A citation-based method for searching scientific literature

Raffaele Falsaperla, Xena Giada Pappalardo, Catia Romano, Simona Domenica Marino, Giovanni Corsello, Martino Ruggieri, Enrico Parano, Piero Pavone. Front Pediatr 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


CNTNAP2 variants affect early language development in the general population.
A J O Whitehouse, D V M Bishop, Q W Ang, C E Pennell, S E Fisher. Genes Brain Behav 2011
114
50

CNTNAP2 is significantly associated with schizophrenia and major depression in the Han Chinese population.
Weidong Ji, Tao Li, Yaosheng Pan, Hua Tao, Kang Ju, Zujia Wen, Yingchun Fu, Zhiguo An, Qian Zhao, Ti Wang,[...]. Psychiatry Res 2013
38
50

CNTNAP2 Is Significantly Associated With Speech Sound Disorder in the Chinese Han Population.
Yun-Jing Zhao, Yue-Ping Wang, Wen-Zhu Yang, Hong-Wei Sun, Hong-Wei Ma, Ya-Ru Zhao. J Child Neurol 2015
8
50

Eight further individuals with intellectual disability and epilepsy carrying bi-allelic CNTNAP2 aberrations allow delineation of the mutational and phenotypic spectrum.
Mateja Smogavec, Alison Cleall, Juliane Hoyer, Damien Lederer, Marie-Cécile Nassogne, Elizabeth E Palmer, Marie Deprez, Valérie Benoit, Isabelle Maystadt, Charlotte Noakes,[...]. J Med Genet 2016
32
50

Children with borderline intellectual functioning and autism spectrum disorder: developmental trajectories from 4 to 11 years of age.
Martina Barnevik Olsson, Anette Holm, Joakim Westerlund, Åsa Lundholm Hedvall, Christopher Gillberg, Elisabeth Fernell. Neuropsychiatr Dis Treat 2017
5
25

Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population.
Xiaoping Li, Zhengmao Hu, Yiqun He, Zhimin Xiong, Zhigao Long, Yu Peng, Fengxiao Bu, Jie Ling, Guanglei Xun, Xiaoyun Mo,[...]. Psychiatr Genet 2010
41
25

Analysis of two language-related genes in autism: a case-control association study of FOXP2 and CNTNAP2.
Claudio Toma, Amaia Hervás, Bàrbara Torrico, Noemí Balmaña, Marta Salgado, Marta Maristany, Elisabet Vilella, Rafael Martínez-Leal, Ma Inmaculada Planelles, Ivon Cuscó,[...]. Psychiatr Genet 2013
39
25

Association between CNTNAP2 polymorphisms and autism: A family-based study in the chinese han population and a meta-analysis combined with GWAS data of psychiatric genomics consortium.
Tian Zhang, Jishui Zhang, Ziqi Wang, Meixiang Jia, Tianlan Lu, Han Wang, Weihua Yue, Dai Zhang, Jun Li, Lifang Wang. Autism Res 2019
11
25

Synaptic proteins and receptors defects in autism spectrum disorders.
Jianling Chen, Shunying Yu, Yingmei Fu, Xiaohong Li. Front Cell Neurosci 2014
100
25

The association of CNTNAP2 rs7794745 gene polymorphism and autism in Iranian population.
Sahar Zare, Farhad Mashayekhi, Elham Bidabadi. J Clin Neurosci 2017
13
25

Association study between autistic-like traits and polymorphisms in the autism candidate regions RELN, CNTNAP2, SHANK3, and CDH9/10.
Lina Jonsson, Anna Zettergren, Erik Pettersson, Daniel Hovey, Henrik Anckarsäter, Lars Westberg, Paul Lichtenstein, Sebastian Lundström, Jonas Melke. Mol Autism 2014
25
25

Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders.
Claudio Toma, Kerrie D Pierce, Alex D Shaw, Anna Heath, Philip B Mitchell, Peter R Schofield, Janice M Fullerton. PLoS Genet 2018
17
25

Widespread differences in cortex DNA methylation of the "language gene" CNTNAP2 between humans and chimpanzees.
Eberhard Schneider, Nady El Hajj, Steven Richter, Justin Roche-Santiago, Indrajit Nanda, Werner Schempp, Peter Riederer, Bianca Navarro, Ronald E Bontrop, Ivanela Kondova,[...]. Epigenetics 2014
16
25

Association study of IL10 gene polymorphisms (rs1800872 and rs1800896) with cervical cancer in the Bangladeshi women.
Anamika Datta, Fatema Tuz Zahora, Md Abdul Aziz, Mohammad Sarowar Uddin, Mahmuda Ferdous, Md Shalahuddin Millat, Md Shahid Sarwar, Md Abdul Barek, Sarah Jafrin, Shamsun Nahar,[...]. Int Immunopharmacol 2020
5
25

Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals.
Heather C Whalley, Garret O'Connell, Jessika E Sussmann, Anna Peel, Andrew C Stanfield, Marianna E Hayiou-Thomas, Eve C Johnstone, Stephen M Lawrie, Andrew M McIntosh, Jeremy Hall. Am J Med Genet B Neuropsychiatr Genet 2011
71
25

