A citation-based method for searching scientific literature

Arndt Rolfs, Arnulf H Koeppen, Ingrid Bauer, Peter Bauer, Sven Buhlmann, Helge Topka, Ludger Schöls, Olaf Riess. Ann Neurol 2003
Times Cited: 151







List of co-cited articles
1357 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
450
55

A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?
R Koide, S Kobayashi, T Shimohata, T Ikeuchi, M Maruyama, M Saito, M Yamada, H Takahashi, S Tsuji. Hum Mol Genet 1999
274
44

Behavioral disorder, dementia, ataxia, and rigidity in a large family with TATA box-binding protein mutation.
Amalia C Bruni, Junko Takahashi-Fujigasaki, Francesca Maltecca, Jean Francois Foncin, Antonio Servadio, Giorgio Casari, Pio D'Adamo, Raffaele Maletta, Sabrina A M Curcio, Giuseppe De Michele,[...]. Arch Neurol 2004
61
49

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
643
29

SCA17 homozygote showing Huntington's disease-like phenotype.
Yasuko Toyoshima, Mitsunori Yamada, Osamu Onodera, Mitsuteru Shimohata, Chikanori Inenaga, Nobuya Fujita, Masahiro Morita, Shoji Tsuji, Hitoshi Takahashi. Ann Neurol 2004
75
37

Polyglutamine domain modulates the TBP-TFIIB interaction: implications for its normal function and neurodegeneration.
Meyer J Friedman, Anjali G Shah, Zhi-Hui Fang, Elizabeth G Ward, Stephen T Warren, Shihua Li, Xiao-Jiang Li. Nat Neurosci 2007
115
25

Intergenerational instability and marked anticipation in SCA-17.
F Maltecca, A Filla, I Castaldo, G Coppola, N A Fragassi, M Carella, A Bruni, S Cocozza, G Casari, A Servadio,[...]. Neurology 2003
69
33

Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington's disease-like phenotype.
P Bauer, F Laccone, A Rolfs, U Wüllner, S Bösch, H Peters, S Liebscher, M Scheible, J T Epplen, B H F Weber,[...]. J Med Genet 2004
66
33

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
22

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
106
19

Spinocerebellar ataxia type 17 (SCA17): oculomotor phenotype and clinical characterization of 15 Italian patients.
Caterina Mariotti, Dario Alpini, Roberto Fancellu, Paola Soliveri, Marina Grisoli, Sabrina Ravaglia, Carlo Lovati, Vincenza Fetoni, Giorgio Giaccone, Alessia Castucci,[...]. J Neurol 2007
37
48

CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia.
H Fujigasaki, J J Martin, P P De Deyn, A Camuzat, D Deffond, G Stevanin, B Dermaut, C Van Broeckhoven, A Dürr, A Brice. Brain 2001
113
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
17

Morphological basis for the spectrum of clinical deficits in spinocerebellar ataxia 17 (SCA17).
K Lasek, R Lencer, C Gaser, J Hagenah, U Walter, A Wolters, N Kock, S Steinlechner, M Nagel, C Zühlke,[...]. Brain 2006
61
26

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
16

Case of spinocerebellar ataxia type 17 (SCA17) associated with only 41 repeats of the TATA-binding protein (TBP) gene.
Ashish Nanda, Sarah A Jackson, John D Schwankhaus, W Steven Metzer. Mov Disord 2007
26
61

Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.
Masaya Oda, Hirofumi Maruyama, Osamu Komure, Hiroyuki Morino, Hideo Terasawa, Yuishin Izumi, Tohru Imamura, Minoru Yasuda, Keiji Ichikawa, Masafumi Ogawa,[...]. Arch Neurol 2004
41
39



Trinucleotide repeat disorders.
Harry T Orr, Huda Y Zoghbi. Annu Rev Neurosci 2007
951
15

Spinocerebellar ataxia type 17 mutation as a causative and susceptibility gene in parkinsonism.
J-Y Kim, S Y Kim, J-M Kim, Y K Kim, K-Y Yoon, J Y Kim, B C Lee, J S Kim, S H Paek, S S Park,[...]. Neurology 2009
49
30

