A citation-based method for searching scientific literature

Carla Marini, Alessandro Porro, Agnès Rastetter, Carine Dalle, Ilaria Rivolta, Daniel Bauer, Renske Oegema, Caroline Nava, Elena Parrini, Davide Mei, Catherine Mercer, Radhika Dhamija, Chelsea Chambers, Christine Coubes, Julien Thévenon, Paul Kuentz, Sophie Julia, Laurent Pasquier, Christèle Dubourg, Wilfrid Carré, Anna Rosati, Federico Melani, Tiziana Pisano, Maria Giardino, A Micheil Innes, Yves Alembik, Sophie Scheidecker, Manuela Santos, Sonia Figueiroa, Cristina Garrido, Carlo Fusco, Daniele Frattini, Carlotta Spagnoli, Anna Binda, Tiziana Granata, Francesca Ragona, Elena Freri, Silvana Franceschetti, Laura Canafoglia, Barbara Castellotti, Cinzia Gellera, Raffaella Milanesi, Maria Margherita Mancardi, Damien R Clark, Fernando Kok, Katherine L Helbig, Shoji Ichikawa, Laurie Sadler, Jana Neupauerová, Petra Laššuthova, Katalin Šterbová, Annick Laridon, Eva Brilstra, Bobby Koeleman, Johannes R Lemke, Federico Zara, Pasquale Striano, Julie Soblet, Guillaume Smits, Nicolas Deconinck, Andrea Barbuti, Dario DiFrancesco, Eric LeGuern, Renzo Guerrini, Bina Santoro, Kay Hamacher, Gerhard Thiel, Anna Moroni, Jacopo C DiFrancesco, Christel Depienne. Brain 2018
Times Cited: 47







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



Times Cited
  Times     Co-cited
Similarity


De novo mutations in HCN1 cause early infantile epileptic encephalopathy.
Caroline Nava, Carine Dalle, Agnès Rastetter, Pasquale Striano, Carolien G F de Kovel, Rima Nabbout, Claude Cancès, Dorothée Ville, Eva H Brilstra, Giuseppe Gobbi,[...]. Nat Genet 2014
130
44

Hyperpolarization-activated cation channels: from genes to function.
Martin Biel, Christian Wahl-Schott, Stylianos Michalakis, Xiangang Zong. Physiol Rev 2009
658
38

A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability.
Mattia Bonzanni, Jacopo C DiFrancesco, Raffaella Milanesi, Giulia Campostrini, Barbara Castellotti, Annalisa Bucchi, Mirko Baruscotti, Carlo Ferrarese, Silvana Franceschetti, Laura Canafoglia,[...]. Neurobiol Dis 2018
24
66

Augmented currents of an HCN2 variant in patients with febrile seizure syndromes.
Leanne M Dibbens, Christopher A Reid, Bree Hodgson, Evan A Thomas, Alison M Phillips, Elena Gazina, Brett A Cromer, Alison L Clarke, Tallie Z Baram, Ingrid E Scheffer,[...]. Ann Neurol 2010
75
21

Loss of dendritic HCN1 subunits enhances cortical excitability and epileptogenesis.
Zhuo Huang, Matthew C Walker, Mala M Shah. J Neurosci 2009
118
21

Absence epilepsy and sinus dysrhythmia in mice lacking the pacemaker channel HCN2.
Andreas Ludwig, Thomas Budde, Juliane Stieber, Sven Moosmang, Christian Wahl, Knut Holthoff, Anke Langebartels, Carsten Wotjak, Thomas Munsch, Xiangang Zong,[...]. EMBO J 2003
384
19

HCN channels: function and clinical implications.
Eduardo E Benarroch. Neurology 2013
125
19

Increased seizure severity and seizure-related death in mice lacking HCN1 channels.
Bina Santoro, Janet Y Lee, Dario J Englot, Sandra Gildersleeve, Rebecca A Piskorowski, Steven A Siegelbaum, Melodie R Winawer, Hal Blumenfeld. Epilepsia 2010
58
19

Gain-of-function HCN2 variants in genetic epilepsy.
Melody Li, Snezana Maljevic, A Marie Phillips, Slave Petrovski, Michael S Hildebrand, Rosemary Burgess, Therese Mount, Federico Zara, Pasquale Striano, Julian Schubert,[...]. Hum Mutat 2018
17
52

Recessive loss-of-function mutation in the pacemaker HCN2 channel causing increased neuronal excitability in a patient with idiopathic generalized epilepsy.
Jacopo C DiFrancesco, Andrea Barbuti, Raffaella Milanesi, Stefania Coco, Annalisa Bucchi, Georgia Bottelli, Carlo Ferrarese, Silvana Franceschetti, Benedetta Terragni, Mirko Baruscotti,[...]. J Neurosci 2011
67
19

