These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
141 related articles for article (PubMed ID: 22750301)
1. Disruption of Contactin 4 in two subjects with autism in Chinese population. Guo H; Xun G; Peng Y; Xiang X; Xiong Z; Zhang L; He Y; Xu X; Liu Y; Lu L; Long Z; Pan Q; Hu Z; Zhao J; Xia K Gene; 2012 Sep; 505(2):201-5. PubMed ID: 22750301 [TBL] [Abstract][Full Text] [Related]
2. Intragenic CNTN4 copy number variants associated with a spectrum of neurobehavioral phenotypes. Zhang SQ; Fleischer J; Al-Kateb H; Mito Y; Amarillo I; Shinawi M Eur J Med Genet; 2020 Mar; 63(3):103736. PubMed ID: 31422286 [TBL] [Abstract][Full Text] [Related]
3. Contactin 4 as an autism susceptibility locus. Cottrell CE; Bir N; Varga E; Alvarez CE; Bouyain S; Zernzach R; Thrush DL; Evans J; Trimarchi M; Butter EM; Cunningham D; Gastier-Foster JM; McBride KL; Herman GE Autism Res; 2011 Jun; 4(3):189-99. PubMed ID: 21308999 [TBL] [Abstract][Full Text] [Related]
4. Disruption of contactin 4 in three subjects with autism spectrum disorder. Roohi J; Montagna C; Tegay DH; Palmer LE; DeVincent C; Pomeroy JC; Christian SL; Nowak N; Hatchwell E J Med Genet; 2009 Mar; 46(3):176-82. PubMed ID: 18349135 [TBL] [Abstract][Full Text] [Related]
5. Clinical and Molecular Characterization of Two Patients with CNTN6 Copy Number Variations. Tassano E; Uccella S; Giacomini T; Severino M; Fiorio P; Gimelli G; Ronchetto P Cytogenet Genome Res; 2018; 156(3):144-149. PubMed ID: 30508811 [TBL] [Abstract][Full Text] [Related]
6. Cell Adhesion Molecules Involved in Neurodevelopmental Pathways Implicated in 3p-Deletion Syndrome and Autism Spectrum Disorder. Gandawijaya J; Bamford RA; Burbach JPH; Oguro-Ando A Front Cell Neurosci; 2020; 14():611379. PubMed ID: 33519384 [TBL] [Abstract][Full Text] [Related]
7. Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome. Fernandez T; Morgan T; Davis N; Klin A; Morris A; Farhi A; Lifton RP; State MW Am J Hum Genet; 2008 Jun; 82(6):1385. PubMed ID: 18551756 [No Abstract] [Full Text] [Related]
8. Gene-rich large deletions are overrepresented in POAG patients of Indian and Caucasian origins. Kaurani L; Vishal M; Kumar D; Sharma A; Mehani B; Sharma C; Chakraborty S; Jha P; Ray J; Sen A; Dash D; Ray K; Mukhopadhyay A Invest Ophthalmol Vis Sci; 2014 Apr; 55(5):3258-64. PubMed ID: 24764060 [TBL] [Abstract][Full Text] [Related]
9. CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders. Repnikova EA; Lyalin DA; McDonald K; Astbury C; Hansen-Kiss E; Cooley LD; Pfau R; Herman GE; Pyatt RE; Hickey SE Eur J Med Genet; 2020 Jan; 63(1):103636. PubMed ID: 30836150 [TBL] [Abstract][Full Text] [Related]
10. Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome. Fernandez T; Morgan T; Davis N; Klin A; Morris A; Farhi A; Lifton RP; State MW Am J Hum Genet; 2004 Jun; 74(6):1286-93. PubMed ID: 15106122 [TBL] [Abstract][Full Text] [Related]
11. A current view on contactin-4, -5, and -6: Implications in neurodevelopmental disorders. Oguro-Ando A; Zuko A; Kleijer KTE; Burbach JPH Mol Cell Neurosci; 2017 Jun; 81():72-83. PubMed ID: 28064060 [TBL] [Abstract][Full Text] [Related]
