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Funding Opportunities
The NHGRI Small Business Program awards Small Business Innovation Research (SBIR) and Small Business Technology Transfer (STTR) grants.
… PAR-24-157 : Addressing Health Inequities in Clinical Diagnostics (R41/R42 Clinical Trials Not Allowed) PAR-24-158 : Addressing Health Inequities in Clinical Diagnostics (R43/R44 Clinical Trials Not Allowed) PAR-23-219 …
Event
A joint NHGRI-NCATS hosted meeting bringing together researchers, clinicians, families and patient advocates from around the world to discuss the natural history, disease pathophysiology, genetics and treatments for rare inborn metabolic errors.
Research Training
A mentored, pre-tenure track junior faculty position during which time the incumbent designs and implements an integrated, translational research program.
Genetic Disorders
Autosomal Dominant Polycystic Kidney Disease is a genetic disorder characterized by the growth of numerous cysts in both kidneys.
News Release
Researchers recommend genomic approaches to discovering inherited variants in one or a handful of genes that affect an individual's rare disease risk.
News Release
As researchers uncover millions of DNA differences in genes, doctors struggle to know which of these inherited differences, called variants, really matter.
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.
Staff
Dr. Laura Elnitski is a senior investigator in the Translational and Functional Genomics Branch at the National Human Genome Research Institute.
… substantially different prognostic outcomes. Therefore, diagnostics based on DNA methylation patterns may provide …
Staff
Dr. Leslie Biesecker is a clinical and molecular geneticist in and the chief of NHGRI's Center for Precision Health Research.
News Release
The Telomere-to-Telomere (T2T) Consortium has generated the first truly complete sequence of a human Y chromosome - the final human chromosome to be fully sequenced.
… relevant genomic variants can help us design better diagnostics in the future.” In addition to the complete Y …