142 related articles for article (PubMed ID: 33524775)
1. CNVs inform the biological network of Autism spectrum disorder.
Briuglia S; Calabrò M; Capra AP; La Rosa MA; Crisafulli C
Psychiatry Res; 2021 Mar; 297():113729. PubMed ID: 33524775
[TBL] [Abstract][Full Text] [Related]
2. The landscape of copy number variations in Finnish families with autism spectrum disorders.
Kanduri C; Kantojärvi K; Salo PM; Vanhala R; Buck G; Blancher C; Lähdesmäki H; Järvelä I
Autism Res; 2016 Jan; 9(1):9-16. PubMed ID: 26052927
[TBL] [Abstract][Full Text] [Related]
3. Diagnostic efficacy and new variants in isolated and complex autism spectrum disorder using molecular karyotyping.
Lovrečić L; Rajar P; Volk M; Bertok S; Gnidovec Stražišar B; Osredkar D; Jekovec Vrhovšek M; Peterlin B
J Appl Genet; 2018 May; 59(2):179-185. PubMed ID: 29564645
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights.
Kushima I; Aleksic B; Nakatochi M; Shimamura T; Okada T; Uno Y; Morikawa M; Ishizuka K; Shiino T; Kimura H; Arioka Y; Yoshimi A; Takasaki Y; Yu Y; Nakamura Y; Yamamoto M; Iidaka T; Iritani S; Inada T; Ogawa N; Shishido E; Torii Y; Kawano N; Omura Y; Yoshikawa T; Uchiyama T; Yamamoto T; Ikeda M; Hashimoto R; Yamamori H; Yasuda Y; Someya T; Watanabe Y; Egawa J; Nunokawa A; Itokawa M; Arai M; Miyashita M; Kobori A; Suzuki M; Takahashi T; Usami M; Kodaira M; Watanabe K; Sasaki T; Kuwabara H; Tochigi M; Nishimura F; Yamasue H; Eriguchi Y; Benner S; Kojima M; Yassin W; Munesue T; Yokoyama S; Kimura R; Funabiki Y; Kosaka H; Ishitobi M; Ohmori T; Numata S; Yoshikawa T; Toyota T; Yamakawa K; Suzuki T; Inoue Y; Nakaoka K; Goto YI; Inagaki M; Hashimoto N; Kusumi I; Son S; Murai T; Ikegame T; Okada N; Kasai K; Kunimoto S; Mori D; Iwata N; Ozaki N
Cell Rep; 2018 Sep; 24(11):2838-2856. PubMed ID: 30208311
[TBL] [Abstract][Full Text] [Related]
6. Integrated Functional Analysis Implicates Syndromic and Rare Copy Number Variation Genes as Prominent Molecular Players in Pathogenesis of Autism Spectrum Disorders.
Ashitha SNM; Ramachandra NB
Neuroscience; 2020 Jul; 438():25-40. PubMed ID: 32407977
[TBL] [Abstract][Full Text] [Related]
7. The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.
Merikangas AK; Segurado R; Heron EA; Anney RJ; Paterson AD; Cook EH; Pinto D; Scherer SW; Szatmari P; Gill M; Corvin AP; Gallagher L
Mol Psychiatry; 2015 Nov; 20(11):1366-72. PubMed ID: 25421404
[TBL] [Abstract][Full Text] [Related]
8. Copy number variations independently induce autism spectrum disorder.
Yingjun X; Haiming Y; Mingbang W; Liangying Z; Jiaxiu Z; Bing S; Qibin Y; Xiaofang S
Biosci Rep; 2017 Aug; 37(4):. PubMed ID: 28533427
[TBL] [Abstract][Full Text] [Related]
9. Molecular Pathways within Autism Spectrum Disorder Endophenotypes.
Briuglia S; Calabrò M; Capra AP; Briguori S; La Rosa MA; Crisafulli C
J Mol Neurosci; 2021 Jul; 71(7):1357-1367. PubMed ID: 33492615
[TBL] [Abstract][Full Text] [Related]
10. An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray.
Bacchelli E; Cameli C; Viggiano M; Igliozzi R; Mancini A; Tancredi R; Battaglia A; Maestrini E
Sci Rep; 2020 Feb; 10(1):3198. PubMed ID: 32081867
[TBL] [Abstract][Full Text] [Related]
11. Copy number variants in autism spectrum disorders.
Vicari S; Napoli E; Cordeddu V; Menghini D; Alesi V; Loddo S; Novelli A; Tartaglia M
Prog Neuropsychopharmacol Biol Psychiatry; 2019 Jun; 92():421-427. PubMed ID: 30797015
[TBL] [Abstract][Full Text] [Related]
12. Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees.
Woodbury-Smith M; Zarrei M; Wei J; Thiruvahindrapuram B; O'Connor I; Paterson AD; Yuen RKC; Dastan J; Stavropoulos DJ; Howe JL; Thompson A; Parlier M; Fernandez B; Piven J; Anagnostou E; Scherer SW; Vieland VJ; Szatmari P
Am J Med Genet B Neuropsychiatr Genet; 2020 Jul; 183(5):268-276. PubMed ID: 32372567
[TBL] [Abstract][Full Text] [Related]
13. Clinical correlates in children with autism spectrum disorder and CNVs: Systematic investigation in a clinical setting.
Barone R; Gulisano M; Amore R; Domini C; Milana MC; Giglio S; Madia F; Mattina T; Casabona A; Fichera M; Rizzo R
Int J Dev Neurosci; 2020 Jun; 80(4):276-286. PubMed ID: 32159884
[TBL] [Abstract][Full Text] [Related]
14. Genetics of autism spectrum disorder: an update on copy number variations leading to autism in the next generation sequencing era.
AlSagob M; Colak D; Kaya N
Discov Med; 2015 May; 19(106):367-79. PubMed ID: 26105700
[TBL] [Abstract][Full Text] [Related]
15. Epigenetics of autism-related impairment: copy number variation and maternal infection.
Mazina V; Gerdts J; Trinh S; Ankenman K; Ward T; Dennis MY; Girirajan S; Eichler EE; Bernier R
J Dev Behav Pediatr; 2015; 36(2):61-7. PubMed ID: 25629966
[TBL] [Abstract][Full Text] [Related]
16. Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriers.
Hudac CM; Bove J; Barber S; Duyzend M; Wallace A; Martin CL; Ledbetter DH; Hanson E; Goin-Kochel RP; Green-Snyder L; Chung WK; Eichler EE; Bernier RA
Autism Res; 2020 Aug; 13(8):1300-1310. PubMed ID: 32597026
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Array-CGH Analysis in a Cohort of Phenotypically Well-Characterized Individuals with "Essential" Autism Spectrum Disorders.
Napoli E; Russo S; Casula L; Alesi V; Amendola FA; Angioni A; Novelli A; Valeri G; Menghini D; Vicari S
J Autism Dev Disord; 2018 Feb; 48(2):442-449. PubMed ID: 29027068
[TBL] [Abstract][Full Text] [Related]
20. Identification of Copy Number Variation by Array-CGH in Portuguese Children and Adolescents Diagnosed with Autism Spectrum Disorders.
Monteiro S; Pinto J; Mira Coelho A; Leão M; Dória S
Neuropediatrics; 2019 Dec; 50(6):367-377. PubMed ID: 31398764
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
