A citation-based method for searching scientific literature

Cihan Kaya, Princesca Dorsaint, Stephanie Mercurio, Alexander M Campbell, Kenneth Wha Eng, Marina N Nikiforova, Olivier Elemento, Yuri E Nikiforov, Andrea Sboner. Thyroid 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy.
Tara Klassen, Caleb Davis, Alica Goldman, Dan Burgess, Tim Chen, David Wheeler, John McPherson, Traci Bourquin, Lora Lewis, Donna Villasana,[...]. Cell 2011
213
50

Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.
Jacob J Michaelson, Yujian Shi, Madhusudan Gujral, Hancheng Zheng, Dheeraj Malhotra, Xin Jin, Minghan Jian, Guangming Liu, Douglas Greer, Abhishek Bhandari,[...]. Cell 2012
328
50

RiboSketch: versatile visualization of multi-stranded RNA and DNA secondary structure.
Jacob S Lu, Eckart Bindewald, Wojciech K Kasprzak, Bruce A Shapiro. Bioinformatics 2018
6
50

IntaRNA 2.0: enhanced and customizable prediction of RNA-RNA interactions.
Martin Mann, Patrick R Wright, Rolf Backofen. Nucleic Acids Res 2017
176
50

Structure of an argonaute silencing complex with a seed-containing guide DNA and target RNA duplex.
Yanli Wang, Stefan Juranek, Haitao Li, Gang Sheng, Thomas Tuschl, Dinshaw J Patel. Nature 2008
374
50


Febrile Seizures and Mesial Temporal Sclerosis.
Shlomo Shinnar. Epilepsy Curr 2003
50
50

Fibroblast growth factor (FGF) homologous factors: new members of the FGF family implicated in nervous system development.
P M Smallwood, I Munoz-Sanjuan, P Tong, J P Macke, S H Hendry, D J Gilbert, N G Copeland, N A Jenkins, J Nathans. Proc Natl Acad Sci U S A 1996
310
50

Gain-of-function FHF1 mutation causes early-onset epileptic encephalopathy with cerebellar atrophy.
Aleksandra Siekierska, Mala Isrie, Yue Liu, Chloë Scheldeman, Niels Vanthillo, Lieven Lagae, Peter A M de Witte, Hilde Van Esch, Mitchell Goldfarb, Gunnar M Buyse. Neurology 2016
37
50

Novel and de novo mutations in pediatric refractory epilepsy.
Jing Liu, Lili Tong, Shuangshuang Song, Yue Niu, Jun Li, Xiu Wu, Jie Zhang, Clement C Zai, Fang Luo, Jian Wu,[...]. Mol Brain 2018
25
50

The Vienna RNA websuite.
Andreas R Gruber, Ronny Lorenz, Stephan H Bernhart, Richard Neuböck, Ivo L Hofacker. Nucleic Acids Res 2008
50

A mechanistic overview of translation initiation in eukaryotes.
Colin Echeverría Aitken, Jon R Lorsch. Nat Struct Mol Biol 2012
222
50

Emerging Roles for 3' UTRs in Neurons.
Bongmin Bae, Pedro Miura. Int J Mol Sci 2020
8
50

Evaluation of Seven Different RNA-Seq Alignment Tools Based on Experimental Data from the Model Plant Arabidopsis thaliana.
Stephanie Schaarschmidt, Axel Fischer, Ellen Zuther, Dirk K Hincha. Int J Mol Sci 2020
8
50

Comprehensive modeling of microRNA targets predicts functional non-conserved and non-canonical sites.
Doron Betel, Anjali Koppal, Phaedra Agius, Chris Sander, Christina Leslie. Genome Biol 2010
50

Increased expression of DNA methyltransferase 1 and 3a in human temporal lobe epilepsy.
Qiong Zhu, Liang Wang, Ying Zhang, Feng-hua Zhao, Jing Luo, Zheng Xiao, Guo-jun Chen, Xue-feng Wang. J Mol Neurosci 2012
67
50

Alzheimer-specific variants in the 3'UTR of Amyloid precursor protein affect microRNA function.
Charlotte Delay, Frédéric Calon, Paul Mathews, Sébastien S Hébert. Mol Neurodegener 2011
83
50

