A citation-based method for searching scientific literature

Stefan-M Pulst, Nieves Santos, Dai Wang, Huiying Yang, Duong Huynh, Luis Velazquez, K Pattie Figueroa. Brain 2005
Times Cited: 92







List of co-cited articles
1068 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
867
43

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
701
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
608
28

Age at onset variance analysis in spinocerebellar ataxias: a study in a Dutch-French cohort.
Bart P C van de Warrenburg, Harrie Hendriks, Alexandra Dürr, Martin C A van Zuijlen, Giovanni Stevanin, Agnès Camuzat, Richard J Sinke, Alexis Brice, Berry P H Kremer. Ann Neurol 2005
78
26

Spinocerebellar ataxia 2 (SCA2).
Isabel Lastres-Becker, Udo Rüb, Georg Auburger. Cerebellum 2008
137
22

CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2).
S Hayes, G Turecki, K Brisebois, I Lopes-Cendes, C Gaspar, O Riess, L P Ranum, S M Pulst, G A Rouleau. Hum Mol Genet 2000
68
29

Deranged calcium signaling and neurodegeneration in spinocerebellar ataxia type 2.
Jing Liu, Tie-Shan Tang, Huiping Tu, Omar Nelson, Emily Herndon, Duong P Huynh, Stefan M Pulst, Ilya Bezprozvanny. J Neurosci 2009
182
21

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
750
21

A novel protein with RNA-binding motifs interacts with ataxin-2.
H Shibata, D P Huynh, S M Pulst. Hum Mol Genet 2000
173
19

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
649
19

Ataxin-2 and its Drosophila homolog, ATX2, physically assemble with polyribosomes.
Terrence F Satterfield, Leo J Pallanck. Hum Mol Genet 2006
126
18


Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies.
R Estrada, J Galarraga, G Orozco, A Nodarse, G Auburger. Acta Neuropathol 1999
157
17

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
87
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
16

Mitochondrial complex I gene variant associated with early age at onset in spinocerebellar ataxia type 2.
David K Simon, Kangni Zheng, Luis Velázquez, Nieves Santos, Luis Almaguer, K Pattie Figueroa, Stefan-M Pulst. Arch Neurol 2007
26
57

Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
Sophie Tezenas du Montcel, Alexandra Durr, Peter Bauer, Karla P Figueroa, Yaeko Ichikawa, Alessandro Brussino, Sylvie Forlani, Maria Rakowicz, Ludger Schöls, Caterina Mariotti,[...]. Brain 2014
92
16

An integrative approach to gain insights into the cellular function of human ataxin-2.
Markus Ralser, Mario Albrecht, Ute Nonhoff, Thomas Lengauer, Hans Lehrach, Sylvia Krobitsch. J Mol Biol 2005
107
15

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
190
15

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
907
15

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
15

Expansion of the polyQ repeat in ataxin-2 alters its Golgi localization, disrupts the Golgi complex and causes cell death.
Duong P Huynh, Hai-Tao Yang, Hema Vakharia, Dung Nguyen, Stefan M Pulst. Hum Mol Genet 2003
93
14


Structural and functional analysis of ataxin-2 and ataxin-3.
Mario Albrecht, Michael Golatta, Ullrich Wüllner, Thomas Lengauer. Eur J Biochem 2004
88
14

Ataxin-2 interacts with the DEAD/H-box RNA helicase DDX6 and interferes with P-bodies and stress granules.
Ute Nonhoff, Markus Ralser, Franziska Welzel, Ilaria Piccini, Daniela Balzereit, Marie-Laure Yaspo, Hans Lehrach, Sylvia Krobitsch. Mol Biol Cell 2007
218
14

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
14



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

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
11

Spinocerebellar ataxia type 2 in southern Italy: a clinical and molecular study of 30 families.
A Filla, G De Michele, L Santoro, O Calabrese, I Castaldo, S Giuffrida, D Restivo, L Serlenga, D F Condorelli, U Bonuccelli,[...]. J Neurol 1999
43
25

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
11

Cellular and molecular pathways triggering neurodegeneration in the spinocerebellar ataxias.
Antoni Matilla-Dueñas, Ivelisse Sánchez, Marc Corral-Juan, Antoni Dávalos, Ramiro Alvarez, Pilar Latorre. Cerebellum 2010
62
17


Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic mice.
I A Klement, P J Skinner, M D Kaytor, H Yi, S M Hersch, H B Clark, H Y Zoghbi, H T Orr. Cell 1998
796
10

Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain.
M DiFiglia, E Sapp, K O Chase, S W Davies, G P Bates, J P Vonsattel, N Aronin. Science 1997
10

Non-expanded polyglutamine proteins in intranuclear inclusions of hereditary ataxias--triple-labeling immunofluorescence study.
T Uchihara, H Fujigasaki, S Koyano, A Nakamura, S Yagishita, K Iwabuchi. Acta Neuropathol 2001
63
15


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
146
10

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
10

The natural history of degenerative ataxia: a retrospective study in 466 patients.
T Klockgether, R Lüdtke, B Kramer, M Abele, K Bürk, L Schöls, O Riess, F Laccone, S Boesch, I Lopes-Cendes,[...]. Brain 1998
223
10

Involvement of the cranial nerves and their nuclei in spinocerebellar ataxia type 2 (SCA2).
K Gierga, K Bürk, M Bauer, G Orozco Diaz, G Auburger, C Schultz, M Vuksic, L Schöls, R A I de Vos, H Braak,[...]. Acta Neuropathol 2005
61
16

Ataxin-2 and huntingtin interact with endophilin-A complexes to function in plastin-associated pathways.
Markus Ralser, Ute Nonhoff, Mario Albrecht, Thomas Lengauer, Erich E Wanker, Hans Lehrach, Sylvia Krobitsch. Hum Mol Genet 2005
71
14

Saccade velocity is controlled by polyglutamine size in spinocerebellar ataxia 2.
Luis Velázquez-Pérez, Carola Seifried, Nieves Santos-Falcón, Michael Abele, Ulf Ziemann, Luis Enrique Almaguer, Edilberto Martínez-Góngora, Gilberto Sánchez-Cruz, Nalia Canales, Ruth Pérez-González,[...]. Ann Neurol 2004
65
15

Ataxin-2 associates with the endocytosis complex and affects EGF receptor trafficking.
David Nonis, Mirko H H Schmidt, Simone van de Loo, Florian Eich, Ivan Dikic, Joachim Nowock, Georg Auburger. Cell Signal 2008
73
13

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
11

Deranged calcium signaling and neurodegeneration in spinocerebellar ataxia type 3.
Xi Chen, Tie-Shan Tang, Huiping Tu, Omar Nelson, Mark Pook, Robert Hammer, Nobuyuki Nukina, Ilya Bezprozvanny. J Neurosci 2008
151
10


Heterozygous deletion of ITPR1, but not SUMF1, in spinocerebellar ataxia type 16.
A Iwaki, Y Kawano, S Miura, H Shibata, D Matsuse, W Li, H Furuya, Y Ohyagi, T Taniwaki, J Kira,[...]. J Med Genet 2008
90
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.