A citation-based method for searching scientific literature

Miriam Kessi, Baiyu Chen, Jing Peng, Yulin Tang, Eleonore Olatoutou, Fang He, Lifen Yang, Fei Yin. Front Genet 2020
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


Additional observation of a de novo pathogenic variant in KCNT2 leading to epileptic encephalopathy with clinical features of frontal lobe epilepsy.
Luciana Midori Inuzuka, Lucia Inês Macedo-Souza, Bruno Della-Ripa, Fabiola Paoli Monteiro, Luiza Ramos, João Paulo Kitajima, Eliana Garzon, Fernando Kok. Brain Dev 2020
4
75

De novo gain-of-function variants in KCNT2 as a novel cause of developmental and epileptic encephalopathy.
Paolo Ambrosino, Maria Virginia Soldovieri, Thomas Bast, Peter D Turnpenny, Sabine Uhrig, Saskia Biskup, Miriam Döcker, Thilo Fleck, Ilaria Mosca, Laura Manocchio,[...]. Ann Neurol 2018
16
42

A De Novo Mutation in the Sodium-Activated Potassium Channel KCNT2 Alters Ion Selectivity and Causes Epileptic Encephalopathy.
Sushmitha Gururaj, Elizabeth Emma Palmer, Garrett D Sheehan, Tejaswi Kandula, Rebecca Macintosh, Kevin Ying, Paula Morris, Jiang Tao, Kerith-Rae Dias, Ying Zhu,[...]. Cell Rep 2017
18
42

De novo KCNH1 mutations in four patients with syndromic developmental delay, hypotonia and seizures.
Ryoko Fukai, Hirotomo Saitsu, Yoshinori Tsurusaki, Yasunari Sakai, Kazuhiro Haginoya, Kazumasa Takahashi, Monika Weisz Hubshman, Nobuhiko Okamoto, Mitsuko Nakashima, Fumiaki Tanaka,[...]. J Hum Genet 2016
30
28

Potassium Channels in Epilepsy.
Rüdiger Köhling, Jakob Wolfart. Cold Spring Harb Perspect Med 2016
55
28

Epilepsy in KCNH1-related syndromes.
Mario Mastrangelo, Ingrid E Scheffer, Nuria C Bramswig, Lal D V Nair, Candace T Myers, Maria Lisa Dentici, Georg C Korenke, Kelly Schoch, Philippe M Campeau, Susan M White,[...]. Epileptic Disord 2016
18
28

Genetic potassium channel-associated epilepsies: Clinical review of the Kv family.
Nicholas M Allen, Sarah Weckhuysen, Kathleen Gorman, Mary D King, Holger Lerche. Eur J Paediatr Neurol 2020
19
28

Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy.
Cas Simons, Lachlan D Rash, Joanna Crawford, Linlin Ma, Ben Cristofori-Armstrong, David Miller, Kelin Ru, Gregory J Baillie, Yasemin Alanay, Adeline Jacquinet,[...]. Nat Genet 2015
83
28

Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil.
Kentaro Ohko, Kimiko Nakajima, Hideki Nakajima, Yoko Hiraki, Kazuo Kubota, Toshiyuki Fukao, Satoko Miyatake, Naomichi Matsumoto, Shigetoshi Sano. J Dermatol 2020
6
33

Lack of response to quinidine in KCNT1-related neonatal epilepsy.
Adam L Numis, Umesh Nair, Anita N Datta, Tristan T Sands, Michael S Oldham, Akash Patel, Melody Li, Elena Gazina, Steven Petrou, Maria Roberta Cilio. Epilepsia 2018
27
28

KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel.
H S Wang, Z Pan, W Shi, B S Brown, R S Wymore, I S Cohen, J E Dixon, D McKinnon. Science 1998
915
28

Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain-of-function variant.
John J Millichap, Francesco Miceli, Michela De Maria, Cynthia Keator, Nishtha Joshi, Baouyen Tran, Maria Virginia Soldovieri, Paolo Ambrosino, Vandana Shashi, Mohamad A Mikati,[...]. Epilepsia 2017
37
28

