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



Betul Bakkaloglu, Brian J O'Roak, Angeliki Louvi, Abha R Gupta, Jesse F Abelson, Thomas M Morgan, Katarzyna Chawarska, Ami Klin, A Gulhan Ercan-Sencicek, Althea A Stillman, Gamze Tanriover, Brett S Abrahams, Jackie A Duvall, Elissa M Robbins, Daniel H Geschwind, Thomas Biederer, Murat Gunel, Richard P Lifton, Matthew W State. Am J Hum Genet 2008
Times Cited: 379




List of shared articles



Times cited


Dendritic Integration Dysfunction in Neurodevelopmental Disorders.
Andrew D Nelson, Kevin J Bender. Dev Neurosci 2021
1

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
0


The DSM-5 introduction of the Social (Pragmatic) Communication Disorder as a new mental disorder: a philosophical review.
M Cristina Amoretti, Elisabetta Lalumera, Davide Serpico. Hist Philos Life Sci 2021
0

Colonic dilation and altered ex vivo gastrointestinal motility in the neuroligin-3 knockout mouse.
Anita J L Leembruggen, Gayathri K Balasuriya, Jinghong Zhang, Shana Schokman, Kristy Swiderski, Joel C Bornstein, Jess Nithianantharajah, Elisa L Hill-Yardin. Autism Res 2020
12

Genetic Intersections of Language and Neuropsychiatric Conditions.
Tanner Koomar, Jacob J Michaelson. Curr Psychiatry Rep 2020
3

Genome-wide association study of rate of cognitive decline in Alzheimer's disease patients identifies novel genes and pathways.
Richard Sherva, Alden Gross, Shubhabrata Mukherjee, Ryan Koesterer, Philippe Amouyel, Celine Bellenguez, Carole Dufouil, David A Bennett, Lori Chibnik, Carlos Cruchaga,[...]. Alzheimers Dement 2020
2

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
2


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
6

Suppression of Akt-mTOR pathway rescued the social behavior in Cntnap2-deficient mice.
Xiaoliang Xing, Jing Zhang, Kunyang Wu, Beibei Cao, Xianfeng Li, Fang Jiang, Zhengmao Hu, Kun Xia, Jia-Da Li. Sci Rep 2019
18

Disrupted AMPA Receptor Function upon Genetic- or Antibody-Mediated Loss of Autism-Associated CASPR2.
Dominique Fernandes, Sandra D Santos, Ester Coutinho, Jessica L Whitt, Nuno Beltrão, Tiago Rondão, M Isabel Leite, Camilla Buckley, Hey-Kyoung Lee, Ana Luísa Carvalho. Cereb Cortex 2019
11

Candidate gene variant effects on language disorders in Robinson Crusoe Island.
Hayley S Mountford, Pía Villanueva, María Angélica Fernández, Zulema De Barbieri, Jean-Baptiste Cazier, Dianne F Newbury. Ann Hum Biol 2019
3

The critical role of ASD-related gene CNTNAP3 in regulating synaptic development and social behavior in mice.
Da-Li Tong, Rui-Guo Chen, Yu-Lan Lu, Wei-Ke Li, Yue-Fang Zhang, Jun-Kai Lin, Ling-Jie He, Ting Dang, Shi-Fang Shan, Xiao-Hong Xu,[...]. Neurobiol Dis 2019
6

Maternal Antibody and ASD: Clinical Data and Animal Models.
Adriana Gata-Garcia, Betty Diamond. Front Immunol 2019
6

Common variant of CNTNAP2 gene modulate the social performances and functional connectivity of posterior right temporoparietal junction.
Tongjian Bai, Long Zhang, Xiaohui Xie, Guixian Xiao, Wanling Huang, Dandan Li, Meidan Zu, Lin Wei, Xianbo Zuo, Gong-Jun J I,[...]. Soc Cogn Affect Neurosci 2019
1


Synaptopathology in autism spectrum disorders: Complex effects of synaptic genes on neural circuits.
Xinxing Wang, Rachel Kery, Qiaojie Xiong. Prog Neuropsychopharmacol Biol Psychiatry 2018
4

