A citation-based method for searching scientific literature

Melanie A Knight, R J McKinlay Gardner, Melanie Bahlo, Tohru Matsuura, Judith A Dixon, Susan M Forrest, Elsdon Storey. Brain 2004
Times Cited: 66







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



Times Cited
  Times     Co-cited
Similarity


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
188
46

Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6.
Guo-Yun Yu, Michael J Howell, Matthew J Roller, Ting-Dong Xie, Christopher M Gomez. Ann Neurol 2005
47
53

Spectrin mutations cause spinocerebellar ataxia type 5.
Yoshio Ikeda, Katherine A Dick, Marcy R Weatherspoon, Dan Gincel, Karen R Armbrust, Joline C Dalton, Giovanni Stevanin, Alexandra Dürr, Christine Zühlke, Katrin Bürk,[...]. Nat Genet 2006
242
37

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
175
36

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
342
36

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
36

A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23.
Ming-Yi Chung, Yi-Chun Lu, Nai-Chia Cheng, Bing-Wen Soong. Brain 2003
57
42

Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3.
D S Verbeek, B P van de Warrenburg, P Wesseling, P L Pearson, H P Kremer, R J Sinke. Brain 2004
47
51

SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2.
Claudia Cagnoli, Caterina Mariotti, Franco Taroni, Marco Seri, Alessandro Brussino, Chiara Michielotto, Marina Grisoli, Daniela Di Bella, Nicola Migone, Cinzia Gellera,[...]. Brain 2006
81
36

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
318
34

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
649
33

Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p.
Giovanni Stevanin, Naima Bouslam, Stéphane Thobois, Hamid Azzedine, Lucas Ravaux, Anne Boland, Martin Schalling, Emmanuel Broussolle, Alexandra Dürr, Alexis Brice. Ann Neurol 2004
49
44

An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)
M D Koob, M L Moseley, L J Schut, K A Benzow, T D Bird, J W Day, L P Ranum. Nat Genet 1999
445
33

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
453
31

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
31

A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1.
Isabelle Vuillaume, David Devos, Susanna Schraen-Maschke, Christian Dina, Arnaud Lemainque, Francis Vasseur, Guy Bocquillon, Patrick Devos, Carole Kocinski, Christiane Marzys,[...]. Ann Neurol 2002
45
46

A novel autosomal dominant spinocerebellar ataxia (SCA16) linked to chromosome 8q22.1-24.1.
Y Miyoshi, T Yamada, M Tanimura, T Taniwaki, K Arakawa, Y Ohyagi, H Furuya, K Yamamoto, K Sakai, T Sasazuki,[...]. Neurology 2001
65
30

Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3.
P F Worth, P Giunti, C Gardner-Thorpe, P H Dixon, M B Davis, N W Wood. Am J Hum Genet 1999
90
30

Identification of a novel SCA locus ( SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21.
Dineke S Verbeek, Jurgen H Schelhaas, Elly F Ippel, Frits A Beemer, Peter L Pearson, Richard J Sinke. Hum Genet 2002
49
38

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
28


Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1.
K Flanigan, K Gardner, K Alderson, B Galster, B Otterud, M F Leppert, C Kaplan, L J Ptácek. Am J Hum Genet 1996
184
28

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
599
28

Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes.
Michael F Waters, Natali A Minassian, Giovanni Stevanin, Karla P Figueroa, John P A Bannister, Dagmar Nolte, Allan F Mock, Virgilio Gerald H Evidente, Dominic B Fee, Ulrich Müller,[...]. Nat Genet 2006
200
27

Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.
Zoran Brkanac, Magali Fernandez, Mark Matsushita, Hilary Lipe, John Wolff, Thomas D Bird, Wendy H Raskind. Am J Med Genet 2002
48
35

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
867
24

Clinical features and genetic analysis of a new form of spinocerebellar ataxia.
D Devos, S Schraen-Maschke, I Vuillaume, K Dujardin, P Nazé, C Willoteaux, A Destée, B Sablonnière. Neurology 2001
49
32

Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11.
Henry Houlden, Janel Johnson, Christopher Gardner-Thorpe, Tammaryn Lashley, Dena Hernandez, Paul Worth, Andrew B Singleton, David A Hilton, Janice Holton, Tamas Revesz,[...]. Nat Genet 2007
115
24

