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… APOE genetic testing as a predictive test for Alzheimer disease. 3. Do not order MTHFR genetic testing for the risk … Resources). The topics of the meeting included: curating gene-disease relationships, initiatives facilitating clinical … to laboratory practices. Multiple professional medical associations with interests in laboratory testing have been …
Fact Sheets
Data used to estimate the cost of sequencing the human genome over time since the Human Genome Project.
Event
On November 16-17, 2023, the National Human Genome Institute will co-sponsor a workshop, Advances in the Genetic Architecture of Complex Human Traits, to take a historically grounded and forward-looking approach towards dissecting the genetic architecture of complex traits in humans.
… phenotypes” have simpler genetic architectures than disease traits or outcomes. Yet, even low-level molecular … University of California, San Francisco Robinson, Gene Director, Carl R. Woese Institute for … Hopkins University 10:15 a.m. Social Inequality and Gene-Environment Correlations Abdel Abdellaoui, Amsterdam UMC …
News Release
Researchers have now identified three health conditions for which people with SCT are at increased risk.
… United States, an estimated 2.5 to 3 million people have a gene variant associated sickle cell trait (SCT) and most … pulmonary embolism , proteinuria and chronic kidney disease . Findings from this first comprehensive review of … SCT means that a person has inherited the sickle cell gene from a parent. … Related Content … Systematic review …
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… of results leading to inappropriate choices for disease management or prevention and inadequate follow-up,Ó … metric to score the clinical actionability of gene-disease-intervention triads. The ClinGen curation … and systematically evaluate the clinical validity of gene-disease pairs. Successful 4 outreach efforts occurred at …
Healthcare Provider Genomics Education Resource
Genomics plays a role in every area of nursing, whether nurses are at the bedside providing one-on-one care, treating entire populations, teaching the next generation of nurses, or making discoveries in the lab.
… in the lab. … Genomic principles form the foundation for disease pathophysiology Genomics underlies all diseases … contributes to our understanding of the mechanisms of disease Genomics principles influence clinical actions … Nurses can help patients understand how genomics affects disease risk. Ethical nursing care includes understanding …
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.
… by which people can learn about their risk of developing a disease, based on the total number of changes related to the … into two classes: those that are associated with a single gene and those that are influenced by multiple genes and … inherited diseases can be traced to variants in a single gene. Cystic fibrosis, a progressive genetic disease that …
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… 9% (1) 0% DD/ID 122 21% (1) 21% (1) 1.6% (4.5) 0% Heart disease 104 23% (1) 26% (1) 1.0% (3) 1.0% (1) Hematology 13 … of Neurology. • Establish list of adult “actionable” gene-disease pairs • Classify all Exome Variant Server (EVS) … in the realm of public health genomics. 10. Henderson. Gene- Screen: A report on a pilot study implementing targeted …
Research Funding
Applications demonstrating excellent grantsmanship, grant mechanisms and research methodologies common to ethical, legal and social implications research.
… Monitoring in Clinical Trials of Germline Gene Editing: Ethical, Legal, and Social Issues Bryan Cwik …
The Genomics Landscape
In the June 2021 issue of The Genomics Landscape, NHGRI Director, Eric Green, M.D., Ph.D. details the upcoming appointment of acting NHGRI Deputy Director, Vence Bonham Jr., J.D. and what it means for the institute.
… such projects, including positional cloning of a fusion gene in leukemia, the identification of the familial Mediterranean fever gene MEFV, and our current natural history study on patients with a rare genetic disease, familial platelet disorder. Our goals – …