Search Results
Staff
Dr. ​Eric D. Green is the Director of the National Human Genome Research Institute at the National Institutes of Health.
… of candidate genes involved in coronary artery calcification by transcriptome sequencing of cell lines. BMC … and protein evidence connects TREML4 to coronary artery calcification. Am J Hum Genet , 95:66-76. 2014. [ PubMed ] …
Event
On March 12-16, 2024, the National Human Genome Research Institute (NHGRI) will participate in the 2024 ACMG Annual Clinical Genetics Meeting - an annual medical and scientific conference continues to provide groundbreaking research and the latest advances in medical genetics, genomics and personalized medicine.
News Release
NIH researchers have created a data resource show how differences in an individual's genome can affect gene activity and contribute to disease.
Staff
Dr. Michael Erdos is an Associate Investigator in the Molecular Genetics Section of the Center for Precision Health Research.
… of vascular smooth muscle cells (VSMCs) and stiffening of arterial walls. In the homozygous state the mouse presents … Children’s Hospital. That trial showed improvement in arterial stiffness, and ultimately a modest extension in …
Graduate Medical Education
An opportunity for a 4-to-8-week elective in the National Human Genome Research Institute (NHGRI) at the NIH Clinical Center in Bethesda, MD.
… and Adolescent Gynecology Pediatric Oncology Pulmonary Arterial Hypertension Service Rheumatology … Chris Ours, M.D. …
Genetic Disorders
Progeria is an extremely rare genetic disease of childhood characterized by dramatic, premature aging.
Research Funding
The PAGE Consortium investigates ancestrally diverse populations to gain a better understanding of how genetic factors influence susceptibility to disease.
News Release
Supporting early career investigators at the cutting edge of genomics.
Careers and Training
NHGRI provides funding to support the development and implementation of modules aimed at providing healthcare professionals with genomic medicine training.
Genetic Disorders
Marfan syndrome an inherited disorder of connective tissue occurring once in every 10,000 to 20,000 individuals.