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Author Details
Full Name
Erwin P Bottinger
Affiliation
Hasso Plattner Institute for Digital Health at Mount Sinai
ORCID
Career Start Year
1992
Papers
287
H Index
101
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
37971801
Development of the ehive Digital Health App: Protocol for a Centralized Research Platform.
JMIR Res Protoc
2023
37024752
Genetic susceptibility to diabetic kidney disease is linked to promoter variants of XOR.
Nat Metab
2023
37143859
A machine learning approach to determine resilience utilizing wearable device data: analysis of an observational cohort.
JAMIA Open
2023
37020303
Implementation and evaluation of personal genetic testing as part of genomics analysis courses in German universities.
BMC Med Genomics
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
37384379
Economic Evaluation of Digital Therapeutic Care Apps for Unsupervised Treatment of Low Back Pain: Monte Carlo Simulation.
JMIR Mhealth Uhealth
2023
36787837
Second-Line Biologic Therapy Following Tumor Necrosis Factor Antagonist Failure: A Real-World Propensity Score-Weighted Analysis.
Clin Gastroenterol Hepatol
2023
37971801
Development of the ehive Digital Health App: Protocol for a Centralized Research Platform.
JMIR Res Protoc
2023
37024752
Genetic susceptibility to diabetic kidney disease is linked to promoter variants of XOR.
Nat Metab
2023
37020303
Implementation and evaluation of personal genetic testing as part of genomics analysis courses in German universities.
BMC Med Genomics
2023
37384379
Economic Evaluation of Digital Therapeutic Care Apps for Unsupervised Treatment of Low Back Pain: Monte Carlo Simulation.
JMIR Mhealth Uhealth
2023
37143859
A machine learning approach to determine resilience utilizing wearable device data: analysis of an observational cohort.
JAMIA Open
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
36787837
Second-Line Biologic Therapy Following Tumor Necrosis Factor Antagonist Failure: A Real-World Propensity Score-Weighted Analysis.
Clin Gastroenterol Hepatol
2023
35197815
COVID-19 in German Competitive Sports: Protocol for a Prospective Multicenter Cohort Study (CoSmo-S).
Int J Public Health
2022
36372681
Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics.
Obesity (Silver Spring)
2022
35838765
Inducing and Recording Acute Stress Responses on a Large Scale With the Digital Stress Test (DST): Development and Evaluation Study.
J Med Internet Res
2022
35652341
Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.
Hypertension
2022
35697829
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.
Commun Biol
2022
35551307
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.
Nat Genet
2022
35677186
Evaluation of a machine learning approach utilizing wearable data for prediction of SARS-CoV-2 infection in healthcare workers.
JAMIA Open
2022
35787512
StudyU: A Platform for Designing and Conducting Innovative Digital N-of-1 Trials.
J Med Internet Res
2022
36448021
Predicting hypertension onset from longitudinal electronic health records with deep learning.
JAMIA Open
2022
36572922
StudyMe: a new mobile app for user-centric N-of-1 trials.
Trials
2022
35244702
Effects of Testing and Disclosing Ancestry-Specific Genetic Risk for Kidney Failure on Patients and Health Care Professionals: A Randomized Clinical Trial.
JAMA Netw Open
2022
35129454
Digital Therapeutic Care Apps With Decision-Support Interventions for People With Low Back Pain in Germany: Cost-Effectiveness Analysis.
JMIR Mhealth Uhealth
2022
35197815
COVID-19 in German Competitive Sports: Protocol for a Prospective Multicenter Cohort Study (CoSmo-S).
Int J Public Health
2022
35085396
Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts.
Diabetes Care
2022
35551307
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.
Nat Genet
2022
35652341
Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.
Hypertension
2022
35677186
Evaluation of a machine learning approach utilizing wearable data for prediction of SARS-CoV-2 infection in healthcare workers.
JAMIA Open
2022
35838765
Inducing and Recording Acute Stress Responses on a Large Scale With the Digital Stress Test (DST): Development and Evaluation Study.
J Med Internet Res
2022
35697829
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.
Commun Biol
2022
35787512
StudyU: A Platform for Designing and Conducting Innovative Digital N-of-1 Trials.
J Med Internet Res
2022
36448021
Predicting hypertension onset from longitudinal electronic health records with deep learning.
JAMIA Open
2022
36572922
StudyMe: a new mobile app for user-centric N-of-1 trials.
Trials
2022
36372681
Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics.
Obesity (Silver Spring)
2022
35129454
Digital Therapeutic Care Apps With Decision-Support Interventions for People With Low Back Pain in Germany: Cost-Effectiveness Analysis.
JMIR Mhealth Uhealth
2022
35244702
Effects of Testing and Disclosing Ancestry-Specific Genetic Risk for Kidney Failure on Patients and Health Care Professionals: A Randomized Clinical Trial.
JAMA Netw Open
2022
35085396
Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts.
Diabetes Care
2022
33441424
Kidney disease genetic risk variants alter lysosomal beta-mannosidase (<i>MANBA</i>) expression and disease severity.
Sci Transl Med
2021
33861964
Toward a fine-scale population health monitoring system.
Cell
2021
33626098
Association of SARS-CoV-2 viral load at admission with in-hospital acute kidney injury: A retrospective cohort study.
PLoS One
2021
33529156
Use of Physiological Data From a Wearable Device to Identify SARS-CoV-2 Infection and Symptoms and Predict COVID-19 Diagnosis: Observational Study.
J Med Internet Res
2021
34108472
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes.
Nat Commun
2021
33461682
Using interpretability approaches to update "black-box" clinical prediction models: an external validation study in nephrology.
Artif Intell Med
2021
33727701
Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Nat Genet
2021
34031183
Predictive Approaches for Acute Dialysis Requirement and Death in COVID-19.
Clin J Am Soc Nephrol
2021
1 - 50 of 574
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Icahn School of Medicine at Mount Sinai
Co-authored papers
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Baylor College of Medicine
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Icahn School of Medicine at Mount Sinai
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48
Bruce M Psaty
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Tamara B Harris
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45
Vilmundur Gudnason
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42
Albert V Smith
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The University of Manchester
Co-authored papers
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Kent D Taylor
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40
Xiuqing Guo
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39
Charles Kooperberg
Co-authored papers
39
Caroline Hayward
Co-authored papers
39
Terho Lehtim??ki
Finnish Cardiovascular Research Center-Tampere - FCRCT, Tampere University
Co-authored papers
38
Yii-Der Ida Chen
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37
Cecilia M Lindgren
Co-authored papers
37
Erik Ingelsson
Stanford University School of Medicine
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37
Andres Metspalu
Co-authored papers
36
Michael Boehnke
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36
John C Chambers
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Andr?? G Uitterlinden
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