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.
209 related articles for article (PubMed ID: 38868529)
1. Copy number variations in autistic children. Alhazmi S; Alharthi M; Alzahrani M; Alrofaidi A; Basingab F; Almuhammadi A; Alkhatabi H; Ashi A; Chaudhary A; Elaimi A Biomed Rep; 2024 Jul; 21(1):107. PubMed ID: 38868529 [TBL] [Abstract][Full Text] [Related]
2. Multiple Recurrent Copy Number Variations (CNVs) in Chromosome 22 Including 22q11.2 Associated with Autism Spectrum Disorder. Alhazmi S; Alzahrani M; Farsi R; Alharbi M; Algothmi K; Alburae N; Ganash M; Azhari S; Basingab F; Almuhammadi A; Alqosaibi A; Alkhatabi H; Elaimi A; Jan M; Aldhalaan HM; Alrafiah A; Alrofaidi A Pharmgenomics Pers Med; 2022; 15():705-720. PubMed ID: 35898556 [TBL] [Abstract][Full Text] [Related]
3. The correlation between copy number variation in Chromosome 14 and DNA methylation in Saudi autistic children. Alhazmi S; Aljahdli B; Farsi R; Alharbi M; Algothmi K; Alburae N; Ganash M; Azhari S; Basingab F; Almuhammadi A; Alqosaibi A; Alkhatabi H; Elaimi A; Jan M; Aldhalaan H; Alyoubi R; Alrafiah A; Alrofaidi A Eur Rev Med Pharmacol Sci; 2022 Nov; 26(21):7866-7882. PubMed ID: 36394735 [TBL] [Abstract][Full Text] [Related]
4. Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services. Roberts JL; Hovanes K; Dasouki M; Manzardo AM; Butler MG Gene; 2014 Feb; 535(1):70-8. PubMed ID: 24188901 [TBL] [Abstract][Full Text] [Related]
5. New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants. Cappuccio G; Vitiello F; Casertano A; Fontana P; Genesio R; Bruzzese D; Ginocchio VM; Mormile A; Nitsch L; Andria G; Melis D Ital J Pediatr; 2016 Apr; 42():39. PubMed ID: 27072107 [TBL] [Abstract][Full Text] [Related]
6. Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybridization. Cho SC; Yim SH; Yoo HK; Kim MY; Jung GY; Shin GW; Kim BN; Hwang JW; Kang JJ; Kim TM; Chung YJ Psychiatr Genet; 2009 Aug; 19(4):177-85. PubMed ID: 19407672 [TBL] [Abstract][Full Text] [Related]
7. CGH Findings in Children with Complex and Essential Autistic Spectrum Disorder. Annunziata S; Bulgheroni S; D'Arrigo S; Esposito S; Taddei M; Saletti V; Alfei E; Sciacca FL; Rizzo A; Pantaleoni C; Riva D J Autism Dev Disord; 2023 Feb; 53(2):615-623. PubMed ID: 33394245 [TBL] [Abstract][Full Text] [Related]
8. Nexus between genome-wide copy number variations and autism spectrum disorder in Northeast Han Chinese population. Qiu S; Qiu Y; Li Y; Zhu X; Liu Y; Qiao Y; Cheng Y; Liu Y BMC Psychiatry; 2023 Feb; 23(1):96. PubMed ID: 36750796 [TBL] [Abstract][Full Text] [Related]
9. Copy number variations in Japanese children with autism spectrum disorder. Sakamoto Y; Shimoyama S; Furukawa T; Adachi M; Takahashi M; Mikami T; Kuribayashi M; Osato A; Tsushima D; Saito M; Ueno S; Nakamura K Psychiatr Genet; 2021 Jun; 31(3):79-87. PubMed ID: 33591083 [TBL] [Abstract][Full Text] [Related]
10. Analysis of a Protein Network Related to Copy Number Variations in Autism Spectrum Disorder. Schuch JB; Paixão-Côrtes VR; Longo D; Roman T; Riesgo RDS; Ranzan J; Becker MM; Riegel M; Schuler-Faccini L J Mol Neurosci; 2019 Sep; 69(1):140-149. PubMed ID: 31161481 [TBL] [Abstract][Full Text] [Related]
11. High-resolution SNP genotyping platform identified recurrent and novel CNVs in autism multiplex families. AlAyadhi LY; Hashmi JA; Iqbal M; Albalawi AM; Samman MI; Elamin NE; Bashir S; Basit S Neuroscience; 2016 Dec; 339():561-570. PubMed ID: 27771533 [TBL] [Abstract][Full Text] [Related]
12. The Role of Copy Number Variations and Ünsel Bolat G; Bolat H Mol Syndromol; 2021 Mar; 12(1):12-19. PubMed ID: 33776622 [TBL] [Abstract][Full Text] [Related]
13. Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank. Yap CX; Alvares GA; Henders AK; Lin T; Wallace L; Farrelly A; McLaren T; Berry J; Vinkhuyzen AAE; Trzaskowski M; Zeng J; Yang Y; Cleary D; Grove R; Hafekost C; Harun A; Holdsworth H; Jellett R; Khan F; Lawson L; Leslie J; Levis Frenk M; Masi A; Mathew NE; Muniandy M; Nothard M; Visscher PM; Dawson PA; Dissanayake C; Eapen V; Heussler HS; Whitehouse AJO; Wray NR; Gratten J Mol Autism; 2021 Feb; 12(1):12. PubMed ID: 33568206 [TBL] [Abstract][Full Text] [Related]
14. Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders. Glessner JT; Khan ME; Chang X; Liu Y; Otieno FG; Lemma M; Slaby I; Hain H; Mentch F; Li J; Kao C; Sleiman PMA; March ME; Connolly J; Hakonarson H J Neurodev Disord; 2023 Apr; 15(1):14. PubMed ID: 37120522 [TBL] [Abstract][Full Text] [Related]
15. Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder. Yin CL; Chen HI; Li LH; Chien YL; Liao HM; Chou MC; Chou WJ; Tsai WC; Chiu YN; Wu YY; Lo CZ; Wu JY; Chen YT; Gau SS Mol Autism; 2016; 7():23. PubMed ID: 27042285 [TBL] [Abstract][Full Text] [Related]
17. Identification of copy number variants in children and adolescents with autism spectrum disorder: a study from Turkey. Özaslan A; Kayhan G; İşeri E; Ergün MA; Güney E; Perçin FE Mol Biol Rep; 2021 Nov; 48(11):7371-7378. PubMed ID: 34637094 [TBL] [Abstract][Full Text] [Related]
18. The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay. Wayhelova M; Smetana J; Vallova V; Hladilkova E; Filkova H; Hanakova M; Vilemova M; Nikolova P; Gromesova B; Gaillyova R; Kuglik P BMC Med Genomics; 2019 Jul; 12(1):111. PubMed ID: 31337399 [TBL] [Abstract][Full Text] [Related]
19. Genotype-phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study. Chawner SJRA; Owen MJ; Holmans P; Raymond FL; Skuse D; Hall J; van den Bree MBM Lancet Psychiatry; 2019 Jun; 6(6):493-505. PubMed ID: 31056457 [TBL] [Abstract][Full Text] [Related]
20. Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving Mak ASL; Chiu ATG; Leung GKC; Mak CCY; Chu YWY; Mok GTK; Tang WF; Chan KYK; Tang MHY; Lau Yim ET; So KW; Tao VQ; Fung CW; Wong VCN; Uddin M; Lee SL; Marshall CR; Scherer SW; Kan ASY; Chung BHY Mol Autism; 2017; 8():31. PubMed ID: 28670437 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]