A citation-based method for searching scientific literature

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, Aravinda Chakravarti. Am J Hum Genet 2008
Times Cited: 403

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
Times Cited: 67

List of shared articles

Times cited

Common variants of the autism-associated CNTNAP2 gene contribute to the modulatory effect of social function mediated by temporal cortex.
Dandan Li, Long Zhang, Tongjian Bai, Wanling Huang, Gong-Jun Ji, Tingting Yang, Yifan Zhang, Yanghua Tian, Bensheng Qiu, Kai Wang. Behav Brain Res 2021

Association between Genetic Variants in DUSP15, CNTNAP2, and PCDHA Genes and Risk of Childhood Autism Spectrum Disorder.
Fang Fang, Minxia Ge, Jun Liu, Zengyu Zhang, Hong Yu, Shuilong Zhu, Liwei Xu, Lina Shao. Behav Neurol 2021

Genetic Intersections of Language and Neuropsychiatric Conditions.
Tanner Koomar, Jacob J Michaelson. Curr Psychiatry Rep 2020

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

Altered Auditory Processing, Filtering, and Reactivity in the Cntnap2 Knock-Out Rat Model for Neurodevelopmental Disorders.
Kaela E Scott, Ashley L Schormans, Katharine Y Pacoli, Cleusa De Oliveira, Brian L Allman, Susanne Schmid. J Neurosci 2018

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

A common variant of the CNTNAP2 gene is associated with structural variation in the left superior occipital gyrus.
Julia Uddén, Tineke M Snijders, Simon E Fisher, Peter Hagoort. Brain Lang 2017

Common variation in the autism risk gene CNTNAP2, brain structural connectivity and multisensory speech integration.
Lars A Ross, Victor A Del Bene, Sophie Molholm, Young Jae Woo, Gizely N Andrade, Brett S Abrahams, John J Foxe. Brain Lang 2017

Imaging genetics in neurodevelopmental psychopathology.
Marieke Klein, Marjolein van Donkelaar, Ellen Verhoef, Barbara Franke. Am J Med Genet B Neuropsychiatr Genet 2017

Regulation of neuronal migration, an emerging topic in autism spectrum disorders.
Orly Reiner, Eyal Karzbrun, Aditya Kshirsagar, Kozo Kaibuchi. J Neurochem 2016

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