A citation-based method for searching scientific literature

Martin Poot. Mol Syndromol 2015
Times Cited: 63

D F Newbury, S Paracchini, T S Scerri, L Winchester, L Addis, Alex J Richardson, J Walter, J F Stein, J B Talcott, A P Monaco. Behav Genet 2011
Times Cited: 140

List of shared articles

Times cited

Intragenic CNTNAP2 Deletions: A Bridge Too Far?
Martin Poot. Mol Syndromol 2017

An oscillopathic approach to developmental dyslexia: From genes to speech processing.
Miguel Jiménez-Bravo, Victoria Marrero, Antonio Benítez-Burraco. Behav Brain Res 2017

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

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

Hyperexcitable and Immature-Like Neuronal Activity in the Auditory Cortex of Adult Rats Lacking the Language-Linked CNTNAP2 Gene.
Kaela E Scott, Rajkamalpreet S Mann, Ashley L Schormans, Susanne Schmid, Brian L Allman. Cereb Cortex 2022