A citation-based method for searching scientific literature

Virginie G Peter, Mathieu Quinodoz, Silvia Sadio, Sebastian Held, Márcia Rodrigues, Marta Soares, Ana Berta Sousa, Luisa Coutinho Santos, Markus Damme, Carlo Rivolta. Hum Mutat 2021
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans.
Samer Khateb, Björn Kowalewski, Nicola Bedoni, Markus Damme, Netta Pollack, Ann Saada, Alexey Obolensky, Tamar Ben-Yosef, Menachem Gross, Thomas Dierks,[...]. Genet Med 2018
19
75

Identification of a novel homozygous ARSG mutation as the second cause of Usher syndrome type 4.
Víctor Abad-Morales, Rafael Navarro, Anniken Burés-Jelstrup, Esther Pomares. Am J Ophthalmol Case Rep 2020
8
75

Ataxia is the major neuropathological finding in arylsulfatase G-deficient mice: similarities and dissimilarities to Sanfilippo disease (mucopolysaccharidosis type III).
Björn Kowalewski, Peter Heimann, Theresa Ortkras, Renate Lüllmann-Rauch, Tomo Sawada, Steven U Walkley, Thomas Dierks, Markus Damme. Hum Mol Genet 2015
19
50

Arylsulfatase G inactivation causes loss of heparan sulfate 3-O-sulfatase activity and mucopolysaccharidosis in mice.
Björn Kowalewski, William C Lamanna, Roger Lawrence, Markus Damme, Stijn Stroobants, Michael Padva, Ina Kalus, Marc-André Frese, Torben Lübke, Renate Lüllmann-Rauch,[...]. Proc Natl Acad Sci U S A 2012
41
50

Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
Saima Riazuddin, Sabiha Nazli, Zubair M Ahmed, Yi Yang, Fareeha Zulfiqar, Rehan S Shaikh, Ahmed U Zafar, Shaheen N Khan, Farooq Sabar, Fouzia T Javid,[...]. Hum Mutat 2008
79
50

Genetics of Usher Syndrome: New Insights From a Meta-analysis.
Guillaume Jouret, Céline Poirsier, Marta Spodenkiewicz, Clémence Jaquin, Evan Gouy, Carl Arndt, Marc Labrousse, Dominique Gaillard, Martine Doco-Fenzy, Anne-Sophie Lebre. Otol Neurotol 2019
26
50

Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.
Saima Riazuddin, Inna A Belyantseva, Arnaud P J Giese, Kwanghyuk Lee, Artur A Indzhykulian, Sri Pratima Nandamuri, Rizwan Yousaf, Ghanshyam P Sinha, Sue Lee, David Terrell,[...]. Nat Genet 2012
143
50

Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss.
Prasanthi Namburi, Rinki Ratnapriya, Samer Khateb, Csilla H Lazar, Yael Kinarty, Alexey Obolensky, Inbar Erdinest, Devorah Marks-Ohana, Eran Pras, Tamar Ben-Yosef,[...]. Am J Hum Genet 2016
22
50

Whole USH2A Gene Sequencing Identifies Several New Deep Intronic Mutations.
Alessandro Liquori, Christel Vaché, David Baux, Catherine Blanchet, Christian Hamel, Sue Malcolm, Michel Koenig, Mireille Claustres, Anne-Françoise Roux. Hum Mutat 2016
55
50

Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
J D Eudy, M D Weston, S Yao, D M Hoover, H L Rehm, M Ma-Edmonds, D Yan, I Ahmad, J J Cheng, C Ayuso,[...]. Science 1998
276
50

Usher syndrome type 2 caused by activation of an USH2A pseudoexon: implications for diagnosis and therapy.
Christel Vaché, Thomas Besnard, Pauline le Berre, Gema García-García, David Baux, Lise Larrieu, Caroline Abadie, Catherine Blanchet, Hanno Jörn Bolz, Jose Millan,[...]. Hum Mutat 2012
74
50

Combined genetic approaches yield a 48% diagnostic rate in a large cohort of French hearing-impaired patients.
D Baux, C Vaché, C Blanchet, M Willems, C Baudoin, M Moclyn, V Faugère, R Touraine, B Isidor, D Dupin-Deguine,[...]. Sci Rep 2017
31
50

Comprehensive molecular diagnosis of 67 Chinese Usher syndrome probands: high rate of ethnicity specific mutations in Chinese USH patients.
Lichun Jiang, Xiaofang Liang, Yumei Li, Jing Wang, Jacques Eric Zaneveld, Hui Wang, Shan Xu, Keqing Wang, Binbin Wang, Rui Chen,[...]. Orphanet J Rare Dis 2015
33
50

Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis.
Crystel Bonnet, M'hamed Grati, Sandrine Marlin, Jacqueline Levilliers, Jean-Pierre Hardelin, Marine Parodi, Magali Niasme-Grare, Diana Zelenika, Marc Délépine, Delphine Feldmann,[...]. Orphanet J Rare Dis 2011
72
50

