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Author Details

Nicolas Robine
Sloan-Kettering Institute
2006
46
27
PMIDPaper TitleJournal TitlePublished Year
38047392NIPBL::NACC1 Fusion Hepatic Carcinoma.Am J Surg Pathol2024
38047392NIPBL::NACC1 Fusion Hepatic Carcinoma.Am J Surg Pathol2024
37704749Evolution of structural rearrangements in prostate cancer intracranial metastases.NPJ Precis Oncol2023
37919447Author Correction: Evolution of structural rearrangements in prostate cancer intracranial metastases.NPJ Precis Oncol2023
37704749Evolution of structural rearrangements in prostate cancer intracranial metastases.NPJ Precis Oncol2023
37919447Author Correction: Evolution of structural rearrangements in prostate cancer intracranial metastases.NPJ Precis Oncol2023
34895873New York's Polyethnic-1000: a regional initiative to understand how diverse ancestries influence the risk, progression, and treatment of cancers.Trends Cancer2022
35697697Gene expression signatures of individual ductal carcinoma in situ lesions identify processes and biomarkers associated with progression towards invasive ductal carcinoma.Nat Commun2022
35752636Occult polyclonality of preclinical pancreatic cancer models drives in vitro evolution.Nat Commun2022
35749364Retromer dysfunction in amyotrophic lateral sclerosis.Proc Natl Acad Sci U S A2022
35484108Somatic whole genome dynamics of precancer in Barrett's esophagus reveals features associated with disease progression.Nat Commun2022
36121736African Ancestry-Associated Gene Expression Profiles in Triple-Negative Breast Cancer Underlie Altered Tumor Biology and Clinical Outcome in Women of African Descent.Cancer Discov2022
34895873New York's Polyethnic-1000: a regional initiative to understand how diverse ancestries influence the risk, progression, and treatment of cancers.Trends Cancer2022
35697697Gene expression signatures of individual ductal carcinoma in situ lesions identify processes and biomarkers associated with progression towards invasive ductal carcinoma.Nat Commun2022
35752636Occult polyclonality of preclinical pancreatic cancer models drives in vitro evolution.Nat Commun2022
35749364Retromer dysfunction in amyotrophic lateral sclerosis.Proc Natl Acad Sci U S A2022
35484108Somatic whole genome dynamics of precancer in Barrett's esophagus reveals features associated with disease progression.Nat Commun2022
36121736African Ancestry-Associated Gene Expression Profiles in Triple-Negative Breast Cancer Underlie Altered Tumor Biology and Clinical Outcome in Women of African Descent.Cancer Discov2022
33626341Whole-genome characterization of lung adenocarcinomas lacking alterations in the RTK/RAS/RAF pathway.Cell Rep2021
33626341Whole-genome characterization of lung adenocarcinomas lacking alterations in the RTK/RAS/RAF pathway.Cell Rep2021
32483360Genome-wide cell-free DNA mutational integration enables ultra-sensitive cancer monitoring.Nat Med2020
32483360Genome-wide cell-free DNA mutational integration enables ultra-sensitive cancer monitoring.Nat Med2020
33007263Distinct Classes of Complex Structural Variation Uncovered across Thousands of Cancer Genome Graphs.Cell2020
33007263Distinct Classes of Complex Structural Variation Uncovered across Thousands of Cancer Genome Graphs.Cell2020
30563911Human papillomavirus and the landscape of secondary genetic alterations in oral cancers.Genome Res2019
31836783Deep whole-genome sequencing of 3 cancer cell lines on 2 sequencing platforms.Sci Rep2019
30563911Human papillomavirus and the landscape of secondary genetic alterations in oral cancers.Genome Res2019
31023376Sequencing and curation strategies for identifying candidate glioblastoma treatments.BMC Med Genomics2019
31011208Immunogenic neoantigens derived from gene fusions stimulate T cell responses.Nat Med2019
31197308SCANVIS: a tool for SCoring, ANnotating and VISualizing splice junctions.Bioinformatics2019
31375115Correction to: Sequencing and curation strategies for identifying candidate glioblastoma treatments.BMC Med Genomics2019
31836783Deep whole-genome sequencing of 3 cancer cell lines on 2 sequencing platforms.Sci Rep2019