KCNT1 mutations in seizure disorders: the phenotypic spectrum and functional effects.
Chiao Xin Lim, Michael G Ricos, Leanne M Dibbens, Sarah E Heron. J Med Genet 2016
48
28

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
267
28

Targeted treatment of migrating partial seizures of infancy with quinidine.
David Bearden, Alanna Strong, Jessica Ehnot, Marissa DiGiovine, Dennis Dlugos, Ethan M Goldberg. Ann Neurol 2014
125
28

Functional consequences of a KCNT1 variant associated with status dystonicus and early-onset infantile encephalopathy.
Tracy S Gertler, Christopher H Thompson, Carlos G Vanoye, John J Millichap, Alfred L George. Ann Clin Transl Neurol 2019
10
28

De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy.
Hirotomo Saitsu, Mitsuhiro Kato, Takeshi Mizuguchi, Keisuke Hamada, Hitoshi Osaka, Jun Tohyama, Katsuhisa Uruno, Satoko Kumada, Kiyomi Nishiyama, Akira Nishimura,[...]. Nat Genet 2008
353
28

The Epilepsy of Infancy With Migrating Focal Seizures: Identification of de novo Mutations of the KCNT2 Gene That Exert Inhibitory Effects on the Corresponding Heteromeric KNa1.1/KNa1.2 Potassium Channel.
Xiao Mao, Nadine Bruneau, Quwen Gao, Hélène Becq, Zhengjun Jia, Hui Xi, Li Shu, Hua Wang, Pierre Szepetowski, Laurent Aniksztejn. Front Cell Neurosci 2020
8
28

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
28

New mutations in KCNT2 gene causing early infantile epileptic encephalopathy type 57: Case study and literature review.
Meryem Alagoz, Nasim Kherad, Sureyya Bozkurt, Adnan Yuksel. Acta Biochim Pol 2020
2
100

ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology.
Ingrid E Scheffer, Samuel Berkovic, Giuseppe Capovilla, Mary B Connolly, Jacqueline French, Laura Guilhoto, Edouard Hirsch, Satish Jain, Gary W Mathern, Solomon L Moshé,[...]. Epilepsia 2017
28

Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome.
Christiane K Bauer, Paolo Calligari, Francesca Clementina Radio, Viviana Caputo, Maria Lisa Dentici, Nadia Falah, Frances High, Francesca Pantaleoni, Sabina Barresi, Andrea Ciolfi,[...]. Am J Hum Genet 2018
43
14


Altered expression of small-conductance Ca2+-activated K+ (SK3) channels modulates arterial tone and blood pressure.
Mark S Taylor, Adrian D Bonev, Tobias P Gross, Delrae M Eckman, Joseph E Brayden, Chris T Bond, John P Adelman, Mark T Nelson. Circ Res 2003
217
14

Organization and regulation of small conductance Ca2+-activated K+ channel multiprotein complexes.
Duane Allen, Bernd Fakler, James Maylie, John P Adelman. J Neurosci 2007
116
14

Heritable arrhythmias associated with abnormal function of cardiac potassium channels.
Lia Crotti, Katja E Odening, Michael C Sanguinetti. Cardiovasc Res 2020
6
16

Glibenclamide reverses cardiovascular abnormalities of Cantu syndrome driven by KATP channel overactivity.
Conor McClenaghan, Yan Huang, Zihan Yan, Theresa M Harter, Carmen M Halabi, Rod Chalk, Attila Kovacs, Gijs van Haaften, Maria S Remedi, Colin G Nichols. J Clin Invest 2020
14
14

Dominant missense mutations in ABCC9 cause Cantú syndrome.
Magdalena Harakalova, Jeske J T van Harssel, Paulien A Terhal, Stef van Lieshout, Karen Duran, Ivo Renkens, David J Amor, Louise C Wilson, Edwin P Kirk, Claire L S Turner,[...]. Nat Genet 2012
113
14

Cantú syndrome versus Zimmermann-Laband syndrome: Report of nine individuals with ABCC9 variants.
Fanny Kortüm, Marcello Niceta, Monia Magliozzi, Katja Dumic Kubat, Stephen P Robertson, Angelica Moresco, Maria Lisa Dentici, Anwar Baban, Chiara Leoni, Roberta Onesimo,[...]. Eur J Med Genet 2020
1
100

