A citation-based method for searching scientific literature

Dineke S Verbeek, Sytse J Piersma, Eric F A M Hennekam, Elly F Ippel, Peter L Pearson, Richard J Sinke. Eur J Hum Genet 2004
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype study.
C Gaspar, I Lopes-Cendes, S Hayes, J Goto, K Arvidsson, A Dias, I Silveira, P Maciel, P Coutinho, M Lima,[...]. Am J Hum Genet 2001
85
66

Asian origin for the worldwide-spread mutational event in Machado-Joseph disease.
Sandra Martins, Francesc Calafell, Claudia Gaspar, Virginia C N Wong, Isabel Silveira, Garth A Nicholson, Ewout R Brunt, Lisbeth Tranebjaerg, Giovanni Stevanin, Mingli Hsieh,[...]. Arch Neurol 2007
47
44

Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia.
J Jonasson, V Juvonen, P Sistonen, J Ignatius, D Johansson, E J Björck, J Wahlström, A Melberg, G Holmgren, L Forsgren,[...]. Eur J Hum Genet 2000
40
33

Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation.
Q Saleem, S Choudhry, M Mukerji, L Bashyam, M V Padma, A Chakravarthy, M C Maheshwari, S Jain, S K Brahmachari. Hum Genet 2000
91
33

Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis.
B P C van de Warrenburg, R J Sinke, C C Verschuuren-Bemelmans, H Scheffer, E R Brunt, P F Ippel, J A Maat-Kievit, D Dooijes, N C Notermans, D Lindhout,[...]. Neurology 2002
161
33

Spinocerebellar ataxia type 6: evidence for a strong founder effect among German families.
M Dichgans, L Schöls, J Herzog, G Stevanin, H Weirich-Schwaiger, G Rouleau, K Bürk, T Klockgether, C Zühlke, F Laccone,[...]. Neurology 1999
28
33

Molecular epidemiology of spinocerebellar ataxia type 6.
Kate Craig, Sharon M Keers, Kate Archibald, Ann Curtis, Patrick F Chinnery. Ann Neurol 2004
32
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
33

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
33

Correlation between CAG repeat length and clinical features in Machado-Joseph disease.
P Maciel, C Gaspar, A L DeStefano, I Silveira, P Coutinho, J Radvany, D M Dawson, L Sudarsky, J Guimarães, J E Loureiro. Am J Hum Genet 1995
223
33

Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysis.
J Infante, O Combarros, V Volpini, J Corral, J Llorca, J Berciano. Acta Neurol Scand 2005
36
33

Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
Alfredo Brusco, Cinzia Gellera, Claudia Cagnoli, Alessandro Saluto, Alessia Castucci, Chiara Michielotto, Vincenza Fetoni, Caterina Mariotti, Nicola Migone, Stefano Di Donato,[...]. Arch Neurol 2004
101
33

The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies.
Luis Ruano, Claudia Melo, M Carolina Silva, Paula Coutinho. Neuroepidemiology 2014
286
33

Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gamma.
Ichiro Yabe, Hidenao Sasaki, Dong-Hui Chen, Wendy H Raskind, Thomas D Bird, Isao Yamashita, Shoji Tsuji, Seiji Kikuchi, Kunio Tashiro. Arch Neurol 2003
87
22

Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia.
Dong-Hui Chen, Zoran Brkanac, Christophe L M J Verlinde, Xiao-Jian Tan, Laura Bylenok, David Nochlin, Mark Matsushita, Hillary Lipe, John Wolff, Magali Fernandez,[...]. Am J Hum Genet 2003
177
22

Spinocerebellar ataxia type 6: founder effect in Western Japan.
M Mori, Y Adachi, M Kusumi, K Nakashima. J Neurol Sci 2001
10
22

Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14.
Giovanni Stevanin, Valérie Hahn, Ebba Lohmann, Naima Bouslam, Michel Gouttard, Caroline Soumphonphakdy, Marie-Laure Welter, Elisabeth Ollagnon-Roman, Arnaud Lemainque, Merle Ruberg,[...]. Arch Neurol 2004
69
22

Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family.
B P C van de Warrenburg, D S Verbeek, S J Piersma, F A M Hennekam, P L Pearson, N V A M Knoers, H P H Kremer, R J Sinke. Neurology 2003
78
22

A new statistical method for haplotype reconstruction from population data.
M Stephens, N J Smith, P Donnelly. Am J Hum Genet 2001
22

SCA6 mutation analysis in a large cohort of the Japanese patients with late-onset pure cerebellar ataxia.
I Yabe, H Sasaki, T Matsuura, A Takada, A Wakisaka, Y Suzuki, T Fukazawa, T Hamada, T Oda, A Ohnishi,[...]. J Neurol Sci 1998
49
22

Meiotic CAG repeat instability in spinocerebellar ataxia type 6: maternally transmitted elongation in a presumed sporadic case.
Suzanne Granhøj Lindquist, Anne Nørremølle, Lena Elisabeth Hjermind, Lis Hasholt, Jørgen Erik Nielsen. J Neurol Sci 2006
6
33