De novo mutations in regulatory elements in neurodevelopmental disorders.
Patrick J Short, Jeremy F McRae, Giuseppe Gallone, Alejandro Sifrim, Hyejung Won, Daniel H Geschwind, Caroline F Wright, Helen V Firth, David R FitzPatrick, Jeffrey C Barrett,[...]. Nature 2018
95
50

Novel truncating and missense mutations of the KCC3 gene associated with Andermann syndrome.
G Uyanik, N Elcioglu, J Penzien, C Gross, Y Yilmaz, A Olmez, E Demir, D Wahl, K Scheglmann, B Winner,[...]. Neurology 2006
42
50

Multiplexed RNA structure characterization with selective 2'-hydroxyl acylation analyzed by primer extension sequencing (SHAPE-Seq).
Julius B Lucks, Stefanie A Mortimer, Cole Trapnell, Shujun Luo, Sharon Aviran, Gary P Schroth, Lior Pachter, Jennifer A Doudna, Adam P Arkin. Proc Natl Acad Sci U S A 2011
234
50

Selective changes in single cell GABA(A) receptor subunit expression and function in temporal lobe epilepsy.
A R Brooks-Kayal, M D Shumate, H Jin, T Y Rikhter, D A Coulter. Nat Med 1998
543
50

Correction to: Novel and de novo mutations in pediatric refractory epilepsy.
Jing Liu, Lili Tong, Shuangshuang Song, Yue Niu, Jun Li, Xiu Wu, Jie Zhang, Clement C Zai, Fang Luo, Jian Wu,[...]. Mol Brain 2018
2
50

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.
J I Friedman, T Vrijenhoek, S Markx, I M Janssen, W A van der Vliet, B H W Faas, N V Knoers, W Cahn, R S Kahn, L Edelmann,[...]. Mol Psychiatry 2008
211
50

The variant call format and VCFtools.
Petr Danecek, Adam Auton, Goncalo Abecasis, Cornelis A Albers, Eric Banks, Mark A DePristo, Robert E Handsaker, Gerton Lunter, Gabor T Marth, Stephen T Sherry,[...]. Bioinformatics 2011
50

Prevalence and Incidence of Drug-Resistant Mesial Temporal Lobe Epilepsy in the United States.
Ali A Asadi-Pooya, Gregory R Stewart, Daniel J Abrams, Ashwini Sharan. World Neurosurg 2017
62
50

miRTar: an integrated system for identifying miRNA-target interactions in human.
Justin Bo-Kai Hsu, Chih-Min Chiu, Sheng-Da Hsu, Wei-Yun Huang, Chia-Hung Chien, Tzong-Yi Lee, Hsien-Da Huang. BMC Bioinformatics 2011
88
50

Alpha-synuclein mRNA isoform formation and translation affected by polymorphism in the human SNCA 3'UTR.
Elizabeth S Barrie, Sung-Ha Lee, John T Frater, Maria Kataki, Douglas W Scharre, Wolfgang Sadee. Mol Genet Genomic Med 2018
4
50

Atomic accuracy in predicting and designing noncanonical RNA structure.
Rhiju Das, John Karanicolas, David Baker. Nat Methods 2010
215
50

Origins of temporal lobe epilepsy: febrile seizures and febrile status epilepticus.
Katelin P Patterson, Tallie Z Baram, Shlomo Shinnar. Neurotherapeutics 2014
53
50

Novel de novo EEF1A2 missense mutations causing epilepsy and intellectual disability.
Wayne W K Lam, John J Millichap, Dinesh C Soares, Richard Chin, Ailsa McLellan, David R FitzPatrick, Frances Elmslie, Melissa M Lees, G Bradley Schaefer, Catherine M Abbott. Mol Genet Genomic Med 2016
26
50

NAPB - a novel SNARE-associated protein for early-onset epileptic encephalopathy.
J Conroy, N M Allen, K M Gorman, A Shahwan, S Ennis, S A Lynch, M D King. Clin Genet 2016
10
50

The Sodium Channel B4-Subunits are Dysregulated in Temporal Lobe Epilepsy Drug-Resistant Patients.
Mariam A Sheilabi, Louise Y Takeshita, Edward J Sims, Francesco Falciani, Alessandra P Princivalle. Int J Mol Sci 2020
4
50

