If you're concerned about your own or your family's risk of brain tumors and meet the study requirements, you may be eligible to participate in an International Brain Tumor Family Study called GLIOGENE.
Certain genetic alterations may place individuals at increased risk of developing cancer. This is why some cancers appear to run in families. If you have a particular genetic alteration, you may be at increased risk for certain types of cancer.
By providing a family health history and a small blood sample brain tumor patients and their families significantly improve our ability to understand the hereditary factors of the disease.
Identifying a genetic link may provide information about the disease -- information that one day we hope will lead to improved treatment, as well as preventive strategies.
GLIOGENE is the largest study ever to be conducted on familial gliomas, or primary brain tumors. Researchers aim to screen approximately 15,000 individuals worldwide during the five-year study.
Please proceed to our registration page. Feel free to email us for further information.
The GLIOGENE study is a collaboration among these
participating institutions:
In the United States:
The University of Texas M. D. Anderson Cancer Center
Baylor College of Medicine
Brigham and Women's Hospital
Case Western Reserve University
Columbia University
Duke University
Northshore University HealthSystem
Memorial Sloan-Kettering Cancer Center
Mayo Clinic Rochester
University of California, San Francisco
University of Illinois, Chicago
In Europe and Israel:
Gertner Institute, Israel
Institute of Cancer Epidemiology, Denmark
Institute of Cancer Research, United Kingdom
Umea University Hospital, Sweden
GLIOGENE: Genetic Epidemiology of Glioma International Consortium is funded by the United States National Cancer Institute 1R01CA119215-01A1, the America Brain Tumor Association, and the National Brain Tumor Foundation.