A citation-based method for searching scientific literature

Martin Poot. Mol Syndromol 2015
Times Cited: 63

Christopher M Watson, Laura A Crinnion, Antigoni Tzika, Alison Mills, Andrea Coates, Maria Pendlebury, Sarah Hewitt, Sally M Harrison, Catherine Daly, Paul Roberts, Ian M Carr, Eamonn G Sheridan, David T Bonthron. Am J Med Genet A 2014
Times Cited: 19

List of shared articles

Times cited

Contactin-associated protein-like 2, a protein of the neurexin family involved in several human diseases.
Margaux Saint-Martin, Bastien Joubert, Véronique Pellier-Monnin, Olivier Pascual, Nelly Noraz, Jérôme Honnorat. Eur J Neurosci 2018

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

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

A patient with a novel CNTNAP2 homozygous variant: further delineation of the CASPR2 deficiency syndrome and review of the literature.
Florence Riccardi, Jill Urquhart, Gary McCullagh, Peter Lawrence, Sofia Douzgou. Clin Dysmorphol 2019

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

Disconnecting CNTNAP2.
Martin Poot. Mol Syndromol 2016