Author details

Full Name

Stacey Gabriel

Affiliation

Broad Institute of MIT and Harvard

ORCID

Career Start Year

2001

Papers

290

H Index

155

Expertise

CM4AI Collaborator

Trey Ideker (CM4AI)

PMID	Paper Title	Journal Title	Published Year
36706355	Mechanisms of response and resistance to combined decitabine and ipilimumab for advanced myeloid disease.	Blood	2023
37601969	Multiset correlation and factor analysis enables exploration of multi-omics data.	Cell Genom	2023
37749248	Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.	Nat Genet	2023
37662416	Proteome-Wide Association Studies for Blood Lipids and Comparison with Transcriptome-Wide Association Studies.	bioRxiv	2023
37802043	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.	Am J Hum Genet	2023
37868038	The functional impact of rare variation across the regulatory cascade.	Cell Genom	2023
37348055	Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.	Genetics	2023
37216410	Canonical correlation analysis for multi-omics: Application to cross-cohort analysis.	PLoS Genet	2023
36778406	Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.	bioRxiv	2023
36778386	Structural variation across 138,134 samples in the TOPMed consortium.	Res Sq	2023
36960714	Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program.	Circ Genom Precis Med	2023
36706355	Mechanisms of response and resistance to combined decitabine and ipilimumab for advanced myeloid disease.	Blood	2023
36747810	Structural variation across 138,134 samples in the TOPMed consortium.	bioRxiv	2023
36463326	Gene expression associations with body mass index in the Multi-Ethnic Study of Atherosclerosis.	Int J Obes (Lond)	2023
37231098	Gene expression in African Americans, Puerto Ricans and Mexican Americans reveals ancestry-specific patterns of genetic architecture.	Nat Genet	2023
37425772	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.	medRxiv	2023
37425716	Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effects.	bioRxiv	2023
37802043	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.	Am J Hum Genet	2023
37662416	Proteome-Wide Association Studies for Blood Lipids and Comparison with Transcriptome-Wide Association Studies.	bioRxiv	2023
37749248	Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.	Nat Genet	2023
37601969	Multiset correlation and factor analysis enables exploration of multi-omics data.	Cell Genom	2023
37868038	The functional impact of rare variation across the regulatory cascade.	Cell Genom	2023
37425772	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.	medRxiv	2023
37425716	Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effects.	bioRxiv	2023
37216410	Canonical correlation analysis for multi-omics: Application to cross-cohort analysis.	PLoS Genet	2023
37348055	Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.	Genetics	2023
37231098	Gene expression in African Americans, Puerto Ricans and Mexican Americans reveals ancestry-specific patterns of genetic architecture.	Nat Genet	2023
36960714	Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program.	Circ Genom Precis Med	2023
36747810	Structural variation across 138,134 samples in the TOPMed consortium.	bioRxiv	2023
36778406	Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.	bioRxiv	2023
36778386	Structural variation across 138,134 samples in the TOPMed consortium.	Res Sq	2023
36463326	Gene expression associations with body mass index in the Multi-Ethnic Study of Atherosclerosis.	Int J Obes (Lond)	2023
35087136	Upregulated heme biosynthesis increases obstructive sleep apnea severity: a pathway-based Mendelian randomization study.	Sci Rep	2022
35396579	Rare coding variants in ten genes confer substantial risk for schizophrenia.	Nature	2022
36038634	Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility.	Nat Genet	2022
35647563	Accounting for population structure in genetic studies of cystic fibrosis.	HGG Adv	2022
35385699	Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program.	Am J Hum Genet	2022
36220816	Whole genome sequence analysis of blood lipid levels in >66,000 individuals.	Nat Commun	2022
35982160	Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.	Nat Genet	2022
35716666	Genetic interactions drive heterogeneity in causal variant effect sizes for gene expression and complex traits.	Am J Hum Genet	2022
35087136	Upregulated heme biosynthesis increases obstructive sleep apnea severity: a pathway-based Mendelian randomization study.	Sci Rep	2022
35243413	Combined tumor and immune signals from genomes or transcriptomes predict outcomes of checkpoint inhibition in melanoma.	Cell Rep Med	2022
35647563	Accounting for population structure in genetic studies of cystic fibrosis.	HGG Adv	2022
35396579	Rare coding variants in ten genes confer substantial risk for schizophrenia.	Nature	2022
35716666	Genetic interactions drive heterogeneity in causal variant effect sizes for gene expression and complex traits.	Am J Hum Genet	2022
35385699	Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program.	Am J Hum Genet	2022
36038634	Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility.	Nat Genet	2022
35982160	Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.	Nat Genet	2022
36220816	Whole genome sequence analysis of blood lipid levels in >66,000 individuals.	Nat Commun	2022
35243413	Combined tumor and immune signals from genomes or transcriptomes predict outcomes of checkpoint inhibition in melanoma.	Cell Rep Med	2022

