357 related articles for article (PubMed ID: 27863250)
1. Histone Acetylome-wide Association Study of Autism Spectrum Disorder.
Sun W; Poschmann J; Cruz-Herrera Del Rosario R; Parikshak NN; Hajan HS; Kumar V; Ramasamy R; Belgard TG; Elanggovan B; Wong CCY; Mill J; Geschwind DH; Prabhakar S
Cell; 2016 Nov; 167(5):1385-1397.e11. PubMed ID: 27863250
[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. Epigenomes of Human Hearts Reveal New Genetic Variants Relevant for Cardiac Disease and Phenotype.
Tan WLW; Anene-Nzelu CG; Wong E; Lee CJM; Tan HS; Tang SJ; Perrin A; Wu KX; Zheng W; Ashburn RJ; Pan B; Lee MY; Autio MI; Morley MP; Tam WL; Cheung C; Margulies KB; Chen L; Cappola TP; Loh M; Chambers J; Prabhakar S; Foo RSY;
Circ Res; 2020 Aug; 127(6):761-777. PubMed ID: 32529949
[TBL] [Abstract][Full Text] [Related]
4. Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue.
Wong CCY; Smith RG; Hannon E; Ramaswami G; Parikshak NN; Assary E; Troakes C; Poschmann J; Schalkwyk LC; Sun W; Prabhakar S; Geschwind DH; Mill J
Hum Mol Genet; 2019 Jul; 28(13):2201-2211. PubMed ID: 31220268
[TBL] [Abstract][Full Text] [Related]
5. Common DNA methylation alterations in multiple brain regions in autism.
Ladd-Acosta C; Hansen KD; Briem E; Fallin MD; Kaufmann WE; Feinberg AP
Mol Psychiatry; 2014 Aug; 19(8):862-71. PubMed ID: 23999529
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. Epigenetic Gene-Regulatory Loci in Alu Elements Associated with Autism Susceptibility in the Prefrontal Cortex of ASD.
Saeliw T; Kanlayaprasit S; Thongkorn S; Songsritaya K; Sanannam B; Sae-Lee C; Jindatip D; Hu VW; Sarachana T
Int J Mol Sci; 2023 Apr; 24(8):. PubMed ID: 37108679
[TBL] [Abstract][Full Text] [Related]
8. Histone acetylome-wide associations in immune cells from individuals with active Mycobacterium tuberculosis infection.
Del Rosario RCH; Poschmann J; Lim C; Cheng CY; Kumar P; Riou C; Ong ST; Gerges S; Hajan HS; Kumar D; Marzuki M; Lu X; Lee A; Wijaya GC; Rayan NA; Zhuang Z; Du Bruyn E; Chee CBE; Lee B; Lum J; Zolezzi F; Poidinger M; Rotzschke O; Khor CC; Wilkinson RJ; Wang YT; Chandy GK; De Libero G; Singhal A; Prabhakar S
Nat Microbiol; 2022 Feb; 7(2):312-326. PubMed ID: 35102304
[TBL] [Abstract][Full Text] [Related]
9. Genome-wide histone acetylation analysis reveals altered transcriptional regulation in the Parkinson's disease brain.
Toker L; Tran GT; Sundaresan J; Tysnes OB; Alves G; Haugarvoll K; Nido GS; Dölle C; Tzoulis C
Mol Neurodegener; 2021 May; 16(1):31. PubMed ID: 33947435
[TBL] [Abstract][Full Text] [Related]
10. Genome-wide profiling of histone H3K27 acetylation featured fatty acid signalling in pancreatic beta cells in diet-induced obesity in mice.
Nammo T; Udagawa H; Funahashi N; Kawaguchi M; Uebanso T; Hiramoto M; Nishimura W; Yasuda K
Diabetologia; 2018 Dec; 61(12):2608-2620. PubMed ID: 30284014
[TBL] [Abstract][Full Text] [Related]
11. Understanding the impact of SNPs associated with autism spectrum disorder on biological pathways in the human fetal and adult cortex.
Golovina E; Fadason T; Lints TJ; Walker C; Vickers MH; O'Sullivan JM
Sci Rep; 2021 Aug; 11(1):15867. PubMed ID: 34354167
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Cell-Type-Specific Analysis of Molecular Pathology in Autism Identifies Common Genes and Pathways Affected Across Neocortical Regions.
Velmeshev D; Magistri M; Mazza EMC; Lally P; Khoury N; D'Elia ER; Bicciato S; Faghihi MA
Mol Neurobiol; 2020 May; 57(5):2279-2289. PubMed ID: 32008165
[TBL] [Abstract][Full Text] [Related]
14. Histone 3 lysine 9 acetylation of BRG1 in the medial prefrontal cortex is associated with heroin self‑administration in rats.
Hong Q; Liu J; Lin Z; Zhuang D; Xu W; Xu Z; Lai M; Zhu H; Zhou W; Liu H
Mol Med Rep; 2020 Jan; 21(1):405-412. PubMed ID: 31939625
[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. Five autism-associated transcriptional regulators target shared loci proximal to brain-expressed genes.
Fazel Darbandi S; An JY; Lim K; Page NF; Liang L; Young DM; Ypsilanti AR; State MW; Nord AS; Sanders SJ; Rubenstein JLR
Cell Rep; 2024 Jun; 43(6):114329. PubMed ID: 38850535
[TBL] [Abstract][Full Text] [Related]
17. Quantitative trait locus analysis for endophenotypes reveals genetic substrates of core symptom domains and neurocognitive function in autism spectrum disorder.
Lee IH; Koelliker E; Kong SW
Transl Psychiatry; 2022 Sep; 12(1):407. PubMed ID: 36153334
[TBL] [Abstract][Full Text] [Related]
18. [The considerations for diagnosis of autism spectrum disorders and its pathogenic mechanisms].
Kato H; Ozaki N
Rinsho Shinkeigaku; 2019 Jan; 59(1):13-20. PubMed ID: 30606997
[TBL] [Abstract][Full Text] [Related]
19. Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.
Chen R; Davis LK; Guter S; Wei Q; Jacob S; Potter MH; Cox NJ; Cook EH; Sutcliffe JS; Li B
Mol Autism; 2017; 8():14. PubMed ID: 28344757
[TBL] [Abstract][Full Text] [Related]
20. Deficiency of autism risk factor ASH1L in prefrontal cortex induces epigenetic aberrations and seizures.
Qin L; Williams JB; Tan T; Liu T; Cao Q; Ma K; Yan Z
Nat Commun; 2021 Nov; 12(1):6589. PubMed ID: 34782621
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
