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Lindsey Criswell, who became the director of the National Institute of Arthritis and Musculoskeletal and Skin Diseases in February, 2021 is also an associate investigator in NHGRI's Metabolic, Cardiovascular and Inflammatory Disease Genomics Branch.
Clinical Research
An Observational Prospective Natural History Study of Metabolism, Infection and Immunity During the COVID19 Pandemic (At-home Participation).
… An Observational Prospective Natural History Study of Metabolism, Infection and Immunity During the COVID19 … … An Observational Prospective Natural History Study of Metabolism, Infection and Immunity During the COVID19 …
News Release
NHGRI has appointed Neil Hanchard, M.D., Ph.D., as a clinical investigator within the Medical Genomics and Metabolic Genetics Branch (MGMGB) in the Division of Intramural Research. Dr. Hanchard will head the Childhood Complex Disease Genomics Section within the MGMGB.
Staff
Dr. Ivona Aksentijevich is an associate investigator in NHGRI Metabolic, Cardiovascular and Inflammatory Disease Genomics Branch.
Staff
Dr. Peter McGuire is an investigator in NHGRI's Center for Precision Health Research.
… the care of patients with disorders of mitochondrial metabolism. By combining his training in immunology and … program to understand the interplay between mitochondrial metabolism and the immune system. His NIH Clinical Center … function in patients with disorders of mitochondrial metabolism, which aims to demonstrate that these patients can …
News Release
ASHG members selected Leslie G. Biesecker, M.D., a clinical and molecular geneticist and investigator with NHGRI, as their new president-elect for 2019.
Research Training
Three-year residency program in medical genetics that trains physicians to diagnose, manage and counsel patients with genetic disorders.
FAQ
Addressing the COVID-19 pandemic and what it means to the pediatric mitochondrial disease community.
… which may lead to disease progression.  … The Metabolism, Infection and Immunity (MINI) Section’s mission … … Peter McGuire is an investigator and head of the Metabolism, Infection and Immunity (MINI) Section at NHGRI. … disease, COVID-19, COVID-19 vaccine, inborn errors of metabolism, organ dysfunction, tissue death, MINI Section, …
Research Training
This program offers training in a combined program of maternal-fetal medicine and medical genetics.
Genetic Disorders
Methylmalonic acidemia is a group of inherited disorders in which the body is unable to process certain proteins and fats (lipids) properly.
… be caused by mutations in at least three other genes. The cobalamin A (cblA) type of methylmalonic acidemia is caused by mutations in the MMAA gene. The cobalamin B (cblB) type of methylmalonic acidemia is caused … of methylmalonic acid and homocysteine. These include cobalamin C (cblC), cobalamin D (cblD) and cobalamin F (cblF) …