A citation-based method for searching scientific literature

Christiana L Cheng, Hidayat Djajadi, Robert S Molday. Methods Mol Biol 2013
Times Cited: 13







List of co-cited articles
52 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Proteomics of photoreceptor outer segments identifies a subset of SNARE and Rab proteins implicated in membrane vesicle trafficking and fusion.
Michael C M Kwok, Juha M Holopainen, Laurie L Molday, Leonard J Foster, Robert S Molday. Mol Cell Proteomics 2008
89
30


The cGMP-gated channel of bovine rod photoreceptors is localized exclusively in the plasma membrane.
N J Cook, L L Molday, D Reid, U B Kaupp, R S Molday. J Biol Chem 1989
114
23


Immunocytochemical analysis of the mouse retina.
S Haverkamp, H Wässle. J Comp Neurol 2000
561
23

Effect of gene therapy on visual function in Leber's congenital amaurosis.
James W B Bainbridge, Alexander J Smith, Susie S Barker, Scott Robbie, Robert Henderson, Kamaljit Balaggan, Ananth Viswanathan, Graham E Holder, Andrew Stockman, Nick Tyler,[...]. N Engl J Med 2008
23

The major cell populations of the mouse retina.
C J Jeon, E Strettoi, R H Masland. J Neurosci 1998
881
23

Production and purification of serotype 1, 2, and 5 recombinant adeno-associated viral vectors.
Sergei Zolotukhin, Mark Potter, Irene Zolotukhin, Yoshihisa Sakai, Scott Loiler, Thomas J Fraites, Vince A Chiodo, Tina Phillipsberg, Nicholas Muzyczka, William W Hauswirth,[...]. Methods 2002
439
15

High-efficiency transduction of the mouse retina by tyrosine-mutant AAV serotype vectors.
Hilda Petrs-Silva, Astra Dinculescu, Qiuhong Li, Seok-Hong Min, Vince Chiodo, Ji-Jing Pang, Li Zhong, Sergei Zolotukhin, Arun Srivastava, Alfred S Lewin,[...]. Mol Ther 2009
269
15

ABCA4 is an N-retinylidene-phosphatidylethanolamine and phosphatidylethanolamine importer.
Faraz Quazi, Stepan Lenevich, Robert S Molday. Nat Commun 2012
135
15


Peripherin. A rim-specific membrane protein of rod outer segment discs.
R S Molday, D Hicks, L Molday. Invest Ophthalmol Vis Sci 1987
281
15

RD3 gene delivery restores guanylate cyclase localization and rescues photoreceptors in the Rd3 mouse model of Leber congenital amaurosis 12.
Laurie L Molday, Hidayat Djajadi, Paul Yan, Lukasz Szczygiel, Sanford L Boye, Vince A Chiodo, Kevin Gregory-Evans, Marinko V Sarunic, William W Hauswirth, Robert S Molday. Hum Mol Genet 2013
38
15




Atp8a1 deficiency is associated with phosphatidylserine externalization in hippocampus and delayed hippocampus-dependent learning.
Kelly Levano, Vineet Punia, Michael Raghunath, Priya Ranjan Debata, Gina Marie Curcio, Amit Mogha, Sudarshana Purkayastha, Dan McCloskey, Jimmie Fata, Probal Banerjee. J Neurochem 2012
44
15

Heteromeric interactions required for abundance and subcellular localization of human CDC50 proteins and class 1 P4-ATPases.
Lieke M van der Velden, Catharina G K Wichers, Adriana E D van Breevoort, Jonathan A Coleman, Robert S Molday, Ruud Berger, Leo W J Klomp, Stan F J van de Graaf. J Biol Chem 2010
68
15

Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion.
Onur Emre Onat, Suleyman Gulsuner, Kaya Bilguvar, Ayse Nazli Basak, Haluk Topaloglu, Meliha Tan, Uner Tan, Murat Gunel, Tayfun Ozcelik. Eur J Hum Genet 2013
72
15

Phospholipid flippases: building asymmetric membranes and transport vesicles.
Tessy T Sebastian, Ryan D Baldridge, Peng Xu, Todd R Graham. Biochim Biophys Acta 2012
140
15

Mutations in a P-type ATPase gene cause axonal degeneration.
Xianjun Zhu, Richard T Libby, Wilhelmine N de Vries, Richard S Smith, Dana L Wright, Roderick T Bronson, Kevin L Seburn, Simon W M John. PLoS Genet 2012
58
15

Mechanism and significance of P4 ATPase-catalyzed lipid transport: lessons from a Na+/K+-pump.
Catheleyne F Puts, Joost C M Holthuis. Biochim Biophys Acta 2009
40
15

ATP8B1 is essential for maintaining normal hearing.
Janneke M Stapelbroek, Theo A Peters, Denis H A van Beurden, Jo H A J Curfs, Anneke Joosten, Andy J Beynon, Bibian M van Leeuwen, Lieke M van der Velden, Laura Bull, Ronald P Oude Elferink,[...]. Proc Natl Acad Sci U S A 2009
68
15

Disruption of the ATP8A2 gene in a patient with a t(10;13) de novo balanced translocation and a severe neurological phenotype.
Pierre Cacciagli, Marie-Reine Haddad, Cécile Mignon-Ravix, Bilal El-Waly, Anne Moncla, Chantal Missirian, Brigitte Chabrol, Laurent Villard. Eur J Hum Genet 2010
41
15

