Omri Gottesman

发表

Incorporating temporal EHR data in predictive models for risk stratification of renal function deterioration

Girish N. Nadkarni, John V. Guttag, Anima Singh, 2014, J. Biomed. Informatics.

Disease progression subtype discovery from longitudinal EMR data with a majority of missing values and unknown initial time points

Girish N. Nadkarni, Ilkka Huopaniemi, Vaneet Lotay, 2014, AMIA.

Development and validation of an electronic phenotyping algorithm for chronic kidney disease

George Hripcsak, Girish N. Nadkarni, Chunhua Weng, 2014, AMIA.

PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability

Paul A. Harris, Gerard Tromp, Joshua C. Denny, 2016, J. Am. Medical Informatics Assoc..

ePhenotyping for Abdominal Aortic Aneurysm in the Electronic Medical Records and Genomics (eMERGE) Network: Algorithm Development and Konstanz Information Miner Workflow

Jyotishman Pathak, Joshua C Denny, Peggy L Peissig, 2015, International journal of biomedical data mining.

Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function

Åsa Johansson, Morris Swertz, John Attia, 2017, Scientific Reports.

Genetic identification of familial hypercholesterolemia within a single U.S. health care system

Marylyn D. Ritchie, Alan R. Shuldiner, Laney K. Jones, 2016, Science.

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

Inês Barroso, Jiyoung Heo, Beverley Balkau, 2015, Nature communications.

Design and Anticipated Outcomes of the eMERGE-PGx Project: A Multi-Center Pilot for Pre-Emptive Pharmacogenomics in Electronic Health Record Systems

Suzette J. Bielinski, Christopher G. Chute, Marylyn D. Ritchie, 2014, Clinical pharmacology and therapeutics.

A collaborative approach to developing an electronic health record phenotyping algorithm for drug-induced liver injury.

George Hripcsak, Carol Friedman, Yufeng Shen, 2013, Journal of the American Medical Informatics Association : JAMIA.

A Meta-Analysis Identifies New Loci Associated with Body Mass index in Individuals of African Ancestry

Xiaofeng Zhu, Olufunmilayo I. Olopade, Alex P. Reiner, 2013, Nature Genetics.

Genetic Background of Patients from a University Medical Center in Manhattan: Implications for Personalized Medicine

Xiaofeng Zhu, Huaizhen Qin, Erwin P. Bottinger, 2011, PloS one.

KaryoScan: abnormal karyotype detection from whole-exome sequence

Jeffrey Staples, Frederick E. Dewey, Alexander E. Lopez, 2017 .

Genetic fine-mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

Christian Gieger, Jason Carey, Steven Wiltshire, 2016 .

Directional dominance on stature and cognition in diverse human populations

Laura J. Scott, Claude Bouchard, Christian Gieger, 2015, Nature.

Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study

Marylyn D. Ritchie, Scott Mellis, Alan R. Shuldiner, 2016, Science.

Genetic polymorphisms associated with intervertebral disc degeneration.

James C. Iatridis, Omri Gottesman, O. Gottesman, 2013, The spine journal : official journal of the North American Spine Society.

Profiling copy number variation and disease associations from 50,726 DiscovEHR Study exomes

Marylyn D. Ritchie, Alan R. Shuldiner, Jeffrey Staples, 2017, bioRxiv.

Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

Claude Bouchard, Uwe Völker, Todd L Edwards, 2016, Nature Genetics.

Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin.

Xiaofeng Zhu, Todd L Edwards, Dana C Crawford, 2016, American journal of human genetics.

Can Genetic Pleiotropy Replicate Common Clinical Constellations of Cardiovascular Disease and Risk?

Vaneet Lotay, Omri Gottesman, Inga Peter, 2012, PloS one.

Systems Pharmacology of Adverse Event Mitigation by Drug Combinations

Ravi Iyengar, Joseph Goldfarb, Omri Gottesman, 2013, Science Translational Medicine.

Physician Attitudes toward Adopting Genome-Guided Prescribing through Clinical Decision Support

Joseph L. Kannry, George Hripcsak, Casey Lynnette Overby, 2014, Journal of personalized medicine.

Loss-of-function mutations in APOC3, triglycerides, and coronary disease.

He Zhang, Thomas Meitinger, Raimund Erbel, 2014, The New England journal of medicine.

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Taesung Park, Christian Gieger, Tien Yin Wong, 2017, Scientific Data.

Opportunities for genomic clinical decision support interventions

George Hripcsak, Chunhua Weng, Joshua C Denny, 2013, Genetics in Medicine.

Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci

Gerard Tromp, Marylyn D. Ritchie, Dana C. Crawford, 2017, Circulation research.

Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations.

Xiaofeng Zhu, Todd L Edwards, Wei Guo, 2013, American journal of human genetics.

Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets

Christian Gieger, Ingo Ruczinski, H Lester Kirchner, 2017, Nature Genetics.