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Author Details

Boris Reva
Icahn School of Medicine at Mount Sinai
1990
62
27
PMIDPaper TitleJournal TitlePublished Year
37057291The most likely but largely ignored triggering factor for breast (or all) cancer invasion.J Cancer2023
37057291The most likely but largely ignored triggering factor for breast (or all) cancer invasion.J Cancer2023
37541199Proteogenomic analysis of chemo-refractory high-grade serous ovarian cancer.Cell2023
37541199Proteogenomic analysis of chemo-refractory high-grade serous ovarian cancer.Cell2023
35881881Reprogrammed Schwann Cells Organize into Dynamic Tracks that Promote Pancreatic Cancer Invasion.Cancer Discov2022
35881881Reprogrammed Schwann Cells Organize into Dynamic Tracks that Promote Pancreatic Cancer Invasion.Cancer Discov2022
35681714Association between Incidental Pelvic Inflammation and Aggressive Prostate Cancer.Cancers (Basel)2022
35681714Association between Incidental Pelvic Inflammation and Aggressive Prostate Cancer.Cancers (Basel)2022
33577785Proteogenomic and metabolomic characterization of human glioblastoma.Cancer Cell2021
33577785Proteogenomic and metabolomic characterization of human glioblastoma.Cancer Cell2021
32510176ProTrack: An Interactive Multi-Omics Data Browser for Proteogenomic Studies.Proteomics2020
31923397Integrated Proteogenomic Characterization of Clear Cell Renal Cell Carcinoma.Cell2020
33446324Immune Escape in Prostate Cancer: Known and Predicted Mechanisms and Targets.Urol Clin North Am2020
32510176ProTrack: An Interactive Multi-Omics Data Browser for Proteogenomic Studies.Proteomics2020
31923397Integrated Proteogenomic Characterization of Clear Cell Renal Cell Carcinoma.Cell2020
33446324Immune Escape in Prostate Cancer: Known and Predicted Mechanisms and Targets.Urol Clin North Am2020
30651579Nonsyndromic craniosynostosis: novel coding variants.Pediatr Res2019
31675502Integrated Proteogenomic Characterization of Clear Cell Renal Cell Carcinoma.Cell2019
30651579Nonsyndromic craniosynostosis: novel coding variants.Pediatr Res2019
31675502Integrated Proteogenomic Characterization of Clear Cell Renal Cell Carcinoma.Cell2019
30301868Detection of endometrial precancer by a targeted gynecologic cancer liquid biopsy.Cold Spring Harb Mol Case Stud2018
30301868Detection of endometrial precancer by a targeted gynecologic cancer liquid biopsy.Cold Spring Harb Mol Case Stud2018
28974674Insights into beta cell regeneration for diabetes via integration of molecular landscapes in human insulinomas.Nat Commun2017
32913967Identification and Functional Characterization of <i>EGFR</i> V769M, a Novel Germline Variant Associated With Multiple Lung Adenocarcinomas.JCO Precis Oncol2017
28974674Insights into beta cell regeneration for diabetes via integration of molecular landscapes in human insulinomas.Nat Commun2017
32913967Identification and Functional Characterization of <i>EGFR</i> V769M, a Novel Germline Variant Associated With Multiple Lung Adenocarcinomas.JCO Precis Oncol2017
26910679Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis.Plast Reconstr Surg2016
27245685Development and clinical application of an integrative genomic approach to personalized cancer therapy.Genome Med2016
27098033A new molecular signature method for prediction of driver cancer pathways from transcriptional data.Nucleic Acids Res2016
26910679Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis.Plast Reconstr Surg2016
26619149Strand-specific in vivo screen of cancer-associated miRNAs unveils a role for miR-21(â¿¿) in SCC progression.Nat Cell Biol2016
28027320Genomic Analysis of Uterine Lavage Fluid Detects Early Endometrial Cancers and Reveals a Prevalent Landscape of Driver Mutations in Women without Histopathologic Evidence of Cancer: A Prospective Cross-Sectional Study.PLoS Med2016
26619149Strand-specific in vivo screen of cancer-associated miRNAs unveils a role for miR-21(â¿¿) in SCC progression.Nat Cell Biol2016
