307 related articles for article (PubMed ID: 32034290)
1. Nuclear receptor corepressors in intellectual disability and autism.
Kong Y; Zhou W; Sun Z
Mol Psychiatry; 2020 Oct; 25(10):2220-2236. PubMed ID: 32034290
[TBL] [Abstract][Full Text] [Related]
2. Epigenetics of Autism Spectrum Disorder: Histone Deacetylases.
Tseng CJ; McDougle CJ; Hooker JM; Zürcher NR
Biol Psychiatry; 2022 Jun; 91(11):922-933. PubMed ID: 35120709
[TBL] [Abstract][Full Text] [Related]
3. Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants.
Siu MT; Butcher DT; Turinsky AL; Cytrynbaum C; Stavropoulos DJ; Walker S; Caluseriu O; Carter M; Lou Y; Nicolson R; Georgiades S; Szatmari P; Anagnostou E; Scherer SW; Choufani S; Brudno M; Weksberg R
Clin Epigenetics; 2019 Jul; 11(1):103. PubMed ID: 31311581
[TBL] [Abstract][Full Text] [Related]
4. Nuclear Receptor Coactivators (NCOAs) and Corepressors (NCORs) in the Brain.
Sun Z; Xu Y
Endocrinology; 2020 Aug; 161(8):. PubMed ID: 32449767
[TBL] [Abstract][Full Text] [Related]
5. Genetic analysis of intellectual disability and autism.
Chiurazzi P; Kiani AK; Miertus J; Paolacci S; Barati S; Manara E; Stuppia L; Gurrieri F; Bertelli M
Acta Biomed; 2020 Nov; 91(13-S):e2020003. PubMed ID: 33170170
[TBL] [Abstract][Full Text] [Related]
6. Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.
Noor A; Whibley A; Marshall CR; Gianakopoulos PJ; Piton A; Carson AR; Orlic-Milacic M; Lionel AC; Sato D; Pinto D; Drmic I; Noakes C; Senman L; Zhang X; Mo R; Gauthier J; Crosbie J; Pagnamenta AT; Munson J; Estes AM; Fiebig A; Franke A; Schreiber S; Stewart AF; Roberts R; McPherson R; Guter SJ; Cook EH; Dawson G; Schellenberg GD; Battaglia A; Maestrini E; ; Jeng L; Hutchison T; Rajcan-Separovic E; Chudley AE; Lewis SM; Liu X; Holden JJ; Fernandez B; Zwaigenbaum L; Bryson SE; Roberts W; Szatmari P; Gallagher L; Stratton MR; Gecz J; Brady AF; Schwartz CE; Schachar RJ; Monaco AP; Rouleau GA; Hui CC; Lucy Raymond F; Scherer SW; Vincent JB
Sci Transl Med; 2010 Sep; 2(49):49ra68. PubMed ID: 20844286
[TBL] [Abstract][Full Text] [Related]
7. Genetic Variation across Phenotypic Severity of Autism.
Toma C
Trends Genet; 2020 Apr; 36(4):228-231. PubMed ID: 32037010
[TBL] [Abstract][Full Text] [Related]
8. [Epigenetics' implication in autism spectrum disorders: A review].
Hamza M; Halayem S; Mrad R; Bourgou S; Charfi F; Belhadj A
Encephale; 2017 Aug; 43(4):374-381. PubMed ID: 27692350
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior.
Harris HK; Nakayama T; Lai J; Zhao B; Argyrou N; Gubbels CS; Soucy A; Genetti CA; Suslovitch V; Rodan LH; Tiller GE; Lesca G; Gripp KW; Asadollahi R; Hamosh A; Applegate CD; Turnpenny PD; Simon MEH; Volker-Touw CML; Gassen KLIV; Binsbergen EV; Pfundt R; Gardeitchik T; Vries BBA; Immken LL; Buchanan C; Willing M; Toler TL; Fassi E; Baker L; Vansenne F; Wang X; Ambrus JL; Fannemel M; Posey JE; Agolini E; Novelli A; Rauch A; Boonsawat P; Fagerberg CR; Larsen MJ; Kibaek M; Labalme A; Poisson A; Payne KK; Walsh LE; Aldinger KA; Balciuniene J; Skraban C; Gray C; Murrell J; Bupp CP; Pascolini G; Grammatico P; Broly M; Küry S; Nizon M; Rasool IG; Zahoor MY; Kraus C; Reis A; Iqbal M; Uguen K; Audebert-Bellanger S; Ferec C; Redon S; Baker J; Wu Y; Zampino G; Syrbe S; Brosse I; Jamra RA; Dobyns WB; Cohen LL; Blomhoff A; Mignot C; Keren B; Courtin T; Agrawal PB; Beggs AH; Yu TW
Genet Med; 2021 Jun; 23(6):1028-1040. PubMed ID: 33658631
[TBL] [Abstract][Full Text] [Related]
11. Autism Spectrum Disorder/Intellectual Disability-Associated Mutations in Trio Disrupt Neuroligin 1-Mediated Synaptogenesis.
