A citation-based method for searching scientific literature

G SCHUBERT, H BORNSCHEIN. Ophthalmologica 1952
Times Cited: 227



Isabelle Audo, Anthony G Robson, Graham E Holder, Anthony T Moore. Surv Ophthalmol 2008
Times Cited: 91




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


Transgenic Expression of Cacna1f Rescues Vision and Retinal Morphology in a Mouse Model of Congenital Stationary Night Blindness 2A (CSNB2A).
Derek M Waldner, Kenichi Ito, Li-Li Chen, Lisa Nguyen, Robert L Chow, Amy Lee, Derrick E Rancourt, Francois Tremblay, William K Stell, N Torben Bech-Hansen. Transl Vis Sci Technol 2020
3

Expanded Retinal Disease Spectrum Associated With Autosomal Recessive Mutations in GUCY2D.
Maria L Stunkel, Scott E Brodie, Artur V Cideciyan, Wanda L Pfeifer, Elizabeth L Kennedy, Edwin M Stone, Samuel G Jacobson, Arlene V Drack. Am J Ophthalmol 2018
11

Channeling Vision: CaV1.4-A Critical Link in Retinal Signal Transmission.
D M Waldner, N T Bech-Hansen, W K Stell. Biomed Res Int 2018
16


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

Next-generation sequencing confirms the implication of SLC24A1 in autosomal-recessive congenital stationary night blindness.
M Neuillé, S Malaichamy, M Vadalà, C Michiels, C Condroyer, R Sachidanandam, S Srilekha, T Arokiasamy, M Letexier, V Démontant,[...]. Clin Genet 2016
9


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

Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness.
Christina Zeitz, Samuel G Jacobson, Christian P Hamel, Kinga Bujakowska, Marion Neuillé, Elise Orhan, Xavier Zanlonghi, Marie-Elise Lancelot, Christelle Michiels, Sharon B Schwartz,[...]. Am J Hum Genet 2013
89

Arrayed primer extension microarray for the analysis of genes associated with congenital stationary night blindness.
Kadri Vaidla, Janne Uksti, Christina Zeitz, Eneli Oitmaa. Methods Mol Biol 2013
2

Photoreceptor and postreceptor responses in congenital stationary night blindness.
Aparna Raghuram, Ronald M Hansen, Anne Moskowitz, Anne B Fulton. Invest Ophthalmol Vis Sci 2013
11

A phenotypic study of congenital stationary night blindness (CSNB) associated with mutations in the GRM6 gene.
Panagiotis I Sergouniotis, Anthony G Robson, Zheng Li, Sophie Devery, Graham E Holder, Anthony T Moore, Andrew R Webster. Acta Ophthalmol 2012
24

GNAT1 associated with autosomal recessive congenital stationary night blindness.
Muhammad Asif Naeem, Venkata R M Chavali, Shahbaz Ali, Muhammad Iqbal, Saima Riazuddin, Shaheen N Khan, Tayyab Husnain, Paul A Sieving, Radha Ayyagari, Sheikh Riazuddin,[...]. Invest Ophthalmol Vis Sci 2012
44

Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness.
Isabelle Audo, Kinga Bujakowska, Elise Orhan, Charlotte M Poloschek, Sabine Defoort-Dhellemmes, Isabelle Drumare, Susanne Kohl, Tien D Luu, Odile Lecompte, Eberhart Zrenner,[...]. Am J Hum Genet 2012
89

Assessing retinal structure in complete congenital stationary night blindness and Oguchi disease.
Pooja Godara, Robert F Cooper, Panagiotis I Sergouniotis, Melissa A Diederichs, Megan R Streb, Mohamed A Genead, J Jason McAnany, Andrew R Webster, Anthony T Moore, Adam M Dubis,[...]. Am J Ophthalmol 2012
44

A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness.
S Amer Riazuddin, Amber Shahzadi, Christina Zeitz, Zubair M Ahmed, Radha Ayyagari, Venkata R M Chavali, Virgilio G Ponferrada, Isabelle Audo, Christelle Michiels, Marie-Elise Lancelot,[...]. Am J Hum Genet 2010
50

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
163