1 - 50 of 580

Hao Hu

Aerospace Center Hospital

Career Start Year 2011

Number of shared co-authors 9

Christopher DeBoever

Stanford University

Career Start Year 2010

Number of shared co-authors 17

Daryl Waggott

Ontario Institute for Cancer Research

Career Start Year 2009

Number of shared co-authors 72

Christian Gilissen

Radboud University Medical Center

Career Start Year 2009

Number of shared co-authors 60

Sofie Ashford

University of Cambridge

Career Start Year 2008

Number of shared co-authors 34

John D Overton

Regeneron Pharmaceuticals

Career Start Year 2008

Number of shared co-authors 55

Martin Kircher

Berlin Institute of Health (BIH) at Charite-Universitatsmedizin Berlin

Career Start Year 2008

Number of shared co-authors 31

Selina Vattathil

Emory University School of Medicine

Career Start Year 2007

Number of shared co-authors 56

Kurt N Hetrick

Center for Inherited Disease Research, Johns Hopkins School of Medicine

Career Start Year 2007

Number of shared co-authors 53

Chad D Huff

University of Texas M.D. Anderson Cancer Center

Career Start Year 2007

Number of shared co-authors 68

Mark J Cowley

Children's Cancer Institute, Lowy Cancer Research Centre

Career Start Year 2006

Number of shared co-authors 29

Alison Meynert

Institute of Genetics and Cancer, University of Edinburgh

Career Start Year 2006

Number of shared co-authors 27

Praveen F Cherukuri

Sanford School of Medicine, University of South Dakota

Career Start Year 2005

Number of shared co-authors 22

Ali Torkamani

Scripps Science Institute

Career Start Year 2005

Number of shared co-authors 39

Laurie Burdett

National Cancer Institute, Frederick National Laboratory for Cancer Research

Career Start Year 2005

Number of shared co-authors 24

David W Craig

University of Southern California

Career Start Year 2004

Number of shared co-authors 71

Scott J Hebbring

Marshfield Clinic Research Institute

Career Start Year 2003

Number of shared co-authors 69

Sek Won Kong

Boston Children's Hospital, Seoul National University, Seoul National University Hospital

Career Start Year 2003

Number of shared co-authors 28

Yufeng Shen

Columbia University

Career Start Year 2002

Number of shared co-authors 70

Eric W Klee

Mayo Clinic College of Medicine and Science

Career Start Year 2001

Number of shared co-authors 40

Kai Wang

University of Pennsylvania

Career Start Year 2001

Number of shared co-authors 102

Nancy F Hansen

National Human Genome Research Institute, National Institutes of Health

Career Start Year 2000

Number of shared co-authors 76

Hugues Sicotte

Mayo Clinic

Career Start Year 1999

Number of shared co-authors 29

Michael O Dorschner

University of Washington

Career Start Year 1997

Number of shared co-authors 85

Szabolcs Szelinger

College of American Pathologists

Career Start Year 1996

Number of shared co-authors 50

Sean McGrath

Harvard T.H. Chan School of Public Health

Career Start Year 1996

Number of shared co-authors 35

John V Pearson

QIMR Berghofer Medical Research Institute

Career Start Year 1996

Number of shared co-authors 52

Jenny C Taylor

University of Oxford

Career Start Year 1996

Number of shared co-authors 42

David B Goldstein

Institute for Genomic Medicine, Columbia University Irving Medical Center

Career Start Year 1992

Number of shared co-authors 119

Stephen J Chanock

National Cancer Institute, National Institutes of Health

Career Start Year 1983

Number of shared co-authors 284

row(s) 1 - 30 of 30

Eric S Lander

Vanderbilt-Ingram Cancer Center, Vanderbilt University

Co-authored papers 78

Gad Getz

Broad Institute of the Massachusetts Institute of Technology and Harvard

Co-authored papers 64

Mark J Daly

Massachusetts General Hospital

Co-authored papers 56

David Altshuler

Broad Institute of Harvard and Massachusetts Institute of Technology (MIT)

Co-authored papers 56

Namrata Gupta

Co-authored papers 50

Sekar Kathiresan

Co-authored papers 49

Kristian Cibulskis

Co-authored papers 47

Carrie Sougnez

The Broad Institute of Harvard and MIT

Co-authored papers 46

Matthew Meyerson

Broad Institute

Co-authored papers 45

James G Wilson

Beth Israel Deaconess Medical Center

Co-authored papers 38

Michael S Lawrence

Co-authored papers 38

Eric Boerwinkle

Baylor College of Medicine

Co-authored papers 36

Levi A Garraway

Broad Institute of Harvard and MIT

Co-authored papers 35

Stephen S Rich

Co-authored papers 32

Scott L Carter

Co-authored papers 29

Gon??alo R Abecasis

Regeneron Pharmaceuticals Inc.

Co-authored papers 28

Bruce M Psaty

Co-authored papers 26

Robert C Onofrio

The Broad Institute of Harvard and MIT

Co-authored papers 26

Deborah A Nickerson

University of Washington

Co-authored papers 25

Jerome I Rotter

Co-authored papers 25

Gina M Peloso

Co-authored papers 25

Russell P Tracy

Co-authored papers 24

Richard A Gibbs

Baylor College of Medicine

Co-authored papers 24

Joseph G Gleeson

University of California

Co-authored papers 23

Daniel J Rader

Co-authored papers 22

Pradeep Natarajan

Co-authored papers 22

Kristin G Ardlie

Co-authored papers 22

Tim Fennell

Co-authored papers 22

Andrey Sivachenko

Cystic Fibrosis Foundation

Co-authored papers 22

Jason Flannick

Co-authored papers 21

1 - 30

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