Author details

Full Name

Melissa A Basford

Affiliation

Vanderbilt University

ORCID

Career Start Year

1997

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36540961	How Fitbit data are being made available to registered researchers in All of Us Research Program.	Pac Symp Biocomput	2023
37669985	Demonstrating paths for unlocking the value of cloud genomics through cross cohort analysis.	Nat Commun	2023
37561600	The <i>All of Us</i> Data and Research Center: Creating a Secure, Scalable, and Sustainable Ecosystem for Biomedical Research.	Annu Rev Biomed Data Sci	2023
37218289	De-black-boxing health AI: demonstrating reproducible machine learning computable phenotypes using the N3C-RECOVER Long COVID model in the All of Us data repository.	J Am Med Inform Assoc	2023
36809550	Managing re-identification risks while providing access to the All of Us research program.	J Am Med Inform Assoc	2023
35266088	Workflow Integration of Research AI Tools into a Hospital Radiology Rapid Prototyping Environment.	J Digit Imaging	2022
28222112	Genome-wide study of resistant hypertension identified from electronic health records.	PLoS One	2017
27026615	PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability.	J Am Med Inform Assoc	2016
26628336	A prognostic model based on readily available clinical data enriched a pre-emptive pharmacogenetic testing program.	J Clin Epidemiol	2016
27881091	Conducting a large, multi-site survey about patients' views on broad consent: challenges and solutions.	BMC Med Res Methodol	2016
27472449	Electronic Health Record Based Algorithm to Identify Patients with Autism Spectrum Disorder.	PLoS One	2016
26857349	Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network.	Clin Pharmacol Ther	2016
26265699	Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemia.	Blood	2015
24456567	The CTSA Consortium's Catalog of Assets for Translational and Clinical Health Research (CATCHR).	Clin Transl Sci	2014
25436638	Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network.	PLoS One	2014
25590050	Replication of <i>SCN5A</i> Associations with Electrocardio-graphic Traits in African Americans from Clinical and Epidemiologic Studies.	Evol Comput Mach Learn Data Min Bioinform	2014
24821742	The Mid-South clinical Data Research Network.	J Am Med Inform Assoc	2014
24960519	Design and anticipated outcomes of the eMERGE-PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systems.	Clin Pharmacol Ther	2014
24534443	Secondary use of clinical data: the Vanderbilt approach.	J Biomed Inform	2014
24595071	Admixture mapping and subsequent fine-mapping suggests a biologically relevant and novel association on chromosome 11 for type 2 diabetes in African Americans.	PLoS One	2014
23531748	Validation of electronic medical record-based phenotyping algorithms: results and lessons learned from the eMERGE network.	J Am Med Inform Assoc	2013
24270849	Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data.	Nat Biotechnol	2013
23651022	Assessment of a pharmacogenomic marker panel in a polypharmacy population identified from electronic medical records.	Pharmacogenomics	2013
23743551	The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future.	Genet Med	2013
23463857	Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.	Circulation	2013
23424142	Enabling high-throughput genotype-phenotype associations in the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) project as part of the Population Architecture using Genomics and Epidemiology (PAGE) study.	Pac Symp Biocomput	2013
23534349	Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans.	Ann Hum Genet	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
22329724	Predicting warfarin dosage in European-Americans and African-Americans using DNA samples linked to an electronic health record.	Pharmacogenomics	2012
22108237	The use of a DNA biobank linked to electronic medical records to characterize pharmacogenomic predictors of tacrolimus dose requirement in kidney transplant recipients.	Pharmacogenet Genomics	2012
21044898	Modulators of normal electrocardiographic intervals identified in a large electronic medical record.	Heart Rhythm	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
21632745	Ethical and practical challenges of sharing data from genome-wide association studies: the eMERGE Consortium experience.	Genome Res	2011
21597104	Mapping clinical phenotype data elements to standardized metadata repositories and controlled terminologies: the eMERGE Network experience.	J Am Med Inform Assoc	2011
21672908	Facilitating pharmacogenetic studies using electronic health records and natural-language processing: a case study of warfarin.	J Am Med Inform Assoc	2011
20335276	PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations.	Bioinformatics	2010
21347153	An automated approach to calculating the daily dose of tacrolimus in electronic health records.	Summit Transl Bioinform	2010
21041692	Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science.	Circulation	2010
20733501	Assessing the accuracy of observer-reported ancestry in a biorepository linked to electronic medical records.	Genet Med	2010
20688191	An analytical approach to characterize morbidity profile dissimilarity between distinct cohorts using electronic medical records.	J Biomed Inform	2010
20362271	Robust replication of genotype-phenotype associations across multiple diseases in an electronic medical record.	Am J Hum Genet	2010
18500243	Development of a large-scale de-identified DNA biobank to enable personalized medicine.	Clin Pharmacol Ther	2008
10351837	How can leaders ensure organizational integrity?	Trustee	1999
10173678	Get yourself a dog: a strategy for avoiding acquisition.	Trustee	1997

