138 related articles for article (PubMed ID: 34906518)
1. ImprintSeq, a novel tool to interrogate DNA methylation at human imprinted regions and diagnose multilocus imprinting disturbance.
Ochoa E; Lee S; Lan-Leung B; Dias RP; Ong KK; Radley JA; Pérez de Nanclares G; Martinez R; Clark G; Martin E; Castaño L; Bottolo L; Maher ER
Genet Med; 2022 Feb; 24(2):463-474. PubMed ID: 34906518
[TBL] [Abstract][Full Text] [Related]
2. Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach.
Bilo L; Ochoa E; Lee S; Dey D; Kurth I; Kraft F; Rodger F; Docquier F; Toribio A; Bottolo L; Binder G; Fekete G; Elbracht M; Maher ER; Begemann M; Eggermann T
Clin Epigenetics; 2023 Mar; 15(1):35. PubMed ID: 36859312
[TBL] [Abstract][Full Text] [Related]
3. ZNF445: a homozygous truncating variant in a patient with Temple syndrome and multilocus imprinting disturbance.
Kagami M; Hara-Isono K; Matsubara K; Nakabayashi K; Narumi S; Fukami M; Ohkubo Y; Saitsu H; Takada S; Ogata T
Clin Epigenetics; 2021 May; 13(1):119. PubMed ID: 34039421
[TBL] [Abstract][Full Text] [Related]
4. Uncovering the phenotypic consequences of multi-locus imprinting disturbances using genome-wide methylation analysis in genomic imprinting disorders.
Kim HY; Shin CH; Shin CH; Ko JM
PLoS One; 2023; 18(8):e0290450. PubMed ID: 37594968
[TBL] [Abstract][Full Text] [Related]
5. Comprehensive methylation analysis of imprinting-associated differentially methylated regions in colorectal cancer.
Hidaka H; Higashimoto K; Aoki S; Mishima H; Hayashida C; Maeda T; Koga Y; Yatsuki H; Joh K; Noshiro H; Iwakiri R; Kawaguchi A; Yoshiura KI; Fujimoto K; Soejima H
Clin Epigenetics; 2018 Dec; 10(1):150. PubMed ID: 30509319
[TBL] [Abstract][Full Text] [Related]
6. Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders.
Fontana L; Bedeschi MF; Maitz S; Cereda A; Faré C; Motta S; Seresini A; D'Ursi P; Orro A; Pecile V; Calvello M; Selicorni A; Lalatta F; Milani D; Sirchia SM; Miozzo M; Tabano S
Epigenetics; 2018; 13(9):897-909. PubMed ID: 30221575
[TBL] [Abstract][Full Text] [Related]
7. Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences.
Eggermann T; Yapici E; Bliek J; Pereda A; Begemann M; Russo S; Tannorella P; Calzari L; de Nanclares GP; Lombardi P; Temple IK; Mackay D; Riccio A; Kagami M; Ogata T; Lapunzina P; Monk D; Maher ER; Tümer Z
Clin Epigenetics; 2022 Mar; 14(1):41. PubMed ID: 35296332
[TBL] [Abstract][Full Text] [Related]
8. The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype.
Sparago A; Verma A; Patricelli MG; Pignata L; Russo S; Calzari L; De Francesco N; Del Prete R; Palumbo O; Carella M; Mackay DJG; Rezwan FI; Angelini C; Cerrato F; Cubellis MV; Riccio A
Clin Epigenetics; 2019 Dec; 11(1):190. PubMed ID: 31829238
[TBL] [Abstract][Full Text] [Related]
9. Genome-wide multilocus imprinting disturbance analysis in Temple syndrome and Kagami-Ogata syndrome.
Kagami M; Matsubara K; Nakabayashi K; Nakamura A; Sano S; Okamura K; Hata K; Fukami M; Ogata T
Genet Med; 2017 Apr; 19(4):476-482. PubMed ID: 27632690
[TBL] [Abstract][Full Text] [Related]
10. NLRP7 variants in spontaneous abortions with multilocus imprinting disturbances from women with recurrent pregnancy loss.
