A citation-based method for searching scientific literature

Wei Du, Jocelyn F Bautista, Huanghe Yang, Ana Diez-Sampedro, Sun-Ah You, Lejin Wang, Prakash Kotagal, Hans O Lüders, Jingyi Shi, Jianmin Cui, George B Richerson, Qing K Wang. Nat Genet 2005
Times Cited: 369







List of co-cited articles
1332 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


De novo KCNMA1 mutations in children with early-onset paroxysmal dyskinesia and developmental delay.
Zhong-Bin Zhang, Mao-Qiang Tian, Kai Gao, Yu-Wu Jiang, Ye Wu. Mov Disord 2015
32
75

BK channel beta4 subunit reduces dentate gyrus excitability and protects against temporal lobe seizures.
Robert Brenner, Qing H Chen, Alex Vilaythong, Glenn M Toney, Jeffrey L Noebels, Richard W Aldrich. Nat Neurosci 2005
259
22

An epilepsy/dyskinesia-associated mutation enhances BK channel activation by potentiating Ca2+ sensing.
Junqiu Yang, Gayathri Krishnamoorthy, Akansha Saxena, Guohui Zhang, Jingyi Shi, Huanghe Yang, Kelli Delaloye, David Sept, Jianmin Cui. Neuron 2010
68
27

Homozygous KCNMA1 mutation as a cause of cerebellar atrophy, developmental delay and seizures.
Brahim Tabarki, Nabil AlMajhad, Amal AlHashem, Ranad Shaheen, Fowzan S Alkuraya. Hum Genet 2016
28
57

Multiple regulatory sites in large-conductance calcium-activated potassium channels.
Xiao-Ming Xia, Xuhui Zeng, Christopher J Lingle. Nature 2002
278
14

Cerebellar ataxia and Purkinje cell dysfunction caused by Ca2+-activated K+ channel deficiency.
M Sausbier, H Hu, C Arntz, S Feil, S Kamm, H Adelsberger, U Sausbier, C A Sailer, R Feil, F Hofmann,[...]. Proc Natl Acad Sci U S A 2004
302
14


Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation.
Elena Gardella, Felicitas Becker, Rikke S Møller, Julian Schubert, Johannes R Lemke, Line H G Larsen, Hans Eiberg, Michael Nothnagel, Holger Thiele, Janine Altmüller,[...]. Ann Neurol 2016
101
14

De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy.
Giulia Barcia, Matthew R Fleming, Aline Deligniere, Valeswara-Rao Gazula, Maile R Brown, Maeva Langouet, Haijun Chen, Jack Kronengold, Avinash Abhyankar, Roberta Cilio,[...]. Nat Genet 2012
265
14

KCNMA1-linked channelopathy.
Cole S Bailey, Hans J Moldenhauer, Su Mi Park, Sotirios Keros, Andrea L Meredith. J Gen Physiol 2019
33
42


De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy.
Steffen Syrbe, Ulrike B S Hedrich, Erik Riesch, Tania Djémié, Stephan Müller, Rikke S Møller, Bridget Maher, Laura Hernandez-Hernandez, Matthis Synofzik, Hande S Caglayan,[...]. Nat Genet 2015
142
13

De novo BK channel variant causes epilepsy by affecting voltage gating but not Ca2+ sensitivity.
Xia Li, Sibylle Poschmann, Qiuyun Chen, Walid Fazeli, Nelly Jouayed Oundjian, Francesca M Snoeijen-Schouwenaars, Oliver Fricke, Erik-Jan Kamsteeg, Marjolein Willemsen, Qing Kenneth Wang. Eur J Hum Genet 2018
17
76


Mechanism of increased BK channel activation from a channel mutation that causes epilepsy.
Bin Wang, Brad S Rothberg, Robert Brenner. J Gen Physiol 2009
44
27

Overactive bladder and incontinence in the absence of the BK large conductance Ca2+-activated K+ channel.
Andrea L Meredith, Kevin S Thorneloe, Matthias E Werner, Mark T Nelson, Richard W Aldrich. J Biol Chem 2004
266
11

BK potassium channel modulation by leucine-rich repeat-containing proteins.
Jiusheng Yan, Richard W Aldrich. Proc Natl Acad Sci U S A 2012
129
11

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
11

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
297
11

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
229
11

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
237
11

KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.
Sarah Weckhuysen, Simone Mandelstam, Arvid Suls, Dominique Audenaert, Tine Deconinck, Lieve R F Claes, Liesbet Deprez, Katrien Smets, Dimitrina Hristova, Iglika Yordanova,[...]. Ann Neurol 2012
284
11

A potassium channel mutation in neonatal human epilepsy.
C Biervert, B C Schroeder, C Kubisch, S F Berkovic, P Propping, T J Jentsch, O K Steinlein. Science 1998
789
11

The evolving spectrum of PRRT2-associated paroxysmal diseases.
Darius Ebrahimi-Fakhari, Afshin Saffari, Ana Westenberger, Christine Klein. Brain 2015
128
11