Mammalian P4-ATPases and ABC transporters and their role in phospholipid transport.
Jonathan A Coleman, Faraz Quazi, Robert S Molday. Biochim Biophys Acta 2013
81
15

The murine cone photoreceptor: a single cone type expresses both S and M opsins with retinal spatial patterning.
M L Applebury, M P Antoch, L C Baxter, L L Chun, J D Falk, F Farhangfar, K Kage, M G Krzystolik, L A Lyass, J T Robbins. Neuron 2000
391
15

Treatment of leber congenital amaurosis due to RPE65 mutations by ocular subretinal injection of adeno-associated virus gene vector: short-term results of a phase I trial.
William W Hauswirth, Tomas S Aleman, Shalesh Kaushal, Artur V Cideciyan, Sharon B Schwartz, Lili Wang, Thomas J Conlon, Sanford L Boye, Terence R Flotte, Barry J Byrne,[...]. Hum Gene Ther 2008
688
15

Safety and efficacy of gene transfer for Leber's congenital amaurosis.
Albert M Maguire, Francesca Simonelli, Eric A Pierce, Edward N Pugh, Federico Mingozzi, Jeannette Bennicelli, Sandro Banfi, Kathleen A Marshall, Francesco Testa, Enrico M Surace,[...]. N Engl J Med 2008
15

Identification of molecular markers of bipolar cells in the murine retina.
Douglas S Kim, Sarah E Ross, Jeffrey M Trimarchi, John Aach, Michael E Greenberg, Constance L Cepko. J Comp Neurol 2008
86
15

Complement system dysregulation and inflammation in the retinal pigment epithelium of a mouse model for Stargardt macular degeneration.
Roxana A Radu, Jane Hu, Quan Yuan, Darcy L Welch, Jacob Makshanoff, Marcia Lloyd, Stephen McMullen, Gabriel H Travis, Dean Bok. J Biol Chem 2011
96
15


Rpe65 Leu450Met variant is associated with reduced levels of the retinal pigment epithelium lipofuscin fluorophores A2E and iso-A2E.
So Ra Kim, Nathan Fishkin, Jian Kong, Koji Nakanishi, Rando Allikmets, Janet R Sparrow. Proc Natl Acad Sci U S A 2004
103
15

Light exposure stimulates formation of A2E oxiranes in a mouse model of Stargardt's macular degeneration.
Roxana A Radu, Nathan L Mata, Aarti Bagla, Gabriel H Travis. Proc Natl Acad Sci U S A 2004
110
15




Effective delivery of large genes to the retina by dual AAV vectors.
Ivana Trapani, Pasqualina Colella, Andrea Sommella, Carolina Iodice, Giulia Cesi, Sonia de Simone, Elena Marrocco, Settimio Rossi, Massimo Giunti, Arpad Palfi,[...]. EMBO Mol Med 2014
122
15

Fundus autofluorescence in the Abca4(-/-) mouse model of Stargardt disease--correlation with accumulation of A2E, retinal function, and histology.
Peter Charbel Issa, Alun R Barnard, Mandeep S Singh, Emma Carter, Zhichun Jiang, Roxana A Radu, Ulrich Schraermeyer, Robert E MacLaren. Invest Ophthalmol Vis Sci 2013
64
15

edgeR: a Bioconductor package for differential expression analysis of digital gene expression data.
Mark D Robinson, Davis J McCarthy, Gordon K Smyth. Bioinformatics 2010
15

Cytoplasmic Rbfox1 Regulates the Expression of Synaptic and Autism-Related Genes.
Ji-Ann Lee, Andrey Damianov, Chia-Ho Lin, Mariana Fontes, Neelroop N Parikshak, Erik S Anderson, Daniel H Geschwind, Douglas L Black, Kelsey C Martin. Neuron 2016
107
15


Gene expression changes in the retina following optic nerve transection.
Natik Piri, Jacky M K Kwong, Min Song, David Elashoff, Joseph Caprioli. Mol Vis 2006
29
15

Generating neuronal diversity in the retina: one for nearly all.
Till Marquardt, Peter Gruss. Trends Neurosci 2002
272
15

The functional diversity of retinal ganglion cells in the mouse.
Tom Baden, Philipp Berens, Katrin Franke, Miroslav Román Rosón, Matthias Bethge, Thomas Euler. Nature 2016
369
15

RNA binding protein with multiple splicing: a new marker for retinal ganglion cells.
Jacky M K Kwong, Joseph Caprioli, Natik Piri. Invest Ophthalmol Vis Sci 2010
106
15

The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene.
Kavita Bhalla, Hilary A Phillips, Joanna Crawford, Olivia L D McKenzie, John C Mulley, Helen Eyre, Alison E Gardner, Gabriel Kremmidiotis, David F Callen. J Hum Genet 2004
111
15

Requirement for cholinergic synaptic transmission in the propagation of spontaneous retinal waves.
M B Feller, D P Wellis, D Stellwagen, F S Werblin, C J Shatz. Science 1996
392
15



Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autism.
Christa Lese Martin, Jacqueline A Duvall, Yesim Ilkin, Jason S Simon, M Gladys Arreaza, Kristin Wilkes, Ana Alvarez-Retuerto, Amy Whichello, Cynthia M Powell, Kathleen Rao,[...]. Am J Med Genet B Neuropsychiatr Genet 2007
151
15


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.