Search Results
Fact Sheets
Genetic mapping offers evidence that a disease transmitted from parent to child is linked to one or more genes and clues about where a gene lies on a chromosome.
… Among the main goals of the Human Genome Project (HGP) was to develop new, better and … identify new genes and to understand their function. One of these tools is genetic mapping. Genetic mapping - also … researchers collect blood or tissue samples from members of families in which a certain disease or trait is prevalent. …
For Patients and Families
​Genetic research is creating new ways for people to take action and prevent disease and new ways to treat disease through personalized medicine.​ ​
… pressure as an adult. Learning about the health history of your family and sharing this information with your health … can help you learn whether you have an increased chance of getting some common diseases. Your health care provider … Initiative . This goal of this campaign is to have all American families learn more about their family health …
Policy Issues
In 2008, the Genetic Information Nondiscrimination Act was passed into law, prohibiting discrimination by employers and health insurers.
… Many Americans wonder if participating in genetics research or undergoing genetic testing will lead to … to participate in the research needed for the development of new tests, therapies, and cures. This page provides an overview of the Genetic Information Nondiscrimination Act (GINA) and …
Fact Sheets
Genetics refers to the study of genes and their roles in inheritance. Genomics refers to the study of all of a person's genes (the genome).
… Genetics and genomics both play roles in health and disease. Genetics refers to the study of genes and the way that certain traits or conditions are … one generation to another. Genomics describes the study of all of a person's genes (the genome). … Genetics is a term that refers to the study of genes and their roles in inheritance - in other words, the …
Research Training
This program offers training in a combined program of maternal-fetal medicine and medical genetics.
… The Metropolitan D.C. Medical Genetics Program also offers new subspecialty training in a combined program of maternal-fetal medicine and med genetics in collaboration with the Washington Hospital Center … seen in prenatally diagnosed anomalies and the impact of genetic and metabolic disease on healthy and high risk …
Educational Resources
Newborn genetic screening is testing performed on newborn babies to detect a wide variety of disorders.
… performed on newborn babies to detect a wide variety of disorders. … Newborn screening is a set of laboratory tests performed on newborn babies to detect a set of known genetic diseases. Typically, this testing is … States, newborn screening is mandatory for a defined set of genetic diseases, although the exact set differs from …
Media Advisory
The NIH-funded Integrative Human Microbiome Project presented at the International Human Microbiome Congress.
… Media Advisory Representatives from the National Institutes of Health (NIH)-funded Integrative Human Microbiome Project (iHMP), which is coordinated by the National Human Genome Research Institute (NHGRI), will present … Representatives from the National Institutes of Health (NIH)-funded Integrative Human Microbiome Project …
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 variation into constituent causal factors. The hope … To support research into the genetic architecture of complex human traits through investigator-initiated projects, … Series: Complex Trait Genetics Following on the heels of NHGRI’s workshop “Advances in the Genetic Architecture of …
Genetic Disorders
Cri du chat syndrome is a rare genetic condition that is caused by the deletion of genetic material on the the p arm of chromosome 5.
… is a rare genetic condition that is caused by the deletion of genetic material on the the p arm of chromosome 5. … condition that is caused by the deletion (a missing piece) of genetic material on the small arm (the p arm) of chromosome 5. The cause of this rare chromosomal deletion …
Event
The National Museum of African American History and Culture presented an insightful conversation about advancements in genetic research and its implications for ​understanding race.
… Rick Kittles and Vence Bonham on how new findings in genetics tear down old ideas about race, grapple with ​the unfinished business of slavery, inspire meaningful conversation of reparations, … Institutes of Health and support from the National Human Genome Research Institute. …