A citation-based method for searching scientific literature

Shirley Rainier, Donald Thomas, Debra Tokarz, Lei Ming, Melanie Bui, Erin Plein, Xinping Zhao, Rosemary Lemons, Roger Albin, Colin Delaney, David Alvarado, John K Fink. Arch Neurol 2004
Times Cited: 110







List of co-cited articles
1078 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
104
64

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
231
46


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
89
43

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
207
37

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
301
35

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
241
34

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
48
56

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
200
27

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
73

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
373
24

The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein.
L J Ozelius, J W Hewett, C E Page, S B Bressman, P L Kramer, C Shalish, D de Leon, M F Brin, D Raymond, D P Corey,[...]. Nat Genet 1997
750
24


Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome.
A Zimprich, M Grabowski, F Asmus, M Naumann, D Berg, M Bertram, K Scheidtmann, P Kern, J Winkelmann, B Müller-Myhsok,[...]. Nat Genet 2001
314
22

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
22

Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism.
Patricia de Carvalho Aguiar, Kathleen J Sweadner, John T Penniston, Jacek Zaremba, Liu Liu, Marsha Caton, Gurutz Linazasoro, Michel Borg, Marina A J Tijssen, Susan B Bressman,[...]. Neuron 2004
316
21

DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA.
Sarah Camargos, Sonja Scholz, Javier Simón-Sánchez, Coro Paisán-Ruiz, Patrick Lewis, Dena Hernandez, Jinhui Ding, J Raphael Gibbs, Mark R Cookson, Jose Bras,[...]. Lancet Neurol 2008
127
21

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
72
29


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
175
20

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
70

Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene.
H Ichinose, T Ohye, E Takahashi, N Seki, T Hori, M Segawa, Y Nomura, K Endo, H Tanaka, S Tsuji. Nat Genet 1994
586
19



Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia.
Tania Fuchs, Sophie Gavarini, Rachel Saunders-Pullman, Deborah Raymond, Michelle E Ehrlich, Susan B Bressman, Laurie J Ozelius. Nat Genet 2009
211
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
17

Reduced neuron-specific expression of the TAF1 gene is associated with X-linked dystonia-parkinsonism.
Satoshi Makino, Ryuji Kaji, Satoshi Ando, Maiko Tomizawa, Katsuhito Yasuno, Satoshi Goto, Shinnichi Matsumoto, Maria Daisy Tabuena, Elma Maranon, Marita Dantes,[...]. Am J Hum Genet 2007
142
17

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
171
17


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
16

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
118
16

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
84

Secondary paroxysmal dyskinesias.
Jaishri Blakeley, Joseph Jankovic. Mov Disord 2002
89
17

Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect.
Y G Weber, C Kamm, A Suls, J Kempfle, K Kotschet, R Schüle, T V Wuttke, S Maljevic, J Liebrich, T Gasser,[...]. Neurology 2011
57
28

Paroxysmal dyskinesias.
Kailash P Bhatia. Mov Disord 2011
105
16

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

Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.
Wilhelmina G Leen, Joerg Klepper, Marcel M Verbeek, Maike Leferink, Tom Hofste, Baziel G van Engelen, Ron A Wevers, Todd Arthur, Nadia Bahi-Buisson, Diana Ballhausen,[...]. Brain 2010
217
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
48
29


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
75
18

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
64
21

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
112
14

The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene.
Allison Brashear, William B Dobyns, Patricia de Carvalho Aguiar, Michel Borg, C J M Frijns, Seema Gollamudi, Andrew Green, João Guimaraes, Bret C Haake, Christine Klein,[...]. Brain 2007
156
13

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
13

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
17

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
25
52

The evolving spectrum of PRRT2-associated paroxysmal diseases.
Darius Ebrahimi-Fakhari, Afshin Saffari, Ana Westenberger, Christine Klein. Brain 2015
133
13


Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures.
J C Jen, J Wan, T P Palos, B D Howard, R W Baloh. Neurology 2005
224
12


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.