A citation-based method for searching scientific literature

Lizbeth E García-Velázquez, Samuel Canizales-Quinteros, Sandra Romero-Hidalgo, Adriana Ochoa-Morales, Leticia Martínez-Ruano, Carla Márquez-Luna, Víctor Acuña-Alonzo, M Teresa Villarreal-Molina, M Elisa Alonso-Vilatela, Petra Yescas-Gómez. Neurogenetics 2014
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia.
J Jonasson, V Juvonen, P Sistonen, J Ignatius, D Johansson, E J Björck, J Wahlström, A Melberg, G Holmgren, L Forsgren,[...]. Eur J Hum Genet 2000
40
66

Analysis of CAG repeats in five SCA loci in Mexican population: epidemiological evidence of a SCA7 founder effect.
J J Magaña, Y S Tapia-Guerrero, L Velázquez-Pérez, C M Cerecedo-Zapata, M Maldonado-Rodríguez, J S Jano-Ito, N Leyva-García, R González-Piña, E Martínez-Cruz, O Hernández-Hernández,[...]. Clin Genet 2014
25
44

Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7).
G David, A Dürr, G Stevanin, G Cancel, N Abbas, A Benomar, S Belal, A S Lebre, M Abada-Bendib, D Grid,[...]. Hum Mol Genet 1998
208
44

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion.
G David, N Abbas, G Stevanin, A Dürr, G Yvert, G Cancel, C Weber, G Imbert, F Saudou, E Antoniou,[...]. Nat Genet 1997
607
44

The hereditary adult-onset ataxias in South Africa.
Alan Bryer, Amanda Krause, Pierre Bill, Virginia Davids, Daphne Bryant, James Butler, Jeannine Heckmann, Rajkumar Ramesar, Jacquie Greenberg. J Neurol Sci 2003
62
44



Origin of the SCA7 gene mutation in South Africa: implications for molecular diagnostics.
J Greenberg, G A E Solomon, A A Vorster, J Heckmann, A Bryer. Clin Genet 2006
21
33

Inherited polyglutamine spinocerebellar ataxias in South Africa.
D C Smith, A Bryer, L M Watson, L J Greenberg. S Afr Med J 2012
20
33

Autosomal dominant cerebellar ataxia: frequency analysis and clinical characterization of 45 families from Portugal.
J Vale, P Bugalho, I Silveira, J Sequeiros, J Guimarães, P Coutinho. Eur J Neurol 2010
41
33

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
182
33

Origin of the spinocerebellar ataxia type 7 gene mutation in Mexican population.
J J Magaña, R Gómez, M Maldonado-Rodríguez, L Velázquez-Pérez, Y S Tapia-Guerrero, H Cortés, N Leyva-García, O Hernández-Hernández, B Cisneros. Cerebellum 2013
20
33

Spinocerebellar ataxia type 7 associated with pigmentary retinal dystrophy.
A Michalik, J-J Martin, C Van Broeckhoven. Eur J Hum Genet 2004
88
33

Evidence for a common founder effect amongst South African and Zambian individuals with Spinocerebellar ataxia type 7.
Danielle C Smith, Masharip Atadzhanov, Mwila Mwaba, Leslie Jacqueline Greenberg. J Neurol Sci 2015
11
33


Clinical and genetic analysis of spinocerebellar ataxia in Mali.
M Traoré, T Coulibaly, K G Meilleur, A La Pean, M Sangaré, G Landouré, F Mochel, M Karambé, C O Guinto, K H Fischbeck. Eur J Neurol 2011
12
22

The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies.
Luis Ruano, Claudia Melo, M Carolina Silva, Paula Coutinho. Neuroepidemiology 2014
286
22

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1.
Y Kawaguchi, T Okamoto, M Taniwaki, M Aizawa, M Inoue, S Katayama, H Kawakami, S Nakamura, M Nishimura, I Akiguchi. Nat Genet 1994
22

Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
Alfredo Brusco, Cinzia Gellera, Claudia Cagnoli, Alessandro Saluto, Alessia Castucci, Chiara Michielotto, Vincenza Fetoni, Caterina Mariotti, Nicola Migone, Stefano Di Donato,[...]. Arch Neurol 2004
101
22

Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype study.
C Gaspar, I Lopes-Cendes, S Hayes, J Goto, K Arvidsson, A Dias, I Silveira, P Maciel, P Coutinho, M Lima,[...]. Am J Hum Genet 2001
85
22

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
22

CAG repeat instability at SCA2 locus: anchoring CAA interruptions and linked single nucleotide polymorphisms.
S Choudhry, M Mukerji, A K Srivastava, S Jain, S K Brahmachari. Hum Mol Genet 2001
94
22

Molecular and clinical studies in SCA-7 define a broad clinical spectrum and the infantile phenotype.
C S Benton, R de Silva, S L Rutledge, S Bohlega, T Ashizawa, H Y Zoghbi. Neurology 1998
124
22

Genomic context drives SCA7 CAG repeat instability, while expressed SCA7 cDNAs are intergenerationally and somatically stable in transgenic mice.
Randell T Libby, Darren G Monckton, Ying-Hui Fu, Refugio A Martinez, John P McAbney, R Lau, David D Einum, K Nichol, Carol B Ware, Louis J Ptacek,[...]. Hum Mol Genet 2003
55
22

Spinocerebellar ataxias: genotype-phenotype correlations in 104 Brazilian families.
Hélio A G Teive, Renato P Munhoz, Walter O Arruda, Iscia Lopes-Cendes, Salmo Raskin, Lineu C Werneck, Tetsuo Ashizawa. Clinics (Sao Paulo) 2012
48
22

Expanded polyglutamines induce neurodegeneration and trans-neuronal alterations in cerebellum and retina of SCA7 transgenic mice.
G Yvert, K S Lindenberg, S Picaud, G B Landwehrmeyer, J A Sahel, J L Mandel. Hum Mol Genet 2000
120
22

Polyglutamine diseases: where does toxicity come from? what is toxicity? where are we going?
Toshiaki Takahashi, Shinichi Katada, Osamu Onodera. J Mol Cell Biol 2010
105
22

Spinocerebellar ataxia type 7 (SCA7) shows a cone-rod dystrophy phenotype.
Tomas S Aleman, Artur V Cideciyan, Nicholas J Volpe, Giovanni Stevanin, Alexis Brice, Samuel G Jacobson. Exp Eye Res 2002
72
22

Neuro-ophthalmologic features of spinocerebellar ataxia type 7.
Randee C Miller, Aash Tewari, Joel A Miller, James Garbern, Gregory P Van Stavern. J Neuroophthalmol 2009
28
22


Spinocerebellar ataxia type 7 (SCA7) - correlations between phenotype and genotype in one large Belgian family.
J Martin, N Van Regemorter, J Del-Favero, A Löfgren, C Van Broeckhoven. J Neurol Sci 1999
48
22

EMQN Best Practice Guidelines for molecular genetic testing of SCAs.
Jorge Sequeiros, Joanne Martindale, Sara Seneca, Paola Giunti, Outi Kämäräinen, Victor Volpini, Helga Weirich, Kyproula Christodoulou, Nazli Bazak, Richard Sinke,[...]. Eur J Hum Genet 2010
26
22

Somatic instability of expanded CAG repeats of ATXN7 in Japanese patients with spinocerebellar ataxia type 7.
Satoshi Katagiri, Takaaki Hayashi, Tomokazu Takeuchi, Hisashi Yamada, Tamaki Gekka, Kiyokazu Kawabe, Akira Kurita, Hiroshi Tsuneoka. Doc Ophthalmol 2015
6
33

Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia.
E Storey, D du Sart, J H Shaw, P Lorentzos, L Kelly, R J McKinley Gardner, S M Forrest, I Biros, G A Nicholson. Am J Med Genet 2000
53
22

Analysis of spinocerebellar ataxia type 2 gene and haplotype analysis: (CCG)1-2 polymorphism and contribution to founder effect.
K Mizushima, M Watanabe, I Kondo, K Okamoto, M Shizuka, K Abe, M Aoki, M Shoji. J Med Genet 1999
13
22

Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study.
Heike Jacobi, Sophie Tezenas du Montcel, Peter Bauer, Paola Giunti, Arron Cook, Robyn Labrum, Michael H Parkinson, Alexandra Durr, Alexis Brice, Perrine Charles,[...]. Lancet Neurol 2015
127
22


Miglustat in patients with Niemann-Pick disease Type C (NP-C): a multicenter observational retrospective cohort study.
M Pineda, J E Wraith, E Mengel, F Sedel, W-L Hwu, M Rohrbach, B Bembi, M Walterfang, G C Korenke, T Marquardt,[...]. Mol Genet Metab 2009
124
11

Disease and patient characteristics in NP-C patients: findings from an international disease registry.
Marc C Patterson, Eugen Mengel, Frits A Wijburg, Audrey Muller, Barbara Schwierin, Harir Drevon, Marie T Vanier, Mercé Pineda. Orphanet J Rare Dis 2013
122
11

Respiratory disease in Niemann-Pick type C2 is caused by pulmonary alveolar proteinosis.
M Griese, F Brasch, V R Aldana, M M Cabrera, U Goelnitz, E Ikonen, B J Karam, G Liebisch, M D Linder, P Lohse,[...]. Clin Genet 2010
56
11


Genetic screening for Niemann-Pick disease type C in adults with neurological and psychiatric symptoms: findings from the ZOOM study.
Peter Bauer, David J Balding, Hans H Klünemann, David E J Linden, Daniel S Ory, Mercè Pineda, Josef Priller, Frederic Sedel, Audrey Muller, Harbajan Chadha-Boreham,[...]. Hum Mol Genet 2013
58
11

Niemann-Pick disease type C.
Marie T Vanier. Orphanet J Rare Dis 2010
656
11

Miglustat for treatment of Niemann-Pick C disease: a randomised controlled study.
Marc C Patterson, Darleen Vecchio, Helena Prady, Larry Abel, James E Wraith. Lancet Neurol 2007
379
11

Niemann-Pick type C is frequent in adult ataxia with cognitive decline and vertical gaze palsy.
Julia Schicks, Jennifer Müller Vom Hagen, Peter Bauer, Stefanie Beck-Wödl, Saskia Biskup, Ingeborg Krägeloh-Mann, Ludger Schöls, Matthis Synofzik. Neurology 2013
26
11

Cholesterol as a factor regulating intracellular localization of annexin A6 in Niemann-Pick type C human skin fibroblasts.
Malgorzata E Sztolsztener, Agnieszka Strzelecka-Kiliszek, Slawomir Pikula, Anna Tylki-Szymanska, Joanna Bandorowicz-Pikula. Arch Biochem Biophys 2010
22
11

Molecular analysis of NPC1 and NPC2 gene in 34 Niemann-Pick C Italian patients: identification and structural modeling of novel mutations.
Tatiana Fancello, Andrea Dardis, Camillo Rosano, Patrizia Tarugi, Barbara Tappino, Stefania Zampieri, Elisa Pinotti, Fabio Corsolini, Simona Fecarotta, Adele D'Amico,[...]. Neurogenetics 2009
27
11

The videofluoroscopic swallowing study shows a sustained improvement of dysphagia in children with Niemann-Pick disease type C after therapy with miglustat.
Simona Fecarotta, Michele Amitrano, Alfonso Romano, Roberto Della Casa, Diana Bruschini, Luca Astarita, Giancarlo Parenti, Generoso Andria. Am J Med Genet A 2011
28
11

Niemann-Pick C variant detection by altered sphingolipid trafficking and correlation with mutations within a specific domain of NPC1.
X Sun, D L Marks, W D Park, C L Wheatley, V Puri, J F O'Brien, D L Kraft, P A Lundquist, M C Patterson, R E Pagano,[...]. Am J Hum Genet 2001
106
11

Impaired dynamics of the late endosome/lysosome compartment in human Niemann-Pick type C skin fibroblasts carrying mutation in NPC1 gene.
Malgorzata E Sztolsztener, Agnieszka Dobrzyn, Slawomir Pikula, Anna Tylki-Szymanska, Joanna Bandorowicz-Pikula. Mol Biosyst 2012
12
11


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.