Search Results
Facet (Page)
Refine Your Search
Audiences
Content Formats
Events
Sections
Video
Divisions
Programs
- Ethical, Legal and Social Implications (ELSI) Research Program2
- Genomics-Enabled Learning Health Systems (gLHS)2
- Genome Technology Program2
- Impact of Genomic Variation on Function (IGVF) Consortium1
- Molecular Phenotypes of Null Alleles in Cells (MorPhiC)1
- NHGRI Genomic Data Science Analysis, Visualization and Informatics Lab-space (AnVIL)2
- Genomics Research to Elucidate the Genetics of Rare Diseases (GREGOR) Consortium1
- Developmental Genotype-Tissue Expression (dGTEx)1
- Multi-Omics for Health and Disease (Multi-Omics)1
Educational Resources
Carrier screening is a genetic test performed on people who display no symptoms for a genetic disorder but may be at risk for passing it on to their children.
… … Genetic Testing, Genetic Disorder, Alleles, Inheritance, Family Health History … Carrier screening involves testing to see if …
Staff
Shirley Freeman is an Intramural Program Assistant for NHGRI's Center for Research on Genomics and Global Health.
… for the Center for Research on Genomics and Global Health (CRGGH) housed under the Metabolic, Cardiovascular and … Human Genome Research Institute, National Institutes of Health. Shirley brings over 12 years of administrative … Freeman, Center for Research on Genomics and Global Health, zebrafish, biochemistry … Shirley Freeman, Center for …
Educational Resources
Newborn genetic screening is testing performed on newborn babies to detect a wide variety of disorders.
… of disorders. … Newborn Screening, Genetic Disorder, Family Health History, Genetic Counselor, Healthcare … Newborn …
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.
… and examine it for unique patterns that are seen only in family members who have the disease or trait. These … likely be passed on together from parent to child. If each family member with a particular disease or trait also … through databases maintained by the National Institutes of Health and the National Library of Medicine's National Center …
Staff
Dr. Guanjie Chen is a senior research fellow with the NHGRI's Center for Research on Genomics and Global Health.
… and joined the Center for Research on Genomics and Global Health (CRGGH), National Human Genome Research Institute, National Institutes of Health as a senior research fellow. His interests include … Bonney, and Charles Rotimi. Gene Copy Number Analysis For Family data Using Semiparametric Copula Model: Bioinformatics …
Educational Resources
Genomic variation refers to diversity in gene frequencies.
… Genetic Testing, Genetic Counselor, Newborn Screening, Family Health History … Genomic variation refers to DNA sequence …
Educational Resources
Genetic testing is the use of a laboratory test to look for genetic variations associated with a disease.
… Genetic Testing, Genetic Counselor, Newborn Screening, Family Health History … Genetic testing is the use of a laboratory …
Educational Resources
In genomic imprinting the ability of a gene to be expressed depends upon the sex of the parent who passed on the gene.
… on the gene. … Genetic Imprinting, DNA Sequence, Genes, Family Health History, Genealogy, Gene Expression … Genomic …
Educational Resources
Cancer is a group of diseases characterized by uncontrolled cell growth.
… Cell Division, Mutation, DNA Error, Metastasis, Tumor, Family Health History … Cancer is a disease in which some of the …
Educational Resources
Dominant refers to the relationship between two versions of a gene.
… two versions of a gene. … Dominant, Recessive, Alleles, Family Health History, Genetics, Genetic Variation, Mutation, …