HCN ion channels and accessory proteins in epilepsy: genetic analysis of a large cohort of patients and review of the literature.
Jacopo C DiFrancesco, Barbara Castellotti, Raffaella Milanesi, Francesca Ragona, Elena Freri, Laura Canafoglia, Silvana Franceschetti, Carlo Ferrarese, Stefania Magri, Franco Taroni,[...]. Epilepsy Res 2019
14
64

Structures of the Human HCN1 Hyperpolarization-Activated Channel.
Chia-Hsueh Lee, Roderick MacKinnon. Cell 2017
186
19

A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability.
Giulia Campostrini, Jacopo C DiFrancesco, Barbara Castellotti, Raffaella Milanesi, Tomaso Gnecchi-Ruscone, Mattia Bonzanni, Annalisa Bucchi, Mirko Baruscotti, Carlo Ferrarese, Silvana Franceschetti,[...]. Front Mol Neurosci 2018
14
57

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
17


Pharmacological upregulation of h-channels reduces the excitability of pyramidal neuron dendrites.
Nicholas P Poolos, Michele Migliore, Daniel Johnston. Nat Neurosci 2002
307
17

Hyperpolarization-activated cation currents: from molecules to physiological function.
Richard B Robinson, Steven A Siegelbaum. Annu Rev Physiol 2003
829
14

Novel HCN2 mutation contributes to febrile seizures by shifting the channel's kinetics in a temperature-dependent manner.
Yuki Nakamura, Xiuyu Shi, Tomohiro Numata, Yasuo Mori, Ryuji Inoue, Christoph Lossin, Tallie Z Baram, Shinichi Hirose. PLoS One 2013
37
18

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
14

Functional variants in HCN4 and CACNA1H may contribute to genetic generalized epilepsy.
Felicitas Becker, Christopher A Reid, Kerstin Hallmann, Han-Shen Tae, A Marie Phillips, Georgeta Teodorescu, Yvonne G Weber, Ailing Kleefuss-Lie, Christian Elger, Edward Perez-Reyes,[...]. Epilepsia Open 2017
14
50

A behavioral role for dendritic integration: HCN1 channels constrain spatial memory and plasticity at inputs to distal dendrites of CA1 pyramidal neurons.
Matthew F Nolan, Gaël Malleret, Josh T Dudman, Derek L Buhl, Bina Santoro, Emma Gibbs, Svetlana Vronskaya, György Buzsáki, Steven A Siegelbaum, Eric R Kandel,[...]. Cell 2004
352
14

Gabapentin Modulates HCN4 Channel Voltage-Dependence.
Han-Shen Tae, Kelly M Smith, A Marie Phillips, Kieran A Boyle, Melody Li, Ian C Forster, Robert J Hatch, Robert Richardson, David I Hughes, Brett A Graham,[...]. Front Pharmacol 2017
19
36

Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies.
Julia Oyrer, Snezana Maljevic, Ingrid E Scheffer, Samuel F Berkovic, Steven Petrou, Christopher A Reid. Pharmacol Rev 2018
101
12

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.
Markus Wolff, Katrine M Johannesen, Ulrike B S Hedrich, Silvia Masnada, Guido Rubboli, Elena Gardella, Gaetan Lesca, Dorothée Ville, Mathieu Milh, Laurent Villard,[...]. Brain 2017
249
12


Molecular mechanism of cAMP modulation of HCN pacemaker channels.
B J Wainger, M DeGennaro, B Santoro, S A Siegelbaum, G R Tibbs. Nature 2001
363
12

Progressive dendritic HCN channelopathy during epileptogenesis in the rat pilocarpine model of epilepsy.
Sangwook Jung, Terrance D Jones, Joaquin N Lugo, Aaron H Sheerin, John W Miller, Raimondo D'Ambrosio, Anne E Anderson, Nicholas P Poolos. J Neurosci 2007
167
12


Diagnostic Targeted Resequencing in 349 Patients with Drug-Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes.
Elena Parrini, Carla Marini, Davide Mei, Anna Galuppi, Elena Cellini, Daniela Pucatti, Laura Chiti, Domenico Rutigliano, Claudia Bianchini, Simona Virdò,[...]. Hum Mutat 2017
100
12

The genetic landscape of the epileptic encephalopathies of infancy and childhood.
Amy McTague, Katherine B Howell, J Helen Cross, Manju A Kurian, Ingrid E Scheffer. Lancet Neurol 2016
288
12


Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy.
Frank H Yu, Massimo Mantegazza, Ruth E Westenbroek, Carol A Robbins, Franck Kalume, Kimberly A Burton, William J Spain, G Stanley McKnight, Todd Scheuer, William A Catterall. Nat Neurosci 2006
690
12


