A citation-based method for searching scientific literature

Yingwei Wang, Wenmin Sun, Xueshan Xiao, Shiqiang Li, Xiaoyun Jia, Panfeng Wang, Qingjiong Zhang. Am J Ophthalmol 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


A clinical and molecular characterisation of CRB1-associated maculopathy.
Kamron N Khan, Anthony Robson, Omar A R Mahroo, Gavin Arno, Chris F Inglehearn, Monica Armengol, Naushin Waseem, Graham E Holder, Keren J Carss, Lucy F Raymond,[...]. Eur J Hum Genet 2018
31
100

CRB1 mutations may result in retinitis pigmentosa without para-arteriolar RPE preservation.
A J Lotery, A Malik, S A Shami, M Sindhi, B Chohan, C Maqbool, P A Moore, M J Denton, E M Stone. Ophthalmic Genet 2001
48
100

Comprehensive analysis of patients with Stargardt macular dystrophy reveals new genotype-phenotype correlations and unexpected diagnostic revisions.
Jacques Zaneveld, Sorath Siddiqui, Huajin Li, Xia Wang, Hui Wang, Keqing Wang, Hui Li, Huanan Ren, Irma Lopez, Allison Dorfman,[...]. Genet Med 2015
33
100

Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.
A I den Hollander, J R Heckenlively, L I van den Born, Y J de Kok, S D van der Velde-Visser, U Kellner, B Jurklies, M J van Schooneveld, A Blankenagel, K Rohrschneider,[...]. Am J Hum Genet 2001
256
100

Novel TTLL5 Variants Associated with Cone-Rod Dystrophy and Early-Onset Severe Retinal Dystrophy.
Vasily Smirnov, Olivier Grunewald, Jean Muller, Christina Zeitz, Carolin D Obermaier, Aurore Devos, Valérie Pelletier, Béatrice Bocquet, Camille Andrieu, Jean-Louis Bacquet,[...]. Int J Mol Sci 2021
1
100

Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal lamination.
Samuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, Michael J Pianta, Alexander Sumaroka, Sharon B Schwartz, Elaine E Smilko, Ann H Milam, Val C Sheffield, Edwin M Stone. Hum Mol Genet 2003
170
100

Panel-based next generation sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies.
Nicola Glöckle, Susanne Kohl, Julia Mohr, Tim Scheurenbrand, Andrea Sprecher, Nicole Weisschuh, Antje Bernd, Günther Rudolph, Max Schubach, Charlotte Poloschek,[...]. Eur J Hum Genet 2014
188
100

The CRB1 and adherens junction complex proteins in retinal development and maintenance.
Celso Henrique Alves, Lucie P Pellissier, Jan Wijnholds. Prog Retin Eye Res 2014
54
100

Cone rod dystrophies.
Christian P Hamel. Orphanet J Rare Dis 2007
267
100

Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease.
Morag E Shanks, Susan M Downes, Richard R Copley, Stefano Lise, John Broxholme, Karl Az Hudspith, Alexandra Kwasniewska, Wayne Il Davies, Mark W Hankins, Emily R Packham,[...]. Eur J Hum Genet 2013
98
100

High frequency of CRB1 mutations as cause of Early-Onset Retinal Dystrophies in the Spanish population.
Marta Corton, Sorina D Tatu, Almudena Avila-Fernandez, Elena Vallespín, Ignacio Tapias, Diego Cantalapiedra, Fiona Blanco-Kelly, Rosa Riveiro-Alvarez, Sara Bernal, Blanca García-Sandoval,[...]. Orphanet J Rare Dis 2013
46
100

Crumbs homologue 1 is required for maintenance of photoreceptor cell polarization and adhesion during light exposure.
Serge A van de Pavert, Albena Kantardzhieva, Anna Malysheva, Jan Meuleman, Inge Versteeg, Christiaan Levelt, Jan Klooster, Sylvia Geiger, Mathias W Seeliger, Penny Rashbass,[...]. J Cell Sci 2004
182
100