1 - 45 of 45

Brett K Beaulieu-Jones

University of Chicago

Career Start Year 2016

Number of shared co-authors 4

Simon Lin

The Abigail Wexner Research Institute, Nationwide Children's Hospital

Career Start Year 2015

Number of shared co-authors 0

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 9

Laura K Wiley

University of Colorado Anschutz Medical Campus

Career Start Year 2013

Number of shared co-authors 23

Fernanda Polubriaginof

Memorial Sloan Kettering Cancer Center

Career Start Year 2012

Number of shared co-authors 11

Tiffany J Callahan

Columbia University

Career Start Year 2012

Number of shared co-authors 8

Mary Regina Boland

University of Pennsylvania

Career Start Year 2011

Number of shared co-authors 5

Jihoon Kim

university of california san diego

Career Start Year 2009

Number of shared co-authors 0

Keith Marsolo

Duke Clinical Research Institute, Duke University School of Medicine

Career Start Year 2007

Number of shared co-authors 50

Laura Lyman Rodriguez

Patient-Centered Outcomes Research Institute

Career Start Year 2007

Number of shared co-authors 26

Paul Avillach

Harvard Medical School

Career Start Year 2007

Number of shared co-authors 8

Jessica D Tenenbaum

Duke University

Career Start Year 2006

Number of shared co-authors 7

Scott L DuVall

University of Utah

Career Start Year 2006

Number of shared co-authors 17

Joel T Dudley

Institute for Next Generation Healthcare

Career Start Year 2006

Number of shared co-authors 13

Vojtech Huser

Lister Hill National Center for Biomedical Communication

Career Start Year 2005

Number of shared co-authors 8

Jomol Mathew

University of Wisconsin-Madison

Career Start Year 2004

Number of shared co-authors 1

Mark A Hoffman

Children's Mercy Hospital

Career Start Year 2003

Number of shared co-authors 16

Chunhua Weng

Columbia University Irving Medical Center

Career Start Year 2002

Number of shared co-authors 70

Nigam H Shah

Stanford University

Career Start Year 2002

Number of shared co-authors 6

Griffin M Weber

Harvard Medical School

Career Start Year 2001

Number of shared co-authors 9

Robert R Freimuth

Center for Individualized Medicine, Mayo Clinic

Career Start Year 2000

Number of shared co-authors 74

Rachel L Richesson

University of Michigan Medical School ann arbor

Career Start Year 1998

Number of shared co-authors 16

Stanley C Ahalt

Renaissance Computing Institute, University of North Carolina at Chapel Hill

Career Start Year 1993

Number of shared co-authors 4

Lucila Ohno-Machado

Escola de Administracao de Empresas - FGV, Stanford University, University of California San Diego, University of Sao Paulo, Yale School of Medicine

Career Start Year 1993

Number of shared co-authors 21

Peter Tarczy-Hornoch

University of Washington School of Medicine, University of Washington

Career Start Year 1992

Number of shared co-authors 35

Kenneth D Mandl

Boston Children's Hospital

Career Start Year 1991

Number of shared co-authors 9

William R Hogan

College of Medicine, University of Florida

Career Start Year 1990

Number of shared co-authors 13

Shawn N Murphy

Harvard Medical School

Career Start Year 1986

Number of shared co-authors 57

John H Holmes

University of Pennsylvania Perelman School of Medicine

Career Start Year 1985

Number of shared co-authors 4

Geoffrey S Ginsburg

National Institutes of Health

Career Start Year 1981

Number of shared co-authors 28

row(s) 1 - 30 of 30

Joshua C Denny

Vanderbilt University

Co-authored papers 31

Dan M Roden

Vanderbilt University Medical Center

Co-authored papers 28

Marylyn D Ritchie

Center for Systems Genomics, Pennsylvania State University, University Park

Co-authored papers 22

Dana C Crawford

Cleveland Institute for Computational Biology, Case Western Reserve University

Co-authored papers 19

Jill M Pulley

Vanderbilt University School of Medicine

Co-authored papers 17

Daniel R Masys

University of Washington School of Medicine.

Co-authored papers 16

Rongling Li

National Human Genome Research Institute, National Institutes of Health

Co-authored papers 13

Andrea H Ramirez

Vanderbilt University Medical Center

Co-authored papers 12

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 12

Rex L Chisholm

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

Co-authored papers 11

Abel N Kho

Northwestern University Feinberg School of Medicine

Co-authored papers 11

Iftikhar J Kullo

Mayo Clinic

Co-authored papers 10

Catherine A McCarty

University of Minnesota Medical School, 1035 University Drive duluth