A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity




Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria.
M K Bruno, M Hallett, K Gwinn-Hardy, B Sorensen, E Considine, S Tucker, D R Lynch, K D Mathews, K J Swoboda, J Harris,[...]. Neurology 2004
258
41


Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation of the syndrome and gene mapping to chromosome 16p12-11.2.
R Guerrini, P Bonanni, N Nardocci, L Parmeggiani, M Piccirilli, M De Fusco, P Aridon, A Ballabio, R Carrozzo, G Casari. Ann Neurol 1999
119
32

Paroxysmal exercise-induced dystonia: eight new sporadic cases and a review of the literature.
K P Bhatia, V L Soland, M H Bhatt, N P Quinn, C D Marsden. Mov Disord 1997
76
40

Familial paroxysmal dystonia induced by exercise.
G T Plant, A C Williams, C J Earl, C D Marsden. J Neurol Neurosurg Psychiatry 1984
69
39

Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11.2-q12.1.
H a Tomita, S Nagamitsu, K Wakui, Y Fukushima, K Yamada, M Sadamatsu, A Masui, T Konishi, T Matsuishi, M Aihara,[...]. Am J Hum Genet 1999
122
27

Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies.
K J Swoboda, B Soong, C McKenna, E R Brunt, M Litt, J F Bale, T Ashizawa, L B Bennett, A M Bowcock, E S Roach,[...]. Neurology 2000
94
27


Myofibrillogenesis regulator 1 gene mutations cause paroxysmal dystonic choreoathetosis.
Shirley Rainier, Donald Thomas, Debra Tokarz, Lei Ming, Melanie Bui, Erin Plein, Xinping Zhao, Rosemary Lemons, Roger Albin, Colin Delaney,[...]. Arch Neurol 2004
110
25

A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study.
A Münchau, E M Valente, G A Shahidi, L H Eunson, M G Hanna, N P Quinn, A H Schapira, N W Wood, K P Bhatia. J Neurol Neurosurg Psychiatry 2000
49
48

Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia.
M K Bruno, H-Y Lee, G W J Auburger, A Friedman, J E Nielsen, A E Lang, E Bertini, P Van Bogaert, Y Averyanov, M Hallett,[...]. Neurology 2007
91
26

Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.
Arvid Suls, Peter Dedeken, Karolien Goffin, Hilde Van Esch, Patrick Dupont, David Cassiman, Judith Kempfle, Thomas V Wuttke, Yvonne Weber, Holger Lerche,[...]. Brain 2008
210
24


The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway.
Hsien-Yang Lee, Ying Xu, Yong Huang, Andrew H Ahn, Georg W J Auburger, Massimo Pandolfo, Hubert Kwiecinski, David A Grimes, Anthony E Lang, Jorgen E Nielsen,[...]. Hum Mol Genet 2004
106
23


Paroxysmal kinesigenic choreoathetosis: a report of 26 patients.
M K Houser, V L Soland, K P Bhatia, N P Quinn, C D Marsden. J Neurol 1999
83
26

The paroxysmal dyskinesias.
K P Bhatia. J Neurol 1999
82
26

Secondary paroxysmal dyskinesias.
Jaishri Blakeley, Joseph Jankovic. Mov Disord 2002
93
23

Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia.
Wan-Jin Chen, Yu Lin, Zhi-Qi Xiong, Wei Wei, Wang Ni, Guo-He Tan, Shun-Ling Guo, Jin He, Ya-Fang Chen, Qi-Jie Zhang,[...]. Nat Genet 2011
320
22

GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak.
Yvonne G Weber, Alexander Storch, Thomas V Wuttke, Knut Brockmann, Judith Kempfle, Snezana Maljevic, Lucia Margari, Christoph Kamm, Susanne A Schneider, Stephan M Huber,[...]. J Clin Invest 2008
234
21

A locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16.
L B Bennett, E S Roach, A M Bowcock. Neurology 2000
95
21

A gene for familial paroxysmal dyskinesia (FPD1) maps to chromosome 2q.
G T Fouad, S Servidei, S Durcan, E Bertini, L J Ptácek. Am J Hum Genet 1996
110
18

Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q.
J K Fink, S Rainer, J Wilkowski, S M Jones, A Kume, P Hedera, R Albin, J Mathay, L Girbach, T Varvil,[...]. Am J Hum Genet 1996
100
18


