A citation-based method for searching scientific literature

U Rüb, E R Brunt, E Petrasch-Parwez, L Schöls, D Theegarten, G Auburger, K Seidel, C Schultz, K Gierga, H Paulson, C van Broeckhoven, T Deller, R A I de Vos. Neuropathol Appl Neurobiol 2006
Times Cited: 58







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



Times Cited
  Times     Co-cited
Similarity


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
50

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
650
34

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
45

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
31

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
29

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
29

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
63
27

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
43

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
27

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
22

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
30

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
29

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
20

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
30

Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies.
R Estrada, J Galarraga, G Orozco, A Nodarse, G Auburger. Acta Neuropathol 1999
157
20




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
18

Brain pathology of spinocerebellar ataxias.
Kay Seidel, Sonny Siswanto, Ewout R P Brunt, Wilfred den Dunnen, Horst-Werner Korf, Udo Rüb. Acta Neuropathol 2012
209
18

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
18

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

Involvement of precerebellar nuclei in multiple system atrophy.
H Braak, U Rüb, K Del Tredici. Neuropathol Appl Neurobiol 2003
72
17

An isoform of ataxin-3 accumulates in the nucleus of neuronal cells in affected brain regions of SCA3 patients.
T Schmidt, G B Landwehrmeyer, I Schmitt, Y Trottier, G Auburger, F Laccone, T Klockgether, M Völpel, J T Epplen, L Schöls,[...]. Brain Pathol 1998
156
17

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

Involvement of the auditory brainstem system in spinocerebellar ataxia type 2 (SCA2), type 3 (SCA3) and type 7 (SCA7).
F Hoche, K Seidel, E R Brunt, G Auburger, L Schöls, K Bürk, R A de Vos, W den Dunnen, I Bechmann, R Egensperger,[...]. Neuropathol Appl Neurobiol 2008
21
47

Pathoanatomy of cerebellar degeneration in spinocerebellar ataxia type 2 (SCA2) and type 3 (SCA3).
W Scherzed, E R Brunt, H Heinsen, R A de Vos, K Seidel, K Bürk, L Schöls, G Auburger, D Del Turco, T Deller,[...]. Cerebellum 2012
56
17

Spinocerebellar ataxia type 7 (SCA7): first report of a systematic neuropathological study of the brain of a patient with a very short expanded CAG-repeat.
U Rüb, E R Brunt, K Gierga, K Seidel, C Schultz, L Schöls, G Auburger, H Heinsen, P F Ippel, W F Glimmerveen,[...]. Brain Pathol 2005
27
33


CAG repeat disorder models and human neuropathology: similarities and differences.
Mitsunori Yamada, Toshiya Sato, Shoji Tsuji, Hitoshi Takahashi. Acta Neuropathol 2008
100
15

Spinocerebellar ataxia 2 (SCA2).
Isabel Lastres-Becker, Udo Rüb, Georg Auburger. Cerebellum 2008
137
15

Ataxin-2 associates with rough endoplasmic reticulum.
Simone van de Loo, Florian Eich, David Nonis, Georg Auburger, Joachim Nowock. Exp Neurol 2009
56
16

Saccade velocity is reduced in presymptomatic spinocerebellar ataxia type 2.
L Velázquez-Pérez, C Seifried, M Abele, F Wirjatijasa, R Rodríguez-Labrada, N Santos-Falcón, G Sánchez-Cruz, L Almaguer-Mederos, R Tejeda, N Canales-Ochoa,[...]. Clin Neurophysiol 2009
54
16

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
21

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
13

Autosomal dominant spinocerebellar degenerations. Clinical, pathological, and genetic correlations.
K Iwabuchi, K Tsuchiya, T Uchihara, S Yagishita. Rev Neurol (Paris) 1999
75
13

SCA3: neurological features, pathogenesis and animal models.
Olaf Riess, Udo Rüb, Annalisa Pastore, Peter Bauer, Ludger Schöls. Cerebellum 2008
148
13

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
13

Stages of sleep pathology in spinocerebellar ataxia type 2 (SCA2).
I Tuin, U Voss, J-S Kang, K Kessler, U Rüb, D Nolte, H Lochmüller, S Tinschert, D Claus, K Krakow,[...]. Neurology 2006
46
17

Axonal inclusions in spinocerebellar ataxia type 3.
Kay Seidel, Wilfred F A den Dunnen, Christian Schultz, Henry Paulson, Stefanie Frank, Rob A de Vos, Ewout R Brunt, Thomas Deller, Harm H Kampinga, Udo Rüb. Acta Neuropathol 2010
66
13

Spinocerebellar ataxia type 2.
Georg W J Auburger. Handb Clin Neurol 2012
49
16

Estimation of the age at onset in spinocerebellar ataxia type 2 Cuban patients by survival analysis.
L E Almaguer-Mederos, N S Falcón, Y R Almira, Y G Zaldivar, D C Almarales, E M Góngora, M P Herrera, K E Batallán, R R Armiñán, M V Manresa,[...]. Clin Genet 2010
37
21

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
13

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
13

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
13

Progression of early features of spinocerebellar ataxia type 2 in individuals at risk: a longitudinal study.
Luis Velázquez-Pérez, Roberto Rodríguez-Labrada, Nalia Canales-Ochoa, Jacqueline Medrano Montero, Gilberto Sánchez-Cruz, Raúl Aguilera-Rodríguez, Luis E Almaguer-Mederos, José M Laffita-Mesa. Lancet Neurol 2014
54
14

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
16

Therapeutic reduction of ataxin-2 extends lifespan and reduces pathology in TDP-43 mice.
Lindsay A Becker, Brenda Huang, Gregor Bieri, Rosanna Ma, David A Knowles, Paymaan Jafar-Nejad, James Messing, Hong Joo Kim, Armand Soriano, Georg Auburger,[...]. Nature 2017
226
13

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
15


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.