Reduced Prefrontal Synaptic Connectivity and Disturbed Oscillatory Population Dynamics in the CNTNAP2 Model of Autism.
Maria T Lazaro, Jiannis Taxidis, Tristan Shuman, Iris Bachmutsky, Taruna Ikrar, Rommel Santos, G Mark Marcello, Apoorva Mylavarapu, Swasty Chandra, Allison Foreman,[...]. Cell Rep 2019
42
25

On the Nature of Monozygotic Twin Concordance and Discordance for Autistic Trait Severity: A Quantitative Analysis.
Lauren Castelbaum, Chad M Sylvester, Yi Zhang, Qiongru Yu, John N Constantino. Behav Genet 2020
36
25

Bias in meta-analysis detected by a simple, graphical test.
M Egger, G Davey Smith, M Schneider, C Minder. BMJ 1997
25

Lung cancer risk in relation to nicotinic acetylcholine receptor, CYP2A6 and CYP1A1 genotypes in the Bangladeshi population.
Mohammad Safiqul Islam, Maizbha Uddin Ahmed, Muhammad Shahdaat Bin Sayeed, Abdullah Al Maruf, A G M Mostofa, Syed Md Akram Hussain, Yearul Kabir, Ann K Daly, Abul Hasnat. Clin Chim Acta 2013
43
25

Quantifying the Optimal Structure of the Autism Phenotype: A Comprehensive Comparison of Dimensional, Categorical, and Hybrid Models.
Hyunsik Kim, Cara Keifer, Craig Rodriguez-Seijas, Nicholas Eaton, Matthew Lerner, Kenneth Gadow. J Am Acad Child Adolesc Psychiatry 2019
20
25

Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample.
Beate Peter, Wendy H Raskind, Mark Matsushita, Mark Lisowski, Tiffany Vu, Virginia W Berninger, Ellen M Wijsman, Zoran Brkanac. J Neurodev Disord 2011
77
25

Interaction effect between handedness and CNTNAP2 polymorphism (rs7794745 genotype) on voice-specific frontotemporal activity in healthy individuals: an fMRI study.
Michihiko Koeda, Atsushi Watanabe, Kumiko Tsuda, Miwako Matsumoto, Yumiko Ikeda, Woochan Kim, Amane Tateno, Banyar Than Naing, Hiroyuki Karibe, Takashi Shimada,[...]. Front Behav Neurosci 2015
11
25

Autism spectrum disorder.
Catherine Lord, Traolach S Brugha, Tony Charman, James Cusack, Guillaume Dumas, Thomas Frazier, Emily J H Jones, Rebecca M Jones, Andrew Pickles, Matthew W State,[...]. Nat Rev Dis Primers 2020
295
25

Autism spectrum disorder: definition, epidemiology, causes, and clinical evaluation.
Holly Hodges, Casey Fealko, Neelkamal Soares. Transl Pediatr 2020
75
25

Mapping the distribution of language related genes FoxP1, FoxP2, and CntnaP2 in the brains of vocal learning bat species.
Pedro M Rodenas-Cuadrado, Janine Mengede, Laura Baas, Paolo Devanna, Tobias A Schmid, Michael Yartsev, Uwe Firzlaff, Sonja C Vernes. J Comp Neurol 2018
13
25

Single nucleotide polymorphisms in the CNTNAP2 gene in Brazilian patients with autistic spectrum disorder.
P P Nascimento, A L Bossolani-Martins, D B A Rosan, L C Mattos, C Brandão-Mattos, A C Fett-Conte. Genet Mol Res 2016
12
25

What does CNTNAP2 reveal about autism spectrum disorder?
Olga Peñagarikano, Daniel H Geschwind. Trends Mol Med 2012
92
25

A Study of Single Nucleotide Polymorphisms of the SLC19A1/RFC1 Gene in Subjects with Autism Spectrum Disorder.
Naila Al Mahmuda, Shigeru Yokoyama, Jian-Jun Huang, Li Liu, Toshio Munesue, Hideo Nakatani, Kenshi Hayashi, Kunimasa Yagi, Masakazu Yamagishi, Haruhiro Higashida. Int J Mol Sci 2016
8
25

Family-based association study of ZNF533, DOCK4 and IMMP2L gene polymorphisms linked to autism in a northeastern Chinese Han population.
Shuang Liang, Xue-lai Wang, Ming-yang Zou, Han Wang, Xue Zhou, Cai-hong Sun, Wei Xia, Li-jie Wu, Takashi X Fujisawa, Akemi Tomoda. J Zhejiang Univ Sci B 2014
26
25

Genome-wide analyses of human perisylvian cerebral cortical patterning.
B S Abrahams, D Tentler, J V Perederiy, M C Oldham, G Coppola, D H Geschwind. Proc Natl Acad Sci U S A 2007
132
25

Ensembl 2018.
Daniel R Zerbino, Premanand Achuthan, Wasiu Akanni, M Ridwan Amode, Daniel Barrell, Jyothish Bhai, Konstantinos Billis, Carla Cummins, Astrid Gall, Carlos García Girón,[...]. Nucleic Acids Res 2018
25