Whole exome sequencing identifies CRB1 defect in an unusual maculopathy phenotype.
Stephen H Tsang, Tomas Burke, Maris Oll, Suzanne Yzer, Winston Lee, Yajing Angela Xie, Rando Allikmets. Ophthalmology 2014
46
100

Genomic Landscape of Sporadic Retinitis Pigmentosa: Findings from 877 Spanish Cases.
Inmaculada Martin-Merida, Almudena Avila-Fernandez, Marta Del Pozo-Valero, Fiona Blanco-Kelly, Olga Zurita, Raquel Perez-Carro, Domingo Aguilera-Garcia, Rosa Riveiro-Alvarez, Ana Arteche, Maria Jose Trujillo-Tiebas,[...]. Ophthalmology 2019
22
100

Microarray-based mutation detection and phenotypic characterization of patients with Leber congenital amaurosis.
Suzanne Yzer, Bart P Leroy, Elfride De Baere, Thomy J de Ravel, Marijke N Zonneveld, Krysta Voesenek, Ulrich Kellner, Jose P Martinez Ciriano, Jan-Tjeerd H N de Faber, Klaus Rohrschneider,[...]. Invest Ophthalmol Vis Sci 2006
71
100

MPP5 recruits MPP4 to the CRB1 complex in photoreceptors.
Albena Kantardzhieva, Ilse Gosens, Svetlana Alexeeva, Ingrid M Punte, Inge Versteeg, Elmar Krieger, Carla A Neefjes-Mol, Anneke I den Hollander, Stef J F Letteboer, Jan Klooster,[...]. Invest Ophthalmol Vis Sci 2005
55
100

Detailed clinical characterisation, unique features and natural history of autosomal recessive RDH12-associated retinal degeneration.
Abigail T Fahim, Zaina Bouzia, Kari H Branham, Neruban Kumaran, Mauricio E Vargas, Kecia L Feathers, N Dayanthi Perera, Kelly Young, Naheed W Khan, John R Heckenlively,[...]. Br J Ophthalmol 2019
13
100

Relative frequencies of inherited retinal dystrophies and optic neuropathies in Southern France: assessment of 21-year data management.
Beatrice Bocquet, Annie Lacroux, Marie-Odile Surget, Corinne Baudoin, Virginie Marquette, Gael Manes, Maxime Hebrard, Audrey Sénéchal, Cecile Delettre, Anne-Francoise Roux,[...]. Ophthalmic Epidemiol 2013
36
100

Novel human pathological mutations. Gene symbol: CRB1. Disease: Leber congenital amaurosis.
Elena Vallespin, A Avila-Fernandez, C Velez-Monsalve, B Almoguera, M Martinez-Garcia, B Gomez-Dominguez, C Gonzalez-Roubaud, D Cantalapiedra, M J Trujillo-Tiebas, C Ayuso. Hum Genet 2010
4
100

Molecular genetics of Leber congenital amaurosis in Chinese: New data from 66 probands and mutation overview of 159 probands.
Yan Xu, Xueshan Xiao, Shiqiang Li, Xiaoyun Jia, Wei Xin, Panfeng Wang, Wenmin Sun, Li Huang, Xiangming Guo, Qingjiong Zhang. Exp Eye Res 2016
23
100

CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina.
Adrienne K Mehalow, Shuhei Kameya, Richard S Smith, Norman L Hawes, James M Denegre, James A Young, Lesley Bechtold, Neena B Haider, Ulrich Tepass, John R Heckenlively,[...]. Hum Mol Genet 2003
273
100

Clinical and genetic characteristics of 251 consecutive patients with macular and cone/cone-rod dystrophy.
Johannes Birtel, Tobias Eisenberger, Martin Gliem, Philipp L Müller, Philipp Herrmann, Christian Betz, Diana Zahnleiter, Christine Neuhaus, Steffen Lenzner, Frank G Holz,[...]. Sci Rep 2018
76
100

