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
33

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
39

Intragenic CNTNAP2 Deletions: A Bridge Too Far?
Martin Poot. Mol Syndromol 2017
20

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
2

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
31

Disconnecting CNTNAP2.
Martin Poot. Mol Syndromol 2016
0