A citation-based method for searching scientific literature

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, K Gwinn-Hardy, B Sorenson, M Pandolfo, H Kwiecinski, S Servidei, Y-H Fu, L Ptácek. Neurology 2007
Times Cited: 91







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



Times Cited
  Times     Co-cited
Similarity



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
51

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
50

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
42

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
39

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
34

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
32



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
25


Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions.
Hsien-Yang Lee, Yong Huang, Nadine Bruneau, Patrice Roll, Elisha D O Roberson, Mark Hermann, Emily Quinn, James Maas, Robert Edwards, Tetsuo Ashizawa,[...]. Cell Rep 2012
181
24

Paroxysmal dyskinesias.
Kailash P Bhatia. Mov Disord 2011
110
24

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
21

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
27


Paroxysmal non-kinesigenic dyskinesia is caused by mutations of the MR-1 mitochondrial targeting sequence.
Daniele Ghezzi, Carlo Viscomi, Alessandra Ferlini, Francesca Gualandi, Paolo Mereghetti, Domenico DeGrandis, Massimo Zeviani. Hum Mol Genet 2009
50
38

Secondary paroxysmal dyskinesias.
Jaishri Blakeley, Joseph Jankovic. Mov Disord 2002
93
19

Genetic heterogeneity in paroxysmal nonkinesigenic dyskinesia.
S D Spacey, P J Adams, P C P Lam, L A Materek, A J Stoessl, T P Snutch, G-Y R Hsiung. Neurology 2006
27
66

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
19

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
19


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
23

Mutations in PRRT2 result in paroxysmal dyskinesias with marked variability in clinical expression.
Qing Liu, Zhan Qi, Xin-Hua Wan, Jing-Yun Li, Lei Shi, Qiang Lu, Xiang-Qin Zhou, Lei Qiao, Li-Wen Wu, Xiu-Qin Liu,[...]. J Med Genet 2012
75
22


Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: confirmation in 2 kindreds.
Dong-Hui Chen, Mark Matsushita, Shirley Rainier, Brandon Meaney, Lisa Tisch, Abreham Feleke, John Wolff, Hillary Lipe, John Fink, Thomas D Bird,[...]. Arch Neurol 2005
34
47

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
17

Clinical characteristics of paroxysmal nonkinesigenic dyskinesia in Serbian family with Myofibrillogenesis regulator 1 gene mutation.
Elka Stefanova, Ana Djarmati, Dragana Momcilović, Natasa Dragasević, Marina Svetel, Christine Klein, Vladimir S Kostić. Mov Disord 2006
20
75

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
16

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
31

Myofibrillogenesis regulator 1 gene (MR-1) mutation in an Omani family with paroxysmal nonkinesigenic dyskinesia.
Anne Hempelmann, Santosh Kumar, Shanmugakonar Muralitharan, Thomas Sander. Neurosci Lett 2006
19
73

PRRT2 phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsions.
Rianne van Vliet, Guido Breedveld, Johanneke de Rijk-van Andel, Eva Brilstra, Nienke Verbeek, Corien Verschuuren-Bemelmans, Maartje Boon, Johnny Samijn, Karin Diderich, Ingrid van de Laar,[...]. Neurology 2012
63
22

Familial paroxysmal dystonia induced by exercise.
G T Plant, A C Williams, C J Earl, C D Marsden. J Neurol Neurosurg Psychiatry 1984
69
18

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
14

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
15

Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions.
Shinji Ono, Koh-ichiro Yoshiura, Akira Kinoshita, Taeko Kikuchi, Yoshibumi Nakane, Nobumasa Kato, Miyuki Sadamatsu, Tohru Konishi, Shinichiro Nagamitsu, Masato Matsuura,[...]. J Hum Genet 2012
67
19

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
15

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
24

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
15

A locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16.
L B Bennett, E S Roach, A M Bowcock. Neurology 2000
95
13

Paroxysmal kinesigenic choreoathetosis (PKC): confirmation of linkage to 16p11-q21, but unsuccessful detection of mutations among 157 genes at the PKC-critical region in seven PKC families.
Taeko Kikuchi, Masayo Nomura, Hiroaki Tomita, Naoki Harada, Kazuaki Kanai, Tohru Konishi, Ayako Yasuda, Masato Matsuura, Nobumasa Kato, Koh-Ichiro Yoshiura,[...]. J Hum Genet 2007
33
36

The paroxysmal dyskinesias.
K P Bhatia. J Neurol 1999
82
14

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
13

Targeted genomic sequencing identifies PRRT2 mutations as a cause of paroxysmal kinesigenic choreoathetosis.
Jingyun Li, Xilin Zhu, Xin Wang, Wei Sun, Bing Feng, Te Du, Bei Sun, Fenghe Niu, Hua Wei, Xiaopan Wu,[...]. J Med Genet 2012
76
15

Identification of a novel PRRT2 mutation in patients with paroxysmal kinesigenic dyskinesias and c.649dupC as a mutation hot-spot.
Li Cao, Xiao-Jun Huang, Lan Zheng, Qin Xiao, Xi-Jin Wang, Sheng-Di Chen. Parkinsonism Relat Disord 2012
46
26

Dopamine dysregulation in a mouse model of paroxysmal nonkinesigenic dyskinesia.
Hsien-yang Lee, Junko Nakayama, Ying Xu, Xueliang Fan, Maha Karouani, Yiguo Shen, Emmanuel N Pothos, Ellen J Hess, Ying-Hui Fu, Robert H Edwards,[...]. J Clin Invest 2012
36
33

Mutations in PNKD causing paroxysmal dyskinesia alters protein cleavage and stability.
Yiguo Shen, Hsien-Yang Lee, Joel Rawson, Sunil Ojha, Patricia Babbitt, Ying-Hui Fu, Louis J Ptácek. Hum Mol Genet 2011
30
40

Familial PRRT2 mutation with heterogeneous paroxysmal disorders including paroxysmal torticollis and hemiplegic migraine.
Russell C Dale, Alice Gardiner, Jayne Antony, Henry Houlden. Dev Med Child Neurol 2012
73
16


A family with paroxysmal nonkinesigenic dyskinesia: genetic and treatment issues.
Krzysztof Szczałuba, Marta Jurek, Elzbieta Szczepanik, Andrzej Friedman, Michał Milewski, Jerzy Bal, Tadeusz Mazurczak. Pediatr Neurol 2009
15
73


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.