Search Results

31 - 40 of 520
News Release
A new study by scientists at NHGRI, suggests that iPSCs do not develop more mutations than cells that are duplicated by subcloning.
Health
A polygenic risk score is one way by which people can learn what their risk of developing a disease is, based on the total number of genomics variants related to the disease.
News Release
Stomach cancers fall into four distinct molecular subtypes researchers with The Cancer Genome Atlas Network have found.
For Patients and Families
The partnership engages communities on genomics, informs and shares perspectives, and impacts the focus of research.
… Washington Health Equity Circle, Sound Alliance, Seattle Christine Wilson, M.S., Health Care Communications …
For Health Professionals
The ISCC-PEG Pharmacogenomics (PGx) Project Group has developed peer-reviewed online education for healthcare practitioners to advance pharmacogenomics in clinical practice.
… Coverage in Medicare Populations Authors: Ben Brown, BS, Christine Formea, Pharm.D., and Sara Rogers, Pharm.D. …
Health
Information about genomics competencies, patient care, and related partnership and outreach activities at NHGRI.
About Genomics
A introduction to basic concepts in genomics to help you understand your genome, how it works, and how it impacts your health.
Professional Development Programs
The JHU/NHGRI Genetic Counseling Training Program trains students to conduct research and provides clinical rotations to learn about genetic conditions.
… Weiyi Mu, Sc.M.   Prenatal Clinic Ginny Corson, M.S. Christine Hertenstein, M.S. Cathy Lawson, M.S. Katie Rock, … Muskett, M.S. St. Joseph's Hospital Prenatal Diagnosis Christine Hertenstein, M.S. Katelynn Sagaser, M.S. University …
News Release
NHGRI researchers will present four platform talks and 55 posters to highlight the institute's diverse portfolio at the 65th annual meeting of ASHG.
… Fanconi anemia group FA-G. (Cancer Genetics) 2976T. May Christine Malicdan: Cell adhesion and migration defects in …
Educational Resources
A point mutation is when a single base pair is altered.