12. Effect Sizes of Deletions and Duplications on Autism Risk Across the Genome. Douard E; Zeribi A; Schramm C; Tamer P; Loum MA; Nowak S; Saci Z; Lord MP; Rodríguez-Herreros B; Jean-Louis M; Moreau C; Loth E; Schumann G; Pausova Z; Elsabbagh M; Almasy L; Glahn DC; Bourgeron T; Labbe A; Paus T; Mottron L; Greenwood CMT; Huguet G; Jacquemont S Am J Psychiatry; 2021 Jan; 178(1):87-98. PubMed ID: 32911998 [TBL] [Abstract][Full Text] [Related]
13. Mutation analysis of the NRXN1 gene in a Chinese autism cohort. Liu Y; Hu Z; Xun G; Peng Y; Lu L; Xu X; Xiong Z; Xia L; Liu D; Li W; Zhao J; Xia K J Psychiatr Res; 2012 May; 46(5):630-4. PubMed ID: 22405623 [TBL] [Abstract][Full Text] [Related]
14. A case report of Chinese brothers with inherited MECP2-containing duplication: autism and intellectual disability, but not seizures or respiratory infections. Xu X; Xu Q; Zhang Y; Zhang X; Cheng T; Wu B; Ding Y; Lu P; Zheng J; Zhang M; Qiu Z; Yu X BMC Med Genet; 2012 Aug; 13():75. PubMed ID: 22909152 [TBL] [Abstract][Full Text] [Related]
15. Schizophrenia and epilepsy as a result of maternally inherited CNTN6 copy number variant. Juan-Perez C; Farrand S; Velakoulis D Schizophr Res; 2018 Dec; 202():111-112. PubMed ID: 29983269 [TBL] [Abstract][Full Text] [Related]
16. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Glessner JT; Wang K; Cai G; Korvatska O; Kim CE; Wood S; Zhang H; Estes A; Brune CW; Bradfield JP; Imielinski M; Frackelton EC; Reichert J; Crawford EL; Munson J; Sleiman PM; Chiavacci R; Annaiah K; Thomas K; Hou C; Glaberson W; Flory J; Otieno F; Garris M; Soorya L; Klei L; Piven J; Meyer KJ; Anagnostou E; Sakurai T; Game RM; Rudd DS; Zurawiecki D; McDougle CJ; Davis LK; Miller J; Posey DJ; Michaels S; Kolevzon A; Silverman JM; Bernier R; Levy SE; Schultz RT; Dawson G; Owley T; McMahon WM; Wassink TH; Sweeney JA; Nurnberger JI; Coon H; Sutcliffe JS; Minshew NJ; Grant SF; Bucan M; Cook EH; Buxbaum JD; Devlin B; Schellenberg GD; Hakonarson H Nature; 2009 May; 459(7246):569-73. PubMed ID: 19404257 [TBL] [Abstract][Full Text] [Related]
17. The genetics of autism. Muhle R; Trentacoste SV; Rapin I Pediatrics; 2004 May; 113(5):e472-86. PubMed ID: 15121991 [TBL] [Abstract][Full Text] [Related]
18. No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins. Murdoch JD; Gupta AR; Sanders SJ; Walker MF; Keaney J; Fernandez TV; Murtha MT; Anyanwu S; Ober GT; Raubeson MJ; DiLullo NM; Villa N; Waqar Z; Sullivan C; Gonzalez L; Willsey AJ; Choe SY; Neale BM; Daly MJ; State MW PLoS Genet; 2015 Jan; 11(1):e1004852. PubMed ID: 25621974 [TBL] [Abstract][Full Text] [Related]
19. CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders. Hu J; Liao J; Sathanoori M; Kochmar S; Sebastian J; Yatsenko SA; Surti U J Neurodev Disord; 2015; 7(1):26. PubMed ID: 26257835 [TBL] [Abstract][Full Text] [Related]
20. CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders. Mercati O; Huguet G; Danckaert A; André-Leroux G; Maruani A; Bellinzoni M; Rolland T; Gouder L; Mathieu A; Buratti J; Amsellem F; Benabou M; Van-Gils J; Beggiato A; Konyukh M; Bourgeois JP; Gazzellone MJ; Yuen RK; Walker S; Delépine M; Boland A; Régnault B; Francois M; Van Den Abbeele T; Mosca-Boidron AL; Faivre L; Shimoda Y; Watanabe K; Bonneau D; Rastam M; Leboyer M; Scherer SW; Gillberg C; Delorme R; Cloëz-Tayarani I; Bourgeron T Mol Psychiatry; 2017 Apr; 22(4):625-633. PubMed ID: 27166760 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]