Author details

Full Name

Lisa Bastarache

Affiliation

Vanderbilt University Medical Center

ORCID

Career Start Year

2009

Papers

117

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
38056484	The Use of Electronic Health Records for Behavioral Phenotyping of School-Age Children With Unilateral Hearing Loss: A Methodological Approach.	J Speech Lang Hear Res	2024
38056484	The Use of Electronic Health Records for Behavioral Phenotyping of School-Age Children With Unilateral Hearing Loss: A Methodological Approach.	J Speech Lang Hear Res	2024
36861341	Human Immunodeficiency Virus Status, Tenofovir Exposure, and the Risk of Poor Coronavirus Disease 19 Outcomes: Real-World Analysis From 6 United States Cohorts Before Vaccine Rollout.	Clin Infect Dis	2023
35393523	Bronchopulmonary dysplasia is associated with polyhydramnios in a scan for novel perinatal risk factors.	Pediatr Res	2023
37607538	The phenotype-genotype reference map: Improving biobank data science through replication.	Am J Hum Genet	2023
37651384	Population genetic testing and SERPINA1 sequencing identifies unidentified alpha-1 antitrypsin deficiency alleles and gene-environment interaction with hepatitis C infection.	PLoS One	2023
37885303	Systematic replication of smoking disease associations using survey responses and EHR data in the All of Us Research Program.	J Am Med Inform Assoc	2023
37622442	A test of automated use of electronic health records to aid in diagnosis of genetic disease.	Genet Med	2023
37337966	Phenotypic presentation of Mendelian disease across the diagnostic trajectory in electronic health records.	Genet Med	2023
36875690	Linking rare and common disease vocabularies by mapping between the human phenotype ontology and phecodes.	JAMIA Open	2023
37246601	The contribution of mosaicism to genetic diseases and de novo pathogenic variants.	Am J Med Genet A	2023
37435729	CTLA-4 Pathway Is Instrumental in Giant Cell Arteritis.	Circ Res	2023
36861341	Human Immunodeficiency Virus Status, Tenofovir Exposure, and the Risk of Poor Coronavirus Disease 19 Outcomes: Real-World Analysis From 6 United States Cohorts Before Vaccine Rollout.	Clin Infect Dis	2023
37164621	Knowledgebase strategies to aid interpretation of clinical correlation research.	J Am Med Inform Assoc	2023
37622442	A test of automated use of electronic health records to aid in diagnosis of genetic disease.	Genet Med	2023
37651384	Population genetic testing and SERPINA1 sequencing identifies unidentified alpha-1 antitrypsin deficiency alleles and gene-environment interaction with hepatitis C infection.	PLoS One	2023
37885303	Systematic replication of smoking disease associations using survey responses and EHR data in the All of Us Research Program.	J Am Med Inform Assoc	2023
37607538	The phenotype-genotype reference map: Improving biobank data science through replication.	Am J Hum Genet	2023
35393523	Bronchopulmonary dysplasia is associated with polyhydramnios in a scan for novel perinatal risk factors.	Pediatr Res	2023
37246601	The contribution of mosaicism to genetic diseases and de novo pathogenic variants.	Am J Med Genet A	2023
37337966	Phenotypic presentation of Mendelian disease across the diagnostic trajectory in electronic health records.	Genet Med	2023
37435729	CTLA-4 Pathway Is Instrumental in Giant Cell Arteritis.	Circ Res	2023
37164621	Knowledgebase strategies to aid interpretation of clinical correlation research.	J Am Med Inform Assoc	2023
