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- 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
- Ethical, Legal and Social Implications (ELSI) Research Program2
- Genomics-Enabled Learning Health Systems (gLHS)1
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 …
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, …
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 …
Staff
Dr. Charles Rotimi is the scientific director of and NIH Distinguished Investigator in the Division of Intramural Research. He also serves as the director of the Center for Research on Genomics and Global Health (CRGGH).
… of Mississippi, where he obtained a master's degree in health care administration. He obtained a second master's … pressure (BP) in AA using data from the Howard University Family Study, a population-based sample of ~2,000 related and … of Podo. CRGGH has conducted a multi-generational family study in Ethiopia and estimated heritability of Podo …