Meiotic instability of the CAG repeats in the SCA6/CACNA1A gene in two Japanese SCA6 families.
H Shimazaki, Y Takiyama, K Sakoe, M Amaike, H Nagaki, M Namekawa, H Sasaki, I Nakano, M Nishizawa. J Neurol Sci 2001
11
22

Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds.
L Schöls, R Krüger, G Amoiridis, H Przuntek, J T Epplen, O Riess. J Neurol Neurosurg Psychiatry 1998
126
22

Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.
K K Sinha, P F Worth, D K Jha, S Sinha, V J Stinton, M B Davis, N W Wood, M G Sweeney, K P Bhatia. J Neurol Neurosurg Psychiatry 2004
50
22




Spinocerebellar ataxia type 6 in Mainland China: molecular and clinical features in four families.
Hong Jiang, Beisha Tang, Kun Xia, Yongxin Zhou, Bo Xu, Guohua Zhao, Haiyan Li, Lu Shen, Qian Pan, Fang Cai. J Neurol Sci 2005
25
22


Gly118Asp is a SCA14 founder mutation in the Dutch ataxia population.
Dineke S Verbeek, Bart P C van de Warrenburg, F A M Hennekam, Dennis Dooijes, P F Ippel, Corien C Verschuuren-Bemelmans, H P H Kremer, Richard J Sinke. Hum Genet 2005
27
22

Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxia.
Yoshio Ikeda, Joline C Dalton, Melinda L Moseley, Kathy L Gardner, Thomas D Bird, Tetsuo Ashizawa, William K Seltzer, Massimo Pandolfo, Aubrey Milunsky, Nicholas T Potter,[...]. Am J Hum Genet 2004
63
22



The hereditary spinocerebellar ataxias in Japan.
H Sasaki, I Yabe, K Tashiro. Cytogenet Genome Res 2003
38
22

Portuguese families with dentatorubropallidoluysian atrophy (DRPLA) share a common haplotype of Asian origin.
Sandra Martins, Teresa Matamá, Laura Guimarães, José Vale, João Guimarães, Lina Ramos, Paula Coutinho, Jorge Sequeiros, Isabel Silveira. Eur J Hum Genet 2003
25
22

Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.
T Matsuura, T Yamagata, D L Burgess, A Rasmussen, R P Grewal, K Watase, M Khajavi, A E McCall, C F Davis, L Zu,[...]. Nat Genet 2000
355
22

Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)n.
Nozomu Sato, Takeshi Amino, Kazuhiro Kobayashi, Shuichi Asakawa, Taro Ishiguro, Taiji Tsunemi, Makoto Takahashi, Tohru Matsuura, Kevin M Flanigan, Sawa Iwasaki,[...]. Am J Hum Genet 2009
180
22

Absence of spinocerebellar ataxia type 3/Machado-Joseph disease within ataxic patients in the Czech population.
P O Bauer, A Zumrova, V Matoska, T Marikova, S Krilova, A Boday, B Singh, P Goetz. Eur J Neurol 2005
12
22

Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family.
Isabel Alonso, José Barros, Assunção Tuna, João Coelho, Jorge Sequeiros, Isabel Silveira, Paula Coutinho. Arch Neurol 2003
60
22

A survey of spinocerebellar ataxia in South Brazil - 66 new cases with Machado-Joseph disease, SCA7, SCA8, or unidentified disease-causing mutations.
L B Jardim, I Silveira, M L Pereira, A Ferro, I Alonso, M do Céu Moreira, P Mendonça, F Ferreirinha, J Sequeiros, R Giugliani. J Neurol 2001
61
22

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
R A Ophoff, G M Terwindt, M N Vergouwe, R van Eijk, P J Oefner, S M Hoffman, J E Lamerdin, H W Mohrenweiser, D E Bulman, M Ferrari,[...]. Cell 1996
22

Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locus.
G Cancel, N Abbas, G Stevanin, A Dürr, H Chneiweiss, C Néri, C Duyckaerts, C Penet, H M Cann, Y Agid. Am J Hum Genet 1995
87
22

Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group.
M A Pujana, J Corral, M Gratacòs, O Combarros, J Berciano, D Genís, I Banchs, X Estivill, V Volpini. Hum Genet 1999
107
22

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
667
22

Evidence of a common founder for SCA12 in the Indian population.
S Bahl, K Virdi, U Mittal, M P Sachdeva, A K Kalla, S E Holmes, E O'Hearn, R L Margolis, S Jain, A K Srivastava,[...]. Ann Hum Genet 2005
42
22


The shortest expanded allele of the MJD1 gene in a Chinese MJD kindred with autonomic dysfunction.
Weihong Gu, Huizi Ma, Kang Wang, Miao Jin, Yongxing Zhou, Xingzhou Liu, Guoxiang Wang, Yan Shen. Eur Neurol 2004
19
22

Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansions.
M Frontali, G Sabbadini, A Novelletto, C Jodice, F Naso, M Spadaro, P Giunti, A G Jacopini, L Veneziano, E Mantuano,[...]. Ann Hum Genet 1996
16
22

The hereditary adult-onset ataxias in South Africa.
Alan Bryer, Amanda Krause, Pierre Bill, Virginia Davids, Daphne Bryant, James Butler, Jeannine Heckmann, Rajkumar Ramesar, Jacquie Greenberg. J Neurol Sci 2003
62
22

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
199
22


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.