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Author Details
Full Name
Omri Gottesman
Affiliation
Icahn School of Medicine at Mount Sinai
ORCID
Career Start Year
2011
Papers
71
H Index
45
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36372942
Prescriber Adoption of SLCO1B1 Genotype-Guided Simvastatin Clinical Decision Support in a Clinical Pharmacogenetics Program.
Clin Pharmacol Ther
2023
36372942
Prescriber Adoption of SLCO1B1 Genotype-Guided Simvastatin Clinical Decision Support in a Clinical Pharmacogenetics Program.
Clin Pharmacol Ther
2023
37669284
iCVS-Inferring Cardio-Vascular hidden States from physiological signals available at the bedside.
PLoS Comput Biol
2023
37196047
Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm.
PLoS One
2023
36781985
Apolipoprotein C3 induces inflammasome activation only in its delipidated form.
Nat Immunol
2023
37669284
iCVS-Inferring Cardio-Vascular hidden States from physiological signals available at the bedside.
PLoS Comput Biol
2023
37196047
Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm.
PLoS One
2023
36781985
Apolipoprotein C3 induces inflammasome activation only in its delipidated form.
Nat Immunol
2023
33168928
Rapid response to the alpha-1 adrenergic agent phenylephrine in the perioperative period is impacted by genomics and ancestry.
Pharmacogenomics J
2021
33692434
Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn's Disease.
Sci Rep
2021
33713608
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.
Am J Hum Genet
2021
33168928
Rapid response to the alpha-1 adrenergic agent phenylephrine in the perioperative period is impacted by genomics and ancestry.
Pharmacogenomics J
2021
33713608
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.
Am J Hum Genet
2021
33692434
Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn's Disease.
Sci Rep
2021
31836692
Clinical and Molecular Prevalence of Lipodystrophy in an Unascertained Large Clinical Care Cohort.
Diabetes
2020
31836692
Clinical and Molecular Prevalence of Lipodystrophy in an Unascertained Large Clinical Care Cohort.
Diabetes
2020
29290336
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.
Am J Hum Genet
2018
30044860
The 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 One
2018
29899519
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes.
Nat Commun
2018
29562163
A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease.
N Engl J Med
2018
29290336
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.
Am J Hum Genet
2018
29360107
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
Sci Data
2018
30044860
The 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 One
2018
29899519
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes.
Nat Commun
2018
29360107
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
Sci Data
2018
29562163
A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease.
N Engl J Med
2018
27920155
<i>SOS2</i> and <i>ACP1</i> Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function.
J Am Soc Nephrol
2017
28548086
Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.
Sci Rep
2017
28895531
Genetic identification of a common collagen disease in puerto ricans via identity-by-descent mapping in a health system.
Elife
2017
28452372
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.
Sci Rep
2017
28538136
Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease.
N Engl J Med
2017
28566273
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.
Diabetes
2017
29257133
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
Sci Data
2017
27899403
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci.
Circ Res
2017
28203683
Identification of unique venous thromboembolism-susceptibility variants in African-Americans.
Thromb Haemost
2017
27920155
<i>SOS2</i> and <i>ACP1</i> Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function.
J Am Soc Nephrol
2017
28166213
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets.
Nat Genet
2017
28166213
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets.
Nat Genet
2017
28452372
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.
Sci Rep
2017
28203683
Identification of unique venous thromboembolism-susceptibility variants in African-Americans.
Thromb Haemost
2017
29257133
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
Sci Data
2017
28538136
Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease.
N Engl J Med
2017
28566273
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.
Diabetes
2017
28895531
Genetic identification of a common collagen disease in puerto ricans via identity-by-descent mapping in a health system.
Elife
2017
28548086
Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.
Sci Rep
2017
27899403
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci.
Circ Res
2017
27026615
PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability.
J Am Med Inform Assoc
2016
28426890
Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci.
Hum Mol Genet
2016
27393744
Implementing Algorithm-Guided Warfarin Dosing in an Ethnically Diverse Patient Population Using Electronic Health Records and Preemptive CYP2C9 and VKORC1 Genetic Testing.
Clin Pharmacol Ther
2016
27026615
PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability.
J Am Med Inform Assoc
2016
1 - 50 of 142
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row(s) 1 - 30 of 30
Collaborators
Erwin P Bottinger
Hasso Plattner Institute for Digital Health at Mount Sinai
Co-authored papers
57
Ruth J F Loos
Co-authored papers
33
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Co-authored papers
28
Ingrid B Borecki
Co-authored papers
23
Eric Boerwinkle
Baylor College of Medicine
Co-authored papers
20
Tamara B Harris
National Institute on Aging
Co-authored papers
17
Jerome I Rotter
Co-authored papers
17
Yii-Der Ida Chen
Co-authored papers
16
Tõnu Esko
Co-authored papers
16
Andres Metspalu
Co-authored papers
16
Panos Deloukas
William Harvey Research Institute, Queen Mary University of London
Co-authored papers
15
Andr?? G Uitterlinden
Erasmus University Medical Center
Co-authored papers
15
Andrew P Morris
The University of Manchester
Co-authored papers
15
Evelin Mihailov
Co-authored papers
15
Christian Gieger
German Research Center for Cardiovascular Disease (DZHK)
Co-authored papers
15
Nicholas J Wareham
Co-authored papers
15
Albert V Smith
University of Michigan School of Public Health ann arbor
Co-authored papers
14
Michael Boehnke
Co-authored papers
14
Vilmundur Gudnason
Co-authored papers
14
Marylyn D Ritchie
Center for Systems Genomics, Pennsylvania State University, University Park
Co-authored papers
14
Daniel I Chasman
Harvard Medical School, Harvard University
Co-authored papers
14
Caroline S Fox
Lung and Blood Institute's (NHLBI) Framingham Heart Study
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14
Alan R Shuldiner
University of Maryland School of Medicine
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14
Mary F Feitosa
Co-authored papers
14
Bruce M Psaty
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Paul M Ridker
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Albert Hofman
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