28027320Genomic Analysis of Uterine Lavage Fluid Detects Early Endometrial Cancers and Reveals a Prevalent Landscape of Driver Mutations in Women without Histopathologic Evidence of Cancer: A Prospective Cross-Sectional Study.PLoS Med2016
27245685Development and clinical application of an integrative genomic approach to personalized cancer therapy.Genome Med2016
27098033A new molecular signature method for prediction of driver cancer pathways from transcriptional data.Nucleic Acids Res2016
25351745MAP2K1 (MEK1) Mutations Define a Distinct Subset of Lung Adenocarcinoma Associated with Smoking.Clin Cancer Res2015
25351745MAP2K1 (MEK1) Mutations Define a Distinct Subset of Lung Adenocarcinoma Associated with Smoking.Clin Cancer Res2015
24436421Direct in vivo RNAi screen unveils myosin IIa as a tumor suppressor of squamous cell carcinomas.Science2014
25521405Clinical and in vivo evidence that EGFR S768I mutant lung adenocarcinomas are sensitive to erlotinib.J Thorac Oncol2014
24346104Unsuspected collision of synchronous lung adenocarcinomas: a potential cause of aberrant driver mutation profiles.J Thorac Oncol2014
24436421Direct in vivo RNAi screen unveils myosin IIa as a tumor suppressor of squamous cell carcinomas.Science2014
25010664Genetic variation in DNA repair pathways and risk of non-Hodgkin's lymphoma.PLoS One2014
25521405Clinical and in vivo evidence that EGFR S768I mutant lung adenocarcinomas are sensitive to erlotinib.J Thorac Oncol2014
25010664Genetic variation in DNA repair pathways and risk of non-Hodgkin's lymphoma.PLoS One2014
24346104Unsuspected collision of synchronous lung adenocarcinomas: a potential cause of aberrant driver mutation profiles.J Thorac Oncol2014
23371856EGFR exon 20 insertion mutations in lung adenocarcinomas: prevalence, molecular heterogeneity, and clinicopathologic characteristics.Mol Cancer Ther2013
24220575Identification of a pan-cancer oncogenic microRNA superfamily anchored by a central core seed motif.Nat Commun2013
23819556Revealing selection in cancer using the predicted functional impact of cancer mutations. Application to nomination of cancer drivers.BMC Genomics2013
23900255Computational approaches to identify functional genetic variants in cancer genomes.Nat Methods2013
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Collaborators

Chris Sander
Broad Institute of MIT and Harvard
Co-authored papers 12
Eric E Schadt
Icahn School of Medicine at Mount Sinai
Co-authored papers 6
Arthur J Olson
Co-authored papers 6
Marc Ladanyi
Memorial Sloan Kettering Cancer Center
Co-authored papers 6
Dmitry Rykunov
Co-authored papers 6
Li Ding
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 5
Tatiana Omelchenko
Co-authored papers 5
Francesca Petralia
Co-authored papers 5
Azra Krek
Co-authored papers 4
Pei Wang
Co-authored papers 4
Seungyeul Yoo
Co-authored papers 4
Bing Zhang
Baylor College of Medicine
Co-authored papers 4
Alexey I Nesvizhskii
University of Michigan ann arbor
Co-authored papers 4
Mehdi Mesri
Co-authored papers 4
Nikolaus Schultz
Memorial Sloan Kettering Cancer Center
Co-authored papers 4
David Feny??
Institute for Systems Genetics, NYU Grossman School of Medicine
Co-authored papers 4
Weiping Ma
Co-authored papers 4
Yize Li
Co-authored papers 3
Barry S Taylor
Memorial Sloan Kettering Cancer Center
Co-authored papers 3
Marcin Cieslik
Co-authored papers 3
Andrew V Uzilov
University of California Santa Cruz
Co-authored papers 3
Kelly V Ruggles
Co-authored papers 3
Felipe da Veiga Leprevost
University of Michigan ann arbor
Co-authored papers 3
Maciej Wiznerowicz
Co-authored papers 3
Jiayi Ji
Co-authored papers 3
Robert Sebra
Icahn School of Medicine at Mount Sinai
Co-authored papers 3
Tara Hiltke
Office of Cancer Clinical Proteomics Research, National Cancer Institute
Co-authored papers 3
Mathangi Thiagarajan
Co-authored papers 3
James J Hsieh
Washington University
Co-authored papers 3
Saravana M Dhanasekaran
Co-authored papers 3
Release 1.2