166 related articles for article (PubMed ID: 29601581)
1. Widespread domain-like perturbations of DNA methylation in whole blood of Down syndrome neonates.
Henneman P; Bouman A; Mul A; Knegt L; van der Kevie-Kersemaekers AM; Zwaveling-Soonawala N; Meijers-Heijboer HEJ; van Trotsenburg ASP; Mannens MM
PLoS One; 2018; 13(3):e0194938. PubMed ID: 29601581
[TBL] [Abstract][Full Text] [Related]
2. Epigenomic signature of major congenital heart defects in newborns with Down syndrome.
Mouat JS; Li S; Myint SS; Laufer BI; Lupo PJ; Schraw JM; Woodhouse JP; de Smith AJ; LaSalle JM
Hum Genomics; 2023 Oct; 17(1):92. PubMed ID: 37803336
[TBL] [Abstract][Full Text] [Related]
3. Meta-Analysis of DNA Methylation Datasets Shows Aberrant DNA Methylation of Thyroid Development or Function Genes in Down Syndrome.
Lauffer P; Zwaveling-Soonawala N; Li S; Bacalini MG; Naumova OY; Wiemels J; Boelen A; Henneman P; de Smith AJ; van Trotsenburg ASP
Thyroid; 2023 Jan; 33(1):53-62. PubMed ID: 36326208
[No Abstract] [Full Text] [Related]
4. Whole genome bisulfite sequencing of Down syndrome brain reveals regional DNA hypermethylation and novel disorder insights.
Laufer BI; Hwang H; Vogel Ciernia A; Mordaunt CE; LaSalle JM
Epigenetics; 2019 Jul; 14(7):672-684. PubMed ID: 31010359
[TBL] [Abstract][Full Text] [Related]
5. Low-pass whole genome bisulfite sequencing of neonatal dried blood spots identifies a role for RUNX1 in Down syndrome DNA methylation profiles.
Laufer BI; Hwang H; Jianu JM; Mordaunt CE; Korf IF; Hertz-Picciotto I; LaSalle JM
Hum Mol Genet; 2021 Jan; 29(21):3465-3476. PubMed ID: 33001180
[TBL] [Abstract][Full Text] [Related]
6. Epigenome-wide base-resolution profiling of DNA methylation in chorionic villi of fetuses with Down syndrome by methyl-capture sequencing.
Lim JH; Kang YJ; Lee BY; Han YJ; Chung JH; Kim MY; Kim MH; Kim JW; Cho YH; Ryu HM
Clin Epigenetics; 2019 Dec; 11(1):180. PubMed ID: 31801612
[TBL] [Abstract][Full Text] [Related]
7. Comparative genome-wide DNA methylation analysis in myocardial tissue from donors with and without Down syndrome.
Cejas RB; Wang J; Hageman-Blair R; Liu S; Blanco JG
Gene; 2021 Jan; 764():145099. PubMed ID: 32861879
[TBL] [Abstract][Full Text] [Related]
8. Identification of a DNA methylation signature in blood cells from persons with Down Syndrome.
Bacalini MG; Gentilini D; Boattini A; Giampieri E; Pirazzini C; Giuliani C; Fontanesi E; Scurti M; Remondini D; Capri M; Cocchi G; Ghezzo A; Del Rio A; Luiselli D; Vitale G; Mari D; Castellani G; Fraga M; Di Blasio AM; Salvioli S; Franceschi C; Garagnani P
Aging (Albany NY); 2015 Feb; 7(2):82-96. PubMed ID: 25701644
[TBL] [Abstract][Full Text] [Related]
9. Stable DNMT3L overexpression in SH-SY5Y neurons recreates a facet of the genome-wide Down syndrome DNA methylation signature.
Laufer BI; Gomez JA; Jianu JM; LaSalle JM
Epigenetics Chromatin; 2021 Mar; 14(1):13. PubMed ID: 33750431
[TBL] [Abstract][Full Text] [Related]
10. Distinct DNA methylation patterns of cognitive impairment and trisomy 21 in Down syndrome.
Jones MJ; Farré P; McEwen LM; Macisaac JL; Watt K; Neumann SM; Emberly E; Cynader MS; Virji-Babul N; Kobor MS
BMC Med Genomics; 2013 Dec; 6():58. PubMed ID: 24373378
[TBL] [Abstract][Full Text] [Related]
11. DNA methylation changes in Down syndrome derived neural iPSCs uncover co-dysregulation of ZNF and HOX3 families of transcription factors.