Using bioinformatics to predict the functional impact of SNVs.
Melissa S Cline, Rachel Karchin. Bioinformatics 2011
56
50

Rare variants and de novo variants in mesial temporal lobe epilepsy with hippocampal sclerosis.
John K L Wong, Hongsheng Gui, Maxwell Kwok, Ping Wing Ng, Colin H T Lui, Larry Baum, Pak Chung Sham, Patrick Kwan, Stacey S Cherny. Neurol Genet 2018
8
50

miRBase: from microRNA sequences to function.
Ana Kozomara, Maria Birgaoanu, Sam Griffiths-Jones. Nucleic Acids Res 2019
845
50

Beyond the Exome: The Non-coding Genome and Enhancers in Neurodevelopmental Disorders and Malformations of Cortical Development.
Elena Perenthaler, Soheil Yousefi, Eva Niggl, Tahsin Stefan Barakat. Front Cell Neurosci 2019
16
50

Mesial temporal lobe epilepsy with hippocampal sclerosis: study of 42 children.
Ricardo Cersósimo, Santiago Flesler, Marcelo Bartuluchi, Ana María Soprano, Hugo Pomata, Roberto Caraballo. Seizure 2011
22
50


Epilepsy-associated genes.
Jie Wang, Zhi-Jian Lin, Liu Liu, Hai-Qing Xu, Yi-Wu Shi, Yong-Hong Yi, Na He, Wei-Ping Liao. Seizure 2017
117
50

A de novo MAPRE2 variant in a patient with congenital symmetric circumferential skin creases type 2.
Jincai Feng, Xiaoping Lan, Jun Shen, Xiaozhen Song, Xiaojun Tang, Wuhen Xu, Xiang Ren, Hong Zhang, Guangjun Yu, Shengnan Wu. Mol Genet Genomic Med 2020
4
50

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
238
50

Genome-wide investigation of an ID cohort reveals de novo 3'UTR variants affecting gene expression.
Paolo Devanna, Maartje van de Vorst, Rolph Pfundt, Christian Gilissen, Sonja C Vernes. Hum Genet 2018
10
50

Fast gapped-read alignment with Bowtie 2.
Ben Langmead, Steven L Salzberg. Nat Methods 2012
50

De novo FGF12 mutation in 2 patients with neonatal-onset epilepsy.
Ilaria Guella, Linda Huh, Marna B McKenzie, Eric B Toyota, E Martina Bebin, Michelle L Thompson, Gregory M Cooper, Daniel M Evans, Sarah E Buerki, Shelin Adam,[...]. Neurol Genet 2016
19
50

A review of databases predicting the effects of SNPs in miRNA genes or miRNA-binding sites.
Tobias Fehlmann, Shashwat Sahay, Andreas Keller, Christina Backes. Brief Bioinform 2019
10
50

Genetic and environmental factors in epilepsy: a population-based study of 11900 Danish twin pairs.
M J Kjeldsen, K O Kyvik, K Christensen, M L Friis. Epilepsy Res 2001
62
50

A peroxisomal disorder of severe intellectual disability, epilepsy, and cataracts due to fatty acyl-CoA reductase 1 deficiency.
Rebecca Buchert, Hasan Tawamie, Christopher Smith, Steffen Uebe, A Micheil Innes, Bassam Al Hallak, Arif B Ekici, Heinrich Sticht, Bernd Schwarze, Ryan E Lamont,[...]. Am J Hum Genet 2014
69
50

Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families.
Pasquale Striano, Antonio Gambardella, Antonietta Coppola, Carlo Di Bonaventura, Giorgia Bovo, Erica Diani, Francesca Boaretto, Gabriella Egeo, Clotilde Ciampa, Angelo Labate,[...]. J Neurol 2008
40
50

GRIN2B gain of function mutations are sensitive to radiprodil, a negative allosteric modulator of GluN2B-containing NMDA receptors.
Brice Mullier, Christian Wolff, Zara Amanda Sands, Philippe Ghisdal, Pierandrea Muglia, Rafal Marian Kaminski, Véronique Marie André. Neuropharmacology 2017
22
50

Genetic variants in mRNA untranslated regions.
Maristella Steri, M Laura Idda, Michael B Whalen, Valeria Orrù. Wiley Interdiscip Rev RNA 2018
30
50


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.