Elise Orhan

Whole-Exome Sequencing Identifies LRIT3 Mutations as a Cause of Autosomal-Recessive Complete Congenital Stationary Night Blindness

Christina Zeitz, Samuel G. Jacobson, Christian Hamel et al. · The American Journal of Human Genetics · 2012 · 135 citations · Full text

Mendelian Disorder, Ophthalmology, Genetic Disorder +5

Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness

Isabelle Audo, Kinga M. Bujakowska, Elise Orhan et al. · The American Journal of Human Genetics · 2012 · 132 citations · Full text

Ocular Disease, Developmental Biology, Mendelian Disorder +6

<scp>LRIT</scp>3 is essential to localize <scp>TRPM</scp>1 to the dendritic tips of depolarizing bipolar cells and may play a role in cone synapse formation

Marion Neuillé, Catherine W. Morgans, Yan Cao et al. · European Journal of Neuroscience · 2015 · 62 citations · Full text

Lrit3 Deficient Mouse (nob6): A Novel Model of Complete Congenital Stationary Night Blindness (cCSNB)

Marion Neuillé, Saïd El Shamieh, Elise Orhan et al. · PLoS ONE · 2014 · 61 citations · Full text

Genetics, Optogenetics, Signaling Pathway +18

Whole-Exome Sequencing Identifies KIZ as a Ciliary Gene Associated with Autosomal-Recessive Rod-Cone Dystrophy

Saïd El Shamieh, Marion Neuillé, Angélique Terray et al. · The American Journal of Human Genetics · 2014 · 59 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +7