Human Genome Epidemiology Literature Finder
|
Records 1 - 7 (of 7 Records) |
| Query Trace: Epilepsy and CNTNAP2[original query] |
|---|
| CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy. Molecular psychiatry 2008 Mar 13 (3): 261-6. Friedman J I, Vrijenhoek T, Markx S, Janssen I M, van der Vliet W A, Faas B H W, Knoers N V, Cahn W, Kahn R S, Edelmann L, Davis K L, Silverman J M, Brunner H G, van Kessel A Geurts, Wijmenga C, Ophoff R A, Veltman J |
| Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies. PLoS genetics 2010 May 6 (5): e1000962. Mefford Heather C, Muhle Hiltrud, Ostertag Philipp, von Spiczak Sarah, Buysse Karen, Baker Carl, Franke Andre, Malafosse Alain, Genton Pierre, Thomas Pierre, Gurnett Christina A, Schreiber Stefan, Bassuk Alexander G, Guipponi Michel, Stephani Ulrich, Helbig Ingo, Eichler Evan |
| Single nucleotide polymorphisms in the CNTNAP2 gene in Brazilian patients with autistic spectrum disorder. Genetics and molecular research : GMR 2016 Feb 15 (1): . Nascimento P P, Bossolani-Martins A L, Rosan D B A, Mattos L C, Brandão-Mattos C, Fett-Conte A |
| Targeted next-generation sequencing provides novel clues for associated epilepsy and cardiac conduction disorder/SUDEP. PloS one 2017 12 12 (12): e0189618. Coll Monica, Striano Pasquale, Ferrer-Costa Carles, Campuzano Oscar, Matés Jesús, Del Olmo Bernat, Iglesias Anna, Pérez-Serra Alexandra, Mademont Irene, Picó Ferran, Oliva Antonio, Brugada Ram |
| Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders. PLoS genetics 2018 12 14 (12): e1007535. Toma Claudio, Pierce Kerrie D, Shaw Alex D, Heath Anna, Mitchell Philip B, Schofield Peter R, Fullerton Janice |
| Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations. Human mutation 2019 Feb . Zhou Wei-Zhen, Zhang Jie, Li Ziyi, Lin Xiaojing, Li Jiarui, Wang Sheng, Yang Changhong, Wu Qixi, Ye Adam Yongxin, Wang Meng, Wang Dandan, Pu Tad Zhengzhang, Wu Yu-Yu, Wei Lipi |
| Genotype-phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder. Human genetics 2023 5 . Gianluca D'Onofrio, Andrea Accogli, Mariasavina Severino, Haluk Caliskan, Tomislav Kokotovi?, Antonela Blazekovic, Kristina Gotovac Jercic, Silvana Markovic, Tamara Zigman, Krnjak Goran, Nina Bariši?, Vlasta Duranovic, Ana Ban, Fran Borovecki, Danijela Petkovi? Ramadža, Ivo Bari?, Walid Fazeli, Peter Herkenrath, Carla Marini, Roberta Vittorini, Vykuntaraju Gowda, Arjan Bouman, Clarissa Rocca, Issam Azmi Alkhawaja, Bibi Nazia Murtaza, Malik Mujaddad Ur Rehman, Chadi Al Alam, Gisele Nader, Maria Margherita Mancardi, Thea Giacomini, Siddharth Srivastava, Javeria Raza Alvi, Hoda Tomoum, Sara Matricardi, Michele Iacomino, Antonella Riva, Marcello Scala, Francesca Madia, Angela Pistorio, Vincenzo Salpietro, Carlo Minetti, Jean-Baptiste Rivière, Myriam Srour, Stephanie Efthymiou, Reza Maroofian, Henry Houlden, Sonja Catherine Vernes, Federico Zara, Pasquale Striano, Vanja Na |
- Page last reviewed:Feb 1, 2024
- Content source: