A citation-based method for searching scientific literature

Tian Zhang, Jishui Zhang, Ziqi Wang, Meixiang Jia, Tianlan Lu, Han Wang, Weihua Yue, Dai Zhang, Jun Li, Lifang Wang. Autism Res 2019
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


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
54

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
45

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
36

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
36

Autism.
Meng-Chuan Lai, Michael V Lombardo, Simon Baron-Cohen. Lancet 2014
36

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.
Dan E Arking, David J Cutler, Camille W Brune, Tanya M Teslovich, Kristen West, Morna Ikeda, Alexis Rea, Moltu Guy, Shin Lin, Edwin H Cook,[...]. Am J Hum Genet 2008
415
36

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.
Olga Peñagarikano, Brett S Abrahams, Edward I Herman, Kellen D Winden, Amos Gdalyahu, Hongmei Dong, Lisa I Sonnenblick, Robin Gruver, Joel Almajano, Anatol Bragin,[...]. Cell 2011
635
36


Autism and serotonin transporter gene polymorphisms: a systematic review and meta-analysis.
Christine H Huang, Susan L Santangelo. Am J Med Genet B Neuropsychiatr Genet 2008
87
27

Association between genetic variants in SLC25A12 and risk of autism spectrum disorders: An integrated meta-analysis.
Jun Liu, Aiping Yang, Qunwei Zhang, Guohui Yang, Wenjun Yang, Heyue Lei, Jianjun Quan, Fei Qu, Min Wang, Zengyu Zhang,[...]. Am J Med Genet B Neuropsychiatr Genet 2015
14
27


Meta-analysis and association of two common polymorphisms of the human oxytocin receptor gene in autism spectrum disorder.
Thorsten M Kranz, Marnie Kopp, Regina Waltes, Michael Sachse, Eftichia Duketis, Tomasz A Jarczok, Franziska Degenhardt, Katharina Görgen, Jobst Meyer, Christine M Freitag,[...]. Autism Res 2016
30
27

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
27


Prevalence and Characteristics of Autism Spectrum Disorder Among Children Aged 8 Years--Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2012.
Deborah L Christensen, Jon Baio, Kim Van Naarden Braun, Deborah Bilder, Jane Charles, John N Constantino, Julie Daniels, Maureen S Durkin, Robert T Fitzgerald, Margaret Kurzius-Spencer,[...]. MMWR Surveill Summ 2016
881
27

Reelin gene variants and risk of autism spectrum disorders: an integrated meta-analysis.
Zhenling Wang, Yuan Hong, Li Zou, Rong Zhong, Beibei Zhu, Na Shen, Wei Chen, Jiao Lou, Juntao Ke, Ti Zhang,[...]. Am J Med Genet B Neuropsychiatr Genet 2014
62
27

Meta-analyses of RELN variants in neuropsychiatric disorders.
Na Chen, Yanping Bao, Yanxue Xue, Yan Sun, Die Hu, Shiqiu Meng, Lin Lu, Jie Shi. Behav Brain Res 2017
27
27



Meta-analysis of GABRB3 Gene Polymorphisms and Susceptibility to Autism Spectrum Disorder.
Rezvan Noroozi, Mohammad Taheri, Soudeh Ghafouri-Fard, Zeinab Bidel, Mir Davood Omrani, Ali Sanjari Moghaddam, Parisa Sarabi, Alireza Mosavi Jarahi. J Mol Neurosci 2018
7
42

The association of CNTNAP2 rs7794745 gene polymorphism and autism in Iranian population.
Sahar Zare, Farhad Mashayekhi, Elham Bidabadi. J Clin Neurosci 2017
13
27

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
27

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
27

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
27

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
27

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
Brian J O'Roak, Pelagia Deriziotis, Choli Lee, Laura Vives, Jerrod J Schwartz, Santhosh Girirajan, Emre Karakoc, Alexandra P Mackenzie, Sarah B Ng, Carl Baker,[...]. Nat Genet 2011
798
27

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.
Maricela Alarcón, Brett S Abrahams, Jennifer L Stone, Jacqueline A Duvall, Julia V Perederiy, Jamee M Bomar, Jonathan Sebat, Michael Wigler, Christa L Martin, David H Ledbetter,[...]. Am J Hum Genet 2008
564
27

Loss of Cntnap2 in the Rat Causes Autism-Related Alterations in Social Interactions, Stereotypic Behavior, and Sensory Processing.
Kaela E Scott, Karnig Kazazian, Rajkamalpreet S Mann, Dorit Möhrle, Ashley L Schormans, Susanne Schmid, Brian L Allman. Autism Res 2020
13
27

Shining a light on CNTNAP2: complex functions to complex disorders.
Pedro Rodenas-Cuadrado, Joses Ho, Sonja C Vernes. Eur J Hum Genet 2014
155
27

Neuroglial activation and neuroinflammation in the brain of patients with autism.
Diana L Vargas, Caterina Nascimbene, Chitra Krishnan, Andrew W Zimmerman, Carlos A Pardo. Ann Neurol 2005
18

Elevated immune response in the brain of autistic patients.
Xiaohong Li, Abha Chauhan, Ashfaq M Sheikh, Sangita Patil, Ved Chauhan, Xiu-Min Li, Lina Ji, Ted Brown, Mazhar Malik. J Neuroimmunol 2009
466
18

Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism.
S Jill James, Stepan Melnyk, Stefanie Jernigan, Mario A Cleves, Charles H Halsted, Donna H Wong, Paul Cutler, Kenneth Bock, Marvin Boris, J Jeffrey Bradstreet,[...]. Am J Med Genet B Neuropsychiatr Genet 2006
371
18

Increased oxidative stress in the cerebellum and peripheral immune cells leads to exaggerated autism-like repetitive behavior due to deficiency of antioxidant response in BTBR T + tf/J mice.
Ahmed Nadeem, Sheikh F Ahmad, Naif O Al-Harbi, Sabry M Attia, Musaad A Alshammari, Khalid S Alzahrani, Saleh A Bakheet. Prog Neuropsychopharmacol Biol Psychiatry 2019
32
18

Evidence of oxidative damage and inflammation associated with low glutathione redox status in the autism brain.
S Rose, S Melnyk, O Pavliv, S Bai, T G Nick, R E Frye, S J James. Transl Psychiatry 2012
266
18

Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability.
Bàrbara Torrico, Noèlia Fernàndez-Castillo, Amaia Hervás, Montserrat Milà, Marta Salgado, Isabel Rueda, Jan K Buitelaar, Nanda Rommelse, Anoek M Oerlemans, Janita Bralten,[...]. Eur J Hum Genet 2015
22
18

An integrated meta-analysis of two variants in HOXA1/HOXB1 and their effect on the risk of autism spectrum disorders.
Ran-Ran Song, Li Zou, Rong Zhong, Xia-Wen Zheng, Bei-Bei Zhu, Wei Chen, Li Liu, Xiao-Ping Miao. PLoS One 2011
9
22

Clinical utility of folate pathway genetic polymorphisms in the diagnosis of autism spectrum disorders.
Naushad Shaik Mohammad, P Sai Shruti, Venkat Bharathi, Chintakindi Krishna Prasad, Tajamul Hussain, Salman A Alrokayan, Usha Naik, Akella Radha Rama Devi. Psychiatr Genet 2016
26
18

Environmental risk factors and biomarkers for autism spectrum disorder: an umbrella review of the evidence.
Jong Yeob Kim, Min Ji Son, Chei Yun Son, Joaquim Radua, Michael Eisenhut, Florence Gressier, Ai Koyanagi, Andre F Carvalho, Brendon Stubbs, Marco Solmi,[...]. Lancet Psychiatry 2019
92
18

Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders.
Regina Waltes, Eftichia Duketis, Michael Knapp, Richard J L Anney, Guillaume Huguet, Sabine Schlitt, Tomasz A Jarczok, Michael Sachse, Laura M Kämpfer, Tina Kleinböck,[...]. Hum Genet 2014
42
18

Common genetic variants on 1p13.2 associate with risk of autism.
K Xia, H Guo, Z Hu, G Xun, L Zuo, Y Peng, K Wang, Y He, Z Xiong, L Sun,[...]. Mol Psychiatry 2014
60
18

The potential role of the antioxidant and detoxification properties of glutathione in autism spectrum disorders: a systematic review and meta-analysis.
Penelope Ae Main, Manya T Angley, Catherine E O'Doherty, Philip Thomas, Michael Fenech. Nutr Metab (Lond) 2012
53
18

A comprehensive meta-analysis of common genetic variants in autism spectrum conditions.
Varun Warrier, Vivienne Chee, Paula Smith, Bhismadev Chakrabarti, Simon Baron-Cohen. Mol Autism 2015
28
18

Autism spectrum disorders and autistic traits: a decade of new twin studies.
Angelica Ronald, Rosa A Hoekstra. Am J Med Genet B Neuropsychiatr Genet 2011
333
18

Meta-Analysis of the Association between GABA Receptor Polymorphisms and Autism Spectrum Disorder (ASD).
Manijeh Mahdavi, Majid Kheirollahi, Roya Riahi, Fariborz Khorvash, Mehdi Khorrami, Maryam Mirsafaie. J Mol Neurosci 2018
18
18

STRING v10: protein-protein interaction networks, integrated over the tree of life.
Damian Szklarczyk, Andrea Franceschini, Stefan Wyder, Kristoffer Forslund, Davide Heller, Jaime Huerta-Cepas, Milan Simonovic, Alexander Roth, Alberto Santos, Kalliopi P Tsafou,[...]. Nucleic Acids Res 2015
18

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
18

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
18

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
18

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
18

Bias in meta-analysis detected by a simple, graphical test.
M Egger, G Davey Smith, M Schneider, C Minder. BMJ 1997
18


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.