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Very Rare Cancer Consortium Tumor Board Meeting

Please join us for the Very Rare Cancer Consortium Tumor Board Meeting. This new initiative aims to bring cancer researchers across New York to the table to discuss compelling rare cancer cases presented by physicians and scientists from the New York Genome Center’s partner institutions. Click here to learn more about the Very Rare Cancer Consortium.

Case Conference and Research Cohort Review

Introduction – Molecular and Clinical Background
Institute Cohort Review
Case Review
Critical Questions


  • Michael V. Ortiz, MD

    Pediatric Oncologist
    Assistant Professor of Pediatrics
    Memorial Sloan Kettering Cancer Center 

  • Brian Robinson, MD

    Chief of Surgical Pathology,
    Co-Chief,  Urologic Pathology
    Weill Cornell Medicine

  • Daniel Ramirez, MD

    Chief, Bone and Soft Tissue Pathology, Division of Anatomic Pathology, Department of Pathology and Laboratory Medicine
    Northwell Health

  • Helen Remotti, MD

    GI, Pancreatobiliary, and Hepatic Pathology Fellowship Director
    Department of Pathology and Cell Biology
    Columbia University Irving Medical Center

  • Darrell J. Yamashiro, MD, PhD

    Chief of the Division of Hematology, Oncology and Stem Cell Transplantation
    Columbia University Irving Medical Center

    "Patient diagnosed at age 5 with recurrence at age 21"
  • Carolyn Fein Levy, MD

    Pediatric Hematologist/Oncologist
    Assistant Professor of Pediatrics
    Zucker School of Medicine at Hofstra/Northwell Health

    "Twins with Wilms Tumor"
  • Gary Crouch, MD

    Professor of Pediatrics in the Jack Martin Division of Pediatric Hematology-Oncology
    Icahn School of Medicine at Mount Sinai

    "Teenager with stage IV Wilms Tumor"
  • Katharine Offer, MD

    Pediatric Hematology-Oncology, Children’s Cancer Institute, Joseph M. Sanzari Children’s Hospital
    Hackensack University Medical Center

    "Beckwith–Wiedemann Syndrome – Bilateral Wilms Tumor"
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