Changes in perfusion pattern using ECD-SPECT indicate frontal lobe and cerebellar involvement in exercise-induced paroxysmal dystonia.
A Kluge, B Kettner, R Zschenderlein, D Sandrock, D L Munz, S Hesse, H Meierkord. Mov Disord 1998
44
38


Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder.
Wei Du, Jocelyn F Bautista, Huanghe Yang, Ana Diez-Sampedro, Sun-Ah You, Lejin Wang, Prakash Kotagal, Hans O Lüders, Jingyi Shi, Jianmin Cui,[...]. Nat Genet 2005
387
17

Paroxysmal dyskinesias.
Kailash P Bhatia. Mov Disord 2011
110
16

Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias.
Jun-Ling Wang, Li Cao, Xun-Hua Li, Zheng-Mao Hu, Jia-Da Li, Jian-Guo Zhang, Yu Liang, San-A, Nan Li, Su-Qin Chen,[...]. Brain 2011
206
16






Typical and atypical forms of paroxysmal choreoathetosis.
N Nardocci, E Lamperti, V Rumi, L Angelini. Dev Med Child Neurol 1989
36
36

Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene.
Sian D Spacey, Enza-Maria Valente, Gurusidheshwar M Wali, Thomas T Warner, Paul R Jarman, Anthony H V Schapira, Peter H Dixon, Mary B Davis, Kailash P Bhatia, Nicholas W Wood. Mov Disord 2002
45
28


PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome.
Sarah E Heron, Bronwyn E Grinton, Sara Kivity, Zaid Afawi, Sameer M Zuberi, James N Hughes, Clair Pridmore, Bree L Hodgson, Xenia Iona, Lynette G Sadleir,[...]. Am J Hum Genet 2012
185
13

PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European population.
Aurélie Méneret, David Grabli, Christel Depienne, Cécile Gaudebout, Fabienne Picard, Alexandra Dürr, Isabelle Lagroua, Delphine Bouteiller, Cyril Mignot, Diane Doummar,[...]. Neurology 2012
72
18

Familial paroxysmal kinesigenic choreoathetosis: an electrophysiologic and genotypic analysis.
M Sadamatsu, A Masui, T Sakai, H Kunugi, S Nanko, N Kato. Epilepsia 1999
27
44

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1.
D L Browne, S T Gancher, J G Nutt, E R Brunt, E A Smith, P Kramer, M Litt. Nat Genet 1994
593
12

PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine.
Alice R Gardiner, Kailash P Bhatia, Maria Stamelou, Russell C Dale, Manju A Kurian, Susanne A Schneider, G M Wali, Tim Counihan, Anthony H Schapira, Sian D Spacey,[...]. Neurology 2012
118
12

The clinical and genetic heterogeneity of paroxysmal dyskinesias.
Alice R Gardiner, Fatima Jaffer, Russell C Dale, Robyn Labrum, Roberto Erro, Esther Meyer, Georgia Xiromerisiou, Maria Stamelou, Matthew Walker, Dimitri Kullmann,[...]. Brain 2015
85
14

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
11

Familial paroxysmal dystonic choreoathetosis: clinical findings in a large Japanese family and genetic linkage to 2q.
H Matsuo, K Kamakura, M Saito, M Okano, T Nagase, Y Tadano, K Kaida, A Hirata, N Miyamoto, T Masaki,[...]. Arch Neurol 1999
32
34

Further localization of a gene for paroxysmal dystonic choreoathetosis to a 5-cM region on chromosome 2q34.
W H Raskind, T Bolin, J Wolff, J Fink, M Matsushita, M Litt, H Lipe, T D Bird. Hum Genet 1998
28
39

Epilepsy and paroxysmal movement disorders in families: evidence for shared mechanisms.
R Singh, R A Macdonell, I E Scheffer, K M Crossland, S F Berkovic. Epileptic Disord 1999
34
32

GLUT1 gene mutations cause sporadic paroxysmal exercise-induced dyskinesias.
Susanne A Schneider, Coro Paisan-Ruiz, Ines Garcia-Gorostiaga, Niall P Quinn, Yvonne G Weber, Holger Lerche, John Hardy, Kailash P Bhatia. Mov Disord 2009
73
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.