Jillian N. Pearring

Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness

Maria M. van Genderen, Mieke M. C. Bijveld, Y. Claassen et al. · The American Journal of Human Genetics · 2009 · 237 citations · Full text

Developmental Biology, Ophthalmology, Genetic Disorder +3

GPR179 Is Required for Depolarizing Bipolar Cell Function and Is Mutated in Autosomal-Recessive Complete Congenital Stationary Night Blindness

Neal S. Peachey, Thomas A. Ray, Ralph Florijn et al. · The American Journal of Human Genetics · 2012 · 158 citations · Full text

Is Mutated, Bipolar Cell Function, Photoreceptor Cell +7

Photoreceptor discs form through peripherin-dependent suppression of ciliary ectosome release

Raquel Y. Salinas, Jillian N. Pearring, Jindong Ding et al. · The Journal of Cell Biology · 2017 · 141 citations · Full text

A Role for Nyctalopin, a Small Leucine-Rich Repeat Protein, in Localizing the TRP Melastatin 1 Channel to Retinal Depolarizing Bipolar Cell Dendrites

Jillian N. Pearring, Pasano Bojang, Yin Shen et al. · Journal of Neuroscience · 2011 · 114 citations · Full text

De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome

Lindsay C. Burrage, Wu‐Lin Charng, Mohammad K. Eldomery et al. · The American Journal of Human Genetics · 2015 · 76 citations · Full text

Meier-gorlin Syndrome, Developmental Biology, Somatic Variant +8