Sazhenova EA; Nikitina TV; Vasilyev SA; Tolmacheva EN; Vasilyeva OY; Markov AV; Yuryev SY; Skryabin NA; Zarubin AA; Kolesnikov NA; Stepanov VA; Lebedev IN
J Assist Reprod Genet; 2021 Nov; 38(11):2893-2908. PubMed ID: 34554362
[TBL] [Abstract][Full Text] [Related]
11. The loss of imprinted DNA methylation in mouse blastocysts is inflicted to a similar extent by in vitro follicle culture and ovulation induction.
Saenz-de-Juano MD; Billooye K; Smitz J; Anckaert E
Mol Hum Reprod; 2016 Jun; 22(6):427-41. PubMed ID: 26908643
[TBL] [Abstract][Full Text] [Related]
12. A patient with multilocus imprinting disturbance involving hypomethylation at 11p15 and 14q32, and phenotypic features of Beckwith-Wiedemann and Temple syndromes.
Grosvenor SE; Davies JH; Lever M; Sillibourne J; Mackay DJG; Temple IK
Am J Med Genet A; 2022 Jun; 188(6):1896-1903. PubMed ID: 35266280
[TBL] [Abstract][Full Text] [Related]
13. Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans.
Sanchez-Delgado M; Riccio A; Eggermann T; Maher ER; Lapunzina P; Mackay D; Monk D
Trends Genet; 2016 Jul; 32(7):444-455. PubMed ID: 27235113
[TBL] [Abstract][Full Text] [Related]
14. Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes.
Docherty LE; Rezwan FI; Poole RL; Jagoe H; Lake H; Lockett GA; Arshad H; Wilson DI; Holloway JW; Temple IK; Mackay DJ
J Med Genet; 2014 Apr; 51(4):229-38. PubMed ID: 24501229
[TBL] [Abstract][Full Text] [Related]
15. Asymmetric DNA methylation of CpG dyads is a feature of secondary DMRs associated with the
Guntrum M; Vlasova E; Davis TL
Epigenetics Chromatin; 2017; 10():31. PubMed ID: 28649282
[TBL] [Abstract][Full Text] [Related]
16. Molecular characterization of temple syndrome families with 14q32 epimutations.
Brück J; Begemann M; Dey D; Elbracht M; Eggermann T
Eur J Med Genet; 2020 Dec; 63(12):104077. PubMed ID: 33010492
[TBL] [Abstract][Full Text] [Related]
17. Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbances.
Bens S; Kolarova J; Beygo J; Buiting K; Caliebe A; Eggermann T; Gillessen-Kaesbach G; Prawitt D; Thiele-Schmitz S; Begemann M; Enklaar T; Gutwein J; Haake A; Paul U; Richter J; Soellner L; Vater I; Monk D; Horsthemke B; Ammerpohl O; Siebert R
Epigenomics; 2016 Jun; 8(6):801-16. PubMed ID: 27323310
[TBL] [Abstract][Full Text] [Related]
18. DNA Methylation Dynamics in the Female Germline and Maternal-Effect Mutations That Disrupt Genomic Imprinting.
Anvar Z; Chakchouk I; Demond H; Sharif M; Kelsey G; Van den Veyver IB
Genes (Basel); 2021 Aug; 12(8):. PubMed ID: 34440388
[TBL] [Abstract][Full Text] [Related]
19. Disturbed methylation at multiple imprinted loci: an increasing observation in imprinting disorders.
Eggermann T; Leisten I; Binder G; Begemann M; Spengler S
Epigenomics; 2011 Oct; 3(5):625-37. PubMed ID: 22126250
[TBL] [Abstract][Full Text] [Related]
20. Exploring the unique function of imprinting control centers in the PWS/AS-responsible region: finding from array-based methylation analysis in cases with variously sized microdeletions.
Matsubara K; Itoh M; Shimizu K; Saito S; Enomoto K; Nakabayashi K; Hata K; Kurosawa K; Ogata T; Fukami M; Kagami M
Clin Epigenetics; 2019 Feb; 11(1):36. PubMed ID: 30819260
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
