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Staff
Barbara Thomas is a scientific review officer for the Center for Inherited Disease Research (CIDR).
… Review Officer and Executive Director of the NIH Center for Inherited Disease Research (CIDR) , a trans-NIH program that …
For Patients and Families
The Genetic and Rare Diseases Information Center helps people find useful information about genetic and rare diseases.
… The Genetic and Rare Diseases Information Center helps people find useful information about genetic and … and teachers who work with people with a genetic or rare disease. Even scientists who are studying a genetic or rare disease and who need information for their research have contacted GARD, as have people who …
Educational Resources
Mendelian inheritance refers to certain patterns of how traits are passed from parents to offspring.
Diversity Center
The Pacific Center for Genome Research (PCGR) at the University of Hawaii at Manoa (UHM) aims to grow and support Genomic Research workforce at UHM, a Minority Serving Institution (MSI), which has a mission to serve historically underrepresented population in biomedical research, namely, Native Hawaiians and other Pacific Islanders.
… The Pacific Center for Genome Research (PCGR) at the University of Hawaii at … identified and established markers and known non-genetic disease risk factors. Knowledge generated by this project …
Diversity Center
The University of Texas Rio Grande Valley (UTRGV) has established a Diversity Center for Genome Research that will build UTRGV’s genomics research capacity by 1) expanding genomic research capabilities and discoveries in two innovative research projects; and 2) enhancing the size and quality of the available genomics workforce.
… Rio Grande Valley (UTRGV) has established a Diversity Center for Genome Research that will build UTRGV’s genomics research … Hepatocellular Genetic Epidemiology of Fatty Liver Disease in Hispanics  Co-Leads: Joanne Curran, Ph.D., and …
Research at NHGRI
The Center for Precision Health Research, formerly Medical Genomics and Metabolic Genetics Branch, studies how health and disease are related to genetic, genomic and metabolic variation.
… The investigators in the Center for Precision Health Research (CPHR) develop and evaluate … with rare variants. They also study disorders that are not inherited and instead are due to new genetic mutations and …
Research Funding
A collaborative large-scale genome sequencing effort to identify rare risk and protective variants contributing to multiple common disease phenotypes.
… The Centers for Common Disease Genomics (CCDG) are a collaborative … of genomic architecture underlying common, complex inherited diseases. Understand how best to design rare … including publications, can be found on the Coordinating Center managed website:  http://ccdg.rutgers.edu/ . … …
News Release
NHGRI will fund a set of genome sequencing and analysis centers whose research will focus on understanding the genomic bases of common and rare human diseases.
… Institute (NHGRI), part of NIH, today launched the Centers for Common Disease Genomics (CCDG), which will use genome … investigating the genomic underpinnings of rare, typically inherited diseases, such as cystic fibrosis and muscular … over four years. NHGRI will also fund a new Coordinating Center for approximately $4 million over four years to …
Research Training
The Clinical Center Genomics Opportunity promotes precision medicine and development of infrastructure to support clinical genomics at the NIH Clinical Center.
… The Clinical Center Genomics Opportunity promotes precision medicine and … Center. … The program provides an exciting opportunity for the Institutes that participate in the NIH Clinical … Institutes to effectively use genomic data in clinical research and clinical care. The NIH Office of Intramural …
Genetic Disorders
Sickle cell disease is a group of inherited red blood cells disorders.
… Sickle cell disease is a group of inherited red blood cell disorders. … … A baby born with sickle cell disease inherits a gene for the disorder from both parents. When both parents have …