Laan L; Klar J; Sobol M; Hoeber J; Shahsavani M; Kele M; Fatima A; Zakaria M; Annerén G; Falk A; Schuster J; Dahl N
Clin Epigenetics; 2020 Jan; 12(1):9. PubMed ID: 31915063
[TBL] [Abstract][Full Text] [Related]
12. Epigenomic signature of major congenital heart defects in newborns with Down syndrome.
Mouat JS; Li S; Myint SS; Laufer BI; Lupo PJ; Schraw JM; Woodhouse JP; de Smith AJ; LaSalle JM
medRxiv; 2023 May; ():. PubMed ID: 37205408
[TBL] [Abstract][Full Text] [Related]
13. DNA Methylation Alterations in Blood Cells of Toddlers with Down Syndrome.
Naumova OY; Lipschutz R; Rychkov SY; Zhukova OV; Grigorenko EL
Genes (Basel); 2021 Jul; 12(8):. PubMed ID: 34440289
[TBL] [Abstract][Full Text] [Related]
14. Accelerated epigenetic aging in newborns with Down syndrome.
Xu K; Li S; Muskens IS; Elliott N; Myint SS; Pandey P; Hansen HM; Morimoto LM; Kang AY; Ma X; Metayer C; Mueller BA; Roberts I; Walsh KM; Horvath S; Wiemels JL; de Smith AJ
Aging Cell; 2022 Jul; 21(7):e13652. PubMed ID: 35661546
[TBL] [Abstract][Full Text] [Related]
15. Epigenetic dysregulation in the developing Down syndrome cortex.
El Hajj N; Dittrich M; Böck J; Kraus TF; Nanda I; Müller T; Seidmann L; Tralau T; Galetzka D; Schneider E; Haaf T
Epigenetics; 2016 Aug; 11(8):563-78. PubMed ID: 27245352
[TBL] [Abstract][Full Text] [Related]
16. Genome-wide survey reveals dynamic widespread tissue-specific changes in DNA methylation during development.
Liang P; Song F; Ghosh S; Morien E; Qin M; Mahmood S; Fujiwara K; Igarashi J; Nagase H; Held WA
BMC Genomics; 2011 May; 12(1):231. PubMed ID: 21569359
[TBL] [Abstract][Full Text] [Related]
17. Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes.
Mordaunt CE; Jianu JM; Laufer BI; Zhu Y; Hwang H; Dunaway KW; Bakulski KM; Feinberg JI; Volk HE; Lyall K; Croen LA; Newschaffer CJ; Ozonoff S; Hertz-Picciotto I; Fallin MD; Schmidt RJ; LaSalle JM
Genome Med; 2020 Oct; 12(1):88. PubMed ID: 33054850
[TBL] [Abstract][Full Text] [Related]
18. DNA Hydroxymethylation Levels Are Altered in Blood Cells From Down Syndrome Persons Enrolled in the MARK-AGE Project.
Ciccarone F; Valentini E; Malavolta M; Zampieri M; Bacalini MG; Calabrese R; Guastafierro T; Reale A; Franceschi C; Capri M; Breusing N; Grune T; Moreno-Villanueva M; Bürkle A; Caiafa P
J Gerontol A Biol Sci Med Sci; 2018 May; 73(6):737-744. PubMed ID: 29069286
[TBL] [Abstract][Full Text] [Related]
19. Novel DNA methylation profiles associated with key gene regulation and transcription pathways in blood and placenta of growth-restricted neonates.
Hillman SL; Finer S; Smart MC; Mathews C; Lowe R; Rakyan VK; Hitman GA; Williams DJ
Epigenetics; 2015; 10(1):50-61. PubMed ID: 25496377
[TBL] [Abstract][Full Text] [Related]
20. Non-invasive epigenetic detection of fetal trisomy 21 in first trimester maternal plasma.
Lim JH; Kim SY; Park SY; Lee SY; Kim MJ; Han YJ; Lee SW; Chung JH; Kim MY; Yang JH; Ryu HM
PLoS One; 2011; 6(11):e27709. PubMed ID: 22132128
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]