Francis S. Collins - Genetic Mutations

Author Information

Francis S. Collins is a prominent researcher affiliated with the National Human Genome Research Institute at the National Institutes of Health in Bethesda, MD. His work primarily focuses on genetics and genomics, contributing significantly to our understanding of human genetic variation and its implications for health and disease.

Research Contributions

Francis S. Collins has made substantial contributions to the field of genetics, with a particular focus on genome-wide association studies (GWAS) and precision medicine. His research includes identifying genetic variants associated with human height, cardiometabolic traits, and diseases such as diabetes and Hutchinson-Gilford Progeria Syndrome. Collins also explores the potential of genetic insights to transform healthcare by 2030, highlighting the importance of precision medicine. His work emphasizes the role of molecular genetics in revealing biological mechanisms underlying human diseases, offering promising avenues for therapeutic interventions.

Aliases

Francis S. Collins is also known by several aliases, including Francis Collins, F. S. Collins, F S Collins, F. Collins, and F Collins. These variations may appear in different publications and contexts, reflecting his widespread recognition in the scientific community.

Publication and Citation Metrics

Metric Value
Total Papers Published 668
Total Citations 156,502
H-index 155

Publications:

DOI: 10.1016/j.cell.2021.01.015

Year: 2021

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