Author details

Full Name

Rex L Chisholm

Affiliation

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

ORCID

Career Start Year

1976

Papers

139

H Index

Expertise

CM4AI Collaborator

Nevan J Krogan (CM4AI)

PMID	Paper Title	Journal Title	Published Year
36866529	The Gene Ontology knowledgebase in 2023.	Genetics	2023
37758692	Proteomic and genetic analyses of influenza A viruses identify pan-viral host targets.	Nat Commun	2023
38065071	Genomic medicine year in review: 2023.	Am J Hum Genet	2023
37883979	Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing.	Am J Hum Genet	2023
37246632	Education and electronic medical records and genomics network, challenges, and lessons learned from a large-scale clinical trial using polygenic risk scores.	Genet Med	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
36621880	Returning integrated genomic risk and clinical recommendations: The eMERGE study.	Genet Med	2023
35031602	The genetic architecture underlying prey-dependent performance in a microbial predator.	Nat Commun	2022
35835913	Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries.	Nat Genet	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
36459977	Genomic Medicine Year in Review: 2022.	Am J Hum Genet	2022
34429112	Mutant resources for functional genomics in Dictyostelium discoideum using REMI-seq technology.	BMC Biol	2021
35837266	NUcore at 10: A Decade of Experience Developing a Core Facilities Management Application.	J Biomol Tech	2021
33861960	Is genetic ancestry a tool to combat health disparities?	Cell	2021
34861172	Genomic medicine year in review: 2021.	Am J Hum Genet	2021
33275910	Genomic Medicine Year in Review: 2020.	Am J Hum Genet	2020
32009526	Pathogenic and Uncertain Genetic Variants Have Clinical Cardiac Correlates in Diverse Biobank Participants.	J Am Heart Assoc	2020
30298529	The eMERGE genotype set of 83,717 subjects imputed to ~40â¿¿million variants genome wide and association with the herpes zoster medical record phenotype.	Genet Epidemiol	2019
32027834	Genomic Medicine Year in Review: 2019.	Am J Hum Genet	2019
31840793	dictyBase and the Dicty Stock Center (version 2.0) - a progress report.	Int J Dev Biol	2019
31395439	Opportunities, resources, and techniques for implementing genomics in clinical care.	Lancet	2019
30778576	An ancillary genomics system to support the return of pharmacogenomic results.	J Am Med Inform Assoc	2019
29460415	Research Directions in the Clinical Implementation of Pharmacogenomics: An Overview of US Programs and Projects.	Clin Pharmacol Ther	2018
28222112	Genome-wide study of resistant hypertension identified from electronic health records.	PLoS One	2017
28340351	Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research.	Cell	2017
28335839	Apolipoprotein L1 VariantsÂ and Blood Pressure Traits inÂ African Americans.	J Am Coll Cardiol	2017
26169577	A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough.	Pharmacogenomics J	2016
26912863	The phenotypic legacy of admixture between modern humans and Neandertals.	Science	2016
26746457	Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.	JAMA	2016
26857349	Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network.	Clin Pharmacol Ther	2016
26112289	Data Safe Havens in health research and healthcare.	Bioinformatics	2015
26041702	Global implementation of genomic medicine: We are not alone.	Sci Transl Med	2015
26088819	dictyBase 2015: Expanding data and annotations in a new software environment.	Genesis	2015
24026423	A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects.	Hum Genet	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
25177340	Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index.	Front Genet	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
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
24634402	Characterizing genetic variants for clinical action.	Am J Med Genet C Semin Med Genet	2014
23306799	Implementing genomic medicine in the clinic: the future is here.	Genet Med	2013
24270849	Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data.	Nat Biotechnol	2013
23882410	At the Interface between Medical Informatics and Personalized Medicine: The eMERGE Network Experience.	Healthc Inform Res	2013
23872829	The opportunities and challenges of implementing genomics-informed personalized medicine.	Clin Pharmacol Ther	2013
23696099	Genetic variants that confer resistance to malaria are associated with red blood cell traits in African-Americans: an electronic medical record-based genome-wide association study.	G3 (Bethesda)	2013
23657386	A P3G generic access agreement for population genomic studies.	Nat Biotechnol	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
23534349	Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans.	Ann Hum Genet	2013
23494302	One stop shop for everything Dictyostelium: dictyBase and the Dicty Stock Center in 2012.	Methods Mol Biol	2013

