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Clinical Research
The CLINSEQ® Study seeks to learn about the role that your genes play in your health.
… and protein evidence connects TREML4 to coronary artery calcification. Am J Hum Genet , 95(1):66-76. 2014. [ PubMed … of candidate genes involved in coronary artery calcification by transcriptome sequencing of cell lines. BMC …
News Release
NHGRI researchers will present four platform talks and 55 posters to highlight the institute's diverse portfolio at the 65th annual meeting of ASHG.
… on chromosome 9p21, is downregulated in coronary artery calcification. (Cardiovascular Genetics) 1381T. Anthony M. …
Staff
Abdel Elkahloun is an associate investigator in NHGRI's Office of Scientific Core Facilities.
… of candidate genes involved in coronary artery calcification by transcriptome sequencing of cell lines. BMC …
The Genomics Landscape
In the February 2019 edition of The Genomics Landscape, NHGRI Director Eric Green recognizes Dr. Bill Gahl's achievements as Clinical Director.
… recalls the discovery of the program's first new disease - Arterial Calcification due to Deficiency of CD73; this work was …
Talking Glossary
Un rasgo, en lo que se relaciona a la genética, es una caracterÃstica especÃfica de una persona.
Clinical Research
NHGRI researchers work with patients and families to explore how genes cause or influence diseases, and develop more effective diagnostics and treatments.
… Molecular Investigations into Ciliopathies Coronary Artery Calcification ClinSeq: A Large-Scale Medical Sequencing …
Genetic Disorders
Familial hypercholesterolemia is an inherited condition causing increased low density lipoprotein cholesterol at birth and heart attacks at an early age.
Staff
Dr. Leslie Biesecker is a clinical and molecular geneticist in and the chief of NHGRI's Center for Precision Health Research.
… discovery of a gene associated with coronary artery calcification using transcriptome sequencing and the use of a …
Health
A polygenic risk score is one way by which people can learn what their risk of developing a disease is, based on the total number of genomics variants related to the disease.
Genetic Disorders
Poland anomaly is an underdevelopment or absence of the chest muscle on one side of the body and webbing of the fingers of the hand on the same side.