A citation-based method for searching scientific literature

Mario-Ubaldo Manto. Cerebellum 2005
Times Cited: 186







List of co-cited articles
1397 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
650
20

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
17

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
16


The cerebellar cognitive affective syndrome.
J D Schmahmann, J C Sherman. Brain 1998
13

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
184
13

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
12

Neurodegeneration in Lurcher mice caused by mutation in delta2 glutamate receptor gene.
J Zuo, P L De Jager, K A Takahashi, W Jiang, D J Linden, N Heintz. Nature 1997
418
12

Cognitive deficits in spinocerebellar ataxia type 1, 2, and 3.
K Bürk, C Globas, S Bösch, T Klockgether, C Zühlke, I Daum, J Dichgans. J Neurol 2003
131
11

The spinocerebellar ataxias.
Henry L Paulson. J Neuroophthalmol 2009
108
10

Mesenchymal stem cells rescue Purkinje cells and improve motor functions in a mouse model of cerebellar ataxia.
Jonathan Jones, Jesús Jaramillo-Merchán, Carlos Bueno, Diego Pastor, Maricarmen Viso-León, Salvador Martínez. Neurobiol Dis 2010
66
15

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

Gray matter volume deficits in spinocerebellar ataxia: an optimized voxel based morphometric study.
Gaurav Goel, Pramod Kumar Pal, Shivashankar Ravishankar, Ganesan Venkatasubramanian, Peruvumba N Jayakumar, Nithin Krishna, Meera Purushottam, Jitender Saini, Mohammed Faruq, Mitali Mukherji,[...]. Parkinsonism Relat Disord 2011
44
20


Grafting neural precursor cells promotes functional recovery in an SCA1 mouse model.
Satyan Chintawar, Raphael Hourez, Ajay Ravella, David Gall, David Orduz, Myriam Rai, Don Patrick Bishop, Stefano Geuna, Serge N Schiffmann, Massimo Pandolfo. J Neurosci 2009
50
18

Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17).
Arndt Rolfs, Arnulf H Koeppen, Ingrid Bauer, Peter Bauer, Sven Buhlmann, Helge Topka, Ludger Schöls, Olaf Riess. Ann Neurol 2003
151
9

Structural and quantitative studies on the normal C3H and Lurcher mutant mouse.
K W Caddy, T J Biscoe. Philos Trans R Soc Lond B Biol Sci 1979
403
9

Cognitive deficits in spinocerebellar ataxia 2.
K Bürk, C Globas, S Bösch, S Gräber, M Abele, A Brice, J Dichgans, I Daum, T Klockgether. Brain 1999
95
9


Cognitive findings in spinocerebellar ataxia type 2: relationship to genetic and clinical variables.
Francesco Le Pira, Giuseppe Zappalà, Riccardo Saponara, Elisabetta Domina, Domenico Restivo, Ester Reggio, Alessandra Nicoletti, Salvatore Giuffrida. J Neurol Sci 2002
49
16


Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies.
R Estrada, J Galarraga, G Orozco, A Nodarse, G Auburger. Acta Neuropathol 1999
157
8

Molecular pathogenesis of spinocerebellar ataxias.
Antoni Matilla Dueñas, Robert Goold, Paola Giunti. Brain 2006
153
8

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
798
8

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
193
8

Trinucleotide repeat disorders.
Harry T Orr, Huda Y Zoghbi. Annu Rev Neurosci 2007
966
8




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
117
8

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
455
8

Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data.
Heike Jacobi, Kathrin Reetz, Sophie Tezenas du Montcel, Peter Bauer, Caterina Mariotti, Lorenzo Nanetti, Maria Rakowicz, Anna Sulek, Alexandra Durr, Perrine Charles,[...]. Lancet Neurol 2013
106
8

