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



Christiane Zweier, Eiko K de Jong, Markus Zweier, Alfredo Orrico, Lilian B Ousager, Amanda L Collins, Emilia K Bijlsma, Merel A W Oortveld, Arif B Ekici, André Reis, Annette Schenck, Anita Rauch. Am J Hum Genet 2009
Times Cited: 234




List of shared articles



Times cited


Molecular networks of the FOXP2 transcription factor in the brain.
Joery den Hoed, Karthikeyan Devaraju, Simon E Fisher. EMBO Rep 2021
0

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

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

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


Dysregulation of Parvalbumin Expression in the Cntnap2-/- Mouse Model of Autism Spectrum Disorder.
Emanuel Lauber, Federica Filice, Beat Schwaller. Front Mol Neurosci 2018
24

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


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

Structural Chromosomal Rearrangements Require Nucleotide-Level Resolution: Lessons from Next-Generation Sequencing in Prenatal Diagnosis.
Zehra Ordulu, Tammy Kammin, Harrison Brand, Vamsee Pillalamarri, Claire E Redin, Ryan L Collins, Ian Blumenthal, Carrie Hanscom, Shahrin Pereira, India Bradley,[...]. Am J Hum Genet 2016
30