Genetic Risk of Autism Spectrum Disorder in a Pakistani Population.
Madiha Khalid, Hashim Raza, Terri M Driessen, Paul J Lee, Leon Tejwani, Abdul Sami, Muhammad Nawaz, Shahid Mehmood Baig, Janghoo Lim, Ghazala Kaukab Raja. Genes (Basel) 2020
2
50


Identification of common genetic risk variants for autism spectrum disorder.
Jakob Grove, Stephan Ripke, Thomas D Als, Manuel Mattheisen, Raymond K Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A Andreassen, Richard Anney,[...]. Nat Genet 2019
744
25

Defining the contribution of CNTNAP2 to autism susceptibility.
Srirangan Sampath, Shambu Bhat, Simone Gupta, Ashley O'Connor, Andrew B West, Dan E Arking, Aravinda Chakravarti. PLoS One 2013
25
25

Melatonin treatment of repetitive behavioral deficits in the Cntnap2 mouse model of autism spectrum disorder.
Huei Bin Wang, Yu Tahara, Shu Hon Christopher Luk, Yoon-Sik Kim, Olivia N Hitchcock, Zoe A MacDowell Kaswan, Yang In Kim, Gene D Block, Cristina A Ghiani, Dawn H Loh,[...]. Neurobiol Dis 2020
7
25

Individual common variants exert weak effects on the risk for autism spectrum disorders.
Richard Anney, Lambertus Klei, Dalila Pinto, Joana Almeida, Elena Bacchelli, Gillian Baird, Nadia Bolshakova, Sven Bölte, Patrick F Bolton, Thomas Bourgeron,[...]. Hum Mol Genet 2012
239
25

Variants of the CNTNAP2 5' promoter as risk factors for autism spectrum disorders: a genetic and functional approach.
A G Chiocchetti, M Kopp, R Waltes, D Haslinger, E Duketis, T A Jarczok, F Poustka, A Voran, U Graab, J Meyer,[...]. Mol Psychiatry 2015
25
25

Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2.
Ashley A Scott-Van Zeeland, Brett S Abrahams, Ana I Alvarez-Retuerto, Lisa I Sonnenblick, Jeffrey D Rudie, Dara Ghahremani, Jeanette A Mumford, Russell A Poldrack, Mirella Dapretto, Daniel H Geschwind,[...]. Sci Transl Med 2010
179
25

Normal variation in fronto-occipital circuitry and cerebellar structure with an autism-associated polymorphism of CNTNAP2.
Geoffrey C Y Tan, Thomas F Doke, John Ashburner, Nicholas W Wood, Richard S J Frackowiak. Neuroimage 2010
82
25

What Is the Male-to-Female Ratio in Autism Spectrum Disorder? A Systematic Review and Meta-Analysis.
Rachel Loomes, Laura Hull, William Polmear Locke Mandy. J Am Acad Child Adolesc Psychiatry 2017
729
25

CNTNAP2 gene in high functioning autism: no association according to family and meta-analysis approaches.
Anna Maria Werling, Elise Bobrowski, Regina Taurines, Ronnie Gundelfinger, Marcel Romanos, Edna Grünblatt, Susanne Walitza. J Neural Transm (Vienna) 2016
13
25

Contactin-associated protein-like 2, a protein of the neurexin family involved in several human diseases.
Margaux Saint-Martin, Bastien Joubert, Véronique Pellier-Monnin, Olivier Pascual, Nelly Noraz, Jérôme Honnorat. Eur J Neurosci 2018
36
25

Neocortical excitation/inhibition balance in information processing and social dysfunction.
Ofer Yizhar, Lief E Fenno, Matthias Prigge, Franziska Schneider, Thomas J Davidson, Daniel J O'Shea, Vikaas S Sohal, Inbal Goshen, Joel Finkelstein, Jeanne T Paz,[...]. Nature 2011
25


Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1.
Sebastian Poliak, Daniela Salomon, Hadas Elhanany, Helena Sabanay, Brent Kiernan, Larysa Pevny, Colin L Stewart, Xiaorong Xu, Shing-Yan Chiu, Peter Shrager,[...]. J Cell Biol 2003
386
25

CUL3 Deficiency Causes Social Deficits and Anxiety-like Behaviors by Impairing Excitation-Inhibition Balance through the Promotion of Cap-Dependent Translation.
Zhaoqi Dong, Wenbing Chen, Chao Chen, Hongsheng Wang, Wanpeng Cui, Zhibing Tan, Heath Robinson, Nannan Gao, Bin Luo, Lei Zhang,[...]. Neuron 2020
40
25


The action potential.
Mark W Barnett, Philip M Larkman. Pract Neurol 2007
25
25

Modulation of prefrontal cortex excitation/inhibition balance rescues social behavior in CNTNAP2-deficient mice.
Aslihan Selimbeyoglu, Christina K Kim, Masatoshi Inoue, Soo Yeun Lee, Alice S O Hong, Isaac Kauvar, Charu Ramakrishnan, Lief E Fenno, Thomas J Davidson, Matthew Wright,[...]. Sci Transl Med 2017
158
25


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.