36875690	Linking rare and common disease vocabularies by mapping between the human phenotype ontology and phecodes.	JAMIA Open	2023
34643670	Laboratory Predictors of Hemolytic Anemia in Patients With Systemic Loxoscelism.	Am J Clin Pathol	2022
36372681	Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics.	Obesity (Silver Spring)	2022
35654975	A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.	Nat Genet	2022
35642720	Frequency of benign neutropenia among Black versus White individuals undergoing a bone marrow assessment.	J Cell Mol Med	2022
35579648	Penetrance of Deleterious Clinical Variants.	JAMA	2022
36083022	The phers R package: using phenotype risk scores based on electronic health records to study Mendelian disease and rare genetic variants.	Bioinformatics	2022
36271344	Limited clinical utility for GWAS or polygenic risk score for postoperative acute kidney injury in non-cardiac surgery in European-ancestry patients.	BMC Nephrol	2022
35679511	New Insights into Clinical and Mechanistic Heterogeneity of the Acute Respiratory Distress Syndrome: Summary of the Aspen Lung Conference 2021.	Am J Respir Cell Mol Biol	2022
35485600	A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources.	J Am Med Inform Assoc	2022
35308936	Mapping the Read2/CTV3 controlled clinical terminologies to Phecodes in UK Biobank primary care electronic health records: implementation and evaluation.	AMIA Annu Symp Proc	2022
34982132	Phenome-Wide Association Studies.	JAMA	2022
34643670	Laboratory Predictors of Hemolytic Anemia in Patients With Systemic Loxoscelism.	Am J Clin Pathol	2022
35195574	SARS-CoV-2 Testing and Positivity Among Persons With and Without HIV in 6 US Cohorts.	J Acquir Immune Defic Syndr	2022
35157022	Cox regression is robust to inaccurate EHR-extracted event time: an application to EHR-based GWAS.	Bioinformatics	2022
35679511	New Insights into Clinical and Mechanistic Heterogeneity of the Acute Respiratory Distress Syndrome: Summary of the Aspen Lung Conference 2021.	Am J Respir Cell Mol Biol	2022
35642720	Frequency of benign neutropenia among Black versus White individuals undergoing a bone marrow assessment.	J Cell Mol Med	2022
35579648	Penetrance of Deleterious Clinical Variants.	JAMA	2022
35485600	A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources.	J Am Med Inform Assoc	2022
35654975	A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.	Nat Genet	2022
36372681	Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics.	Obesity (Silver Spring)	2022
36271344	Limited clinical utility for GWAS or polygenic risk score for postoperative acute kidney injury in non-cardiac surgery in European-ancestry patients.	BMC Nephrol	2022
36083022	The phers R package: using phenotype risk scores based on electronic health records to study Mendelian disease and rare genetic variants.	Bioinformatics	2022
35157022	Cox regression is robust to inaccurate EHR-extracted event time: an application to EHR-based GWAS.	Bioinformatics	2022
34982132	Phenome-Wide Association Studies.	JAMA	2022
35308936	Mapping the Read2/CTV3 controlled clinical terminologies to Phecodes in UK Biobank primary care electronic health records: implementation and evaluation.	AMIA Annu Symp Proc	2022
35195574	SARS-CoV-2 Testing and Positivity Among Persons With and Without HIV in 6 US Cohorts.	J Acquir Immune Defic Syndr	2022