Longitudinal study of cognitive and psychiatric functions in spinocerebellar ataxia types 1 and 2.
Roberto Fancellu, Dominga Paridi, Chiara Tomasello, Marta Panzeri, Anna Castaldo, Silvia Genitrini, Paola Soliveri, Floriano Girotti. J Neurol 2013
52
15

Disruption of visual and motor connectivity in spinocerebellar ataxia type 7.
Carlos R Hernandez-Castillo, Sarael Alcauter, Victor Galvez, Fernando A Barrios, Petra Yescas, Adriana Ochoa, Lizbeth Garcia, Rosalinda Diaz, Wei Gao, Juan Fernandez-Ruiz. Mov Disord 2013
28
28

International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome. The Ataxia Neuropharmacology Committee of the World Federation of Neurology.
P Trouillas, T Takayanagi, M Hallett, R D Currier, S H Subramony, K Wessel, A Bryer, H C Diener, S Massaquoi, C M Gomez,[...]. J Neurol Sci 1997
879
8

Survival of interneurons and parallel fiber synapses in a cerebellar cortex deprived of Purkinje cells: studies in the double mutant mouse Grid2Lc/+;Bax(-/-).
S Hadi Zanjani, Fekrije Selimi, Michael W Vogel, Anne-Marie Haeberlé, Julien Boeuf, Jean Mariani, Yannick J Bailly. J Comp Neurol 2006
21
38

Atrophy pattern in SCA2 determined by voxel-based morphometry.
Christian Brenneis, Sylvia M Bösch, Michael Schocke, Gregor K Wenning, Werner Poewe. Neuroreport 2003
77
9

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
7

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
7

Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant CaV2.1 channels.
Kei Watase, Curtis F Barrett, Taisuke Miyazaki, Taro Ishiguro, Kinya Ishikawa, Yuanxin Hu, Toshinori Unno, Yaling Sun, Sayumi Kasai, Masahiko Watanabe,[...]. Proc Natl Acad Sci U S A 2008
104
7

Diagnosis and management of early- and late-onset cerebellar ataxia.
E Brusse, J A Maat-Kievit, J C van Swieten. Clin Genet 2007
68
10

RNAi suppresses polyglutamine-induced neurodegeneration in a model of spinocerebellar ataxia.
Haibin Xia, Qinwen Mao, Steven L Eliason, Scott Q Harper, Inês H Martins, Harry T Orr, Henry L Paulson, Linda Yang, Robert M Kotin, Beverly L Davidson. Nat Med 2004
485
7

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
7

The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study.
H Jacobi, P Bauer, P Giunti, R Labrum, M G Sweeney, P Charles, A Dürr, C Marelli, C Globas, C Linnemann,[...]. Neurology 2011
120
7

Purkinje cell degeneration, a new neurological mutation in the mouse.
R J Mullen, E M Eicher, R L Sidman. Proc Natl Acad Sci U S A 1976
455
7

Mesenchymal stem cell transplantation ameliorates motor function deterioration of spinocerebellar ataxia by rescuing cerebellar Purkinje cells.
You-Kang Chang, Ming-Hsiang Chen, Yi-Hung Chiang, Yu-Fan Chen, Wei-Hsien Ma, Chian-You Tseng, Bin-Wen Soong, Jennifer H Ho, Oscar K Lee. J Biomed Sci 2011
47
14

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
152
7

Non-ATG-initiated translation directed by microsatellite expansions.
Tao Zu, Brian Gibbens, Noelle S Doty, Mário Gomes-Pereira, Aline Huguet, Matthew D Stone, Jamie Margolis, Mark Peterson, Todd W Markowski, Melissa A C Ingram,[...]. Proc Natl Acad Sci U S A 2011
531
7

Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.
Jörg B Schulz, Johannes Borkert, Stefanie Wolf, Tanja Schmitz-Hübsch, Maryla Rakowicz, Caterina Mariotti, Ludger Schöls, Dagmar Timmann, Bart van de Warrenburg, Alexandra Dürr,[...]. Neuroimage 2010
110
7

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
7


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.