A citation-based method for searching scientific literature

Tristan T Sands, Francesco Miceli, Gaetan Lesca, Anita E Beck, Lynette G Sadleir, Daniel K Arrington, Bitten Schönewolf-Greulich, Sébastien Moutton, Anna Lauritano, Piera Nappi, Maria Virginia Soldovieri, Ingrid E Scheffer, Heather C Mefford, Nicholas Stong, Erin L Heinzen, David B Goldstein, Ana Grijalvo Perez, Eric H Kossoff, Amber Stocco, Jennifer A Sullivan, Vandana Shashi, Benedicte Gerard, Christine Francannet, Anne-Marie Bisgaard, Zeynep Tümer, Marjolaine Willems, François Rivier, Antonio Vitobello, Kavita Thakkar, Deepa S Rajan, A James Barkovich, Sarah Weckhuysen, Edward C Cooper, Maurizio Taglialatela, M Roberta Cilio. Ann Neurol 2019
Times Cited: 23







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



Times Cited
  Times     Co-cited
Similarity


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
290
52

Early-onset epileptic encephalopathy caused by gain-of-function mutations in the voltage sensor of Kv7.2 and Kv7.3 potassium channel subunits.
Francesco Miceli, Maria Virginia Soldovieri, Paolo Ambrosino, Michela De Maria, Michele Migliore, Rosanna Migliore, Maurizio Taglialatela. J Neurosci 2015
89
43

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
39

Dominant-negative effects of KCNQ2 mutations are associated with epileptic encephalopathy.
Gökce Orhan, Merle Bock, Dorien Schepers, Elena I Ilina, Stephanie Nadine Reichel, Heidi Löffler, Nicole Jezutkovic, Sarah Weckhuysen, Simone Mandelstam, Arvid Suls,[...]. Ann Neurol 2014
124
34

A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability.
Francesco Miceli, Pasquale Striano, Maria Virginia Soldovieri, Antonina Fontana, Rosaria Nardello, Angela Robbiano, Giulia Bellini, Maurizio Elia, Federico Zara, Maurizio Taglialatela,[...]. Epilepsia 2015
42
30

Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patients.
Sarah Weckhuysen, Vanja Ivanovic, Rik Hendrickx, Rudy Van Coster, Helle Hjalgrim, Rikke S Møller, Sabine Grønborg, An-Sofie Schoonjans, Berten Ceulemans, Sinead B Heavin,[...]. Neurology 2013
130
30

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
30

Loss-of-Function and Gain-of-Function Mutations in KCNQ5 Cause Intellectual Disability or Epileptic Encephalopathy.
Anna Lehman, Samrat Thouta, Grazia M S Mancini, Sakkubai Naidu, Marjon van Slegtenhorst, Kirsty McWalter, Richard Person, Jill Mwenifumbo, Ramona Salvarinova, Ilaria Guella,[...]. Am J Hum Genet 2017
52
30

Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance.
Federico Zara, Nicola Specchio, Pasquale Striano, Angela Robbiano, Elena Gennaro, Roberta Paravidino, Nicola Vanni, Francesca Beccaria, Giuseppe Capovilla, Amedeo Bianchi,[...]. Epilepsia 2013
74
26

Genotype-phenotype correlations in neonatal epilepsies caused by mutations in the voltage sensor of K(v)7.2 potassium channel subunits.
Francesco Miceli, Maria Virginia Soldovieri, Paolo Ambrosino, Vincenzo Barrese, Michele Migliore, Maria Roberta Cilio, Maurizio Taglialatela. Proc Natl Acad Sci U S A 2013
109
26

KCNQ2 encephalopathy: Features, mutational hot spots, and ezogabine treatment of 11 patients.
John J Millichap, Kristen L Park, Tammy Tsuchida, Bruria Ben-Zeev, Lionel Carmant, Robert Flamini, Nishtha Joshi, Paul M Levisohn, Eric Marsh, Srishti Nangia,[...]. Neurol Genet 2016
99
26

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.
C Charlier, N A Singh, S G Ryan, T B Lewis, B E Reus, R J Leach, M Leppert. Nat Genet 1998
728
26


Developmental changes in KCNQ2 and KCNQ3 expression in human brain: possible contribution to the age-dependent etiology of benign familial neonatal convulsions.
Takeshi Kanaumi, Sachio Takashima, Hiroshi Iwasaki, Masayuki Itoh, Akihisa Mitsudome, Shinichi Hirose. Brain Dev 2008
44
26

Kv7.3 Compound Heterozygous Variants in Early Onset Encephalopathy Reveal Additive Contribution of C-Terminal Residues to PIP2-Dependent K+ Channel Gating.
Paolo Ambrosino, Elena Freri, Barbara Castellotti, Maria Virginia Soldovieri, Ilaria Mosca, Laura Manocchio, Cinzia Gellera, Laura Canafoglia, Silvana Franceschetti, Barbara Salis,[...]. Mol Neurobiol 2018
12
50

Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain-of-function variants R201C and R201H.
Sarah B Mulkey, Bruria Ben-Zeev, Joost Nicolai, John L Carroll, Sabine Grønborg, Yong-Hui Jiang, Nishtha Joshi, Megan Kelly, David A Koolen, Mohamad A Mikati,[...]. Epilepsia 2017
33
26

Clinical spectrum of early onset epileptic encephalopathies caused by KCNQ2 mutation.
Mitsuhiro Kato, Takanori Yamagata, Masaya Kubota, Hiroshi Arai, Sumimasa Yamashita, Taku Nakagawa, Takanari Fujii, Kenji Sugai, Kaoru Imai, Tami Uster,[...]. Epilepsia 2013
132
26


A novel homozygous KCNQ3 loss-of-function variant causes non-syndromic intellectual disability and neonatal-onset pharmacodependent epilepsy.
Anna Lauritano, Sebastien Moutton, Elena Longobardi, Frédéric Tran Mau-Them, Giusy Laudati, Piera Nappi, Maria Virginia Soldovieri, Paolo Ambrosino, Mauro Cataldi, Thibaud Jouan,[...]. Epilepsia Open 2019
17
35


Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, Thomas Wieland, Sabine Endele, Thomas Schwarzmayr, Beate Albrecht, Deborah Bartholdi, Jasmin Beygo, Nataliya Di Donato,[...]. Lancet 2012
677
21

A recurrent KCNQ2 pore mutation causing early onset epileptic encephalopathy has a moderate effect on M current but alters subcellular localization of Kv7 channels.
Affef Abidi, Jérôme J Devaux, Florence Molinari, Gisèle Alcaraz, François-Xavier Michon, Julie Sutera-Sardo, Hélène Becq, Caroline Lacoste, Cécilia Altuzarra, Alexandra Afenjar,[...]. Neurobiol Dis 2015
40
21

De novo mutations in epileptic encephalopathies.
Andrew S Allen, Samuel F Berkovic, Patrick Cossette, Norman Delanty, Dennis Dlugos, Evan E Eichler, Michael P Epstein, Tracy Glauser, David B Goldstein, Yujun Han,[...]. Nature 2013
935
21


KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes.
B A Neubauer, S Waldegger, J Heinzinger, A Hahn, G Kurlemann, B Fiedler, F Eberhard, H Muhle, U Stephani, S Garkisch,[...]. Neurology 2008
64
21

Potassium Channel Gain of Function in Epilepsy: An Unresolved Paradox.
Zachary Niday, Anastasios V Tzingounis. Neuroscientist 2018
38
21

Neurodevelopmental Disorders Caused by De Novo Variants in KCNB1 Genotypes and Phenotypes.
Carolien G F de Kovel, Steffen Syrbe, Eva H Brilstra, Nienke Verbeek, Bronwyn Kerr, Holly Dubbs, Allan Bayat, Sonal Desai, Sakkubai Naidu, Siddharth Srivastava,[...]. JAMA Neurol 2017
40
21

Early and effective treatment of KCNQ2 encephalopathy.
Tiziana Pisano, Adam L Numis, Sinéad B Heavin, Sarah Weckhuysen, Marco Angriman, Arvid Suls, Barbara Podesta, Ronald L Thibert, Kevin A Shapiro, Renzo Guerrini,[...]. Epilepsia 2015
111
21

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
876
21

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, Michael S Breen, Silvia De Rubeis, Joon-Yong An, Minshi Peng, Ryan Collins, Jakob Grove, Lambertus Klei,[...]. Cell 2020
419
21


KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum.
Nanda A Singh, Peter Westenskow, Carole Charlier, Chris Pappas, Jonathan Leslie, Jessica Dillon, V Elving Anderson, Michael C Sanguinetti, Mark F Leppert. Brain 2003
199
17

Diagnostic yield of targeted massively parallel sequencing in children with epileptic encephalopathy.
Kavitha Kothur, Katherine Holman, Elizabeth Farnsworth, Gladys Ho, Michelle Lorentzos, Christopher Troedson, Sachin Gupta, Richard Webster, Peter G Procopis, Manoj P Menezes,[...]. Seizure 2018
34
17

Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome.
Bronwyn E Grinton, Sarah E Heron, James T Pelekanos, Sameer M Zuberi, Sara Kivity, Zaid Afawi, Tristiana C Williams, Dan M Casalaz, Simone Yendle, Ilan Linder,[...]. Epilepsia 2015
52
17

Novel genetic causes for cerebral visual impairment.
Daniëlle G M Bosch, F Nienke Boonstra, Nicole de Leeuw, Rolph Pfundt, Willy M Nillesen, Joep de Ligt, Christian Gilissen, Shalini Jhangiani, James R Lupski, Frans P M Cremers,[...]. Eur J Hum Genet 2016
82
17

Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies.
Silvia Masnada, Ulrike B S Hedrich, Elena Gardella, Julian Schubert, Charu Kaiwar, Eric W Klee, Brendan C Lanpher, Ralitza H Gavrilova, Matthis Synofzik, Thomas Bast,[...]. Brain 2017
56
17

Epileptic Encephalopathy In A Patient With A Novel Variant In The Kv7.2 S2 Transmembrane Segment: Clinical, Genetic, and Functional Features.
Maria Virginia Soldovieri, Paolo Ambrosino, Ilaria Mosca, Francesco Miceli, Cristina Franco, Lorella Maria Teresa Canzoniero, Beth Kline-Fath, Edward C Cooper, Charu Venkatesan, Maurizio Taglialatela. Int J Mol Sci 2019
8
50

Intragenic duplication of KCNQ5 gene results in aberrant splicing leading to a premature termination codon in a patient with intellectual disability.
Giulia Rosti, Elisa Tassano, Simone Bossi, Maria Teresa Divizia, Patrizia Ronchetto, Martina Servetti, Margherita Lerone, Livia Pisciotta, Maria Margherita Mancardi, Edvige Veneselli,[...]. Eur J Med Genet 2019
9
44

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
17

Autism with seizures and intellectual disability: possible causative role of gain-of-function of the inwardly-rectifying K+ channel Kir4.1.
Federico Sicca, Paola Imbrici, Maria Cristina D'Adamo, Francesca Moro, Fabrizia Bonatti, Paola Brovedani, Alessandro Grottesi, Renzo Guerrini, Gabriele Masi, Filippo Maria Santorelli,[...]. Neurobiol Dis 2011
82
17

KCNQ5, a novel potassium channel broadly expressed in brain, mediates M-type currents.
B C Schroeder, M Hechenberger, F Weinreich, C Kubisch, T J Jentsch. J Biol Chem 2000
283
17

KCNQ2 is a nodal K+ channel.
Jérôme J Devaux, Kleopas A Kleopa, Edward C Cooper, Steven S Scherer. J Neurosci 2004
306
17

Heteromeric Kv7.2/7.3 channels differentially regulate action potential initiation and conduction in neocortical myelinated axons.
Arne Battefeld, Baouyen T Tran, Jason Gavrilis, Edward C Cooper, Maarten H P Kole. J Neurosci 2014
99
17

Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability.
Detelina Grozeva, Keren Carss, Olivera Spasic-Boskovic, Maria-Isabel Tejada, Jozef Gecz, Marie Shaw, Mark Corbett, Eric Haan, Elizabeth Thompson, Kathryn Friend,[...]. Hum Mutat 2015
106
13

Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: first evidence for an altered channel regulation by syntaxin-1A.
Maria Virginia Soldovieri, Nadia Boutry-Kryza, Mathieu Milh, Diane Doummar, Benedicte Heron, Emilie Bourel, Paolo Ambrosino, Francesco Miceli, Michela De Maria, Nathalie Dorison,[...]. Hum Mutat 2014
54
13

Early-onset epileptic encephalopathy caused by a reduced sensitivity of Kv7.2 potassium channels to phosphatidylinositol 4,5-bisphosphate.
Maria Virginia Soldovieri, Paolo Ambrosino, Ilaria Mosca, Michela De Maria, Edoardo Moretto, Francesco Miceli, Alessandro Alaimo, Nunzio Iraci, Laura Manocchio, Alessandro Medoro,[...]. Sci Rep 2016
27
13

Decreased subunit stability as a novel mechanism for potassium current impairment by a KCNQ2 C terminus mutation causing benign familial neonatal convulsions.
Maria Virginia Soldovieri, Pasqualina Castaldo, Luisa Iodice, Francesco Miceli, Vincenzo Barrese, Giulia Bellini, Emanuele Miraglia del Giudice, Antonio Pascotto, Stefano Bonatti, Lucio Annunziato,[...]. J Biol Chem 2006
52
13

The C-terminus of Kv7 channels: a multifunctional module.
Yoni Haitin, Bernard Attali. J Physiol 2008
103
13

Epilepsy-causing mutations in Kv7.2 C-terminus affect binding and functional modulation by calmodulin.
Paolo Ambrosino, Alessandro Alaimo, Silvia Bartollino, Laura Manocchio, Michela De Maria, Ilaria Mosca, Carolina Gomis-Perez, Araitz Alberdi, Giovanni Scambia, Gaetan Lesca,[...]. Biochim Biophys Acta 2015
28
13

Driving with no brakes: molecular pathophysiology of Kv7 potassium channels.
Maria Virginia Soldovieri, Francesco Miceli, Maurizio Taglialatela. Physiology (Bethesda) 2011
98
13


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.