Search Results
Facet (Page)
Refine Your Search
Audiences
Content Formats
Events
Sections
Divisions
Event
NHGRI, National Institute of Environmental Health Sciences (NIEHS) and National Cancer Institute (NCI) will host a pre-application interactive webinar for the Multi-Omics for Health and Disease program funding opportunity announcements (FOAs): RFA-HG-22-008,
RFA-HG-22-009 and RFA-HG-22-010.
… of Environmental Health Sciences (NIEHS) and National Cancer Institute (NCI) will host a pre-application … of Environmental Health Sciences (NIEHS) and National Cancer Institute (NCI) will host a pre-application … of Environmental Health Sciences (NIEHS) and National Cancer Institute (NCI) will host a pre-application …
Educational Resources
Gene therapy is an experimental technique for treating disease by altering the patient's genetic material.
… … Genetic Disease, Genetic Disorder, Gene Mutation, Cancer Treatment, Healthcare … Gene therapy is a technique …
Staff
Dr. Bailey-Wilson is a scientist emeritus in NHGRI's Division of Intramural Research.
… and is especially interested in risk factors for lung cancer, prostate cancer, eye disorders, autism and oral clefts. Dr. … served on many scientific advisory boards including the Cancer Family Registry CFRCCS Advisory Board, the World Trade …
Staff
Dr. Carolyn M. Hutter was the director of the Division of Genome Sciences at the National Human Genome Research Institute.​
… NIH in 2012, serving as a program director in the National Cancer Institute (NCI) Epidemiology and Genomics Research … a program director, serving as the NHGRI team lead for The Cancer Genome Atlas (TCGA) . Prior to NIH, she was a senior staff scientist at the Fred Hutchinson Cancer Research Center and lecturer at the University of …
Educational Resources
A retrovirus is a virus that uses RNA as its genetic material.
… material. … Acquired Immunodeficiency Syndrome (AIDS), Cancer, Cell, Deoxyribonucleic Acid (DNA), Genome, … associated with diseases, including AIDS and some forms of cancer. … A retrovirus is a virus that uses RNA as its …
News Release
NHGRI appointed Carolyn Hutter, Ph.D., director of the Division of Genome Sciences, which researches human genome function in health and disease.
… research programs. Most recently, she co-managed The Cancer Genome Atlas (TCGA) - a collaboration between NHGRI and the National Cancer Institute (NCI) - which generated over 2.5 petabytes of publically available genomic data used by the cancer research community to improve the prevention, …
Outreach
15 examples of how genomics has and continues to transform our world in myriad ways.
… Complete Genome Sequence, Genomics Impact On Society, Cancer Genomics, Genomic Testing, Enhanced Forensics, Genome …
Clinical Research
The CLINSEQ® Study seeks to learn about the role that your genes play in your health.
… to a variety of conditions, including heart disease, breast cancer, and hearing loss. … Our goal is to enroll 1500 … High incidence of unrecognized visceral/neurological late-onset Niemann-Pick disease, type C1, predicted by analysis of … participants in the ClinSeq genome sequencing cohort as early adopters of a new health technology. PLoS One, …
Research at NHGRI
Families Sharing Health Assessment and Risk Evaluation (SHARE) helps you and your family learn how your family health history affects your risk for diseases.
… Colorectal Cancer Breast Cancer Prostate Cancer Type 2 Diabetes Heart … guidelines to reduce risk of heart disease, diabetes, breast cancer, and colorectal cancer . BMC Public Health,  …
Genomics and Medicine
Starting in 2019, the American Journal of Human Genetics has published an annual feature identifying ten key advances in applying genomic information to clinical care that were reported in the previous 12 months of published literature. The Genomic Medicine Working Group has authored these reviews, based on its broader effort to identify notable accomplishments in genomic medicine on a monthly basis. From this larger set of published accomplishments, the working group has continued to select ten papers annually to be highlighted as the most significant.
… method of choice for detecting repeat expansion disorders Early genome sequencing in acutely ill infants improves … frequently identifies susceptibility variants in early-onset atrial fibrillation Germline genomic screening for … … Population screening for hereditary breast and ovarian cancer is cost effective Australian …