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
608
22

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
701
22

Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation.
A Herman-Bert, G Stevanin, J C Netter, O Rascol, D Brassat, P Calvas, A Camuzat, Q Yuan, M Schalling, A Dürr,[...]. Am J Hum Genet 2000
96
22

Clinical and genetic analysis of a four-generation family with a distinct autosomal dominant cerebellar ataxia.
H J Schelhaas, P F Ippel, G Hageman, R J Sinke, E N van der Laan, F A Beemer. J Neurol 2001
41
34

Spinocerebellar ataxia type 5: clinical and molecular genetic features of a German kindred.
K Bürk, C Zühlke, I R König, A Ziegler, E Schwinger, C Globas, J Dichgans, Y Hellenbroich. Neurology 2004
43
32

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
192
21

A form of inherited cerebellar ataxia with saccadic intrusions, increased saccadic speed, sensory neuropathy, and myoclonus.
Barbara E Swartz, Margit Burmeister, Jeffrey T Somers, Klaus G Rottach, Irina N Bespalova, R John Leigh. Ann N Y Acad Sci 2002
29
44

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
77
18

A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter.
Zoran Brkanac, Laura Bylenok, Magali Fernandez, Mark Matsushita, Hillary Lipe, John Wolff, David Nochlin, Wendy H Raskind, Thomas D Bird. Arch Neurol 2002
46
26

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA).
R Koide, T Ikeuchi, O Onodera, H Tanaka, S Igarashi, K Endo, H Takahashi, R Kondo, A Ishikawa, T Hayashi. Nat Genet 1994
975
18

Clinical and MRI findings in spinocerebellar ataxia type 5.
G Stevanin, A Herman, A Brice, A Dürr. Neurology 1999
55
21

An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains.
Kinya Ishikawa, Shuta Toru, Taiji Tsunemi, Mingshun Li, Kazuhiro Kobayashi, Takanori Yokota, Takeshi Amino, Kiyoshi Owada, Hiroto Fujigasaki, Masaki Sakamoto,[...]. Am J Hum Genet 2005
96
18

Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus.
T E Dudding, K Friend, P W Schofield, S Lee, I A Wilkinson, R I Richards. Neurology 2004
58
20

A duplication at chromosome 11q12.2-11q12.3 is associated with spinocerebellar ataxia type 20.
Melanie A Knight, Dena Hernandez, Scott J Diede, Hans G Dauwerse, Ian Rafferty, Joyce van de Leemput, Susan M Forrest, R J McKinlay Gardner, Elsdon Storey, Gert-Jan B van Ommen,[...]. Hum Mol Genet 2008
34
35

A novel locus for dominant cerebellar ataxia (SCA14) maps to a 10.2-cM interval flanked by D19S206 and D19S605 on chromosome 19q13.4-qter.
I Yamashita, H Sasaki, I Yabe, T Fukazawa, S Nogoshi, K Komeichi, A Takada, K Shiraishi, Y Takiyama, M Nishizawa,[...]. Ann Neurol 2000
83
16

Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter: exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutant.
Melanie A Knight, Marina L Kennerson, Richard J Anney, Tohru Matsuura, Garth A Nicholson, Peyman Salimi-Tari, R J McKinlay Gardner, Elsdon Storey, Susan M Forrest. Neurobiol Dis 2003
51
21

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
276
16

A new autosomal dominant pure cerebellar ataxia.
E Storey, R J Gardner, M A Knight, M L Kennerson, R R Tuck, S M Forrest, G A Nicholson. Neurology 2001
50
22

SCA-12: Tremor with cerebellar and cortical atrophy is associated with a CAG repeat expansion.
E O'Hearn, S E Holmes, P C Calvert, C A Ross, R L Margolis. Neurology 2001
80
16

Mutation analysis in the fibroblast growth factor 14 gene: frameshift mutation and polymorphisms in patients with inherited ataxias.
Andreas Dalski, Jassemien Atici, Friedmar R Kreuz, Yorck Hellenbroich, Eberhard Schwinger, Christine Zühlke. Eur J Hum Genet 2005
66
16

Molecular pathogenesis of spinocerebellar ataxias.
Antoni Matilla Dueñas, Robert Goold, Paola Giunti. Brain 2006
153
16

Clinical and genetic analysis of four Mexican families with spinocerebellar ataxia type 10.
A Rasmussen, T Matsuura, L Ruano, P Yescas, A Ochoa, T Ashizawa, E Alonso. Ann Neurol 2001
87
16


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.