A citation-based method for searching scientific literature

Antoni Matilla-Dueñas. Adv Exp Med Biol 2012
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity



SCA3: neurological features, pathogenesis and animal models.
Olaf Riess, Udo Rüb, Annalisa Pastore, Peter Bauer, Ludger Schöls. Cerebellum 2008
149
42

The spinocerebellar ataxias: clinical aspects and molecular genetics.
Antoni Matilla-Dueñas, Marc Corral-Juan, Victor Volpini, Ivelisse Sanchez. Adv Exp Med Biol 2012
40
35

Clinical features, neurogenetics and neuropathology of the polyglutamine spinocerebellar ataxias type 1, 2, 3, 6 and 7.
Udo Rüb, Ludger Schöls, Henry Paulson, Georg Auburger, Pawel Kermer, Joanna C Jen, Kay Seidel, Horst-Werner Korf, Thomas Deller. Prog Neurobiol 2013
177
35

Chronic treatment with 17-DMAG improves balance and coordination in a new mouse model of Machado-Joseph disease.
Anabela Silva-Fernandes, Sara Duarte-Silva, Andreia Neves-Carvalho, Marina Amorim, Carina Soares-Cunha, Pedro Oliveira, Kenneth Thirstrup, Andreia Teixeira-Castro, Patrícia Maciel. Neurotherapeutics 2014
67
28

Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data.
Heike Jacobi, Kathrin Reetz, Sophie Tezenas du Montcel, Peter Bauer, Caterina Mariotti, Lorenzo Nanetti, Maria Rakowicz, Anna Sulek, Alexandra Durr, Perrine Charles,[...]. Lancet Neurol 2013
108
28

Update on degenerative ataxias.
Thomas Klockgether. Curr Opin Neurol 2011
66
28

Brain pathology of spinocerebellar ataxias.
Kay Seidel, Sonny Siswanto, Ewout R P Brunt, Wilfred den Dunnen, Horst-Werner Korf, Udo Rüb. Acta Neuropathol 2012
214
28

Machado-Joseph disease/spinocerebellar ataxia type 3.
Henry Paulson. Handb Clin Neurol 2012
80
28

Neuropathology of degenerative ataxias.
Jonathan D Fratkin, P J S Vig. Handb Clin Neurol 2012
16
28

New subtype of spinocerebellar ataxia with altered vertical eye movements mapping to chromosome 1p32.
Carmen Serrano-Munuera, Marc Corral-Juan, Giovanni Stevanin, Hector San Nicolás, Carles Roig, Jordi Corral, Berta Campos, Laura de Jorge, Carlos Morcillo-Suárez, Arcadi Navarro,[...]. JAMA Neurol 2013
24
21

Nonmotor and extracerebellar features in Machado-Joseph disease: a review.
José Luiz Pedroso, Marcondes C França, Pedro Braga-Neto, Anelyssa D'Abreu, Maria Luiza Saraiva-Pereira, Jonas A Saute, Hélio A Teive, Paulo Caramelli, Laura Bannach Jardim, Iscia Lopes-Cendes,[...]. Mov Disord 2013
61
21

Endocannabinoid signalling and the deteriorating brain.
Vincenzo Di Marzo, Nephi Stella, Andreas Zimmer. Nat Rev Neurosci 2015
197
21

Polyglutamine-expanded ataxin-3 causes cerebellar dysfunction of SCA3 transgenic mice by inducing transcriptional dysregulation.
An-Hsun Chou, Tu-Hsueh Yeh, Pin Ouyang, Ying-Ling Chen, Si-Ying Chen, Hung-Li Wang. Neurobiol Dis 2008
123
21

Endocannabinoid-hydrolysing enzymes in the post-mortem cerebellum of humans affected by hereditary autosomal dominant ataxias.
Carmen Rodríguez-Cueto, Cristina Benito, Julián Romero, Mariluz Hernández-Gálvez, María Gómez-Ruiz, Javier Fernández-Ruiz. Pathobiology 2014
9
33

Cannabinoid CB2 receptor: a new target for controlling neural cell survival?
Javier Fernández-Ruiz, Julián Romero, Guillermo Velasco, Rosa M Tolón, José A Ramos, Manuel Guzmán. Trends Pharmacol Sci 2007
270
21

