A citation-based method for searching scientific literature

G SCHUBERT, H BORNSCHEIN. Ophthalmologica 1952
Times Cited: 226



Yin Shen, J Alexander Heimel, Maarten Kamermans, Neal S Peachey, Ronald G Gregg, Scott Nawy. J Neurosci 2009
Times Cited: 154




List of shared articles



Times cited

A New Mouse Model for Complete Congenital Stationary Night Blindness Due to Gpr179 Deficiency.
Elise Orhan, Marion Neuillé, Miguel de Sousa Dias, Thomas Pugliese, Christelle Michiels, Christel Condroyer, Aline Antonio, José-Alain Sahel, Isabelle Audo, Christina Zeitz. Int J Mol Sci 2021
1

LRIT3 Differentially Affects Connectivity and Synaptic Transmission of Cones to ON- and OFF-Bipolar Cells.
Marion Neuillé, Yan Cao, Romain Caplette, Debbie Guerrero-Given, Connon Thomas, Naomi Kamasawa, José-Alain Sahel, Christian P Hamel, Isabelle Audo, Serge Picaud,[...]. Invest Ophthalmol Vis Sci 2017
12

Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness.
Ajoy Vincent, Isabelle Audo, Erika Tavares, Jason T Maynes, Anupreet Tumber, Thomas Wright, Shuning Li, Christelle Michiels, Christel Condroyer, Heather MacDonald,[...]. Am J Hum Genet 2016
29

Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristics.
Virginie Dinet, Giuseppe D Ciccotosto, Kimberley Delaunay, Céline Borras, Isabelle Ranchon-Cole, Corinne Kostic, Michèle Savoldelli, Mohamed El Sanharawi, Laurent Jonet, Caroline Pirou,[...]. Mol Brain 2016
7


A Naturally Occurring Canine Model of Autosomal Recessive Congenital Stationary Night Blindness.
Mineo Kondo, Gautami Das, Ryoetsu Imai, Evelyn Santana, Tomio Nakashita, Miho Imawaka, Kosuke Ueda, Hirohiko Ohtsuka, Kazuhiko Sakai, Takehiro Aihara,[...]. PLoS One 2015
15

Lrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB).
Marion Neuillé, Said El Shamieh, Elise Orhan, Christelle Michiels, Aline Antonio, Marie-Elise Lancelot, Christel Condroyer, Kinga Bujakowska, Olivier Poch, José-Alain Sahel,[...]. PLoS One 2014
36

Further insights into GPR179: expression, localization, and associated pathogenic mechanisms leading to complete congenital stationary night blindness.
Elise Orhan, Laurent Prézeau, Said El Shamieh, Kinga M Bujakowska, Christelle Michiels, Yvrick Zagar, Claire Vol, Shomi S Bhattacharya, José-Alain Sahel, Florian Sennlaub,[...]. Invest Ophthalmol Vis Sci 2013
16

Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation.
Neal S Peachey, Jillian N Pearring, Pasano Bojang, Matthew E Hirschtritt, Gwen Sturgill-Short, Thomas A Ray, Takahisa Furukawa, Chieko Koike, Andrew F X Goldberg, Yin Shen,[...]. J Neurophysiol 2012
34

TRPM1 mutations are associated with the complete form of congenital stationary night blindness.
Makoto Nakamura, Rikako Sanuki, Tetsuhiro R Yasuma, Akishi Onishi, Koji M Nishiguchi, Chieko Koike, Mikiko Kadowaki, Mineo Kondo, Yozo Miyake, Takahisa Furukawa. Mol Vis 2010
74

Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses.
Rebecca R Bellone, George Forsyth, Tosso Leeb, Sheila Archer, Snaevar Sigurdsson, Freyja Imsland, Evan Mauceli, Martina Engensteiner, Ernest Bailey, Lynne Sandmeyer,[...]. Brief Funct Genomics 2010
31

TRPM1: a vertebrate TRP channel responsible for retinal ON bipolar function.
Chieko Koike, Tomohiro Numata, Hiroshi Ueda, Yasuo Mori, Takahisa Furukawa. Cell Calcium 2010
61


TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.
Isabelle Audo, Susanne Kohl, Bart P Leroy, Francis L Munier, Xavier Guillonneau, Saddek Mohand-Saïd, Kinga Bujakowska, Emeline F Nandrot, Birgit Lorenz, Markus Preising,[...]. Am J Hum Genet 2009
161