A citation-based method for searching scientific literature

Mineo Kondo, Gautami Das, Ryoetsu Imai, Evelyn Santana, Tomio Nakashita, Miho Imawaka, Kosuke Ueda, Hirohiko Ohtsuka, Kazuhiko Sakai, Takehiro Aihara, Kumiko Kato, Masahiko Sugimoto, Shinji Ueno, Yuji Nishizawa, Gustavo D Aguirre, Keiko Miyadera. PLoS One 2015
Times Cited: 13







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



Times Cited
  Times     Co-cited
Similarity


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
88
38

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
35
38

A large animal model for CNGB1 autosomal recessive retinitis pigmentosa.
Paige A Winkler, Kari J Ekenstedt, Laurence M Occelli, Anton V Frattaroli, Joshua T Bartoe, Patrick J Venta, Simon M Petersen-Jones. PLoS One 2013
30
38

cGMP phosphodiesterase-alpha mutation causes progressive retinal atrophy in the Cardigan Welsh corgi dog.
S M Petersen-Jones, D D Entz, D R Sargan. Invest Ophthalmol Vis Sci 1999
97
38

Canine CNGB3 mutations establish cone degeneration as orthologous to the human achromatopsia locus ACHM3.
Duska J Sidjanin, Jennifer K Lowe, John L McElwee, Bruce S Milne, Taryn M Phippen, David R Sargan, Gustavo D Aguirre, Gregory M Acland, Elaine A Ostrander. Hum Mol Genet 2002
136
38


Congenital stationary night blindness with negative electroretinogram. A new classification.
Y Miyake, K Yagasaki, M Horiguchi, Y Kawase, T Kanda. Arch Ophthalmol 1986
347
30

Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.
Zheng Li, Panagiotis I Sergouniotis, Michel Michaelides, Donna S Mackay, Genevieve A Wright, Sophie Devery, Anthony T Moore, Graham E Holder, Anthony G Robson, Andrew R Webster. Am J Hum Genet 2009
120
30

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
N T Bech-Hansen, M J Naylor, T A Maybaum, R L Sparkes, B Koop, D G Birch, A A Bergen, C F Prinsen, R C Polomeno, A Gal,[...]. Nat Genet 2000
234
30

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
C M Pusch, C Zeitz, O Brandau, K Pesch, H Achatz, S Feil, C Scharfe, J Maurer, F K Jacobi, A Pinckers,[...]. Nat Genet 2000
183
30

Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6.
Thaddeus P Dryja, Terri L McGee, Eliot L Berson, Gerald A Fishman, Michael A Sandberg, Kenneth R Alexander, Deborah J Derlacki, Aruna S Rajagopalan. Proc Natl Acad Sci U S A 2005
163
30


Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse.
Rebecca R Bellone, Heather Holl, Vijayasaradhi Setaluri, Sulochana Devi, Nityanand Maddodi, Sheila Archer, Lynne Sandmeyer, Arne Ludwig, Daniel Foerster, Melanie Pruvost,[...]. PLoS One 2013
58
30

Irish setter dogs affected with rod/cone dysplasia contain a nonsense mutation in the rod cGMP phosphodiesterase beta-subunit gene.
M L Suber, S J Pittler, N Qin, G C Wright, V Holcombe, R H Lee, C M Craft, R N Lolley, W Baehr, R L Hurwitz. Proc Natl Acad Sci U S A 1993
210
30

Canine RPGRIP1 mutation establishes cone-rod dystrophy in miniature longhaired dachshunds as a homologue of human Leber congenital amaurosis.
C S Mellersh, M E G Boursnell, L Pettitt, E J Ryder, N G Holmes, D Grafham, O P Forman, J Sampson, K C Barnett, S Blanton,[...]. Genomics 2006
74
30


LRIT3 is essential to localize TRPM1 to the dendritic tips of depolarizing bipolar cells and may play a role in cone synapse formation.
Marion Neuillé, Catherine W Morgans, Yan Cao, Elise Orhan, Christelle Michiels, José-Alain Sahel, Isabelle Audo, Robert M Duvoisin, Kirill A Martemyanov, Christina Zeitz. Eur J Neurosci 2015
26
23

[Analysis of the human electroretinogram].
G SCHUBERT, H BORNSCHEIN. Ophthalmologica 1952
223
23

Night blindness-associated mutations in the ligand-binding, cysteine-rich, and intracellular domains of the metabotropic glutamate receptor 6 abolish protein trafficking.
Christina Zeitz, Ursula Forster, John Neidhardt, Silke Feil, Stefan Kälin, Dorothee Leifert, Peter J Flor, Wolfgang Berger. Hum Mutat 2007
44
23

