A citation-based method for searching scientific literature

Martin Poot. Mol Syndromol 2015
Times Cited: 64



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: 389




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
36

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

The Interaction Between Contactin and Amyloid Precursor Protein and Its Role in Alzheimer's Disease.
Rosemary A Bamford, Jocelyn Widagdo, Natsuki Takamura, Madeline Eve, Victor Anggono, Asami Oguro-Ando. Neuroscience 2020
12

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
33

Cntnap2 Knockout Rats and Mice Exhibit Epileptiform Activity and Abnormal Sleep-Wake Physiology.
Alexia M Thomas, Michael D Schwartz, Michael D Saxe, Thomas S Kilduff. Sleep 2017
32


Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures.
Raffaele Falsaperla, Xena Giada Pappalardo, Catia Romano, Simona Domenica Marino, Giovanni Corsello, Martino Ruggieri, Enrico Parano, Piero Pavone. Front Pediatr 2020
4

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
38



Shed CNTNAP2 ectodomain is detectable in CSF and regulates Ca2+ homeostasis and network synchrony via PMCA2/ATP2B2.
M Dolores Martín-de-Saavedra, Marc Dos Santos, Lorenza Culotta, Olga Varea, Benjamin P Spielman, Euan Parnell, Marc P Forrest, Ruoqi Gao, Sehyoun Yoon, Emmarose McCoig,[...]. Neuron 2022
3

Intragenic CNTNAP2 Deletions: A Bridge Too Far?
Martin Poot. Mol Syndromol 2017
22

An oscillopathic approach to developmental dyslexia: From genes to speech processing.
Miguel Jiménez-Bravo, Victoria Marrero, Antonio Benítez-Burraco. Behav Brain Res 2017
12

Structural mapping of hot spots within human CASPR2 discoidin domain for autoantibody recognition.
Wenjun Liang, Junying Zhang, Margaux Saint-Martin, Fei Xu, Nelly Noraz, Jianmei Liu, Jérôme Honnorat, Heli Liu. J Autoimmun 2019
1

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
11

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
32

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
12

Genetic variants in autism-related CNTNAP2 impair axonal growth of cortical neurons.
Giorgia Canali, Marta Garcia, Bruno Hivert, Delphine Pinatel, Aline Goullancourt, Ksenia Oguievetskaia, Margaux Saint-Martin, Jean-Antoine Girault, Catherine Faivre-Sarrailh, Laurence Goutebroze. Hum Mol Genet 2018
23

A white paper on a neurodevelopmental framework for drug discovery in autism and other neurodevelopmental disorders.
C M Díaz-Caneja, M W State, R J Hagerman, S Jacquemont, O Marín, C Bagni, D Umbricht, E Simonoff, F de Andrés-Trelles, A Kaale,[...]. Eur Neuropsychopharmacol 2021
14