Autophagy induction reduces mutant ataxin-3 levels and toxicity in a mouse model of spinocerebellar ataxia type 3.
Fiona M Menzies, Jeannette Huebener, Maurizio Renna, Michael Bonin, Olaf Riess, David C Rubinsztein. Brain 2010
183
21

Silencing ataxin-3 mitigates degeneration in a rat model of Machado-Joseph disease: no role for wild-type ataxin-3?
Sandro Alves, Isabel Nascimento-Ferreira, Noëlle Dufour, Raymonde Hassig, Gwennaëlle Auregan, Clévio Nóbrega, Emmanuel Brouillet, Philippe Hantraye, Maria C Pedroso de Lima, Nicole Déglon,[...]. Hum Mol Genet 2010
74
21

Cannabinoids in Neurodegenerative Disorders and Stroke/Brain Trauma: From Preclinical Models to Clinical Applications.
Javier Fernández-Ruiz, María A Moro, José Martínez-Orgado. Neurotherapeutics 2015
75
21

Changes in CB(1) and CB(2) receptors in the post-mortem cerebellum of humans affected by spinocerebellar ataxias.
Carmen Rodríguez-Cueto, Cristina Benito, Javier Fernández-Ruiz, Julián Romero, Mariluz Hernández-Gálvez, María Gómez-Ruiz. Br J Pharmacol 2014
33
21

Cell biology of spinocerebellar ataxia.
Harry T Orr. J Cell Biol 2012
106
21

Beclin 1 mitigates motor and neuropathological deficits in genetic mouse models of Machado-Joseph disease.
Isabel Nascimento-Ferreira, Clévio Nóbrega, Ana Vasconcelos-Ferreira, Isabel Onofre, David Albuquerque, Célia Aveleira, Hirokazu Hirai, Nicole Déglon, Luís Pereira de Almeida. Brain 2013
72
21

The pathogenesis of spinocerebellar ataxia.
Arnulf H Koeppen. Cerebellum 2005
148
21

Polyglutamine aggregation in Huntington's disease and spinocerebellar ataxia type 3: similar mechanisms in aggregate formation.
K Seidel, S Siswanto, M Fredrich, M Bouzrou, E R Brunt, F W van Leeuwen, H H Kampinga, H-W Korf, U Rüb, W F A den Dunnen. Neuropathol Appl Neurobiol 2016
27
21

Pathways to motor incoordination: the inherited ataxias.
Franco Taroni, Stefano DiDonato. Nat Rev Neurosci 2004
123
21

Mouse models of spinocerebellar ataxia type 3 (Machado-Joseph disease).
Veronica F Colomer Gould. Neurotherapeutics 2012
23
21

Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms.
T Schmitz-Hübsch, M Coudert, P Bauer, P Giunti, C Globas, L Baliko, A Filla, C Mariotti, M Rakowicz, P Charles,[...]. Neurology 2008
168
14

Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study.
Anne Kjersti Erichsen, Jeanette Koht, Asbjørg Stray-Pedersen, Michael Abdelnoor, Chantal M E Tallaksen. Brain 2009
124
14

Scale for the assessment and rating of ataxia: development of a new clinical scale.
T Schmitz-Hübsch, S Tezenas du Montcel, L Baliko, J Berciano, S Boesch, C Depondt, P Giunti, C Globas, J Infante, J-S Kang,[...]. Neurology 2006
941
14

Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement.
Hatasu Kobayashi, Koji Abe, Tohru Matsuura, Yoshio Ikeda, Toshiaki Hitomi, Yuji Akechi, Toshiyuki Habu, Wanyang Liu, Hiroko Okuda, Akio Koizumi. Am J Hum Genet 2011
166
14

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.
H T Orr, M Y Chung, S Banfi, T J Kwiatkowski, A Servadio, A L Beaudet, A E McCall, L A Duvick, L P Ranum, H Y Zoghbi. Nat Genet 1993
14

The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study.
H Jacobi, P Bauer, P Giunti, R Labrum, M G Sweeney, P Charles, A Dürr, C Marelli, C Globas, C Linnemann,[...]. Neurology 2011
121
14

Locus for familial migrainous vertigo disease maps to chromosome 5q35.
Fayez Bahmad, Steven R DePalma, Saumil N Merchant, Roberta L Bezerra, Carlos A Oliveira, Christine E Seidman, Jonathan G Seidman. Ann Otol Rhinol Laryngol 2009
32
14

Mini-review: spinocerebellar ataxias: an update of SCA genes.
Alexis Trott, Lucien J Houenou. Recent Pat DNA Gene Seq 2012
14
14

