Author details

Full Name

Andrea H Ramirez

Affiliation

Vanderbilt University Medical Center

ORCID

Career Start Year

2010

Papers

H Index

Expertise

CM4AI Collaborator

Andrej Sali (CM4AI)

PMID	Paper Title	Journal Title	Published Year
36474423	Characterizing variability of electronic health record-driven phenotype definitions.	J Am Med Inform Assoc	2023
35090449	Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions.	BMC Med Inform Decis Mak	2022
34870058	Integrated Analysis of the Pancreas and Islets Reveals Unexpected Findings in Human Male With Type 1 Diabetes.	J Endocr Soc	2021
32289280	A genome-wide association study of polycystic ovary syndrome identified from electronic health records.	Am J Obstet Gynecol	2020
32803091	Phenotypic Profiling in Subjects Heterozygous for 1 of 2 Rare Variants in the Hypophosphatasia Gene (<i>ALPL</i>).	J Endocr Soc	2020
30506689	Effect of CYP4F2, VKORC1, and CYP2C9 in Influencing Coumarin Dose: A Single-Patient Data Meta-Analysis in More Than 15,000 Individuals.	Clin Pharmacol Ther	2019
31395443	Building evidence and measuring clinical outcomes for genomic medicine.	Lancet	2019
30895746	IGNITE network: Response of patients to genomic medicine interventions.	Mol Genet Genomic Med	2019
29590070	Phenotype risk scores identify patients with unrecognized Mendelian disease patterns.	Science	2018
30042363	Physician-Reported Benefits and Barriers to Clinical Implementation of Genomic Medicine: A Multi-Site IGNITE-Network Survey.	J Pers Med	2018
29659871	Rare Variants in the Gene ALPL That Cause Hypophosphatasia Are Strongly Associated With Ovarian and Uterine Disorders.	J Clin Endocrinol Metab	2018
29659628	Interactions between genetic variation and cellular environment in skeletal muscle gene expression.	PLoS One	2018
28222112	Genome-wide study of resistant hypertension identified from electronic health records.	PLoS One	2017
27632229	Genetic determinants of variability in warfarin response after the dose-titration phase.	Pharmacogenet Genomics	2016
25564553	Multiplex ligation-dependent probe amplification copy number variant analysis in patients with acquired long QT syndrome.	Europace	2015
24561134	Exome sequencing implicates an increased burden of rare potassium channel variants in the risk of drug-induced long QT interval syndrome.	J Am Coll Cardiol	2014
25352737	Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility loci.	Mol Vis	2014
22584458	Novel rare variants in congenital cardiac arrhythmia genes are frequent in drug-induced torsades de pointes.	Pharmacogenomics J	2013
24270849	Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data.	Nat Biotechnol	2013
23861363	Whole exome sequencing identifies a causal RBM20 mutation in a large pedigree with familial dilated cardiomyopathy.	Circ Cardiovasc Genet	2013
23463857	Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.	Circulation	2013
23534349	Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans.	Ann Hum Genet	2013
23267855	The effect of novel promoter variants in MATE1 and MATE2 on the pharmacokinetics and pharmacodynamics of metformin.	Clin Pharmacol Ther	2013
22190063	Predicting clopidogrel response using DNA samples linked to an electronic health record.	Clin Pharmacol Ther	2012
22739144	Optimizing drug outcomes through pharmacogenetics: a case for preemptive genotyping.	Clin Pharmacol Ther	2012
22588608	Operational implementation of prospective genotyping for personalized medicine: the design of the Vanderbilt PREDICT project.	Clin Pharmacol Ther	2012
22329724	Predicting warfarin dosage in European-Americans and African-Americans using DNA samples linked to an electronic health record.	Pharmacogenomics	2012
21044898	Modulators of normal electrocardiographic intervals identified in a large electronic medical record.	Heart Rhythm	2011
21956618	A common 5'-UTR variant in MATE2-K is associated with poor response to metformin.	Clin Pharmacol Ther	2011
21981779	Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.	Am J Hum Genet	2011
21705400	Carrying one or two reduced-function CYP2C19 alleles is associated with an increased risk of major adverse cardiovascular events in people undergoing percutaneous coronary intervention and treated with clopidogrel.	Evid Based Med	2011
21672908	Facilitating pharmacogenetic studies using electronic health records and natural-language processing: a case study of warfarin.	J Am Med Inform Assoc	2011
20362271	Robust replication of genotype-phenotype associations across multiple diseases in an electronic medical record.	Am J Hum Genet	2010
21041692	Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science.	Circulation	2010

1 - 34 of 34

Heidi E Steiner

Data Science Institute, University of Arizona

Career Start Year 2017

Number of shared co-authors 12

Megan M Shuey

Vanderbilt University Medical Center

Career Start Year 2013

Number of shared co-authors 21

Stephen B Ellis

Icahn School of Medicine at Mount Sinai

Career Start Year 2013

Number of shared co-authors 42

Eric Farber-Eger

Vanderbilt University Medical Center

Career Start Year 2013

Number of shared co-authors 42

John J Connolly

Center for Applied Genomics, Children's Hospital of Philadelphia

Career Start Year 2012

Number of shared co-authors 68

Omri Gottesman

Icahn School of Medicine at Mount Sinai

Career Start Year 2011

Number of shared co-authors 69

Anurag Verma

Corporal Michael J Crescenz VA Medical Center Philadelphia

Career Start Year 2010

Number of shared co-authors 39

Nicholas P Tatonetti

Columbia Universtiy College of Physicians and Surgeons

Career Start Year 2009

Number of shared co-authors 32

James S Floyd

Cardiovascular Health Research Unit, University of Washington

Career Start Year 2008

Number of shared co-authors 22

Adam S Gordon

Northwestern University Feinberg School of Medicine.

