Author details

Full Name

Eric S Lander

Affiliation

Vanderbilt-Ingram Cancer Center, Vanderbilt University

ORCID

Career Start Year

1986

Papers

545

H Index

244

Expertise

CM4AI Collaborator

Emma Lundberg (CM4AI)

PMID	Paper Title	Journal Title	Published Year
36495309	Using the HER2/CEP17 FISH Ratio to Predict Pathologic Complete Response Following Neoadjuvant Anti-HER2 Doublet Therapy in HER2+ Breast Cancer.	Oncologist	2023
37640881	Extremely sparse models of linkage disequilibrium in ancestrally diverse association studies.	Nat Genet	2023
36495309	Using the HER2/CEP17 FISH Ratio to Predict Pathologic Complete Response Following Neoadjuvant Anti-HER2 Doublet Therapy in HER2+ Breast Cancer.	Oncologist	2023
37137305	Massively parallel base editing to map variant effects in human hematopoiesis.	Cell	2023
37443254	Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases.	Nat Genet	2023
37640881	Extremely sparse models of linkage disequilibrium in ancestrally diverse association studies.	Nat Genet	2023
37443254	Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases.	Nat Genet	2023
37137305	Massively parallel base editing to map variant effects in human hematopoiesis.	Cell	2023
36048760	Neurocognitive trajectory and proteomic signature of inherited risk for Alzheimer's disease.	PLoS Genet	2022
36048760	Neurocognitive trajectory and proteomic signature of inherited risk for Alzheimer's disease.	PLoS Genet	2022
35594906	Compatibility rules of human enhancer and promoter sequences.	Nature	2022
36177448	A patient-driven clinicogenomic partnership for metastatic prostate cancer.	Cell Genom	2022
35969771	Inferring gene regulation from stochastic transcriptional variation across single cells at steady state.	Proc Natl Acad Sci U S A	2022
35594906	Compatibility rules of human enhancer and promoter sequences.	Nature	2022
35969771	Inferring gene regulation from stochastic transcriptional variation across single cells at steady state.	Proc Natl Acad Sci U S A	2022
36177448	A patient-driven clinicogenomic partnership for metastatic prostate cancer.	Cell Genom	2022
33349665	The SARS-CoV-2 RNA-protein interactome in infected human cells.	Nat Microbiol	2021
33859401	Compressed sensing for highly efficient imaging transcriptomics.	Nat Biotechnol	2021
33536627	Author Correction: A structural variation reference for medical and population genetics.	Nature	2021
33513366	A regulatory variant at 3q21.1 confers an increased pleiotropic risk for hyperglycemia and altered bone mineral density.	Cell Metab	2021
33828297	Genome-wide enhancer maps link risk variants to disease genes.	Nature	2021
34255846	Cross-Sectional Assessment of SARS-CoV-2 Viral Load by Symptom Status in Massachusetts Congregate Living Facilities.	J Infect Dis	2021
34244402	ARPA-H: Accelerating biomedical breakthroughs.	Science	2021
33349665	The SARS-CoV-2 RNA-protein interactome in infected human cells.	Nat Microbiol	2021
33393745	Human Molecular Genetics and Genomics - Important Advances and Exciting Possibilities.	N Engl J Med	2021
33828297	Genome-wide enhancer maps link risk variants to disease genes.	Nature	2021
33513366	A regulatory variant at 3q21.1 confers an increased pleiotropic risk for hyperglycemia and altered bone mineral density.	Cell Metab	2021
33536627	Author Correction: A structural variation reference for medical and population genetics.	Nature	2021
33859401	Compressed sensing for highly efficient imaging transcriptomics.	Nat Biotechnol	2021
34244402	ARPA-H: Accelerating biomedical breakthroughs.	Science	2021
34255846	Cross-Sectional Assessment of SARS-CoV-2 Viral Load by Symptom Status in Massachusetts Congregate Living Facilities.	J Infect Dis	2021
33393745	Human Molecular Genetics and Genomics - Important Advances and Exciting Possibilities.	N Engl J Med	2021
32199098	Towards a treatment for genetic prion disease: trials and biomarkers.	Lancet Neurol	2020
32144282	Prioritizing disease and trait causal variants at the TNFAIP3 locus using functional and genomic features.	Nat Commun	2020
32199098	Towards a treatment for genetic prion disease: trials and biomarkers.	Lancet Neurol	2020
32015527	Identification of cancer driver genes based on nucleotide context.	Nat Genet	2020
31959994	Control of human hemoglobin switching by LIN28B-mediated regulation of BCL11A translation.	Nat Genet	2020
32053334	The Risk of Corticosteroids in Community-Acquired Pneumonia.	Am Fam Physician	2020
32042194	The Angiosarcoma Project: enabling genomic and clinical discoveries in a rare cancer through patient-partnered research.	Nat Med	2020
33377127	Delivery Mode Affects Stability of Early Infant Gut Microbiota.	Cell Rep Med	2020
33376219	HyPR-seq: Single-cell quantification of chosen RNAs via hybridization and sequencing of DNA probes.	Proc Natl Acad Sci U S A	2020
32820175	Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions.	Nat Commun	2020
32053334	The Risk of Corticosteroids in Community-Acquired Pneumonia.	Am Fam Physician	2020
31959994	Control of human hemoglobin switching by LIN28B-mediated regulation of BCL11A translation.	Nat Genet	2020
32015527	Identification of cancer driver genes based on nucleotide context.	Nat Genet	2020
32042194	The Angiosarcoma Project: enabling genomic and clinical discoveries in a rare cancer through patient-partnered research.	Nat Med	2020
33377127	Delivery Mode Affects Stability of Early Infant Gut Microbiota.	Cell Rep Med	2020
33376219	HyPR-seq: Single-cell quantification of chosen RNAs via hybridization and sequencing of DNA probes.	Proc Natl Acad Sci U S A	2020
32820175	Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions.	Nat Commun	2020
32144282	Prioritizing disease and trait causal variants at the TNFAIP3 locus using functional and genomic features.	Nat Commun	2020