'Splitting versus lumping': Temple-Baraitser and Zimmermann-Laband Syndromes.
Nuria C Bramswig, C W Ockeloen, J C Czeschik, A J van Essen, R Pfundt, J Smeitink, B T Poll-The, H Engels, T M Strom, D Wieczorek,[...]. Hum Genet 2015
16
14

Zimmermann-Laband-1 Syndrome: Clinical, Histological, and Proteomic Findings of a 3-Year-Old Patient with Hereditary Gingival Fibromatosis.
Federica Guglielmi, Edoardo Staderini, Federica Iavarone, Laura Di Tonno, Patrizia Gallenzi. Biomedicines 2019
6
16

Small-conductance Ca2+-activated K+ channels: form and function.
John P Adelman, James Maylie, Pankaj Sah. Annu Rev Physiol 2012
286
14

A second case of severe mental retardation and absent nails of hallux and pollex (Temple-Baraitser syndrome).
Michael T Gabbett, Ronald C Clark, Julie M McGaughran. Am J Med Genet A 2008
14
14

Ether-à-go-go K+ channels: effective modulators of neuronal excitability.
Christiane K Bauer, Jürgen R Schwarz. J Physiol 2018
26
14


Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca2+-Activated K+ Channel SK3 Cause Zimmermann-Laband Syndrome.
Christiane K Bauer, Pauline E Schneeberger, Fanny Kortüm, Janine Altmüller, Fernando Santos-Simarro, Laura Baker, Jennifer Keller-Ramey, Susan M White, Philippe M Campeau, Karen W Gripp,[...]. Am J Hum Genet 2019
16
14


Genetic deficit of SK3 and IK1 channels disrupts the endothelium-derived hyperpolarizing factor vasodilator pathway and causes hypertension.
Sebastian Brähler, Anuradha Kaistha, Volker J Schmidt, Stephanie E Wölfle, Christoph Busch, Brajesh P Kaistha, Michael Kacik, Anna-Lena Hasenau, Ivica Grgic, Han Si,[...]. Circulation 2009
176
14



Expanding the phenotype of gingival fibromatosis-mental retardation-hypertrichosis (Zimmermann-Laband) syndrome.
Oscar F Chacon-Camacho, Johanna Vázquez, Juan C Zenteno. Am J Med Genet A 2011
14
14

Endothelial SK3 channel-associated Ca2+ microdomains modulate blood pressure.
Fui C Yap, David S Weber, Mark S Taylor, Mary I Townsley, Brian S Comer, James Maylie, John P Adelman, Mike T Lin. Am J Physiol Heart Circ Physiol 2016
17
14


Cantú syndrome is caused by mutations in ABCC9.
Bregje W M van Bon, Christian Gilissen, Dorothy K Grange, Raoul C M Hennekam, Hülya Kayserili, Hartmut Engels, Heiko Reutter, John R Ostergaard, Eva Morava, Konstantinos Tsiakas,[...]. Am J Hum Genet 2012
96
14

Cantú syndrome resulting from activating mutation in the KCNJ8 gene.
Paige E Cooper, Heiko Reutter, Joachim Woelfle, Hartmut Engels, Dorothy K Grange, Gijs van Haaften, Bregje W van Bon, Alexander Hoischen, Colin G Nichols. Hum Mutat 2014
65
14




Clinical and genetic study of two patients with Zimmermann-Laband syndrome and literature review.
Marco Castori, Michele Valiante, Giulia Pascolini, Vincenzo Leuzzi, Antonio Pizzuti, Paola Grammatico. Eur J Med Genet 2013
23
14

Cantú syndrome: Findings from 74 patients in the International Cantú Syndrome Registry.
Dorothy K Grange, Helen I Roessler, Conor McClenaghan, Karen Duran, Kathleen Shields, Maria S Remedi, Nine V A M Knoers, Jin-Moo Lee, Edwin P Kirk, Ingrid Scurr,[...]. Am J Med Genet C Semin Med Genet 2019
18
14


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.