Thomas M. Hallam
188 York Way
London, ENG N79AS, United Kingdom
London, ENG N79AS, United Kingdom
Last Updated: 09/26/2026
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Found 9 publications
The role of complement factor I rare genetic variants in age related macular degeneration in Finland.
Journal: Human molecular genetics
Published: May 09, 2024
Comprehensive functional characterization of complement factor I rare variant genotypes identified in the SCOPE geographic atrophy cohort.
Journal: The Journal of biological chemistry
Published: April 10, 2024
Gene targeting as a therapeutic avenue in diseases mediated by the complement alternative pathway.
Journal: Immunological reviews
Published: November 12, 2022
A novel method for real-time analysis of the complement C3b:FH:FI complex reveals dominant negative CFI variants in age-related macular degeneration.
Journal: Frontiers in immunology
Published: August 26, 2022
Homodimeric Minimal Factor H: In Vivo Tracking and Extended Dosing Studies in Factor H Deficient Mice.
Journal: Frontiers in immunology
Published: August 03, 2021
Insights Into the Structure-Function Relationships of Dimeric C3d Fragments.
Journal: Frontiers in immunology
Published: May 24, 2021
Functional Characterization of Rare Genetic Variants in the N-Terminus of Complement Factor H in aHUS, C3G, and AMD.
Journal: Frontiers in immunology
Published: September 02, 2020
Rare Genetic Variants in Complement Factor I Lead to Low FI Plasma Levels Resulting in Increased Risk of Age-Related Macular Degeneration.
Journal: Investigative ophthalmology & visual science
Published: June 10, 2020
Showing 1-9 of 9
Last Updated: 09/26/2026