1 - 50 of 234

Binglan Li

Stanford University

Career Start Year 2018

Number of shared co-authors 12

Laura K Wiley

University of Colorado Anschutz Medical Campus

Career Start Year 2013

Number of shared co-authors 29

Stephen B Ellis

Icahn School of Medicine at Mount Sinai

Career Start Year 2013

Number of shared co-authors 65

Benjamin S Glicksberg

Hasso Plattner Institute for Digital Health, Icahn School of Medicine at Mount Sinai

Career Start Year 2013

Number of shared co-authors 12

Nicholas B Larson

Mayo Clinic

Career Start Year 2012

Number of shared co-authors 26

Omri Gottesman

Icahn School of Medicine at Mount Sinai

Career Start Year 2011

Number of shared co-authors 146

Chirag J Patel

The University of Texas MD Anderson Cancer Center

Career Start Year 2010

Number of shared co-authors 9

Konrad J Karczewski

Broad Institute of MIT and Harvard

Career Start Year 2010

Number of shared co-authors 37

Nicholas P Tatonetti

Columbia Universtiy College of Physicians and Surgeons

Career Start Year 2009

Number of shared co-authors 31

Jihoon Kim

university of california san diego

Career Start Year 2009

Number of shared co-authors 6

Matthew S Lebo

Harvard Medical School, Brigham and Women's Hospital

Career Start Year 2009

Number of shared co-authors 52

Nathan E Wineinger

Scripps Research Translational Institute, The Scripps Research Institute

Career Start Year 2008

Number of shared co-authors 2

Andrea Ganna

Institute for Molecular Medicine Finland (FIMM), University of Helsinki

Career Start Year 2008

Number of shared co-authors 73

John D Overton

Regeneron Pharmaceuticals

Career Start Year 2008

Number of shared co-authors 32

Paul Avillach

Harvard Medical School

Career Start Year 2007

Number of shared co-authors 16

Elizabeth T Cirulli

Duke University

Career Start Year 2007

Number of shared co-authors 12

Terrie Kitchner

Center for Precision Medicine Research, Marshfield Clinic Research Institute

Career Start Year 2007

Number of shared co-authors 85

Joel T Dudley

Institute for Next Generation Healthcare

Career Start Year 2006

Number of shared co-authors 11

Ali Torkamani

Scripps Science Institute

Career Start Year 2005

Number of shared co-authors 15

Degui Zhi

University of Texas Health Science Center at Houston

Career Start Year 2004

Number of shared co-authors 55

Anthony A Philippakis

Broad Institute of Harvard and the Massachusetts Institute of Technology

Career Start Year 2004

Number of shared co-authors 26

Sarah S Murray

University of California San Diego Health System

Career Start Year 2004

Number of shared co-authors 69

Eimear E Kenny

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

Career Start Year 2003

Number of shared co-authors 85

Brendan J Keating

Perelman School of Medicine, University of Pennsylvania

Career Start Year 2003

Number of shared co-authors 125

Laura J Rasmussen-Torvik

Northwestern University, Center for Genetic Medicine

Career Start Year 2003

Number of shared co-authors 179

Vincenzo Forgetta

5 Prime Sciences Inc.

Career Start Year 2003

Number of shared co-authors 28

Noura S Abul-Husn

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

Career Start Year 2002

Number of shared co-authors 57

Robert R Freimuth

Center for Individualized Medicine, Mayo Clinic

Career Start Year 2000

Number of shared co-authors 69

Michael F Murray

Yale School of Medicine

Career Start Year 1999

Number of shared co-authors 41

Nicole L Washington

Renaissance Computing Institute, University of North Carolina

Career Start Year 1997

Number of shared co-authors 7

row(s) 1 - 30 of 30

Joshua C Denny

Vanderbilt University

Co-authored papers 72

Dan M Roden

Vanderbilt University Medical Center

Co-authored papers 39

Gail P Jarvik

University of Washington Medical Center

Co-authored papers 19

Jonathan D Mosley

Vanderbilt University Medical Center

Co-authored papers 19

Wei-Qi Wei

Vanderbilt University Medical Center

Co-authored papers 17

Eric B Larson

University of Washington

Co-authored papers 16

David R Crosslin

University of Washington Medical Center

Co-authored papers 16

Iftikhar J Kullo

Mayo Clinic

Co-authored papers 14

Murray H Brilliant

Marshfield Clinic Research Institute

Co-authored papers 13

Christian M Shaffer

Vanderbilt University

Co-authored papers 12

Todd L Edwards

Vanderbilt University Medical Center

Co-authored papers 12

Peggy L Peissig

Center for Precision Medicine Research, Marshfield Clinic Research Institute

Co-authored papers 12

Marylyn D Ritchie

Center for Systems Genomics, Pennsylvania State University, University Park

Co-authored papers 11

Catherine A McCarty

University of Minnesota Medical School, 1035 University Drive duluth

Co-authored papers 10

Sara L Van Driest

National Institutes of Health

Co-authored papers 10

Jill M Pulley

Vanderbilt University School of Medicine

Co-authored papers 9

Erwin P Bottinger

Hasso Plattner Institute for Digital Health at Mount Sinai

Co-authored papers 9

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 9

Digna R Velez Edwards

Vanderbilt University Medical Center

Co-authored papers 9

Robert J Carroll

Vanderbilt University Medical Center

Co-authored papers 9

Josh F Peterson

Vanderbilt University Medical Center

Co-authored papers 9

Nancy J Cox

Vanderbilt University Medical Center