A citation-based method for searching scientific literature

Isabel Lastres-Becker, Udo Rüb, Georg Auburger. Cerebellum 2008
Times Cited: 137







List of co-cited articles
1335 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
40

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
38

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
28

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
28

Ataxin-2 and its Drosophila homolog, ATX2, physically assemble with polyribosomes.
Terrence F Satterfield, Leo J Pallanck. Hum Mol Genet 2006
126
27

Ataxin-2 associates with rough endoplasmic reticulum.
Simone van de Loo, Florian Eich, David Nonis, Georg Auburger, Joachim Nowock. Exp Neurol 2009
54
44

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
24


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
22

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
649
21

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
26

The Ataxin-2 protein is required for microRNA function and synapse-specific long-term olfactory habituation.
Cathal McCann, Eimear E Holohan, Sudeshna Das, Adrian Dervan, Aoife Larkin, John Anthony Lee, Veronica Rodrigues, Roy Parker, Mani Ramaswami. Proc Natl Acad Sci U S A 2011
105
19

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
168
19

Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies.
R Estrada, J Galarraga, G Orozco, A Nodarse, G Auburger. Acta Neuropathol 1999
157
18

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
18

Ataxin-2 intermediate-length polyglutamine expansions in European ALS patients.
Teresa Lee, Yun R Li, Caroline Ingre, Markus Weber, Torsten Grehl, Ole Gredal, Mamede de Carvalho, Thomas Meyer, Ole-Björn Tysnes, Georg Auburger,[...]. Hum Mol Genet 2011
99
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
19

The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effect.
Suzana Gispert, Alexander Kurz, Stefan Waibel, Peter Bauer, Inga Liepelt, Christof Geisen, Aaron D Gitler, Tim Becker, Markus Weber, Daniela Berg,[...]. Neurobiol Dis 2012
58
24

Insulin receptor and lipid metabolism pathology in ataxin-2 knock-out mice.
Isabel Lastres-Becker, Susanne Brodesser, Dieter Lütjohann, Mekhman Azizov, Jana Buchmann, Edith Hintermann, Konrad Sandhoff, Annette Schürmann, Joachim Nowock, Georg Auburger. Hum Mol Genet 2008
76
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
13


Trinucleotide repeat disorders.
Harry T Orr, Huda Y Zoghbi. Annu Rev Neurosci 2007
961
13

Brain pathology of spinocerebellar ataxias.
Kay Seidel, Sonny Siswanto, Ewout R P Brunt, Wilfred den Dunnen, Horst-Werner Korf, Udo Rüb. Acta Neuropathol 2012
207
13

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
13

The KRAB-containing zinc-finger transcriptional regulator ZBRK1 activates SCA2 gene transcription through direct interaction with its gene product, ataxin-2.
Linda Hallen, Holger Klein, Carola Stoschek, Silke Wehrmeyer, Ute Nonhoff, Markus Ralser, Jeannine Wilde, Christina Röhr, Michal R Schweiger, Kurt Zatloukal,[...]. Hum Mol Genet 2011
30
40

dAtaxin-2 mediates expanded Ataxin-1-induced neurodegeneration in a Drosophila model of SCA1.
Ismael Al-Ramahi, Alma M Pérez, Janghoo Lim, Minghang Zhang, Rie Sorensen, Maria de Haro, Joana Branco, Stefan M Pulst, Huda Y Zoghbi, Juan Botas. PLoS Genet 2007
70
17

Ataxin-2 repeat-length variation and neurodegeneration.
Owen A Ross, Nicola J Rutherford, Matt Baker, Alexandra I Soto-Ortolaza, Minerva M Carrasquillo, Mariely DeJesus-Hernandez, Jennifer Adamson, Ma Li, Kathryn Volkening, Elizabeth Finger,[...]. Hum Mol Genet 2011
120
12

A comprehensive review of spinocerebellar ataxia type 2 in Cuba.
Luis Velázquez-Pérez, Roberto Rodríguez-Labrada, Julio Cesar García-Rodríguez, Luis Enrique Almaguer-Mederos, Tania Cruz-Mariño, José Miguel Laffita-Mesa. Cerebellum 2011
55
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
12

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
19

Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3.
H L Paulson, M K Perez, Y Trottier, J Q Trojanowski, S H Subramony, S S Das, P Vig, J L Mandel, K H Fischbeck, R N Pittman. Neuron 1997
655
12


Direct binding of Ataxin-2 to distinct elements in 3' UTRs promotes mRNA stability and protein expression.
Moe Yokoshi, Quan Li, Munetaka Yamamoto, Hitomi Okada, Yutaka Suzuki, Yukio Kawahara. Mol Cell 2014
76
15

Extended pathoanatomical studies point to a consistent affection of the thalamus in spinocerebellar ataxia type 2.
U Rüb, D Del Turco, K Bürk, G Orozco Diaz, G Auburger, M Mittelbronn, K Gierga, E Ghebremedhin, C Schultz, L Schöls,[...]. Neuropathol Appl Neurobiol 2005
36
30

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
11

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
12

Thalamic involvement in a spinocerebellar ataxia type 2 (SCA2) and a spinocerebellar ataxia type 3 (SCA3) patient, and its clinical relevance.
U Rüb, D Del Turco, K Del Tredici, R A I de Vos, E R Brunt, G Reifenberger, C Seifried, C Schultz, G Auburger, H Braak. Brain 2003
62
17


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
10

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
10

SCA3: neurological features, pathogenesis and animal models.
Olaf Riess, Udo Rüb, Annalisa Pastore, Peter Bauer, Ludger Schöls. Cerebellum 2008
148
10

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
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
10

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Manuela Neumann, Deepak M Sampathu, Linda K Kwong, Adam C Truax, Matthew C Micsenyi, Thomas T Chou, Jennifer Bruce, Theresa Schuck, Murray Grossman, Christopher M Clark,[...]. Science 2006
10

A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration.
Janghoo Lim, Tong Hao, Chad Shaw, Akash J Patel, Gábor Szabó, Jean-François Rual, C Joseph Fisk, Ning Li, Alex Smolyar, David E Hill,[...]. Cell 2006
553
10

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

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
10


Spinocerebellar ataxia type 2.
Georg W J Auburger. Handb Clin Neurol 2012
49
20



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.