1 - 50 of 1,090

James G D Prendergast

The Roslin Institute, The University of Edinburgh

Career Start Year 2005

Number of shared co-authors 47

Jochen Hecht

The Barcelona Institute of Science and Technology

Career Start Year 2003

Number of shared co-authors 2

Chao Xing

University of Texas Southwestern Medical Center

Career Start Year 1999

Number of shared co-authors 21

Shawn Levy

HudsonAlpha Institute for Biotechnology

Career Start Year 1999

Number of shared co-authors 63

Sarah J Wheelan

National Human Genome Research Institute, National Institutes of Health

Career Start Year 1998

Number of shared co-authors 36

Eric E Schadt

Icahn School of Medicine at Mount Sinai

Career Start Year 1998

Number of shared co-authors 155

Edwin Cuppen

Hartwig Medical Foundation

Career Start Year 1997

Number of shared co-authors 39

Grier P Page

Genomics and Translational Research Center

Career Start Year 1996

Number of shared co-authors 16

Jay Shendure

University of Washington

Career Start Year 1996

Number of shared co-authors 121

Simon Heath

Barcelona Institute of Science and Technology (BIST)

Career Start Year 1995

Number of shared co-authors 108

Ping Liang

College of Chemistry and Chemical Engineering, Hunan University

Career Start Year 1995

Number of shared co-authors 8

Jared C Roach

Institute for Systems Biology

Career Start Year 1995

Number of shared co-authors 33

Len A Pennacchio

Lawrence Berkeley National Laboratory

Career Start Year 1995

Number of shared co-authors 79

Elizabeth A Worthey

Heersink School of Medicine, The University of Alabama at Birmingham

Career Start Year 1995

Number of shared co-authors 30

Alejandro A Sch??ffer

National Cancer Institute, National Institutes of Health

Career Start Year 1993

Number of shared co-authors 22

Kimberly F Doheny

Center for Inherited Disease Research, Johns Hopkins School of Medicine

Career Start Year 1993

Number of shared co-authors 92

David B Goldstein

Institute for Genomic Medicine, Columbia University Irving Medical Center

Career Start Year 1992

Number of shared co-authors 68

Marie-Laure Yaspo

Max Planck Institute for Molecular Genetics

Career Start Year 1992

Number of shared co-authors 28

Samuel Levy

Bluestar Genomics Inc.