SCWRL and MolIDE: computer programs for side-chain conformation prediction and homology modeling.
Qiang Wang, Adrian A Canutescu, Roland L Dunbrack. Nat Protoc 2008
124
100

CRB1-Associated Retinal Dystrophies: A Prospective Natural History Study in Anticipation of Future Clinical Trials.
Xuan-Thanh-An Nguyen, Mays Talib, Mary J van Schooneveld, Jan Wijnholds, Maria M van Genderen, Nicoline E Schalij-Delfos, Caroline C W Klaver, Herman E Talsma, Marta Fiocco, Ralph J Florijn,[...]. Am J Ophthalmol 2021
1
100

Phenotypic features of CRB1-associated early-onset severe retinal dystrophy and the different molecular approaches to identifying the disease-causing variants.
Bohdan Kousal, Lubica Dudakova, Renata Gaillyova, Michaela Hejtmankova, Pavel Diblik, Michel Michaelides, Petra Liskova. Graefes Arch Clin Exp Ophthalmol 2016
11
100

CRB1 mutations in inherited retinal dystrophies.
Kinga Bujakowska, Isabelle Audo, Saddek Mohand-Saïd, Marie-Elise Lancelot, Aline Antonio, Aurore Germain, Thierry Léveillard, Mélanie Letexier, Jean-Paul Saraiva, Christine Lonjou,[...]. Hum Mutat 2012
111
100

Leber congenital amaurosis: comprehensive survey of the genetic heterogeneity, refinement of the clinical definition, and genotype-phenotype correlations as a strategy for molecular diagnosis.
Sylvain Hanein, Isabelle Perrault, Sylvie Gerber, Gaëlle Tanguy, Fabienne Barbet, Dominique Ducroq, Patrick Calvas, Hélène Dollfus, Christian Hamel, Tuija Lopponen,[...]. Hum Mutat 2004
257
100


Study of the involvement of the RGR, CRPB1, and CRB1 genes in the pathogenesis of autosomal recessive retinitis pigmentosa.
S Bernal, M Calaf, M Garcia-Hoyos, B Garcia-Sandoval, J Rosell, A Adan, C Ayuso, M Baiget. J Med Genet 2003
62
100

PALS1 is essential for retinal pigment epithelium structure and neural retina stratification.
Bokyung Park, Celso Henrique Alves, Ditte M Lundvig, Naoyuki Tanimoto, Susanne C Beck, Gesine Huber, Fabrice Richard, Jan Klooster, Till F M Andlauer, Eric C Swindell,[...]. J Neurosci 2011
38
100

Generation of the human iPSC line ESi082-A from a patient with macular dystrophy associated to mutations in the CRB1 gene.
Alberto Cañibano-Hernández, Lourdes Valdes-Sanchez, Ana B Garcia-Delgado, Beatriz Ponte-Zúñiga, Francisco J Diaz-Corrales, Berta de la Cerda. Stem Cell Res 2021
1
100

Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.
Robert H Henderson, Donna S Mackay, Zheng Li, Phillip Moradi, Panagiotis Sergouniotis, Isabelle Russell-Eggitt, Dorothy A Thompson, Anthony G Robson, Graham E Holder, Andrew R Webster,[...]. Br J Ophthalmol 2011
76
100

Expanding the phenotypic spectrum in RDH12-associated retinal disease.
Hilary A Scott, Emily M Place, Kevin Ferenchak, Erin Zampaglione, Naomi E Wagner, Katherine R Chao, Stephanie P DiTroia, Daniel Navarro-Gomez, Shizuo Mukai, Rachel M Huckfeldt,[...]. Cold Spring Harb Mol Case Stud 2020
5
100