31375115Correction to: Sequencing and curation strategies for identifying candidate glioblastoma treatments.BMC Med Genomics2019
31197308SCANVIS: a tool for SCoring, ANnotating and VISualizing splice junctions.Bioinformatics2019
31011208Immunogenic neoantigens derived from gene fusions stimulate T cell responses.Nat Med2019
31023376Sequencing and curation strategies for identifying candidate glioblastoma treatments.BMC Med Genomics2019
29468833Identification of Three Rheumatoid Arthritis Disease Subtypes by Machine Learning Integration of Synovial Histologic Features and RNA Sequencing Data.Arthritis Rheumatol2018
29875142<i>YES1</i> amplification is a mechanism of acquired resistance to EGFR inhibitors identified by transposon mutagenesis and clinical genomics.Proc Natl Acad Sci U S A2018
30138725Analytical Validation of Clinical Whole-Genome and Transcriptome Sequencing of Patient-Derived Tumors for Reporting Targetable Variants in Cancer.J Mol Diagn2018
29853643Organoid Profiling Identifies Common Responders to Chemotherapy in Pancreatic Cancer.Cancer Discov2018
30271907Genome-wide somatic variant calling using localized colored de Bruijn graphs.Commun Biol2018
29468833Identification of Three Rheumatoid Arthritis Disease Subtypes by Machine Learning Integration of Synovial Histologic Features and RNA Sequencing Data.Arthritis Rheumatol2018
29588360taxMaps: comprehensive and highly accurate taxonomic classification of short-read data in reasonable time.Genome Res2018
29853643Organoid Profiling Identifies Common Responders to Chemotherapy in Pancreatic Cancer.Cancer Discov2018
29875142<i>YES1</i> amplification is a mechanism of acquired resistance to EGFR inhibitors identified by transposon mutagenesis and clinical genomics.Proc Natl Acad Sci U S A2018
30138725Analytical Validation of Clinical Whole-Genome and Transcriptome Sequencing of Patient-Derived Tumors for Reporting Targetable Variants in Cancer.J Mol Diagn2018
30271907Genome-wide somatic variant calling using localized colored de Bruijn graphs.Commun Biol2018
29588360taxMaps: comprehensive and highly accurate taxonomic classification of short-read data in reasonable time.Genome Res2018
28740869Comparing sequencing assays and human-machine analyses in actionable genomics for glioblastoma.Neurol Genet2017
28855512ATRX is a regulator of therapy induced senescence in human cells.Nat Commun2017
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Collaborators

Minita Shah
Co-authored papers 12
Eric C Lai
Co-authored papers 11
Kanika Arora
Co-authored papers 11
Anne-Katrin Emde
Variant Bio Inc.
Co-authored papers 10
Michael C Zody
Broad Institute of Harvard and MIT
Co-authored papers 8
Katsutomo Okamura
Co-authored papers 7
Robert B Darnell
Co-authored papers 6
Andrea Sboner
Institute for Computational Biomedicine
Co-authored papers 6
Olivier Elemento
Meyer Cancer Center
Co-authored papers 5
Vladimir Vacic
Stanley Institute for Cognitive Genomics
Co-authored papers 5
Juan Miguel Mosquera
Caryl and Israel Englander Institute for Precision Medicine
Co-authored papers 5
Michael Sigouros
Caryl and Israel Englander Institute for Precision Medicine
Co-authored papers 4
Jakub Orzechowski Westholm
Co-authored papers 4
Raquel Martin
Co-authored papers 3
Qi Dai
Co-authored papers 3
Kahn Rhrissorrakrai
T.J. Watson Research Center
Co-authored papers 3
Diane Bortolamiol-Becet
Co-authored papers 3
Himisha Beltran
Dana-Farber Cancer Institute
Co-authored papers 3
Eugene Berezikov
Co-authored papers 3
Marcin Imielinski
Co-authored papers 3
Cecilia Esteves
Harvard Medical School
Co-authored papers 2
Emmanuel Barillot
Institut Curie, Universite PSL
Co-authored papers 2
Mariza Daras
University of California san francisco
Co-authored papers 2
Will Liao
Co-authored papers 2
Umesh Bhanot
Memorial Sloan Kettering Cancer Center
Co-authored papers 2
Norbert Perrimon
Co-authored papers 2
Kenneth Eng
Caryl and Israel Englander Institute for Precision Medicine
Co-authored papers 2
John A Boockvar
Lenox Hill Hospital
Co-authored papers 2
Alexis Demopoulos
Co-authored papers 2
Erik Ladewig
Memorial Sloan Kettering Cancer Center
Co-authored papers 2
Release 1.2