Career Start Year 2008

Number of shared co-authors 71

Nathan E Wineinger

Scripps Research Translational Institute, The Scripps Research Institute

Career Start Year 2008

Number of shared co-authors 0

Terrie Kitchner

Center for Precision Medicine Research, Marshfield Clinic Research Institute

Career Start Year 2007

Number of shared co-authors 63

William S Bush

Cleveland Institute for Computational Biology, Case Western Reserve University

Career Start Year 2006

Number of shared co-authors 64

Erick R Scott

Icahn School of Medicine at Mount Sinai

Career Start Year 2005

Number of shared co-authors 4

Janey Wang

Vanderbilt University Medical Center

Career Start Year 2005

Number of shared co-authors 11

James K Hicks

H. Lee Moffitt Cancer Center and Research Institute

Career Start Year 2004

Number of shared co-authors 32

Sarah S Murray

University of California San Diego Health System

Career Start Year 2004

Number of shared co-authors 20

Amber L Beitelshees

University of Maryland School of Medicine

Career Start Year 2004

Number of shared co-authors 35

Brendan J Keating

Perelman School of Medicine, University of Pennsylvania

Career Start Year 2003

Number of shared co-authors 59

Laura J Rasmussen-Torvik

Northwestern University, Center for Genetic Medicine

Career Start Year 2003

Number of shared co-authors 86

Noura S Abul-Husn

Institute for Genomic Health, Icahn School of Medicine at Mount Sinai

Career Start Year 2002

Number of shared co-authors 54

Andrew D Johnson

and Blood Institute

Career Start Year 2001

Number of shared co-authors 53

Gregory D Jenkins

Mayo Clinic

Career Start Year 2001

Number of shared co-authors 13

Linnea M Baudhuin

Mayo Clinic

Career Start Year 1999

Number of shared co-authors 5

Deepak Voora

Durham VA Healthcare System and Duke University

Career Start Year 1998

Number of shared co-authors 22

Lara M Mangravite

Children's Hospital Oakland Research Institute

Career Start Year 1998

Number of shared co-authors 12

Ulrich Broeckel

Medical College of Wisconsin

Career Start Year 1998

Number of shared co-authors 31

Sony Tuteja

University of Pennsylvania Perelman School of Medicine

Career Start Year 1996

Number of shared co-authors 24

Michelle Whirl-Carrillo

Stanford University

Career Start Year 1995

Number of shared co-authors 32

Geoffrey S Ginsburg

National Institutes of Health

Career Start Year 1981

Number of shared co-authors 37

row(s) 1 - 30 of 30

Dan M Roden

Vanderbilt University Medical Center

Co-authored papers 22

Joshua C Denny

Vanderbilt University

Co-authored papers 19

Melissa A Basford

Vanderbilt University

Co-authored papers 12

Marylyn D Ritchie

Center for Systems Genomics, Pennsylvania State University, University Park

Co-authored papers 12

Dana C Crawford

Cleveland Institute for Computational Biology, Case Western Reserve University

Co-authored papers 12

Daniel R Masys

University of Washington School of Medicine.

Co-authored papers 11

Jill M Pulley

Vanderbilt University School of Medicine

Co-authored papers 10

Jonathan S Schildcrout

Vanderbilt University Medical Center.

Co-authored papers 8

Luke V Rasmussen

Northwestern University Feinberg School of Medicine

Co-authored papers 7

Erica Bowton

Institute for Clinical and Translational Research, Vanderbilt University

Co-authored papers 7

Catherine A McCarty

University of Minnesota Medical School, 1035 University Drive duluth

Co-authored papers 7

Jennifer A Pacheco

University of Pennsylvania

Co-authored papers 6

Jessica T Delaney

Vanderbilt University

Co-authored papers 6

Russell A Wilke

University of South Dakota Sanford School of Medicine

Co-authored papers 6

Abel N Kho

Northwestern University Feinberg School of Medicine

Co-authored papers 6

Jyotishman Pathak

Cornell University

Co-authored papers 6

David S Carrell

Kaiser Permanente Washington Health Research Institute

Co-authored papers 6

Gail P Jarvik

University of Washington Medical Center

Co-authored papers 6

Iftikhar J Kullo

Mayo Clinic

Co-authored papers 6

Eric B Larson

University of Washington

Co-authored papers 5

Rex L Chisholm

Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University

Co-authored papers 5

Jonathan D Mosley

Vanderbilt University Medical Center

Co-authored papers 5

Christopher G Chute

Brown University, Brown University Warren Alpert Medical School, Dartmouth-Hitchcock Medical Center, Harvard School of Public Health, Johns Hopkins Medicine, Mayo Clinic Minnesota

Co-authored papers 5

Rongling Li

National Human Genome Research Institute, National Institutes of Health

Co-authored papers 5

Peggy L Peissig

Center for Precision Medicine Research, Marshfield Clinic Research Institute

Co-authored papers 5

Lisa Bastarache

Vanderbilt University Medical Center

Co-authored papers 5

Hua Xu

Yale University