Highly accurate protein structure prediction with AlphaFold.
John Jumper, Richard Evans, Alexander Pritzel, Tim Green, Michael Figurnov, Olaf Ronneberger, Kathryn Tunyasuvunakool, Russ Bates, Augustin Žídek, Anna Potapenko,[...]. Nature 2021
400
100

Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12).
A I den Hollander, J B ten Brink, Y J de Kok, S van Soest, L I van den Born, M A van Driel, D J van de Pol, A M Payne, S S Bhattacharya, U Kellner,[...]. Nat Genet 1999
356
100

Genotyping microarray (disease chip) for Leber congenital amaurosis: detection of modifier alleles.
Jana Zernant, Maigi Külm, Sharola Dharmaraj, Anneke I den Hollander, Isabelle Perrault, Markus N Preising, Birgit Lorenz, Josseline Kaplan, Frans P M Cremers, Irene Maumenee,[...]. Invest Ophthalmol Vis Sci 2005
126
100

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
100

Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease.
Keren J Carss, Gavin Arno, Marie Erwood, Jonathan Stephens, Alba Sanchis-Juan, Sarah Hull, Karyn Megy, Detelina Grozeva, Eleanor Dewhurst, Samantha Malka,[...]. Am J Hum Genet 2017
196
100

Comprehensive identification of mRNA isoforms reveals the diversity of neural cell-surface molecules with roles in retinal development and disease.
Thomas A Ray, Kelly Cochran, Chris Kozlowski, Jingjing Wang, Graham Alexander, Martha A Cady, William J Spencer, Philip A Ruzycki, Brian S Clark, Annelies Laeremans,[...]. Nat Commun 2020
19
100

Pals1/Mpp5 is required for correct localization of Crb1 at the subapical region in polarized Muller glia cells.
Agnes G S H van Rossum, Wendy M Aartsen, Jan Meuleman, Jan Klooster, Anna Malysheva, Inge Versteeg, Jean-Pierre Arsanto, André Le Bivic, Jan Wijnholds. Hum Mol Genet 2006
81
100

The phenotypic variability of retinal dystrophies associated with mutations in CRX, with report of a novel macular dystrophy phenotype.
Sarah Hull, Gavin Arno, Vincent Plagnol, Sarah Chamney, Isabelle Russell-Eggitt, Dorothy Thompson, Simon C Ramsden, Graeme C M Black, Anthony Robson, Graham E Holder,[...]. Invest Ophthalmol Vis Sci 2014
39
100

CRB1 mutation spectrum in inherited retinal dystrophies.
Anneke I den Hollander, Jason Davis, Saskia D van der Velde-Visser, Marijke N Zonneveld, Chiara O Pierrottet, Robert K Koenekoop, Ulrich Kellner, L Ingeborgh van den Born, John R Heckenlively, Carel B Hoyng,[...]. Hum Mutat 2004
135
100

Mutations in the CRB1 gene cause Leber congenital amaurosis.
A J Lotery, S G Jacobson, G A Fishman, R G Weleber, A B Fulton, P Namperumalsamy, E Héon, A V Levin, S Grover, J R Rosenow,[...]. Arch Ophthalmol 2001
179
100

Genotypic and Phenotypic Characteristics of CRB1-Associated Retinal Dystrophies: A Long-Term Follow-up Study.
Mays Talib, Mary J van Schooneveld, Maria M van Genderen, Jan Wijnholds, Ralph J Florijn, Jacoline B Ten Brink, Nicoline E Schalij-Delfos, Gislin Dagnelie, Frans P M Cremers, Ron Wolterbeek,[...]. Ophthalmology 2017
37
100

Crumbs proteins regulate layered retinal vascular development required for vision.
Sunggeun Son, Minsub Cho, Junyeop Lee. Biochem Biophys Res Commun 2020
3
100

[Genotype-Phenotype Correlations in Patients with CRB1 Mutations].
C Papadopoulou Laiou, M N Preising, H J Bolz, B Lorenz. Klin Monbl Augenheilkd 2017
2
100


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.