Dementia, ataxia, extrapyramidal features, and epilepsy: phenotype spectrum in two Italian families with spinocerebellar ataxia type 17.
G De Michele, F Maltecca, M Carella, G Volpe, M Orio, A De Falco, S Gombia, A Servadio, G Casari, A Filla,[...]. Neurol Sci 2003
33
42

Instability of expanded CAG/CAA repeats in spinocerebellar ataxia type 17.
Rui Gao, Tohru Matsuura, Mary Coolbaugh, Christine Zühlke, Koichiro Nakamura, Astrid Rasmussen, Michael J Siciliano, Tetsuo Ashizawa, Xi Lin. Eur J Hum Genet 2008
45
31


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
331
13

A novel transgenic rat model for spinocerebellar ataxia type 17 recapitulates neuropathological changes and supplies in vivo imaging biomarkers.
Alexandra Kelp, Arnulf H Koeppen, Elisabeth Petrasch-Parwez, Carsten Calaminus, Claudia Bauer, Esteban Portal, Libo Yu-Taeger, Bernd Pichler, Peter Bauer, Olaf Riess,[...]. J Neurosci 2013
28
46

Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.
I Silveira, C Miranda, L Guimarães, M-C Moreira, I Alonso, P Mendonça, A Ferro, J Pinto-Basto, J Coelho, F Ferreirinha,[...]. Arch Neurol 2002
127
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
595
12

Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxia.
C Zühlke, Y Hellenbroich, A Dalski, N Kononowa, J Hagenah, P Vieregge, O Riess, C Klein, E Schwinger. Eur J Hum Genet 2001
84
14

Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7).
G David, A Dürr, G Stevanin, G Cancel, N Abbas, A Benomar, S Belal, A S Lebre, M Abada-Bendib, D Grid,[...]. Hum Mol Genet 1998
202
12

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
241
11

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
697
11

A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected].
John C van Swieten, Esther Brusse, Bianca M de Graaf, Elmar Krieger, Raoul van de Graaf, Inge de Koning, Anneke Maat-Kievit, Peter Leegwater, Dennis Dooijes, Ben A Oostra,[...]. Am J Hum Genet 2003
187
11

Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease.
Y R Wu, H Y Lin, C M Chen, K Gwinn-Hardy, L S Ro, Y C Wang, S H Li, J C Hwang, K Fang, H M Hsieh-Li,[...]. Clin Genet 2004
62
17

Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8.
Melinda L Moseley, Tao Zu, Yoshio Ikeda, Wangcai Gao, Anne K Mosemiller, Randy S Daughters, Gang Chen, Marcy R Weatherspoon, H Brent Clark, Timothy J Ebner,[...]. Nat Genet 2006
297
11

Spinocerebellar ataxia type 17: extension of phenotype with putaminal rim hyperintensity on magnetic resonance imaging.
Clement T Loy, Mary G Sweeney, Mary B Davis, Adrian J Wills, Guy V Sawle, Andrew J Lees, Sarah J Tabrizi. Mov Disord 2005
27
40


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
792
11



Transcriptional dysregulation of TrkA associates with neurodegeneration in spinocerebellar ataxia type 17.
Anjali G Shah, Meyer J Friedman, Shanshan Huang, Meredith Roberts, Xiao-Jiang Li, Shihua Li. Hum Mol Genet 2009
28
39


The SCA17 phenotype can include features of MSA-C, PSP and cognitive impairment.
I-Sheng Lin, Ruey-Meei Wu, Guey-Jen Lee-Chen, Din-E Shan, Katrina Gwinn-Hardy. Parkinsonism Relat Disord 2007
46
21

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

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
190
10

Spinocerebellar ataxia type 6: gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset.
C M Gomez, R M Thompson, J T Gammack, S L Perlman, W B Dobyns, C L Truwit, D S Zee, H B Clark, J H Anderson. Ann Neurol 1997
201
10

Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12.
S E Holmes, E E O'Hearn, M G McInnis, D A Gorelick-Feldman, J J Kleiderlein, C Callahan, N G Kwak, R G Ingersoll-Ashworth, M Sherr, A J Sumner,[...]. Nat Genet 1999
317
10

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
858
10

Glutamine repeats and neurodegeneration.
H Y Zoghbi, H T Orr. Annu Rev Neurosci 2000
950
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.