Triplication of the Glycine Decarboxylase Gene.Biol Psychiatry2019
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
30774981A phenome-wide association study to discover pleiotropic effects of <i>PCSK9</i>, <i>APOB</i>, and <i>LDLR</i>.NPJ Genom Med2019
29323929Variation in Cilia Protein Genes and Progression of Lung Disease in Cystic Fibrosis.Ann Am Thorac Soc2018
29590070Phenotype risk scores identify patients with unrecognized Mendelian disease patterns.Science2018
28968884Applying family analyses to electronic health records to facilitate genetic research.Bioinformatics2018
29053189Pilot screening study of targeted genetic polymorphisms for association with seasonal influenza hospital admission.J Med Virol2018
27856289RNA-Binding Protein IGF2BP1 in Cutaneous Squamous Cell Carcinoma.J Invest Dermatol2017
28490672Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants.Sci Transl Med2017
28867356Relationship of SULT1A1 copy number variation with estrogen metabolism and human health.J Steroid Biochem Mol Biol2017
26691988A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.Nat Genet2016
26524704Mining Retrospective Data for Virtual Prospective Drug Repurposing: L-DOPA and Age-related Macular Degeneration.Am J Med2016
28018425The Decay of Disease Association with Declining Linkage Disequilibrium: A Fine Mapping Theorem.Front Genet2016
27535653eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants.BMC Med Genomics2016
27287392Phenome-wide association study maps new diseases to the human major histocompatibility complex region.J Med Genet2016
26912863The phenotypic legacy of admixture between modern humans and Neandertals.Science2016
27109359Identifying genetically driven clinical phenotypes using linear mixed models.Nat Commun2016
25074467Phenome-wide association studies (PheWASs) for functional variants.Eur J Hum Genet2015
26109056Comparison of RNA-seq and microarray-based models for clinical endpoint prediction.Genome Biol2015
25850054Opportunities for drug repositioning from phenome-wide association studies.Nat Biotechnol2015
26030142Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy.PLoS One2015
25657332Application of clinical text data for phenome-wide association studies (PheWASs).Bioinformatics2015
25587064SeqHBase: a big data toolset for family based sequencing data analysis.J Med Genet2015
24147732The challenges, advantages and future of phenome-wide association studies.Immunology2014
25250975Use of an electronic medical record to create the marshfield clinic twin/multiple birth cohort.Genet Epidemiol2014
25326128Regulatory polymorphisms in human DBH affect peripheral gene expression and sympathetic activity.Circ Res2014
25177340Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index.Front Genet2014
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Collaborators

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Co-authored papers 25
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Co-authored papers 18
Marshfield Clinic Research Institute
Co-authored papers 17
University of Washington Medical Center
Co-authored papers 17
Vanderbilt University
Co-authored papers 14
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Co-authored papers 13
Vanderbilt University Medical Center
Co-authored papers 12
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University of Washington Medical Center
Co-authored papers 11
Kaiser Permanente Southern California
Co-authored papers 10
University of Washington
Co-authored papers 9
The Brady Urological Institute, The Johns Hopkins School of Medicine
Co-authored papers 9
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Co-authored papers 9
Fred Hutchinson Cancer Research Center
Co-authored papers 8
National Cancer Institute
Co-authored papers 8
Center for Systems Genomics, Pennsylvania State University, University Park
Co-authored papers 8
Vanderbilt University Medical Center
Co-authored papers 8
Vanderbilt University Medical Center
Co-authored papers 8
Kidney Research Institute and Division of Nephrology, University of Washington
Co-authored papers 8
Institute of Biomedicine, University of Turku
Co-authored papers 7
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Cincinnati Children's Hospital
Co-authored papers 7
Duke University School of Medicine, and the Duke Cancer Institute
Co-authored papers 7
University of Wisconsin Madison
Co-authored papers 7
Vanderbilt University Medical Center
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Vanderbilt University
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The Institute of Cancer Research
Co-authored papers 6