MicroRNA expression profiling in blood from fragile X-associated tremor/ataxia syndrome patients.
M I Alvarez-Mora, L Rodriguez-Revenga, I Madrigal, F Torres-Silva, E Mateu-Huertas, E Lizano, M R Friedländer, E Martí, X Estivill, M Milà. Genes Brain Behav 2013
20
14

Ataxia in mitochondrial disorders.
Massimo Zeviani, Alessandro Simonati, Laurence A Bindoff. Handb Clin Neurol 2012
20
14

Suggestive linkage to chromosome 6q in families with bilateral vestibulopathy.
J C Jen, H Wang, H Lee, C Sabatti, R Trent, I Hannigan, K Brantberg, G M Halmagyi, S F Nelson, R W Baloh. Neurology 2004
24
14

PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine.
Alice R Gardiner, Kailash P Bhatia, Maria Stamelou, Russell C Dale, Manju A Kurian, Susanne A Schneider, G M Wali, Tim Counihan, Anthony H Schapira, Sian D Spacey,[...]. Neurology 2012
112
14

Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxia.
Sascha Vermeer, Alexander Hoischen, Rowdy P P Meijer, Christian Gilissen, Kornelia Neveling, Nienke Wieskamp, Arjan de Brouwer, Michel Koenig, Mathieu Anheim, Mirna Assoum,[...]. Am J Hum Genet 2010
83
14

Sensory neuropathy as part of the cerebellar ataxia neuropathy vestibular areflexia syndrome.
D J Szmulewicz, J A Waterston, G M Halmagyi, S Mossman, A M Chancellor, C A McLean, E Storey. Neurology 2011
64
14

Exome sequencing reveals a homozygous SYT14 mutation in adult-onset, autosomal-recessive spinocerebellar ataxia with psychomotor retardation.
Hiroshi Doi, Kunihiro Yoshida, Takao Yasuda, Mitsunori Fukuda, Yoko Fukuda, Hiroshi Morita, Shu-ichi Ikeda, Rumiko Kato, Yoshinori Tsurusaki, Noriko Miyake,[...]. Am J Hum Genet 2011
57
14

Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticity.
Monia B Hammer, Ghada Eleuch-Fayache, Lucia V Schottlaender, Houda Nehdi, J Raphael Gibbs, Sampath K Arepalli, Sean B Chong, Dena G Hernandez, Anna Sailer, Guoxiang Liu,[...]. Am J Hum Genet 2013
88
14

Identification and functional study of a new missense mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11).
Qing Sang, Xukun Yan, Huan Wang, Ruizhi Feng, Xiang Fei, Duan Ma, Qinghe Xing, Qiaoli Li, Xinzhi Zhao, Li Jin,[...]. PLoS One 2013
13
15

Allelic variants in TLR10 gene may influence bilateral affectation and clinical course of Meniere's disease.
Teresa Requena, Irene Gazquez, Antonia Moreno, Angel Batuecas, Ismael Aran, Andres Soto-Varela, Sofia Santos-Perez, Nicolas Perez, Herminio Perez-Garrigues, Alicia Lopez-Nevot,[...]. Immunogenetics 2013
34
14

Phenotypic and genetic analysis of a large family with migraine-associated vertigo.
Hane Lee, Joanna C Jen, Yoon-Hee Cha, Stanley F Nelson, Robert W Baloh. Headache 2008
22
14


A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity.
Hane Lee, Joanna C Jen, Hui Wang, Zugen Chen, Hafsa Mamsa, Chiara Sabatti, Robert W Baloh, Stanley F Nelson. Hum Mol Genet 2006
37
14


Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1).
Melody Caramins, James G Colebatch, Matthew N Bainbridge, Steven S Scherer, Charles K Abrams, Emma L Hackett, Mona M Freidin, Shalini N Jhangiani, Min Wang, Yuanqing Wu,[...]. Hum Mol Genet 2013
15
14

MICA-STR A.4 is associated with slower hearing loss progression in patients with Ménière's disease.
Irene Gazquez, Antonia Moreno, Ismael Aran, Andres Soto-Varela, Sofia Santos, Herminio Perez-Garrigues, Alicia Lopez-Nevot, Teresa Requena, Miguel Angel Lopez-Nevot, Jose Antonio Lopez-Escamez. Otol Neurotol 2012
19
14


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.