Career Start Year 1991

Number of shared co-authors 37

Francisco M De La Vega

Stanford University School of Medicine

Career Start Year 1991

Number of shared co-authors 49

Winston Hide

Harvard Medical School

Career Start Year 1991

Number of shared co-authors 139

Christopher J Porter

Ottawa Hospital Research Institute

Career Start Year 1990

Number of shared co-authors 1

Anthony J Brookes

University of Leicester

Career Start Year 1989

Number of shared co-authors 88

Michael E Zwick

Rutgers University-New Brunswick, Rutgers University

Career Start Year 1989

Number of shared co-authors 16

Stephen F Kingsmore

Rady Children's Institute for Genomic Medicine

Career Start Year 1988

Number of shared co-authors 33

Dieter Weichenhan

German Cancer Research Center (DKFZ)

Career Start Year 1988

Number of shared co-authors 8

Jiannis Ragoussis

McGill University

Career Start Year 1986

Number of shared co-authors 43

Mark Lathrop

Victor Philip Dahdaleh Institute of Genomic Medicine at McGill University

Career Start Year 1975

Number of shared co-authors 153

Mary-Claire King

University of Washington

Career Start Year 1975

Number of shared co-authors 51

Alan F Scott

Johns Hopkins University School of Medicine

Career Start Year 1972

Number of shared co-authors 39

row(s) 1 - 30 of 30

Stacey Gabriel

Broad Institute of MIT and Harvard

Co-authored papers 78

Mark J Daly

Massachusetts General Hospital

Co-authored papers 58

Gad Getz

Broad Institute of the Massachusetts Institute of Technology and Harvard

Co-authored papers 55

Todd R Golub

Broad Institute of MIT and Harvard

Co-authored papers 43

Matthew Meyerson

Broad Institute

Co-authored papers 39

Bruce W Birren

Broad Institute of MIT and Harvard

Co-authored papers 38

Michael S Lawrence

Co-authored papers 36

Kerstin Lindblad-Toh

Uppsala University

Co-authored papers 36

Carrie Sougnez

The Broad Institute of Harvard and MIT

Co-authored papers 34

David B Jaffe

Co-authored papers 34

Chad Nusbaum

Co-authored papers 33

Levi A Garraway

Broad Institute of Harvard and MIT

Co-authored papers 30

Kristian Cibulskis

Co-authored papers 29

David Altshuler

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

Co-authored papers 27

Tarjei S Mikkelsen

Harvard University, USA Broad Institute, USA Harvard Stem Cell Institute

Co-authored papers 26

Thomas J Hudson

Ontario Institute for Cancer Research

Co-authored papers 25

Jill P Mesirov

University of California San Diego

Co-authored papers 24

Stephen F Schaffner

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

Co-authored papers 24

Jesse M Engreitz

Co-authored papers 24

Aviv Regev

Broad Institute of MIT and Harvard

Co-authored papers 23

Andreas Gnirke

The Center for Genome Architecture, Baylor College of Medicine

Co-authored papers 22

John D Rioux

Co-authored papers 22

Scott L Carter

Co-authored papers 21

Nir Hacohen

Broad Institute of MIT and Harvard

Co-authored papers 20

Leonid Kruglyak

Co-authored papers 20

Michael C Zody

Broad Institute of Harvard and MIT

Co-authored papers 20

Andrey Sivachenko

Cystic Fibrosis Foundation

Co-authored papers 20

Robert C Onofrio

The Broad Institute of Harvard and MIT

Co-authored papers 20

Manolis Kellis

Massachusetts Institute of Technology

Co-authored papers 17

Sekar Kathiresan

Co-authored papers 17

1 - 30

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