A citation-based method for searching scientific literature

Hong-Fu Li, Wang Ni, Zhi-Qi Xiong, Jianfeng Xu, Zhi-Ying Wu. CNS Neurosci Ther 2013
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


Novel loss-of-function PRRT2 mutation causes paroxysmal kinesigenic dyskinesia in a Han Chinese family.
Zhisong Ji, Quanxi Su, Lingling Hu, Qi Yang, Cuixian Liu, Jun Xiong, Fu Xiong. BMC Neurol 2014
5
40

Clinical and genetic features of paroxysmal kinesigenic dyskinesia in Italian patients.
Costanza Lamperti, Federica Invernizzi, Roberta Solazzi, Elena Freri, Francesco Carella, Massimo Zeviani, Federica Zibordi, Carlo Fusco, Giovanna Zorzi, Tiziana Granata,[...]. Eur J Paediatr Neurol 2016
11
18

Functional study and pathogenicity classification of PRRT2 missense variants in PRRT2-related disorders.
Shao-Yun Zhao, Li-Xi Li, Yu-Lan Chen, Yi-Jun Chen, Gong-Lu Liu, Hai-Lin Dong, Dian-Fu Chen, Hong-Fu Li, Zhi-Ying Wu. CNS Neurosci Ther 2020
5
40

PRRT2 Regulates Synaptic Fusion by Directly Modulating SNARE Complex Assembly.
Jeff Coleman, Ouardane Jouannot, Sathish K Ramakrishnan, Maria N Zanetti, Jing Wang, Vincenzo Salpietro, Henry Houlden, James E Rothman, Shyam S Krishnakumar. Cell Rep 2018
40
11

A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1B.
Hongying Ma, Shenglei Feng, Xuejun Deng, Li Wang, Sheng Zeng, Cheng Wang, Xixiang Ma, Hao Sun, Rui Chen, Shiyue Du,[...]. Epilepsia 2018
8
25

Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity.
M Malacarne, E Gennaro, F Madia, S Pozzi, D Vacca, B Barone, B dalla Bernardina, A Bianchi, P Bonanni, P De Marco,[...]. Am J Hum Genet 2001
53
5

A comprehensive genetic map of the human genome based on 5,264 microsatellites.
C Dib, S Fauré, C Fizames, D Samson, N Drouot, A Vignal, P Millasseau, S Marc, J Hazan, E Seboun,[...]. Nature 1996
5


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
5

Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families.
Pasquale Striano, Maria Luisa Lispi, Elena Gennaro, Francesca Madia, Monica Traverso, Laura Bordo, Paolo Aridon, Filippo Martinelli Boneschi, Baldassare Barone, Bernardo dalla Bernardina,[...]. Epilepsia 2006
21
5

Linkage mapping of benign familial infantile convulsions (BFIC) to chromosome 19q.
M Guipponi, F Rivier, F Vigevano, C Beck, A Crespel, B Echenne, P Lucchini, R Sebastianelli, M Baldy-Moulinier, A Malafosse. Hum Mol Genet 1997
157
5

A BFIS-like syndrome with late onset and febrile seizures: suggestive linkage to chromosome 16p11.2-16q12.1.
Yvonne G Weber, Miriam Jacob, Gabriele Weber, Holger Lerche. Epilepsia 2008
22
5



Complex Loci in human and mouse genomes.
Pär G Engström, Harukazu Suzuki, Noriko Ninomiya, Altuna Akalin, Luca Sessa, Giovanni Lavorgna, Alessandro Brozzi, Lucilla Luzi, Sin Lam Tan, Liang Yang,[...]. PLoS Genet 2006
240
5

Defining and refining the phenotype of PRRT2 mutations.
Jonathan W Mink. Dev Med Child Neurol 2013
4
25

Benign familial infantile convulsions: linkage to chromosome 16p12-q12 in 14 families.
Yvonne G Weber, Andrea Berger, Nerses Bebek, Sabine Maier, Skevos Karafyllakes, Nancy Meyer, Yukio Fukuyama, Anne Halbach, Christiane Hikel, Gerhard Kurlemann,[...]. Epilepsia 2004
34
5



Refinement of the chromosome 16 locus for benign familial infantile convulsions.
P M C Callenbach, E H van den Boogerd, R F M de Coo, R ten Houten, J C Oosterwijk, G Hageman, R R Frants, O F Brouwer, A M J M van den Maagdenberg. Clin Genet 2005
22
5

Benign infantile familial convulsions.
F Vigevano, L Fusco, M Di Capua, S Ricci, R Sebastianelli, P Lucchini. Eur J Pediatr 1992
181
5

Good outcome in patients with early dietary treatment of GLUT-1 deficiency syndrome: results from a retrospective Norwegian study.
Anette Ramm-Pettersen, Karl O Nakken, Inger M Skogseid, Hans Randby, Erik B Skei, Laurence A Bindoff, Kaja K Selmer. Dev Med Child Neurol 2013
43
5

Milder phenotypes of glucose transporter type 1 deficiency syndrome.
Geetha Anand, Anuruddha Padeniya, Donncha Hanrahan, Hans Scheffer, Zenobia Zaiwalla, Debbie Cox, Nicholas Mann, John Hewertson, Sue Price, Andrea Nemeth,[...]. Dev Med Child Neurol 2011
12
8

