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- Developmental Genotype-Tissue Expression (dGTEx)1
- Multi-Omics for Health and Disease (Multi-Omics)1
- Ethical, Legal and Social Implications (ELSI) Research Program2
- Genomics-Enabled Learning Health Systems (gLHS)1
- Genetic Architecture of Complex Traits1
- Genome Technology Program1
- Impact of Genomic Variation on Function (IGVF) Consortium1
- Clinical Genome (ClinGen) Resource1
- Polygenic RIsk MEthods in Diverse populations (PRIMED) Consortium1
- Genomics Research to Elucidate the Genetics of Rare Diseases (GREGOR) Consortium2
Research Funding
A collaborative large-scale genome sequencing effort to identify rare risk and protective variants contributing to multiple common disease phenotypes.
… disease phenotypes. … The CCDG initiative explores a range of diseases with the goal of: Undertaking variant discovery for … disease phenotypes. ​ … Genome Sequence, Gene Variants, Genetic Risk, Common Disease, Rare Disease, Dna Sequencing, …
Research Funding
​The Undiagnosed Diseases Network accelerates discovery and innovation in how we diagnose and treat patients with previously undiagnosed diseases.
… Applications UDN does not accept all applicants due to the complex nature of the body and the diseases being investigated. However, they do fully review …
Research Funding
Building upon a foundation of quantitative genetics laid over a century ago, applying modern genomic approaches to resolve how genetic and non-genetic factors shape variation in human diseases and traits.
… A major goal of human genetics is to decompose the sources of trait … about how to identify and interpret the interplay of genetic and non-genetic factors on trait variation. These … now being applied towards illuminating contemporary human diseases and traits. This webinar will seek input from the …
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.
… David Conti, Alaina Vidmar, Tanya Alderete University of Southern California Longitudinal integration of … Sofer University of Illinois at Chicago Multi-Omics at the Intersections of Environment, Diabetes, and Kidney … practices, and standards that can be generalized across diseases and populations. It will also generate a …
Fact Sheet
Gene therapy for sickle cell disease is available to you through FDA-approved therapies and through clinical trials.
… ), and through clinical trials . While there are a number of clinical trials for sickle cell gene therapy, the journey can be similar across all treatments. This is a … to have: Certain screenings (e.g., MRI, blood tests). A genetic test to determine if there are changes that would …
Research Funding
The PAGE Consortium investigates ancestrally diverse populations to gain a better understanding of how genetic factors influence susceptibility to disease.
… Genome-wide association studies have identified many genetic variants related to disease and have highlighted the … ( RFA HG-12-010  and RFA HG-12-015 ). The first phase of PAGE examined putative causal genetic variants across … which facilitated trans-ethnic fine mapping of several diseases of public health importance. PAGE II will add to …
Health FAQ
Discuss these questions with your doctor or health care provider.
… these questions with your doctor or clinical trial team. … The Democratizing Education Project welcomes your feedback … only. They are meant to promote your general understanding of gene therapy for sickle cell disease. We encourage you to … child having sickle cell trait or sickle cell disease. Genetic counselors are trained to help you know the risks of …
Fact Sheet
Understanding gene therapy for sickle cell disease
… Sickle cell disease is the most common inherited blood disorder in the United … than 100,000 people. … Presently, there are only a handful of options to manage or treat sickle cell disease.  Now, … and individuals. This group met over the course of four workshops. … The Democratizing Education Project …
Research Funding
The N​on-Coding Variants Program explores which variants in a region associated with a disease or trait cause the higher risk for the disease or trait
… When the genomes of many people are sequenced, millions of sites in the genome differ among those people. Some of these genetic variants are common, such as the variants for blood … this RFA use a range of approaches to study a variety of diseases as test cases. All the data used and produced will …
Research Funding
The primary mission of the Alliance of Genome Resources (the Alliance) is to develop and maintain sustainable genome information resources that facilitate the use of diverse model organisms in understanding the genetic and genomic basis of human biology, health and disease. This understanding is fundamental for advancing genome biology research and for translating human genome data into clinical utility.
… The primary mission of the Alliance of Genome Resources … the use of diverse model organisms in understanding the genetic and genomic basis of human biology, health and … pathways, gene expression, and both protein–protein and genetic interactions. Given the significant use of these …