Tian C; Paskus JD; Fingleton E; Roche KW; Herring BE
J Neurosci; 2021 Sep; 41(37):7768-7778. PubMed ID: 34353896
[TBL] [Abstract][Full Text] [Related]
12. NEXMIF/KIDLIA Knock-out Mouse Demonstrates Autism-Like Behaviors, Memory Deficits, and Impairments in Synapse Formation and Function.
Gilbert J; O'Connor M; Templet S; Moghaddam M; Di Via Ioschpe A; Sinclair A; Zhu LQ; Xu W; Man HY
J Neurosci; 2020 Jan; 40(1):237-254. PubMed ID: 31704787
[TBL] [Abstract][Full Text] [Related]
13. Damaging coding variants within kainate receptor channel genes are enriched in individuals with schizophrenia, autism and intellectual disabilities.
Koromina M; Flitton M; Blockley A; Mellor IR; Knight HM
Sci Rep; 2019 Dec; 9(1):19215. PubMed ID: 31844109
[TBL] [Abstract][Full Text] [Related]
14. School dysfunction in youth with autistic spectrum disorder in Taiwan: The effect of subtype and ADHD.
Chiang HL; Kao WC; Chou MC; Chou WJ; Chiu YN; Wu YY; Gau SS
Autism Res; 2018 Jun; 11(6):857-869. PubMed ID: 29427542
[TBL] [Abstract][Full Text] [Related]
15. Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder.
Latypova X; Vincent M; Mollé A; Adebambo OA; Fourgeux C; Khan TN; Caro A; Rosello M; Orellana C; Niyazov D; Lederer D; Deprez M; Capri Y; Kannu P; Tabet AC; Levy J; Aten E; den Hollander N; Splitt M; Walia J; Immken LL; Stankiewicz P; McWalter K; Suchy S; Louie RJ; Bell S; Stevenson RE; Rousseau J; Willem C; Retiere C; Yang XJ; Campeau PM; Martinez F; Rosenfeld JA; Le Caignec C; Küry S; Mercier S; Moradkhani K; Conrad S; Besnard T; Cogné B; Katsanis N; Bézieau S; Poschmann J; Davis EE; Isidor B
Am J Hum Genet; 2021 May; 108(5):929-941. PubMed ID: 33811806
[TBL] [Abstract][Full Text] [Related]
16. Autism spectrum disorder in a patient with a genomic rearrangement that only involves the EPHA5 gene.
Pascolini G; Majore S; Valiante M; Bottillo I; Laino L; Agolini E; Novelli A; Grammatico B; Calvani M; Grammatico P
Psychiatr Genet; 2019 Jun; 29(3):86-90. PubMed ID: 30724859
[TBL] [Abstract][Full Text] [Related]
17. [Intellectual developmental disability overlapping with autism spectrum disorder and attention deficit-hyperactivity disorder].
Mulas F; Rojas M
Medicina (B Aires); 2018; 78 Suppl 2():63-68. PubMed ID: 30199368
[TBL] [Abstract][Full Text] [Related]
18. The autism spectrum phenotype in ADNP syndrome.
Arnett AB; Rhoads CL; Hoekzema K; Turner TN; Gerdts J; Wallace AS; Bedrosian-Sermone S; Eichler EE; Bernier RA
Autism Res; 2018 Sep; 11(9):1300-1310. PubMed ID: 30107084
[TBL] [Abstract][Full Text] [Related]
19. DNA Methylation Associated with Mitochondrial Dysfunction in a South African Autism Spectrum Disorder Cohort.
Stathopoulos S; Gaujoux R; Lindeque Z; Mahony C; Van Der Colff R; Van Der Westhuizen F; O'Ryan C
Autism Res; 2020 Jul; 13(7):1079-1093. PubMed ID: 32490597
[TBL] [Abstract][Full Text] [Related]
20. The Association Between Somatic Health, Autism Spectrum Disorder, and Autistic Traits.
Pan PY; Tammimies K; Bölte S
Behav Genet; 2020 Jul; 50(4):233-246. PubMed ID: 31811521
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]