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List of co-cited articles
1134 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.
S M Pulst, A Nechiporuk, T Nechiporuk, S Gispert, X N Chen, I Lopes-Cendes, S Pearlman, S Starkman, G Orozco-Diaz, A Lunkes,[...]. Nat Genet 1996
870
53

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats.
G Imbert, F Saudou, G Yvert, D Devys, Y Trottier, J M Garnier, C Weber, J L Mandel, G Cancel, N Abbas,[...]. Nat Genet 1996
703
37

Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families.
G Cancel, A Dürr, O Didierjean, G Imbert, K Bürk, A Lezin, S Belal, A Benomar, M Abada-Bendib, C Vial,[...]. Hum Mol Genet 1997
192
33

Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.
K Sanpei, H Takano, S Igarashi, T Sato, M Oyake, H Sasaki, A Wakisaka, K Tashiro, Y Ishida, T Ikeuchi,[...]. Nat Genet 1996
610
30

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
649
25

Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS.
Andrew C Elden, Hyung-Jun Kim, Michael P Hart, Alice S Chen-Plotkin, Brian S Johnson, Xiaodong Fang, Maria Armakola, Felix Geser, Robert Greene, Min Min Lu,[...]. Nature 2010
755
21

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
18

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
18

Spinocerebellar ataxia 2 (SCA2).
Isabel Lastres-Becker, Udo Rüb, Georg Auburger. Cerebellum 2008
137
18

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
O Zhuchenko, J Bailey, P Bonnen, T Ashizawa, D W Stockton, C Amos, W B Dobyns, S H Subramony, H Y Zoghbi, C C Lee. Nat Genet 1997
17

Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies.
R Estrada, J Galarraga, G Orozco, A Nodarse, G Auburger. Acta Neuropathol 1999
157
16


Spinocerebellar ataxia type 2: polyQ repeat variation in the CACNA1A calcium channel modifies age of onset.
Stefan-M Pulst, Nieves Santos, Dai Wang, Huiying Yang, Duong Huynh, Luis Velazquez, K Pattie Figueroa. Brain 2005
92
17

Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families.
A Dürr, D Smadja, G Cancel, A Lezin, G Stevanin, J Mikol, R Bellance, G G Buisson, H Chneiweiss, J Dellanave. Brain 1995
166
15

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1.
S Gispert, R Twells, G Orozco, A Brice, J Weber, L Heredero, K Scheufler, B Riley, R Allotey, C Nothers. Nat Genet 1993
290
15

SCA2 trinucleotide expansion in German SCA patients.
O Riess, F A Laccone, S Gispert, L Schöls, C Zühlke, A M Vieira-Saecker, S Herlt, K Wessel, J T Epplen, B H Weber,[...]. Neurogenetics 1997
67
22

Cognitive deficits in spinocerebellar ataxia type 1, 2, and 3.
K Bürk, C Globas, S Bösch, T Klockgether, C Zühlke, I Daum, J Dichgans. J Neurol 2003
131
15

The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates.
P Giunti, G Sabbadini, M G Sweeney, M B Davis, L Veneziano, E Mantuano, A Federico, R Plasmati, M Frontali, N W Wood. Brain 1998
80
17

Dominantly inherited olivopontocerebellar atrophy from eastern Cuba. Clinical, neuropathological, and biochemical findings.
G Orozco, R Estrada, T L Perry, J Araña, R Fernandez, A Gonzalez-Quevedo, J Galarraga, S Hansen. J Neurol Sci 1989
147
13

Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese.
K Gwinn-Hardy, J Y Chen, H C Liu, T Y Liu, M Boss, W Seltzer, A Adam, A Singleton, W Koroshetz, C Waters,[...]. Neurology 2000
147
13

SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein.
K Nakamura, S Y Jeong, T Uchihara, M Anno, K Nagashima, T Nagashima, S Ikeda, S Tsuji, I Kanazawa. Hum Mol Genet 2001
454
13

Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds.
L Schöls, S Gispert, M Vorgerd, A M Menezes Vieira-Saecker, P Blanke, G Auburger, G Amoiridis, S Meves, J T Epplen, H Przuntek,[...]. Arch Neurol 1997
97
12

Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis.
B P C van de Warrenburg, R J Sinke, C C Verschuuren-Bemelmans, H Scheffer, E R Brunt, P F Ippel, J A Maat-Kievit, D Dooijes, N C Notermans, D Lindhout,[...]. Neurology 2002
159
12

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
599
12

Generation and characterization of Sca2 (ataxin-2) knockout mice.
Tim-Rasmus Kiehl, Alex Nechiporuk, Karla P Figueroa, Mark T Keating, Duong P Huynh, Stefan-M Pulst. Biochem Biophys Res Commun 2006
89
13

Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.
K Bürk, M Abele, M Fetter, J Dichgans, M Skalej, F Laccone, O Didierjean, A Brice, T Klockgether. Brain 1996
177
11

Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?
L Schöls, G Amoiridis, T Büttner, H Przuntek, J T Epplen, O Riess. Ann Neurol 1997
243
11

An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)
M D Koob, M L Moseley, L J Schut, K A Benzow, T D Bird, J W Day, L P Ranum. Nat Genet 1999
446
11


Childhood-onset ataxia: testing for large CAG-repeats in SCA2 and SCA7.
Rong Mao, Arthur S Aylsworth, Nicholas Potter, William G Wilson, Galen Breningstall, Myra J Wick, Dusica Babovic-Vuksanovic, Martha Nance, Marc C Patterson, Christopher M Gomez,[...]. Am J Med Genet 2002
45
24


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
917
11

SCA-2 presenting as parkinsonism in an Alberta family: clinical, genetic, and PET findings.
S Furtado, M Farrer, Y Tsuboi, M L Klimek, R de la Fuente-Fernández, J Hussey, P Lockhart, D B Calne, O Suchowersky, A J Stoessl,[...]. Neurology 2002
65
15

Changes in Purkinje cell firing and gene expression precede behavioral pathology in a mouse model of SCA2.
Stephen T Hansen, Pratap Meera, Thomas S Otis, Stefan M Pulst. Hum Mol Genet 2013
104
10

Spinocerebellar ataxia type 2 presenting as familial levodopa-responsive parkinsonism.
D E Shan, B W Soong, C M Sun, S J Lee, K K Liao, R S Liu. Ann Neurol 2001
76
11

Neuronal intranuclear inclusions in SCA2: a genetic, morphological and immunohistochemical study of two cases.
Joanna T Pang, Paola Giunti, Susan Chamberlain, Shu F An, Roberta Vitaliani, Tomaso Scaravilli, Lillian Martinian, Nicholas W Wood, Francesco Scaravilli, Olaf Ansorge. Brain 2002
68
13

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
92
9

Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes.
Giovanni Stevanin, Hiroto Fujigasaki, Anne-Sophie Lebre, Agnes Camuzat, Cecile Jeannequin, Catherine Dode, Junko Takahashi, Chankranira San, Robert Bellance, Alexis Brice,[...]. Brain 2003
107
9

A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2.
S E Holmes, E O'Hearn, A Rosenblatt, C Callahan, H S Hwang, R G Ingersoll-Ashworth, A Fleisher, G Stevanin, A Brice, N T Potter,[...]. Nat Genet 2001
191
9


Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion.
D Babovic-Vuksanovic, K Snow, M C Patterson, V V Michels. Am J Med Genet 1998
51
17

Frequency analysis and clinical characterization of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Korean patients.
Won Yong Lee, Dong Kyu Jin, Myung Ryurl Oh, Ji Eun Lee, Seng Mi Song, Eun Ah Lee, Gyeong-Moon Kim, Jin Sang Chung, Kwang Ho Lee. Arch Neurol 2003
59
15

Spinocerebellar ataxia type 2 (SCA2) presenting with ophthalmoplegia and developmental delay in infancy.
Paolo Moretti, Maria Blazo, Leonardo Garcia, Dawna Armstrong, Richard Alan Lewis, Benjamin Roa, Fernando Scaglia. Am J Med Genet A 2004
27
33

Cognitive findings in spinocerebellar ataxia type 2: relationship to genetic and clinical variables.
Francesco Le Pira, Giuseppe Zappalà, Riccardo Saponara, Elisabetta Domina, Domenico Restivo, Ester Reggio, Alessandra Nicoletti, Salvatore Giuffrida. J Neurol Sci 2002
49
18

Cognitive deficits in spinocerebellar ataxia 2.
K Bürk, C Globas, S Bösch, S Gräber, M Abele, A Brice, J Dichgans, I Daum, T Klockgether. Brain 1999
95
9

Ataxin-2 and its Drosophila homolog, ATX2, physically assemble with polyribosomes.
Terrence F Satterfield, Leo J Pallanck. Hum Mol Genet 2006
127
9

A novel protein with RNA-binding motifs interacts with ataxin-2.
H Shibata, D P Huynh, S M Pulst. Hum Mol Genet 2000
174
9

Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans.
Joyce van de Leemput, Jayanth Chandran, Melanie A Knight, Lynne A Holtzclaw, Sonja Scholz, Mark R Cookson, Henry Houlden, Katrina Gwinn-Hardy, Hon-Chung Fung, Xian Lin,[...]. PLoS Genet 2007
192
9

Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?
P Charles, A Camuzat, N Benammar, F Sellal, A Destée, A-M Bonnet, S Lesage, I Le Ber, G Stevanin, A Dürr,[...]. Neurology 2007
90
10



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.