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NHGRI researchers recently published a study using virtual reality simulations to investigate how clinicians might use a type of genomic risk information called polygenic risk scores in medical care.
News Release
NHGRI researchers seek help from people with Sickle Cell Disease to find the factors - environmental, social and genetic - that impact the severity of symptoms.
News Release
NIH Center for Research on Genomics and Global Health is participating in the H3Africa Consortium's effort to develop an African-specific genotyping array.
Event
The Genomics and Health Disparities Lecture Series was formed to enhance opportunities for dialogue about how innovations in genomics research and technology can impact health disparities. Topics will range from basic science to translational research.
News Release
Researchers have now identified three health conditions for which people with SCT are at increased risk.
Genetic Disorders
WAGR syndrome is a genetic condition caused by a deletion of genes located on chromosome 11, often causing eye problems and increased risk of cancer in babies.
… birth history are not unusual. Enlargement of the baby's kidneys may be seen on a prenatal ultrasound. The eye … childhood, and adulthood. These problems can affect the kidneys, eyes, testes or ovaries. The specific symptoms that …
Research at NHGRI
CRGGH facilitates understanding of the relationship between genetic variation and population differences in disease distribution to inform health disparities.
Educational Resources
Sickle cell disease is a hereditary disease seen most often among people of African ancestry.
… experience significant damage to their heart, lungs, and kidneys. … Educational Resources …
News Release
A new phase of the IGNITE Network will conduct clinical trials of genomic medicine interventions.