Robin M. Johnston, Ph.D.
Affiliations: | 2010 | Regent University |
Area:
History of Religion, General Religion, United States History, BiographyGoogle:
"Robin Johnston"Parents
Sign in to add mentorVinson Synan | grad student | 2010 | Regent University | |
(Howard A. Goss: A Pentecostal life.) |
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Publications
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Chirco KR, Lewis CJ, Scheetz TE, et al. (2017) Evaluation of sFLT1 protein levels in human eyes with the FLT1 rs9943922 polymorphism. Ophthalmic Genetics. 1-5 |
DeLuca AP, Whitmore SS, Barnes J, et al. (2015) Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosis. Human Molecular Genetics |
Mullins RF, Schoo DP, Sohn EH, et al. (2014) The membrane attack complex in aging human choriocapillaris: relationship to macular degeneration and choroidal thinning. The American Journal of Pathology. 184: 3142-53 |
Braun TA, Mullins RF, Wagner AH, et al. (2013) Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease. Human Molecular Genetics. 22: 5136-45 |
Tucker BA, Scheetz TE, Mullins RF, et al. (2011) Exome sequencing and analysis of induced pluripotent stem cells identify the cilia-related gene male germ cell-associated kinase (MAK) as a cause of retinitis pigmentosa. Proceedings of the National Academy of Sciences of the United States of America. 108: E569-76 |
Fingert JH, Kwon YH, Moore PA, et al. (2006) The C677T variant in the methylenetetrahydrofolate reductase gene is not associated with disease in cohorts of pseudoexfoliation glaucoma and primary open-angle glaucoma patients from Iowa. Ophthalmic Genetics. 27: 39-41 |