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
78
14

Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy.
Sarah E Heron, Katherine R Smith, Melanie Bahlo, Lino Nobili, Esther Kahana, Laura Licchetta, Karen L Oliver, Aziz Mazarib, Zaid Afawi, Amos Korczyn,[...]. Nat Genet 2012
210
11

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.
N A Singh, C Charlier, D Stauffer, B R DuPont, R J Leach, R Melis, G M Ronen, I Bjerre, T Quattlebaum, J V Murphy,[...]. Nat Genet 1998
871
11

BK Channels in the Central Nervous System.
C Contet, S P Goulding, D A Kuljis, A L Barth. Int Rev Neurobiol 2016
60
18

De novo loss-of-function KCNMA1 variants are associated with a new multiple malformation syndrome and a broad spectrum of developmental and neurological phenotypes.
Lina Liang, Xia Li, Sébastien Moutton, Samantha A Schrier Vergano, Benjamin Cogné, Anne Saint-Martin, Anna C E Hurst, Yushuang Hu, Olaf Bodamer, Julien Thevenon,[...]. Hum Mol Genet 2019
20
55

Presynaptic Ca2+-activated K+ channels in glutamatergic hippocampal terminals and their role in spike repolarization and regulation of transmitter release.
H Hu, L R Shao, S Chavoshy, N Gu, M Trieb, R Behrens, P Laake, O Pongs, H G Knaus, O P Ottersen,[...]. J Neurosci 2001
259
10

BK calcium-activated potassium channels regulate circadian behavioral rhythms and pacemaker output.
Andrea L Meredith, Steven W Wiler, Brooke H Miller, Joseph S Takahashi, Anthony A Fodor, Norman F Ruby, Richard W Aldrich. Nat Neurosci 2006
163
10

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
10

Familial paroxysmal exercise-induced dystonia: atypical presentation of autosomal dominant GTP-cyclohydrolase 1 deficiency.
Russell C Dale, Anna Melchers, Victor S C Fung, Padraic Grattan-Smith, Henry Houlden, John Earl. Dev Med Child Neurol 2010
33
30

KCNT1 gain of function in 2 epilepsy phenotypes is reversed by quinidine.
Carol J Milligan, Melody Li, Elena V Gazina, Sarah E Heron, Umesh Nair, Chantel Trager, Christopher A Reid, Anu Venkat, Donald P Younkin, Dennis J Dlugos,[...]. Ann Neurol 2014
136
10

Association of a functional deficit of the BKCa channel, a synaptic regulator of neuronal excitability, with autism and mental retardation.
Frédéric Laumonnier, Sébastien Roger, Pascaline Guérin, Florence Molinari, Ridha M'rad, Dominique Cahard, Ahlem Belhadj, Mohamed Halayem, Antonio M Persico, Maurizio Elia,[...]. Am J Psychiatry 2006
104
10

BK channels: multiple sensors, one activation gate.
Huanghe Yang, Guohui Zhang, Jianmin Cui. Front Physiol 2015
60
16

Cryo-EM structure of the open high-conductance Ca2+-activated K+ channel.
Xiao Tao, Richard K Hite, Roderick MacKinnon. Nature 2017
111
10


Targeting BK (big potassium) channels in epilepsy.
Prosper N'Gouemo. Expert Opin Ther Targets 2011
60
15




BK channel activators and their therapeutic perspectives.
Bo H Bentzen, Søren-Peter Olesen, Lars C B Rønn, Morten Grunnet. Front Physiol 2014
96
9

Paroxysmal dyskinesias.
Kailash P Bhatia. Mov Disord 2011
105
9

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
109
9

Anticonvulsant effects of the BK-channel antagonist paxilline.
Jesse J Sheehan, Brett L Benedetti, Alison L Barth. Epilepsia 2009
47
19

De novo KCNB1 mutations in epileptic encephalopathy.
Ali Torkamani, Kevin Bersell, Benjamin S Jorge, Robert L Bjork, Jennifer R Friedman, Cinnamon S Bloss, Julie Cohen, Siddharth Gupta, Sakkubai Naidu, Carlos G Vanoye,[...]. Ann Neurol 2014
77
11

Structural basis for gating the high-conductance Ca2+-activated K+ channel.
Richard K Hite, Xiao Tao, Roderick MacKinnon. Nature 2017
86
10

High-conductance potassium channels of the SLO family.
Lawrence Salkoff, Alice Butler, Gonzalo Ferreira, Celia Santi, Aguan Wei. Nat Rev Neurosci 2006
383
9

Expanding the Phenotype of Homozygous KCNMA1 Mutations; Dyskinesia, Epilepsy, Intellectual Disability, Cerebellar and Corticospinal Tract Atrophy
Gözde Yeşil, Ayşe Aralaşmak, Enes Akyüz, Dilara İçağasıoğlu, Türkan Uygur Şahin, Yavuz Bayram. Balkan Med J 2018
13
69


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.