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Author Details

Julian M Hess
Broad Institute of MIT and Harvard
2015
27
21
PMIDPaper TitleJournal TitlePublished Year
36702949Combined PD-1, BRAF and MEK inhibition in BRAF<sup>V600E</sup> colorectal cancer: a phase 2 trial.Nat Med2023
36702949Combined PD-1, BRAF and MEK inhibition in BRAF<sup>V600E</sup> colorectal cancer: a phase 2 trial.Nat Med2023
36697832Author Correction: Analyses of non-coding somatic drivers in 2,658 cancer whole genomes.Nature2023
36624313Evolutionary history of transformation from chronic lymphocytic leukemia to Richter syndrome.Nat Med2023
36697832Author Correction: Analyses of non-coding somatic drivers in 2,658 cancer whole genomes.Nature2023
36624313Evolutionary history of transformation from chronic lymphocytic leukemia to Richter syndrome.Nat Med2023
35398145The Four mRNA Bases Have Quite Different (Un)folding Free Energies, Applications to RNA Splicing and Translation Initiation with BindOligoNet.J Mol Biol2022
35398145The Four mRNA Bases Have Quite Different (Un)folding Free Energies, Applications to RNA Splicing and Translation Initiation with BindOligoNet.J Mol Biol2022
32424350Cas9 activates the p53 pathway and selects for p53-inactivating mutations.Nat Genet2020
32424350Cas9 activates the p53 pathway and selects for p53-inactivating mutations.Nat Genet2020
32587373Author Correction: Cas9 activates the p53 pathway and selects for p53-inactivating mutations.Nat Genet2020
32587373Author Correction: Cas9 activates the p53 pathway and selects for p53-inactivating mutations.Nat Genet2020
31171663RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues.Science2019
31526759Passenger Hotspot Mutations in Cancer.Cancer Cell2019
31171663RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues.Science2019
31068700Next-generation characterization of the Cancer Cell Line Encyclopedia.Nature2019
31526759Passenger Hotspot Mutations in Cancer.Cancer Cell2019
31068700Next-generation characterization of the Cancer Cell Line Encyclopedia.Nature2019
29316429Integrative Analysis Identifies Four Molecular and Clinical Subsets in Uveal Melanoma.Cancer Cell2018
30262473Comment on "DNA damage is a pervasive cause of sequencing errors, directly confounding variant identification".Science2018
30107175Widespread Chromosomal Losses and Mitochondrial DNA Alterations as Genetic Drivers in Hürthle Cell Carcinoma.Cancer Cell2018
30096302Comprehensive Characterization of Cancer Driver Genes and Mutations.Cell2018
29955181Publisher Correction: Molecular subtypes of diffuse large B cell lymphoma are associated with distinct pathogenic mechanisms and outcomes.Nat Med2018
29955182Author Correction: Molecular subtypes of diffuse large B cell lymphoma are associated with distinct pathogenic mechanisms and outcomes.Nat Med2018
29625053Comprehensive Characterization of Cancer Driver Genes and Mutations.Cell2018
29717118Distinct mutational signatures characterize concurrent loss of polymerase proofreading and mismatch repair.Nat Commun2018
29713087Molecular subtypes of diffuse large B cell lymphoma are associated with distinct pathogenic mechanisms and outcomes.Nat Med2018
29596782Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines.Cell Syst2018
29316429Integrative Analysis Identifies Four Molecular and Clinical Subsets in Uveal Melanoma.Cancer Cell2018
30107175Widespread Chromosomal Losses and Mitochondrial DNA Alterations as Genetic Drivers in Hürthle Cell Carcinoma.Cancer Cell2018
30096302Comprehensive Characterization of Cancer Driver Genes and Mutations.Cell2018
29955181Publisher Correction: Molecular subtypes of diffuse large B cell lymphoma are associated with distinct pathogenic mechanisms and outcomes.Nat Med2018
29955182Author Correction: Molecular subtypes of diffuse large B cell lymphoma are associated with distinct pathogenic mechanisms and outcomes.Nat Med2018
