Ross, Kevin D.

TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone.

Huang, L., Szymanska, K., Jensen, V. L., Janecke, A. R., Innes, A. M., Davis, E. E., Frosk, P., Li, C., Willer, J. R., Chodirker, B. N., et al. (2011) · The American Journal of Human Genetics

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

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The lipid elongation enzyme ELOVL2 is a molecular regulator of aging in the retina

Chen, D., Chao, D. L., Rocha, L., Kolar, M., Nguyen Huu, V. A., Krawczyk, M., Dasyani, M., Wang, T., Jafari, M., Jabari, M., et al. (2020) · Aging Cell

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 109

Ankfn1 vestibular defects in zebrafish require mutations in both ancestral and derived paralogs

Ross, K. D., Ren, J., Zhang, R., Chi, N. C., & Hamilton, B. A. (2021) · G3 Genes Genomes Genetics

Developmental Biology and Gene RegulationVestibular and auditory disorders

Cited by 4

Ankfn1 -mutant vestibular defects require loss of both ancestral and derived paralogs for penetrance in zebrafish

Ross, K. D., Ren, J., Zhang, R., Chi, N. C., & Hamilton, B. A. (2022) · G3 Genes|Genomes|Genetics

Developmental Biology and Gene RegulationVestibular and auditory disorders

Cited by 4