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.
T M Strom, G Nyakatura, E Apfelstedt-Sylla, H Hellebrand, B Lorenz, B H Weber, K Wutz, N Gutwillinger, K Rüther, B Drescher,[...]. Nat Genet 1998
343
23

Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.
N T Bech-Hansen, M J Naylor, T A Maybaum, W G Pearce, B Koop, G A Fishman, M Mets, M A Musarella, K M Boycott. Nat Genet 1998
364
23

TRPM1 is a component of the retinal ON bipolar cell transduction channel in the mGluR6 cascade.
Chieko Koike, Takehisa Obara, Yoshitsugu Uriu, Tomohiro Numata, Rikako Sanuki, Kentarou Miyata, Toshiyuki Koyasu, Shinji Ueno, Kazuo Funabiki, Akiko Tani,[...]. Proc Natl Acad Sci U S A 2010
188
23

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
155
23



Dog models for blinding inherited retinal dystrophies.
Simon M Petersen-Jones, András M Komáromy. Hum Gene Ther Clin Dev 2015
31
23

Characterization of a canine model of autosomal recessive retinitis pigmentosa due to a PDE6A mutation.
Nalinee Tuntivanich, Steven J Pittler, Andy J Fischer, Ghezal Omar, Matti Kiupel, Arthur Weber, Suxia Yao, Juan Pedro Steibel, Naheed Wali Khan, Simon M Petersen-Jones. Invest Ophthalmol Vis Sci 2009
35
23

Gene therapy restores vision in a canine model of childhood blindness.
G M Acland, G D Aguirre, J Ray, Q Zhang, T S Aleman, A V Cideciyan, S E Pearce-Kelling, V Anand, Y Zeng, A M Maguire,[...]. Nat Genet 2001
838
23

Bestrophin gene mutations cause canine multifocal retinopathy: a novel animal model for best disease.
Karina E Guziewicz, Barbara Zangerl, Sarah J Lindauer, Robert F Mullins, Lynne S Sandmeyer, Bruce H Grahn, Edwin M Stone, Gregory M Acland, Gustavo D Aguirre. Invest Ophthalmol Vis Sci 2007
82
23

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
87
23

Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humans.
Barbara Zangerl, Orly Goldstein, Alisdair R Philp, Sarah J P Lindauer, Susan E Pearce-Kelling, Robert F Mullins, Alexander S Graphodatsky, Daniel Ripoll, Jeanette S Felix, Edwin M Stone,[...]. Genomics 2006
119
23

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, Lucy B Rowe, Trijntje Sjoerdsma, Susana Contreras-Alcantara, Kenkichi Baba, Gianluca Tosini, Nikita Pozdeyev, P Michael Iuvone,[...]. Am J Hum Genet 2012
90
23

Congenital stationary night blindness in the dog: common mutation in the RPE65 gene indicates founder effect.
G D Aguirre, V Baldwin, S Pearce-Kelling, K Narfström, K Ray, G M Acland. Mol Vis 1998
147
23

Canine RD3 mutation establishes rod-cone dysplasia type 2 (rcd2) as ortholog of human and murine rd3.
Anna V Kukekova, Orly Goldstein, Jennifer L Johnson, Malcolm A Richardson, Susan E Pearce-Kelling, Anand Swaroop, James S Friedman, Gustavo D Aguirre, Gregory M Acland. Mamm Genome 2009
43
23

Generalized progressive retinal atrophy in the Irish Glen of Imaal Terrier is associated with a deletion in the ADAM9 gene.
Regina Kropatsch, Elisabeth Petrasch-Parwez, Dominik Seelow, Annegrit Schlichting, Wanda M Gerding, Denis A Akkad, Joerg T Epplen, Gabriele Dekomien. Mol Cell Probes 2010
16
23

Assessment of canine BEST1 variations identifies new mutations and establishes an independent bestrophinopathy model (cmr3).
Barbara Zangerl, Kaisa Wickström, Julianna Slavik, Sarah J Lindauer, Saija Ahonen, Claude Schelling, Hannes Lohi, Karina E Guziewicz, Gustavo D Aguirre. Mol Vis 2010
32
23

Different RPGR exon ORF15 mutations in Canids provide insights into photoreceptor cell degeneration.
Qi Zhang, Gregory M Acland, Wen X Wu, Jennifer L Johnson, Sue Pearce-Kelling, Brian Tulloch, Raf Vervoort, Alan F Wright, Gustavo D Aguirre. Hum Mol Genet 2002
172
23

Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus).
Rebecca R Bellone, Samantha A Brooks, Lynne Sandmeyer, Barbara A Murphy, George Forsyth, Sheila Archer, Ernest Bailey, Bruce Grahn. Genetics 2008
103
23

Exclusion of RPGRIP1 ins44 from primary causal association with early-onset cone-rod dystrophy in dogs.
Tatyana Kuznetsova, Simone Iwabe, Kathleen Boesze-Battaglia, Sue Pearce-Kelling, Yim Chang-Min, Kendra McDaid, Keiko Miyadera, Andras Komaromy, Gustavo D Aguirre. Invest Ophthalmol Vis Sci 2012
13
23

Genome-wide association study in RPGRIP1(-/-) dogs identifies a modifier locus that determines the onset of retinal degeneration.
Keiko Miyadera, Kumiko Kato, Mike Boursnell, Cathryn S Mellersh, David R Sargan. Mamm Genome 2012
21
23

Genomic deletion of CNGB3 is identical by descent in multiple canine breeds and causes achromatopsia.
Connie Y Yeh, Orly Goldstein, Anna V Kukekova, Debbie Holley, Amy M Knollinger, Heather J Huson, Susan E Pearce-Kelling, Gregory M Acland, András M Komáromy. BMC Genet 2013
18
23

Pathological and electrophysiological features of a canine cone-rod dystrophy in the miniature longhaired dachshund.
Clare Turney, N H Victor Chong, Robert A Alexander, Chris R Hogg, Lorraine Fleming, Deborah Flack, Keith C Barnett, Alan C Bird, Graham E Holder, Philip J Luthert. Invest Ophthalmol Vis Sci 2007
31
23

Functional and structural recovery of the retina after gene therapy in the RPE65 null mutation dog.
Kristina Narfström, Martin L Katz, Ragnheidur Bragadottir, Mathias Seeliger, Ana Boulanger, T Michael Redmond, Lynette Caro, Chooi-May Lai, P Elizabeth Rakoczy. Invest Ophthalmol Vis Sci 2003
188
23

An ADAM9 mutation in canine cone-rod dystrophy 3 establishes homology with human cone-rod dystrophy 9.
Orly Goldstein, Jason G Mezey, Adam R Boyko, Chuan Gao, Wei Wang, Carlos D Bustamante, Lynne J Anguish, Julie Ann Jordan, Susan E Pearce-Kelling, Gustavo D Aguirre,[...]. Mol Vis 2010
36
23

A deletion in nephronophthisis 4 (NPHP4) is associated with recessive cone-rod dystrophy in standard wire-haired dachshund.
Anne Caroline Wiik, Claire Wade, Tara Biagi, Ernst-Otto Ropstad, Ellen Bjerkås, Kerstin Lindblad-Toh, Frode Lingaas. Genome Res 2008
63
23

Long-term effect of gene therapy on Leber's congenital amaurosis.
James W B Bainbridge, Manjit S Mehat, Venki Sundaram, Scott J Robbie, Susie E Barker, Caterina Ripamonti, Anastasios Georgiadis, Freya M Mowat, Stuart G Beattie, Peter J Gardner,[...]. N Engl J Med 2015
403
23

Patients and animal models of CNGβ1-deficient retinitis pigmentosa support gene augmentation approach.
Simon M Petersen-Jones, Laurence M Occelli, Paige A Winkler, Winston Lee, Janet R Sparrow, Mai Tsukikawa, Sanford L Boye, Vince Chiodo, Jenina E Capasso, Elvir Becirovic,[...]. J Clin Invest 2018
26
23

Gene Supplementation Rescues Rod Function and Preserves Photoreceptor and Retinal Morphology in Dogs, Leading the Way Toward Treating Human PDE6A-Retinitis Pigmentosa.
Laurence M Occelli, Christian Schön, Mathias W Seeliger, Martin Biel, Stylianos Michalakis, Simon M Petersen-Jones. Hum Gene Ther 2017
15
23

Topographical characterization of cone photoreceptors and the area centralis of the canine retina.
Freya M Mowat, Simon M Petersen-Jones, Helen Williamson, David L Williams, Philip J Luthert, Robin R Ali, James W Bainbridge. Mol Vis 2008
69
23

Characterization of a novel form of progressive retinal atrophy in Whippet dogs: a clinical, electroretinographic, and breeding study.
André Tavares Somma, Juan Carlos Duque Moreno, Mario Teruo Sato, Blanche Dreher Rodrigues, Marianna Bacellar-Galdino, Laurence Mireille Occelli, Simon Michael Petersen-Jones, Fabiano Montiani-Ferreira. Vet Ophthalmol 2017
11
27


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.