Search Results
Research Funding
ClinGen will advance genomics in clinical care and improve our understanding of phenotypic and functional effects of genetic variants and their clinical value.
… Medical and research centers are increasingly sequencing patient … However, it is difficult to identify which sequence variants are relevant to disease. As a result, information on only a few genomic … including evidence and clinical assertions of genes and variants. Jonathan S. Berg, University of North Carolina …
15 Ways Genomics Influences Our World
​Genomics is helping us understand what makes each of us different and what makes us the same.
… is helping us understand what makes each of us different and what makes us the same. … Did you know that at the base-pair level your genome is 99.9 percent the same as all of the humans around … today, researchers are still discovering new types of variants  within human genomes. Human genomic variation is …
Research at NHGRI
The Genetic Disease Research Branch studies how genetic changes affect the structure and function of gene products leading to human disease.
… The Genetic Disease Research Branch studies the mechanisms by which genetic changes affect the structure and function of gene products leading to human disease. … in understanding how disruptions in signaling pathways and transcription factors contribute to disease. Our …
Research Funding
The Multi-Omics for Health and Disease Consortium aims to advance the application of multi-omic technologies to study health and disease in ancestrally diverse populations.
… integration of environmental exposures, omics, and childhood NAFLD (LEON) Study Disease Study Site** Stephanie Christenson*, Neeta Thakur, … Multi-Omics at the Intersections of Environment, Diabetes, and Kidney Disease: A Multi-Omics for Health and Disease … The Multi-Omics for Health and Disease Consortium aims to advance the application of …
News Release
NIH researchers have discovered a rare and sometimes lethal inflammatory disease - otulipenia - that primarily affects young children.
… Institutes of Health researchers have discovered a rare and sometimes lethal inflammatory disease - otulipenia - that primarily affects young children. … symptoms: fever, skin rashes, diarrhea, joint pain and overall failure to grow or thrive. … to the work were researchers from the National Human Genome Research Institute (NHGRI), the National Institute of …
Talking Glossary
A secondary genomic finding refers to a genomic variant, found through the analysis of a person’s genome, that is of potential medical value yet is unrelated to the initial reason for examining the person’s genome.
… genomic variant, found through the analysis of a person’s genome, that is of potential medical value yet is unrelated to the initial reason for examining the person’s genome. … genomic variant, found through the analysis of a person’s genome, that is of potential medical value yet is unrelated …
Clinical Research
A study with the goal of finding the genetic cause of familial Mediterranean fever (FMF) and several novel and undiagnosed causes of autoinflammatory disease.
… Since then, it has expanded to include several novel and undiagnosed causes of autoinflammatory disease. For more information, see Protocol 94-HG-0105 or … or localized inflammation, without evidence of infection and without the high antibody titers or antigen-specific …
Staff
Dr. Daniel Gilchrist is a program director of Computational Genomics and Data Science in NHGRI's Division of Genome Science.
… Dr. Daniel Gilchrist joined the National Human Genome Research Institute's Extramural Research Program as a … a portfolio of grants focused on functional genomics and computational genomics and data science. He is also part … understanding of the effects of genomic variation on genome function and phenotype. Prior to joining the National …
News Release
The Undiagnosed Diseases Network has opened an online patient application portal called the UDN Gateway.
… The Gateway replaces what had previously been a paper-and-mail application process for the NIH Undiagnosed Diseases … of NIH's Division of Program Coordination, Planning, and Strategic Initiatives (DPCPSI), which provides financial … Additional information about NHGRI can be found at www.genome.gov . …
News Release
A new genome-based technology for demystifying undiagnosed illnesses - even rare childhood diseases - is moving into general medical practice.
… Sooner than almost anyone expected, a new, genome-based technology for demystifying undiagnosed … "This primer illustrates how rapidly the use of genome sequencing has moved into clinical practice," said … DNA and a reference sequence for the human genome. These variants may point to the cause of the patient's disease. In …