Protective chromosome 1q32 haplotypes mitigate risk for age-related macular degeneration associated with the CFH-CFHR5 and ARMS2/HTRA1 loci
Pappas, Chris M, Zouache, Moussa A, Matthews, Stacie, Faust, Caitlin D, Hageman, Jill L, Williams, Brandi L, Richards, Burt T, Hageman, Gregory S
Published in Human genomics (25.09.2021)
Published in Human genomics (25.09.2021)
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Electroconvulsive seizure thresholds and kindling acquisition rates are altered in mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions
Otto, James F., Singh, Nanda A., Dahle, E. Jill, Leppert, Mark F., Pappas, Chris M., Pruess, Timothy H., Wilcox, Karen S., White, H. Steve
Published in Epilepsia (Copenhagen) (01.07.2009)
Published in Epilepsia (Copenhagen) (01.07.2009)
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Chromosome 10q26–driven age-related macular degeneration is associated with reduced levels of HTRA1 in human retinal pigment epithelium
Williams, Brandi L., Seager, Nathan A., Gardiner, Jamie D., Pappas, Chris M., Cronin, Monica C., di San Filippo, Cristina Amat, Anstadt, Robert A., Liu, Jin, Toso, Marc A., Nichols, Lisa, Parnell, Timothy J., Eve, Jacqueline R., Bartel, Paul L., Zouache, Moussa A., Richards, Burt T., Hageman, Gregory S.
Published in Proceedings of the National Academy of Sciences - PNAS (27.07.2021)
Published in Proceedings of the National Academy of Sciences - PNAS (27.07.2021)
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Levels of the HtrA1 Protein in Serum and Vitreous Humor Are Independent of Genetic Risk for Age-Related Macular Degeneration at the 10q26 Locus
Williams, Brandi L, Zouache, Moussa A, Seager, Nathan A, Pappas, Chris M, Liu, Jin, Anstadt, Robert A, Hubbard, William C, Thomas, Julie, Hageman, Jill L, Mohler, Jennifer, Richards, Burt T, Hageman, Gregory S
Published in Investigative ophthalmology & visual science (01.04.2024)
Published in Investigative ophthalmology & visual science (01.04.2024)
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Characterization of West African Crystalline Macular Dystrophy in the Ghanaian Population
Amoaku, Winfried M, Sampalli, Amrit, Silvestri, Vittorio, Cushley, Laura N, Akafo, Stephen, Amissah-Arthur, Kwesi N, Lartey, Seth, Hageman, Courtney N, Hubbard, William C, Pappas, Chris M, Zouache, Moussa A, Stevenson, Michael, Hageman, Gregory S, Silvestri, Giuliana
Published in Ophthalmology retina (01.08.2022)
Published in Ophthalmology retina (01.08.2022)
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Diverse Macular Dystrophy Phenotype Caused by a Novel Complex Mutation in the ELOVL4 Gene
Bernstein, Paul S, Tammur, Jaana, Singh, Nanda, Hutchinson, Amy, Dixon, Missy, Pappas, Chris M, Zabriskie, Norman A, Zhang, Kang, Petrukhin, Konstantin, Leppert, Mark, Allikmets, Rando
Published in Investigative ophthalmology & visual science (01.12.2001)
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Published in Investigative ophthalmology & visual science (01.12.2001)
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126 Complement Factor I protein concentration in human plasma and ocular tissue samples stratified by AMD genotypes and phenotypes
Richards, Burt T., Anstadt, Robert A., Liu, Jin, Corsetti, Tana G., Williams, Brandi L., Zouache, Moussa A., Pappas, Chris M., Hageman, Gregory S.
Published in Immunobiology (1979) (01.09.2023)
Published in Immunobiology (1979) (01.09.2023)
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