1 - 50 of 139

B??rang??re Lombard

Institut Curie, PSL Research University

Career Start Year 2005

Number of shared co-authors 0

Matthew D Sekedat

Columbia University

Career Start Year 2004

Number of shared co-authors 0

Sean R Collins

University of California davis

Career Start Year 2003

Number of shared co-authors 6

Josef D Franke

Creighton University

Career Start Year 2002

Number of shared co-authors 1

Karsten Hokamp

Smurfit Institute of Genetics, Trinity College of Dublin

Career Start Year 1999

Number of shared co-authors 13

David R Powell

Biomedicine Discovery Institute, Monash University

Career Start Year 1998

Number of shared co-authors 1

Damarys Loew

Institut Curie, PSL Research University

Career Start Year 1996

Number of shared co-authors 0

Kristin C Gunsalus

Center for Genomics and Systems Biology, New York University Abu Dhabi (NYUAD)

Career Start Year 1995

Number of shared co-authors 4

Nicolas Bertin

University Bordeaux, CNRS

Career Start Year 1994

Number of shared co-authors 6

Bianca Habermann

Aix Marseille University, CNRS, Turing Center for Living Systems

Career Start Year 1993

Number of shared co-authors 2

Gyorgy Babnigg

Argonne National Laboratory

Career Start Year 1992

Number of shared co-authors 2

Jeffrey J Delrow

Clinical Research Division, Fred Hutchinson Cancer Research Center

Career Start Year 1992

Number of shared co-authors 2

Janos Demeter

Stanford University School of Medicine, Center for Clinical Sciences Research

Career Start Year 1991

Number of shared co-authors 20

Ri-Ichiroh Manabe

Center for Integrative Medical Sciences

Career Start Year 1990

Number of shared co-authors 5

Shankar Subramaniam

University of California

Career Start Year 1989

Number of shared co-authors 7

Chris P Ponting

The University of Edinburgh

Career Start Year 1989

Number of shared co-authors 36

Alasdair Ivens

University of Washington School of Medicine

Career Start Year 1987

Number of shared co-authors 11

Aled M Edwards

University of Toronto

Career Start Year 1984

Number of shared co-authors 4

Hediye Erdjument-Bromage

Neuroscience Institute, NYU Grossman School of Medicine

Career Start Year 1984

Number of shared co-authors 3

Marian J A Groot Koerkamp

Princess Maxima Center for Pediatric Oncology Research

Career Start Year 1983

Number of shared co-authors 1

Michael Snyder

Stanford University

Career Start Year 1981

Number of shared co-authors 58

Pamela A Silver

Harvard Medical School

Career Start Year 1979

Number of shared co-authors 4

Barbara J Wold

Merkin Institute for Translational Research, California Institute of Technology

Career Start Year 1976

Number of shared co-authors 26

Kathleen A Burke

Brown University

Career Start Year 1975

Number of shared co-authors 0

Lawrence S B Goldstein

university of california san diego

Career Start Year 1975

Number of shared co-authors 14

Norma Neff

Stanford University

Career Start Year 1974

Number of shared co-authors 8

Ronald W Davis

Stanford University

Career Start Year 1968

Number of shared co-authors 29

David L Nelson

Baylor College of Medicine

Career Start Year 1968

Number of shared co-authors 28

David Schlessinger

NIH/National Institute of Ageing

Career Start Year 1960

Number of shared co-authors 61

John S Mattick

Australia UNSW RNA Institute

Career Start Year 1951

Number of shared co-authors 24

row(s) 1 - 30 of 30

Dan M Roden

Vanderbilt University Medical Center

Co-authored papers 33

Petra Fey

Center for Genetic Medicine, Northwestern University.

Co-authored papers 32

Gail P Jarvik

University of Washington Medical Center

Co-authored papers 28

Joshua C Denny

Vanderbilt University

Co-authored papers 27

Teri A Manolio

National Human Genome Research Institute

Co-authored papers 27

Pascale Gaudet

University of Geneva

Co-authored papers 26

Marylyn D Ritchie

Center for Systems Genomics, Pennsylvania State University, University Park

Co-authored papers 24

Iftikhar J Kullo

Mayo Clinic

Co-authored papers 21

Jennifer A Pacheco

University of Pennsylvania

Co-authored papers 20

Marc S Williams

University of Washington Medical Center

Co-authored papers 20

Rongling Li

National Human Genome Research Institute, National Institutes of Health

Co-authored papers 18

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 17

David R Crosslin

University of Washington Medical Center

Co-authored papers 16

Abel N Kho

Northwestern University Feinberg School of Medicine

Co-authored papers 15

Eric B Larson

University of Washington

Co-authored papers 14

Laura J Rasmussen-Torvik

Northwestern University, Center for Genetic Medicine