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Author Details

Omri Gottesman
Icahn School of Medicine at Mount Sinai
2011
71
45
PMIDPaper TitleJournal TitlePublished Year
36372942Prescriber Adoption of SLCO1B1 Genotype-Guided Simvastatin Clinical Decision Support in a Clinical Pharmacogenetics Program.Clin Pharmacol Ther2023
36372942Prescriber Adoption of SLCO1B1 Genotype-Guided Simvastatin Clinical Decision Support in a Clinical Pharmacogenetics Program.Clin Pharmacol Ther2023
37669284iCVS-Inferring Cardio-Vascular hidden States from physiological signals available at the bedside.PLoS Comput Biol2023
37196047Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm.PLoS One2023
36781985Apolipoprotein C3 induces inflammasome activation only in its delipidated form.Nat Immunol2023
37669284iCVS-Inferring Cardio-Vascular hidden States from physiological signals available at the bedside.PLoS Comput Biol2023
37196047Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm.PLoS One2023
36781985Apolipoprotein C3 induces inflammasome activation only in its delipidated form.Nat Immunol2023
33168928Rapid response to the alpha-1 adrenergic agent phenylephrine in the perioperative period is impacted by genomics and ancestry.Pharmacogenomics J2021
33692434Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn's Disease.Sci Rep2021
33713608Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.Am J Hum Genet2021
33168928Rapid response to the alpha-1 adrenergic agent phenylephrine in the perioperative period is impacted by genomics and ancestry.Pharmacogenomics J2021
33713608Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.Am J Hum Genet2021
33692434Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn's Disease.Sci Rep2021
31836692Clinical and Molecular Prevalence of Lipodystrophy in an Unascertained Large Clinical Care Cohort.Diabetes2020
31836692Clinical and Molecular Prevalence of Lipodystrophy in an Unascertained Large Clinical Care Cohort.Diabetes2020
29290336Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.Am J Hum Genet2018
30044860The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis.PLoS One2018
29899519Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes.Nat Commun2018
29562163A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease.N Engl J Med2018
29290336Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.Am J Hum Genet2018
29360107Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2018
30044860The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis.PLoS One2018
29899519Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes.Nat Commun2018
29360107Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2018
29562163A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease.N Engl J Med2018
27920155<i>SOS2</i> and <i>ACP1</i> Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function.J Am Soc Nephrol2017
28548086Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.Sci Rep2017
28895531Genetic identification of a common collagen disease in puerto ricans via identity-by-descent mapping in a health system.Elife2017
284523721000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.Sci Rep2017
28538136Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease.N Engl J Med2017
28566273An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.Diabetes2017
29257133Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2017
27899403Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci.Circ Res2017
28203683Identification of unique venous thromboembolism-susceptibility variants in African-Americans.Thromb Haemost2017
27920155<i>SOS2</i> and <i>ACP1</i> Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function.J Am Soc Nephrol2017
28166213Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets.Nat Genet2017
28166213Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets.Nat Genet2017
284523721000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.Sci Rep2017
28203683Identification of unique venous thromboembolism-susceptibility variants in African-Americans.Thromb Haemost2017
29257133Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2017
28538136Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease.N Engl J Med2017
28566273An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.Diabetes2017
28895531Genetic identification of a common collagen disease in puerto ricans via identity-by-descent mapping in a health system.Elife2017
28548086Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.Sci Rep2017
27899403Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci.Circ Res2017
27026615PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability.J Am Med Inform Assoc2016
28426890Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci.Hum Mol Genet2016
27393744Implementing Algorithm-Guided Warfarin Dosing in an Ethnically Diverse Patient Population Using Electronic Health Records and Preemptive CYP2C9 and VKORC1 Genetic Testing.Clin Pharmacol Ther2016
27026615PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability.J Am Med Inform Assoc2016
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Collaborators

Hasso Plattner Institute for Digital Health at Mount Sinai
Co-authored papers 57
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Baylor College of Medicine
Co-authored papers 20
National Institute on Aging
Co-authored papers 17
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William Harvey Research Institute, Queen Mary University of London
Co-authored papers 15
Erasmus University Medical Center
Co-authored papers 15
The University of Manchester
Co-authored papers 15
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German Research Center for Cardiovascular Disease (DZHK)
Co-authored papers 15
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University of Michigan School of Public Health ann arbor
Co-authored papers 14
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Co-authored papers 14
Center for Systems Genomics, Pennsylvania State University, University Park
Co-authored papers 14
Harvard Medical School, Harvard University
Co-authored papers 14
Lung and Blood Institute's (NHLBI) Framingham Heart Study
Co-authored papers 14
University of Maryland School of Medicine
Co-authored papers 14
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Harvard T.H. Chan School of Public Health
Co-authored papers 13
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Geisinger Medical Center
Co-authored papers 13