Primary and secondary dystonic syndromes: an update.
Gavin Charlesworth, Kailash P Bhatia. Curr Opin Neurol 2013
10
10

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
5

Paroxysmal exercise-induced dyskinesia with self-limiting partial epilepsy: a novel GLUT-1 mutation with benign phenotype.
Tommaso Bovi, Alfonso Fasano, Ina Juergenson, Cinzia Gellera, Barbara Castellotti, Elena Fontana, Michele Tinazzi. Parkinsonism Relat Disord 2011
12
8

Glut1 deficiency syndrome and erythrocyte glucose uptake assay.
Hong Yang, Dong Wang, Kristin Engelstad, Leslie Bagay, Ying Wei, Michael Rotstein, Vimla Aggarwal, Brynn Levy, Lijiang Ma, Wendy K Chung,[...]. Ann Neurol 2011
62
5

Fixing the broken system of genetic locus symbols: Parkinson disease and dystonia as examples.
Connie Marras, Katja Lohmann, Anthony Lang, Christine Klein. Neurology 2012
40
5

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
5

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
5

The genetics of dystonia: new twists in an old tale.
Gavin Charlesworth, Kailash P Bhatia, Nicholas W Wood. Brain 2013
68
5

Glut1 deficiency: inheritance pattern determined by haploinsufficiency.
Michael Rotstein, Kristin Engelstad, Hong Yang, Dong Wang, Brynn Levy, Wendy K Chung, Darryl C De Vivo. Ann Neurol 2010
60
5

GLUT1 deficiency syndrome 2013: current state of the art.
Valentina De Giorgis, Pierangelo Veggiotti. Seizure 2013
118
5

Allelic variations of glut-1 deficiency syndrome: the chinese experience.
Yanyan Liu, Xinhua Bao, Dong Wang, Na Fu, Xiaoying Zhang, Guangna Cao, Fuying Song, Shuang Wang, Yuehua Zhang, Jiong Qin,[...]. Pediatr Neurol 2012
7
14

Caffeine improved paroxysmal dyskinesia caused by the PRRT2 mutation.
Virginie Lambrecq, Florence Riant, Elisabeth Tournier-Lasserve, Véronique Michel, Pierre Burbaud. Mov Disord 2013
1
100

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
61
5

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
6

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
5

Familial paroxysmal nonkinesigenic dyskinesia: clinical and genetic analysis of a Taiwanese family.
Tu-Hsueh Yeh, Juei-Jueng Lin, Szu-Chia Lai, Yah-Huei Wu-Chou, An-Chih Chen, Kuo-Chu Yueh, Rou-Shayn Chen, Chin-Song Lu. J Neurol Sci 2012
16
6

Paroxysmal exercise-induced dyskinesia, writer's cramp, migraine with aura and absence epilepsy in twin brothers with a novel SLC2A1 missense mutation.
Aintzane Urbizu, Ester Cuenca-León, Miquel Raspall-Chaure, Margarida Gratacòs, Joan Conill, Susana Redecillas, Manuel Roig-Quilis, Alfons Macaya. J Neurol Sci 2010
38
5

Episodic movement disorders: from phenotype to genotype and back.
Knut Brockmann. Curr Neurol Neurosci Rep 2013
5
20

Paroxysmal movement disorders and episodic ataxias.
Emilio Fernández-Alvarez, Belén Perez-Dueñas. Handb Clin Neurol 2013
5
20

Paroxysmal non-kinesigenic dyskinesia due to a PNKD recurrent mutation: report of two Southern European families.
Roser Pons, Ester Cuenca-León, Elena Miravet, Montse Pons, Athina Xaidara, Sotiris Youroukos, Alfons Macaya. Eur J Paediatr Neurol 2012
15
6

Mild adolescent/adult onset epilepsy and paroxysmal exercise-induced dyskinesia due to GLUT1 deficiency.
Zaid Afawi, Arvid Suls, Dana Ekstein, Sara Kivity, Miriam Y Neufeld, Karen Oliver, Peter De Jonghe, Amos D Korczyn, Samuel F Berkovic. Epilepsia 2010
17
5

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
229
5

Paroxysmal movement disorders in GLUT1 deficiency syndrome.
G Zorzi, B Castellotti, F Zibordi, C Gellera, N Nardocci. Neurology 2008
51
5

Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2.
Rosanna Cardani, Marzia Giagnacovo, Annalisa Botta, Fabrizio Rinaldi, Alessandra Morgante, Bjarne Udd, Olayinka Raheem, Sini Penttilä, Tiina Suominen, Laura V Renna,[...]. J Neurol 2012
33
5

Non-genomic effects of sex hormones on CLC-1 may contribute to gender differences in myotonia congenita.
Doreen Fialho, Dimitri M Kullmann, Michael G Hanna, Stephanie Schorge. Neuromuscul Disord 2008
24
5

Myotonia congenita and myotonic dystrophy: surveillance and management.
Allison Conravey, Lenay Santana-Gould. Curr Treat Options Neurol 2010
8
12

Myotonia congenita.
Christoph Lossin, Alfred L George. Adv Genet 2008
81
5


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.