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genomics

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People and fronts concerned with cancer genomics. 21 records carry it: 20 people, 1 front.

21 records
Aleix Prat
Head of Medical Oncology, Hospital Clínic de Barcelona; Scientific Director, SOLTI · Hospital Clínic de Barcelona / IDIBAPS
Translational oncologist who built genomic tests (HER2DX) to decide which HER2-positive patients can skip chemotherapy.
Benjamin Kile
Executive Director · Garvan Institute of Medical Research / Kinghorn Cancer Centre
Blood cell molecular biologist who has led Sydney's Garvan Institute of Medical Research since 2023, sharpening its focus on genomics, immunology and cancer.
Carlos Caldas
Professor of Cancer Medicine, University of Cambridge; Senior Group Leader, CRUK Cambridge Institute · Cancer Research UK Cambridge Centre / CRUK Cambridge Institute
Led METABRIC, which used 2,000 tumours to define ten genomic subtypes of breast cancer and their long-term outcomes.
Catherine J. Wu
Chief, Division of Stem Cell Transplantation and Cellular Therapies, Dana-Farber Cancer Institute; Professor, Harvard Medical School · Dana-Farber Brigham Cancer Center
Led the first personalised neoantigen peptide vaccine trial in melanoma and mapped how CLL evolves under treatment.
Charles M. Perou
Professor of Genetics and Pathology, UNC Lineberger Comprehensive Cancer Center · UNC Lineberger Comprehensive Cancer Center
Defined the molecular subtypes of breast cancer (luminal, HER2-enriched, basal-like) that clinicians now use every day.
Christina Curtis
Professor of Medicine, Genetics and Biomedical Data Science, Stanford University · Stanford Health Care / Stanford Cancer Institute
Showed that colorectal cancers grow as a 'Big Bang' and that metastasis can be seeded years before diagnosis.
Diagnostics & Biomarkers
Tests on tissue and blood that say what kind of cancer it is, what is driving it, and which drugs might work.
Douglas A. Levine
Director of Gynecologic Oncology, NYU Langone Perlmutter Cancer Center · Laura and Isaac Perlmutter Cancer Center at NYU Langone Health
Surgeon-scientist who led the TCGA endometrial cancer study that created today's four molecular subtypes.
Ewan Birney
Director of EMBL-EBI · EMBL's European Bioinformatics Institute
Computational biologist who directs EMBL-EBI, home of the open genomic and cancer data resources used worldwide.
John M. Maris
Giulio D'Angio Chair in Neuroblastoma Research, Children's Hospital of Philadelphia · Children's Hospital of Philadelphia
Neuroblastoma geneticist whose lab found the ALK mutations and immunotherapy targets now in paediatric trials.
Ludmil B. Alexandrov
Professor of Cellular and Molecular Medicine and Bioengineering, UC San Diego · UC San Diego Moores Cancer Center
Created the mathematical framework for extracting mutational signatures from cancer genomes and the COSMIC signature catalogue.
Matthew Hurles
Director of the Wellcome Sanger Institute and Senior Group Leader · Wellcome Sanger Institute
Human geneticist who directs the Wellcome Sanger Institute, a world centre for cancer genome research.
Michael D. Taylor
Professor of Pediatrics and Neurosurgery, Baylor College of Medicine and Texas Children's Hospital · Texas Children's Cancer and Hematology Center
Neurosurgeon-scientist who defined the four molecular subgroups of medulloblastoma that now guide therapy.
Michael F. Berger
Associate Director, Marie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center · Memorial Sloan Kettering Cancer Center
Built MSK-IMPACT, the tumour sequencing test used on more than 100,000 patients and the first FDA-authorised hospital panel.
Nikhil C. Munshi
Director of Basic and Correlative Science, Jerome Lipper Multiple Myeloma Center, Dana-Farber Cancer Institute · Dana-Farber Brigham Cancer Center
Led KarMMa, which brought idecabtagene vicleucel, the first CAR-T for myeloma, to approval.
Nikolaus Rajewsky
Group Leader, Systems Biology of Gene Regulatory Elements; Scientific Director, Berlin Institute for Medical Systems Biology (MDC-BIMSB) · Max Delbrück Center for Molecular Medicine
Systems biologist at the MDC known for microRNA and circular RNA discoveries and for single-cell and spatial genomics applied to cancer.
Nitzan Rosenfeld
Professor of Cancer Genomics, Barts Cancer Institute; former Senior Group Leader, CRUK Cambridge Institute · Barts Cancer Institute / Barts Health NHS Trust
Showed that whole-exome sequencing of blood can track how a cancer evolves, and co-founded Inivata.
Serena Nik-Zainal
Professor of Genomic Medicine and Bioinformatics, University of Cambridge; Honorary Consultant in Clinical Genetics · Cancer Research UK Cambridge Centre / CRUK Cambridge Institute
Deciphered the mutational signatures written in cancer genomes and turned them into clinical tests like HRDetect.
Silvana Konermann
Executive Director and Core Investigator, Arc Institute · Arc Institute
Neuroscientist and co-founder who runs the Arc Institute, an independent research institute in the San Francisco Bay Area built to tackle complex diseases.
Stephen Scherer
Chief of Research · The Hospital for Sick Children (SickKids)
Genome scientist who heads research at SickKids and co-discovered genome-wide copy number variation in humans.
Steven P. Treon
Director, Bing Center for Waldenström's Macroglobulinemia, Dana-Farber Cancer Institute · Dana-Farber Brigham Cancer Center
Discovered the MYD88 mutation that defines Waldenström macroglobulinaemia and led the trial that made ibrutinib its first approved drug.

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