Mutation analysis of the hyperpolarization-activated cyclic nucleotide-gated channels HCN1 and HCN2 in idiopathic generalized epilepsy.
Bin Tang, Thomas Sander, Kimberley B Craven, Anne Hempelmann, Andrew Escayg. Neurobiol Dis 2008
48
10

MinK-related peptide 1: A beta subunit for the HCN ion channel subunit family enhances expression and speeds activation.
H Yu, J Wu, I Potapova, R T Wymore, B Holmes, J Zuckerman, Z Pan, H Wang, W Shi, R B Robinson,[...]. Circ Res 2001
189
10

Phenotypic spectrum of GABRA1: From generalized epilepsies to severe epileptic encephalopathies.
Katrine Johannesen, Carla Marini, Siona Pfeffer, Rikke S Møller, Thomas Dorn, Cristina Elena Niturad, Elena Gardella, Yvonne Weber, Marianne Søndergård, Helle Hjalgrim,[...]. Neurology 2016
71
10


Mislocalization of h channel subunits underlies h channelopathy in temporal lobe epilepsy.
Minyoung Shin, Darrin Brager, Thomas C Jaramillo, Daniel Johnston, Dane M Chetkovich. Neurobiol Dis 2008
81
10

Reduction of thalamic and cortical Ih by deletion of TRIP8b produces a mouse model of human absence epilepsy.
Robert J Heuermann, Thomas C Jaramillo, Shui-Wang Ying, Benjamin A Suter, Kyle A Lyman, Ye Han, Alan S Lewis, Thomas G Hampton, Gordon M G Shepherd, Peter A Goldstein,[...]. Neurobiol Dis 2016
27
18

Rapid loss of dendritic HCN channel expression in hippocampal pyramidal neurons following status epilepticus.
Sangwook Jung, Lindsay N Warner, Julika Pitsch, Albert J Becker, Nicholas P Poolos. J Neurosci 2011
50
10

Deletion of the hyperpolarization-activated cyclic nucleotide-gated channel auxiliary subunit TRIP8b impairs hippocampal Ih localization and function and promotes antidepressant behavior in mice.
Alan S Lewis, Sachin P Vaidya, Cory A Blaiss, Zhiqiang Liu, Travis R Stoub, Darrin H Brager, Xiangdong Chen, Roland A Bender, Chad M Estep, Andrey B Popov,[...]. J Neurosci 2011
94
10

Alternatively spliced isoforms of TRIP8b differentially control h channel trafficking and function.
Alan S Lewis, Emily Schwartz, C Savio Chan, Yoav Noam, Minyoung Shin, Wytse J Wadman, D James Surmeier, Tallie Z Baram, Robert L Macdonald, Dane M Chetkovich. J Neurosci 2009
106
10


TRIP8b splice variants form a family of auxiliary subunits that regulate gating and trafficking of HCN channels in the brain.
Bina Santoro, Rebecca A Piskorowski, Phillip Pian, Lei Hu, Haiying Liu, Steven A Siegelbaum. Neuron 2009
125
10

Sodium channel SCN1A and epilepsy: mutations and mechanisms.
Andrew Escayg, Alan L Goldin. Epilepsia 2010
232
10

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
309
10

The hyperpolarization-activated HCN1 channel is important for motor learning and neuronal integration by cerebellar Purkinje cells.
Matthew F Nolan, Gaël Malleret, Ka Hung Lee, Emma Gibbs, Joshua T Dudman, Bina Santoro, Deqi Yin, Richard F Thompson, Steven A Siegelbaum, Eric R Kandel,[...]. Cell 2003
236
10

Suppression of Hyperpolarization-Activated Cyclic Nucleotide-Gated Channel Function in Thalamocortical Neurons Prevents Genetically Determined and Pharmacologically Induced Absence Seizures.
François David, Nihan Çarçak, Szabina Furdan, Filiz Onat, Timothy Gould, Ádám Mészáros, Giuseppe Di Giovanni, Vivian M Hernández, C Savio Chan, Magor L Lőrincz,[...]. J Neurosci 2018
17
29

Hyperpolarization-Activated Cyclic Nucleotide-Gated (HCN) Channels in Epilepsy.
Gary P Brennan, Tallie Z Baram, Nicholas P Poolos. Cold Spring Harb Perspect Med 2016
27
18

The hyperpolarization-activated channel HCN4 is required for the generation of pacemaker action potentials in the embryonic heart.
Juliane Stieber, Stefan Herrmann, Susanne Feil, Jana Löster, Robert Feil, Martin Biel, Franz Hofmann, Andreas Ludwig. Proc Natl Acad Sci U S A 2003
335
10


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.