30262473Comment on "DNA damage is a pervasive cause of sequencing errors, directly confounding variant identification".Science2018
29717118Distinct mutational signatures characterize concurrent loss of polymerase proofreading and mismatch repair.Nat Commun2018
29713087Molecular subtypes of diffuse large B cell lymphoma are associated with distinct pathogenic mechanisms and outcomes.Nat Med2018
29625053Comprehensive Characterization of Cancer Driver Genes and Mutations.Cell2018
29596782Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines.Cell Syst2018
27869828Tumor-suppressor genes that escape from X-inactivation contribute to cancer sex bias.Nat Genet2017
28810145Integrative Analysis Identifies Four Molecular and Clinical Subsets in Uveal Melanoma.Cancer Cell2017
28892075Analysis of somatic microsatellite indels identifies driver events in human tumors.Nat Biotechnol2017
28658632Integrative Genomic Analysis of Cholangiocarcinoma Identifies Distinct IDH-Mutant Molecular Profiles.Cell Rep2017
28658208Recurrent and functional regulatory mutations in breast cancer.Nature2017
28297679Integrative Genomic Analysis of Cholangiocarcinoma Identifies Distinct IDH-Mutant Molecular Profiles.Cell Rep2017
27869828Tumor-suppressor genes that escape from X-inactivation contribute to cancer sex bias.Nat Genet2017
28297679Integrative Genomic Analysis of Cholangiocarcinoma Identifies Distinct IDH-Mutant Molecular Profiles.Cell Rep2017
28810145Integrative Analysis Identifies Four Molecular and Clinical Subsets in Uveal Melanoma.Cancer Cell2017
28658632Integrative Genomic Analysis of Cholangiocarcinoma Identifies Distinct IDH-Mutant Molecular Profiles.Cell Rep2017
28892075Analysis of somatic microsatellite indels identifies driver events in human tumors.Nat Biotechnol2017
28658208Recurrent and functional regulatory mutations in breast cancer.Nature2017
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Collaborators

Gad Getz
Broad Institute of the Massachusetts Institute of Technology and Harvard
Co-authored papers 20
Michael S Lawrence
Co-authored papers 14
Jaegil Kim
Co-authored papers 13
Chip Stewart
Broad Institute of MIT and Harvard
Co-authored papers 11
Ignaty Leshchiner
Broad Institute of Massachusetts Institute of Technology and Harvard
Co-authored papers 7
David A Wheeler
Baylor College of Medicine
Co-authored papers 7
Rameen Beroukhim
Co-authored papers 7
Esther Rheinbay
Co-authored papers 7
Dimitri Livitz
Co-authored papers 7
Amaro Taylor-Weiner
Co-authored papers 7
Todd R Golub
Broad Institute of MIT and Harvard
Co-authored papers 7
Daniel Rosebrock
Co-authored papers 7
Atanas Kamburov
Broad Institute of Harvard and MIT
Co-authored papers 6
Nicholas J Haradhvala
Co-authored papers 6
Gordon B Mills
Knight Cancer Institute, Oregon Health and Sciences University
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Aaron R Thorner
Co-authored papers 5
Andrew D Cherniack
Dana-Farber Cancer Institute
Co-authored papers 5
Paz Polak
McGill University
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Mara Rosenberg
Broad Institute of MIT and Harvard
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Rehan Akbani
The University of Texas MD Anderson Cancer Center
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Donna Neuberg
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Joshua M Stuart
University of California at Santa Cruz
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Chandra Sekhar Pedamallu
Broad Institute
Co-authored papers 5
Amy G Robertson
Present address: Dxige Research Inc.
Co-authored papers 4
Kyle R Covington
Baylor College of Medicine
Co-authored papers 4
Katherine A Hoadley
Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill
Co-authored papers 4
Jeremiah Wala
The Broad Institute of MIT and Harvard
Co-authored papers 4
Adam Tracy
Co-authored papers 4
Alexander J Lazar
The University of Texas MD Anderson Cancer Center
Co-authored papers 4
Matthew Meyerson
Broad Institute
Co-authored papers 4
Release 1.2