Genetic mapping and exome sequencing identify variants associated with five novel diseases.
Erik G Puffenberger, Robert N Jinks, Carrie Sougnez, Kristian Cibulskis, Rebecca A Willert, Nathan P Achilly, Ryan P Cassidy, Christopher J Fiorentini, Kory F Heiken, Johnny J Lawrence,[...]. PLoS One 2012
183
50

Variants in CIB2 cause DFNB48 and not USH1J.
K T Booth, K Kahrizi, M Babanejad, H Daghagh, G Bademci, S Arzhangi, D Zareabdollahi, D Duman, A El-Amraoui, M Tekin,[...]. Clin Genet 2018
24
50

Inframe deletion of human ESPN is associated with deafness, vestibulopathy and vision impairment.
Zubair M Ahmed, Thomas J Jaworek, Gowri N Sarangdhar, Lili Zheng, Khitab Gul, Shaheen N Khan, Thomas B Friedman, Robert A Sisk, James R Bartles, Sheikh Riazuddin,[...]. J Med Genet 2018
9
50

Disease mechanisms and gene therapy for Usher syndrome.
Gwenaelle G S Géléoc, Aziz El-Amraoui. Hear Res 2020
18
50

Midbrain tectal stem cells display diverse regenerative capacities in zebrafish.
Benjamin W Lindsey, Georgia E Aitken, Jean K Tang, Mitra Khabooshan, Alon M Douek, Celia Vandestadt, Jan Kaslin. Sci Rep 2019
16
25

Functional correction of CNS lesions in an MPS-IIIA mouse model by intracerebral AAV-mediated delivery of sulfamidase and SUMF1 genes.
Alessandro Fraldi, Kim Hemsley, Allison Crawley, Alessia Lombardi, Adeline Lau, Leanne Sutherland, Alberto Auricchio, Andrea Ballabio, John J Hopwood. Hum Mol Genet 2007
91
25

Prevalence of lysosomal storage disorders.
P J Meikle, J J Hopwood, A E Clague, W F Carey. JAMA 1999
25

MPS-IIIA mice acquire autistic behaviours with age.
Adeline A Lau, Sarah J Tamang, Kim M Hemsley. J Inherit Metab Dis 2018
5
25

Lipid autoreactivity in multiple sclerosis.
M M Blewett. Med Hypotheses 2010
11
25

Two phenotypically and functionally distinct microglial populations in adult zebrafish.
Shuting Wu, Linh T M Nguyen, Hongru Pan, Shaoli Hassan, Yimei Dai, Jin Xu, Zilong Wen. Sci Adv 2020
8
25

Endothelial heparan sulfate in angiogenesis.
Mark M Fuster, Lianchun Wang. Prog Mol Biol Transl Sci 2010
50
25

Distribution of Heparan Sulfate Oligosaccharides in Murine Mucopolysaccharidosis Type IIIA.
Kerryn Mason, Peter Meikle, John Hopwood, Maria Fuller. Metabolites 2014
5
25

Early neurodegeneration progresses independently of microglial activation by heparan sulfate in the brain of mucopolysaccharidosis IIIB mice.
Jérôme Ausseil, Nathalie Desmaris, Stéphanie Bigou, Ruben Attali, Sébastien Corbineau, Sandrine Vitry, Mathieu Parent, David Cheillan, Maria Fuller, Irène Maire,[...]. PLoS One 2008
88
25

Allogeneic stem cell transplantation does not improve neurological deficits in mucopolysaccharidosis type IIIA mice.
Adeline A Lau, Hanan Hannouche, Tina Rozaklis, Sofia Hassiotis, John J Hopwood, Kim M Hemsley. Exp Neurol 2010
29
25

Brain Pathology in Mucopolysaccharidoses (MPS) Patients with Neurological Forms.
Gustavo M Viana, David A Priestman, Frances M Platt, Shaukat Khan, Shunji Tomatsu, Alexey V Pshezhetsky. J Clin Med 2020
16
25

Myeloid/Microglial driven autologous hematopoietic stem cell gene therapy corrects a neuronopathic lysosomal disease.
Ana Sergijenko, Alexander Langford-Smith, Ai Y Liao, Claire E Pickford, John McDermott, Gabriel Nowinski, Kia J Langford-Smith, Catherine L R Merry, Simon A Jones, J Edmond Wraith,[...]. Mol Ther 2013
71
25

SWISS-MODEL: homology modelling of protein structures and complexes.
Andrew Waterhouse, Martino Bertoni, Stefan Bienert, Gabriel Studer, Gerardo Tauriello, Rafal Gumienny, Florian T Heer, Tjaart A P de Beer, Christine Rempfer, Lorenza Bordoli,[...]. Nucleic Acids Res 2018
25

Bone marrow transplantation augments the effect of brain- and spinal cord-directed adeno-associated virus 2/5 gene therapy by altering inflammation in the murine model of globoid-cell leukodystrophy.
Adarsh S Reddy, Joong H Kim, Jacqueline A Hawkins-Salsbury, Shannon L Macauley, Elisabeth T Tracy, Carole A Vogler, Xialin Han, Sheng-Kwei Song, David F Wozniak, Stephen C Fowler,[...]. J Neurosci 2011
56
25

