A citation-based method for searching scientific literature

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
Times Cited: 63







List of co-cited articles
544 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
873
47

Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies.
R Estrada, J Galarraga, G Orozco, A Nodarse, G Auburger. Acta Neuropathol 1999
157
38

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
62
38

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
37
56

Anatomically based guidelines for systematic investigation of the central somatosensory system and their application to a spinocerebellar ataxia type 2 (SCA2) patient.
U Rüb, C Schultz, K Del Tredici, K Gierga, G Reifenberger, R A I de Vos, C Seifried, H Braak, G Auburger. Neuropathol Appl Neurobiol 2003
43
46

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
705
30

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
650
30

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
26

Spinocerebellar ataxias types 2 and 3: degeneration of the pre-cerebellar nuclei isolates the three phylogenetically defined regions of the cerebellum.
U Rüb, K Gierga, E R Brunt, R A I de Vos, M Bauer, L Schöls, K Bürk, G Auburger, J Bohl, C Schultz,[...]. J Neural Transm (Vienna) 2005
42
40

Consistent affection of the central somatosensory system in spinocerebellar ataxia type 2 and type 3 and its significance for clinical symptoms and rehabilitative therapy.
Udo Rüb, Kay Seidel, Inci Ozerden, Kristin Gierga, Ewout R Brunt, Ludger Schöls, Rob A I de Vos, Wilfred den Dunnen, Christian Schultz, Georg Auburger,[...]. Brain Res Rev 2007
42
40

Damage to the reticulotegmental nucleus of the pons in spinocerebellar ataxia type 1, 2, and 3.
U Rüb, K Bürk, L Schöls, E R Brunt, R A I de Vos, G Orozco Diaz, K Gierga, E Ghebremedhin, C Schultz, D Del Turco,[...]. Neurology 2004
37
43

Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7.
U Rüb, E R Brunt, E Petrasch-Parwez, L Schöls, D Theegarten, G Auburger, K Seidel, C Schultz, K Gierga, H Paulson,[...]. Neuropathol Appl Neurobiol 2006
58
27

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
758
23

Autosomal dominant spinocerebellar degenerations. Clinical, pathological, and genetic correlations.
K Iwabuchi, K Tsuchiya, T Uchihara, S Yagishita. Rev Neurol (Paris) 1999
75
22

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
22


Spinocerebellar ataxia type 3 (Machado-Joseph disease): severe destruction of the lateral reticular nucleus.
U Rüb, R A I de Vos, C Schultz, E R Brunt, H Paulson, H Braak. Brain 2002
45
28


Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features.
A Dürr, G Stevanin, G Cancel, C Duyckaerts, N Abbas, O Didierjean, H Chneiweiss, A Benomar, O Lyon-Caen, J Julien,[...]. Ann Neurol 1996
337
19

Involvement of precerebellar nuclei in multiple system atrophy.
H Braak, U Rüb, K Del Tredici. Neuropathol Appl Neurobiol 2003
72
19

The spinocerebellar ataxias.
S Gilman. Clin Neuropharmacol 2000
39
30

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
19

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
19

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
19

Spinocerebellar ataxia 2 (SCA2).
Isabel Lastres-Becker, Udo Rüb, Georg Auburger. Cerebellum 2008
137
19

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
80
19

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
74
19

Ataxin-2 associates with rough endoplasmic reticulum.
Simone van de Loo, Florian Eich, David Nonis, Georg Auburger, Joachim Nowock. Exp Neurol 2009
56
21

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
20

ATXN2-CAG42 sequesters PABPC1 into insolubility and induces FBXW8 in cerebellum of old ataxic knock-in mice.
Ewa Damrath, Melanie V Heck, Suzana Gispert, Mekhman Azizov, Joachim Nowock, Carola Seifried, Udo Rüb, Michael Walter, Georg Auburger. PLoS Genet 2012
50
24

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
17

Autosomal dominant cerebellar ataxia type I: oculomotor abnormalities in families with SCA1, SCA2, and SCA3.
K Bürk, M Fetter, M Abele, F Laccone, A Brice, J Dichgans, T Klockgether. J Neurol 1999
105
17

Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population.
G Auburger, G O Diaz, R F Capote, S G Sanchez, M P Perez, M E del Cueto, M G Meneses, M Farrall, R Williamson, S Chamberlain. Am J Hum Genet 1990
85
17

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
17

Degeneration of the central vestibular system in spinocerebellar ataxia type 3 (SCA3) patients and its possible clinical significance.
U Rüb, E R Brunt, R A I de Vos, D Del Turco, K Del Tredici, K Gierga, C Schultz, E Ghebremedhin, K Bürk, G Auburger,[...]. Neuropathol Appl Neurobiol 2004
40
27

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
17

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
611
17

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
17

Spinocerebellar ataxia type 3 (SCA3): thalamic neurodegeneration occurs independently from thalamic ataxin-3 immunopositive neuronal intranuclear inclusions.
Udo Rüb, Rob A I de Vos, Ewout R Brunt, Tamás Sebestény, Ludger Schöls, Georg Auburger, Jürgen Bohl, Estifanos Ghebremedhin, Kristin Gierga, Kay Seidel,[...]. Brain Pathol 2006
44
25

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
222
17

Ataxin-2 modulates the levels of Grb2 and SRC but not ras signaling.
Jessica Drost, David Nonis, Florian Eich, Oliver Leske, Ewa Damrath, Ewout R Brunt, Isabel Lastres-Becker, Rolf Heumann, Joachim Nowock, Georg Auburger. J Mol Neurosci 2013
36
30


The neuropathology of CAG repeat diseases: review and update of genetic and molecular features.
Y Robitaille, I Lopes-Cendes, M Becher, G Rouleau, A W Clark. Brain Pathol 1997
100
15

Autosomal dominant cerebellar ataxia type I. Nerve conduction and evoked potential studies in families with SCA1, SCA2 and SCA3.
M Abele, K Bürk, F Andres, H Topka, F Laccone, S Bösch, A Brice, G Cancel, J Dichgans, T Klockgether. Brain 1997
92
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
923
15

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

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
172
15

Ataxia and hereditary disorders.
H Paulson, Z Ammache. Neurol Clin 2001
35
25

Neuropathological stageing of Alzheimer-related changes.
H Braak, E Braak. Acta Neuropathol 1991
14

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
658
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.