Mouse Cntnap2 and Human CNTNAP2 ASD Alleles Cell Autonomously Regulate PV+ Cortical Interneurons.
Daniel Vogt, Kathleen K A Cho, Samantha M Shelton, Anirban Paul, Z Josh Huang, Vikaas S Sohal, John L R Rubenstein. Cereb Cortex 2018
34

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
11

Common Ribs of Inhibitory Synaptic Dysfunction in the Umbrella of Neurodevelopmental Disorders.
Rachel Ali Rodriguez, Christina Joya, Rochelle M Hines. Front Mol Neurosci 2018
8

Sociability and synapse subtype-specific defects in mice lacking SRPX2, a language-associated gene.
Breeanne M Soteros, Qifei Cong, Christian R Palmer, Gek-Ming Sia. PLoS One 2018
6


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
10

CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders.
O Mercati, G Huguet, A Danckaert, G André-Leroux, A Maruani, M Bellinzoni, T Rolland, L Gouder, A Mathieu, J Buratti,[...]. Mol Psychiatry 2017
35

Autism genetics - an overview.
Jiani Yin, Christian P Schaaf. Prenat Diagn 2017
23


The association of CNTNAP2 rs7794745 gene polymorphism and autism in Iranian population.
Sahar Zare, Farhad Mashayekhi, Elham Bidabadi. J Clin Neurosci 2017
10

Candidate Genes for Inherited Autism Susceptibility in the Lebanese Population.
Silva Kourtian, Jihane Soueid, Nadine J Makhoul, Dikran Richard Guisso, Maria Chahrour, Rose-Mary N Boustany. Sci Rep 2017
4


Relatively frequent switching of transcription start sites during cerebellar development.
Peter Zhang, Emmanuel Dimont, Thomas Ha, Douglas J Swanson, Winston Hide, Dan Goldowitz. BMC Genomics 2017
11

Features of emotional and social behavioral phenotypes of calsyntenin2 knockout mice.
S V Ranneva, K S Pavlov, A V Gromova, T G Amstislavskaya, T V Lipina. Behav Brain Res 2017
9

Bio-collections in autism research.
Jamie Reilly, Louise Gallagher, June L Chen, Geraldine Leader, Sanbing Shen. Mol Autism 2017
12

Regulatory Mechanisms Controlling Maturation of Serotonin Neuron Identity and Function.
William C Spencer, Evan S Deneris. Front Cell Neurosci 2017
13


Behavioral phenotypes of genetic mouse models of autism.
T M Kazdoba, P T Leach, J N Crawley. Genes Brain Behav 2016
83

Regulation of neuronal migration, an emerging topic in autism spectrum disorders.
Orly Reiner, Eyal Karzbrun, Aditya Kshirsagar, Kozo Kaibuchi. J Neurochem 2016
60

Expression of Cntnap2 (Caspr2) in multiple levels of sensory systems.
Aaron Gordon, Daniela Salomon, Noy Barak, Yefim Pen, Michael Tsoory, Tali Kimchi, Elior Peles. Mol Cell Neurosci 2016
26

Synapse alterations in autism: Review of animal model findings.
Martina Zatkova, Jan Bakos, Julius Hodosy, Daniela Ostatnikova. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub 2016
12


Functional Evaluations of Genes Disrupted in Patients with Tourette's Disorder.
Nawei Sun, Jay A Tischfield, Robert A King, Gary A Heiman. Front Psychiatry 2016
8

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
10

Translational Mouse Models of Autism: Advancing Toward Pharmacological Therapeutics.
Tatiana M Kazdoba, Prescott T Leach, Mu Yang, Jill L Silverman, Marjorie Solomon, Jacqueline N Crawley. Curr Top Behav Neurosci 2016
66

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
27

Clinical and genomic evaluation of a Chinese patient with a novel deletion associated with Phelan-McDermid syndrome.
Dongzhu Lei, Shaoyuan Li, Santasree Banerjee, Haoqing Zhang, Caiyun Li, Shuai Hou, Danjing Chen, Haiying Yan, Hanmei Li, Huan Huan Peng,[...]. Oncotarget 2016
0