A fluorimetric enzyme assay for the diagnosis of Sanfilippo disease type A (MPS IIIA).
E A Karpova, Voznyi YaV, J L Keulemans, A T Hoogeveen, B Winchester, I V Tsvetkova, O P van Diggelen. J Inherit Metab Dis 1996
86
25

Scoring evaluation of the natural course of mucopolysaccharidosis type IIIA (Sanfilippo syndrome type A).
Ann Meyer, Kai Kossow, Andreas Gal, Chris Mühlhausen, Kurt Ullrich, Thomas Braulke, Nicole Muschol. Pediatrics 2007
82
25

Macrophage enzyme and reduced inflammation drive brain correction of mucopolysaccharidosis IIIB by stem cell gene therapy.
Rebecca J Holley, Stuart M Ellison, Daniel Fil, Claire O'Leary, John McDermott, Nishanthi Senthivel, Alexander W W Langford-Smith, Fiona L Wilkinson, Zelpha D'Souza, Helen Parker,[...]. Brain 2018
33
25

The role of neuro-epithelial-like and radial-glial stem and progenitor cells in development, plasticity, and repair.
Benjamin W Lindsey, Zachary J Hall, Aurélie Heuzé, Jean-Stéphane Joly, Vincent Tropepe, Jan Kaslin. Prog Neurobiol 2018
23
25

Use of LysoTracker dyes: a flow cytometric study of autophagy.
Shaheen Chikte, Neelam Panchal, Gary Warnes. Cytometry A 2014
61
25

Characterization of a C57BL/6 congenic mouse strain of mucopolysaccharidosis type IIIA.
Allison C Crawley, Briony L Gliddon, Dyane Auclair, Suzanne L Brodie, Craig Hirte, Barbara M King, Maria Fuller, Kim M Hemsley, John J Hopwood. Brain Res 2006
76
25

Molecular Bases of Neurodegeneration and Cognitive Decline, the Major Burden of Sanfilippo Disease.
Rachel Heon-Roberts, Annie L A Nguyen, Alexey V Pshezhetsky. J Clin Med 2020
18
25


Synthetic Disaccharide Standards Enable Quantitative Analysis of Stored Heparan Sulfate in MPS IIIA Murine Brain Regions.
Qi Qi He, Paul J Trim, Adeline A Lau, Barbara M King, John J Hopwood, Kim M Hemsley, Marten F Snel, Vito Ferro. ACS Chem Neurosci 2019
5
25

Prenatal diagnosis of Sanfilippo syndrome.
John J Hopwood. Prenat Diagn 2005
8
25

Anxiety-related behavioral responses of pentylenetetrazole-treated zebrafish larvae to light-dark transitions.
Xiaolan Peng, Jia Lin, Yingdong Zhu, Xiuyun Liu, Yinglan Zhang, Yongxia Ji, Xue Yang, Yan Zhang, Ning Guo, Qiang Li. Pharmacol Biochem Behav 2016
32
25

Comparative Analyses of Zebrafish Anxiety-Like Behavior Using Conflict-Based Novelty Tests.
Elana V Kysil, Darya A Meshalkina, Erin E Frick, David J Echevarria, Denis B Rosemberg, Caio Maximino, Monica Gomes Lima, Murilo S Abreu, Ana C Giacomini, Leonardo J G Barcellos,[...]. Zebrafish 2017
92
25

Measuring thigmotaxis in larval zebrafish.
S J Schnörr, P J Steenbergen, M K Richardson, D L Champagne. Behav Brain Res 2012
151
25

A novel conditional Sgsh knockout mouse model recapitulates phenotypic and neuropathic deficits of Sanfilippo syndrome.
Adeline A Lau, Barbara M King, Carly L Thorsen, Sofia Hassiotis, Helen Beard, Paul J Trim, Lauren S Whyte, Sarah J Tamang, Stephen K Duplock, Marten F Snel,[...]. J Inherit Metab Dis 2017
8
25


Multimodal imaging and genetic findings in a case of ARSG-related atypical Usher syndrome.
Nicholas H Fowler, May I El-Rashedy, Emad A Chishti, Craig W Vander Kooi, Ramiro S Maldonado. Ophthalmic Genet 2021
1
100

Lysosomal storage diseases.
Frances M Platt, Alessandra d'Azzo, Beverly L Davidson, Elizabeth F Neufeld, Cynthia J Tifft. Nat Rev Dis Primers 2018
214
25

Mucopolysaccharidosis type IIIA: clinical spectrum and genotype-phenotype correlations.
Marlies J Valstar, Sanne Neijs, Hennie T Bruggenwirth, Renske Olmer, George J G Ruijter, Ron A Wevers, Otto P van Diggelen, Ben J Poorthuis, Dicky J Halley, Frits A Wijburg. Ann Neurol 2010
110
25


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.