Chris F. Inglehearn
Papers
1
Total Citations
81
H-Index
1
About
Chris F. Inglehearn is a leading geneticist whose research focuses on the molecular genetics of inherited eye diseases, particularly those causing childhood blindness and retinal degeneration. His major contributions include the identification and mapping of novel genetic loci for disorders such as familial exudative vitreoretinopathy (FEVR) and Leber congenital amaurosis. In his landmark 2001 study, Inglehearn and his team localized a new autosomal dominant FEVR gene to chromosome 11p12-13, a finding that has garnered 81 citations and paved the way for subsequent gene discovery. His work has directly advanced the understanding of retinal development and vascularization, offering crucial insights for genetic counseling and future therapies. With a career spanning decades, Inglehearn has been instrumental in establishing the genetic basis of several blinding conditions, and his studies are widely cited by researchers in ophthalmology and human genetics. His dedication to unraveling the complexities of inherited retinal disease continues to inspire students and clinicians alike.
Research Focus
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Top Papers
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