143 related articles for article (PubMed ID: 38212313)
1. Kagami Ogata syndrome: a small deletion refines critical region for imprinting.
Kilich G; Hassey K; Behrens EM; Falk M; Vanderver A; Rader DJ; Cahill PJ; Raper A; Zhang Z; Westerfer D; Jadhav T; Conlin L; Izumi K; Rajagopalan R; Sullivan KE;
NPJ Genom Med; 2024 Jan; 9(1):5. PubMed ID: 38212313
[TBL] [Abstract][Full Text] [Related]
2. Two infants with mild, atypical clinical features of Kagami-Ogata syndrome caused by epimutation.
Higashiyama H; Ohsone Y; Takatani R; Futatani T; Kosaki R; Kagami M
Eur J Med Genet; 2022 Oct; 65(10):104580. PubMed ID: 35953028
[TBL] [Abstract][Full Text] [Related]
3. Kagami-Ogata syndrome: a clinically recognizable upd(14)pat and related disorder affecting the chromosome 14q32.2 imprinted region.
Ogata T; Kagami M
J Hum Genet; 2016 Feb; 61(2):87-94. PubMed ID: 26377239
[TBL] [Abstract][Full Text] [Related]
4. Maternally inherited deletion encompassing the RTL1as and MEG8 genes of the human 14q32 imprinted region in a patient with a mild Kagami-Ogata syndrome phenotype.
Sirera Sirera P; García-Payá E; Olivas García J; Jadraque Rodríguez R; Hernández Romero SD
Am J Med Genet A; 2023 Aug; 191(8):2225-2231. PubMed ID: 37222159
[TBL] [Abstract][Full Text] [Related]
5. Prenatal Diagnosis of a Mosaic Paternal Uniparental Disomy for Chromosome 14: A Case Report of Kagami-Ogata Syndrome.
Li F; Liu S; Jia B; Wu R; Chang Q
Front Pediatr; 2021; 9():691761. PubMed ID: 34746047
[TBL] [Abstract][Full Text] [Related]
6. New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome.
Beygo J; Küchler A; Gillessen-Kaesbach G; Albrecht B; Eckle J; Eggermann T; Gellhaus A; Kanber D; Kordaß U; Lüdecke HJ; Purmann S; Rossier E; van de Nes J; van der Werf IM; Wenzel M; Wieczorek D; Horsthemke B; Buiting K
Eur J Hum Genet; 2017 Aug; 25(8):935-945. PubMed ID: 28635951
[TBL] [Abstract][Full Text] [Related]
7. Paternal uniparental disomy chromosome 14-like syndrome due a maternal de novo 160 kb deletion at the 14q32.2 region not encompassing the IG- and the MEG3-DMRs: Patient report and genotype-phenotype correlation.
Corsello G; Salzano E; Vecchio D; Antona V; Grasso M; Malacarne M; Carella M; Palumbo P; Piro E; Giuffrè M
Am J Med Genet A; 2015 Dec; 167A(12):3130-8. PubMed ID: 26333487
[TBL] [Abstract][Full Text] [Related]
8. Novel deletions affecting the MEG3-DMR provide further evidence for a hierarchical regulation of imprinting in 14q32.
Beygo J; Elbracht M; de Groot K; Begemann M; Kanber D; Platzer K; Gillessen-Kaesbach G; Vierzig A; Green A; Heller R; Buiting K; Eggermann T
Eur J Hum Genet; 2015 Feb; 23(2):180-8. PubMed ID: 24801763
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. A Male Case of Kagami-Ogata Syndrome Caused by Paternal Unipaternal Disomy 14 as a Result of a Robertsonian Translocation.
Wang X; Pang H; Shah BA; Gu H; Zhang L; Wang H
Front Pediatr; 2020; 8():88. PubMed ID: 32211354
[TBL] [Abstract][Full Text] [Related]
11. Case report: Prenatal diagnosis of Kagami-Ogata syndrome in a Chinese family.
Hu J; Zhang Y; Yang Y; Wang L; Sun Y; Dong M
Front Genet; 2022; 13():959666. PubMed ID: 36035167
[TBL] [Abstract][Full Text] [Related]
12. Kagami-Ogata syndrome in a fetus presenting with polyhydramnios, malformations, and preterm delivery: a case report.
Huang H; Mikami Y; Shigematsu K; Uemura N; Shinsaka M; Iwatani A; Miyake F; Kabe K; Takai Y; Saitoh M; Baba K; Seki H
J Med Case Rep; 2019 Nov; 13(1):340. PubMed ID: 31753000
[TBL] [Abstract][Full Text] [Related]
13. Temple syndrome in a patient with variably methylated CpGs at the primary MEG3/DLK1:IG-DMR and severely hypomethylated CpGs at the secondary MEG3:TSS-DMR.
Kagami M; Yanagisawa A; Ota M; Matsuoka K; Nakamura A; Matsubara K; Nakabayashi K; Takada S; Fukami M; Ogata T
Clin Epigenetics; 2019 Mar; 11(1):42. PubMed ID: 30846001
[TBL] [Abstract][Full Text] [Related]
14. Kagami-Ogata syndrome in a patient with 46,XX,t(2;14)(q11.2;q32.2)mat disrupting MEG3.
Omark J; Masunaga Y; Hannibal M; Shaw B; Fukami M; Kato F; Saitsu H; Kagami M; Ogata T
J Hum Genet; 2021 Apr; 66(4):439-443. PubMed ID: 33067531
[TBL] [Abstract][Full Text] [Related]
15. Epimutations of the IG-DMR and the MEG3-DMR at the 14q32.2 imprinted region in two patients with Silver-Russell Syndrome-compatible phenotype.
Kagami M; Mizuno S; Matsubara K; Nakabayashi K; Sano S; Fuke T; Fukami M; Ogata T
Eur J Hum Genet; 2015 Aug; 23(8):1062-7. PubMed ID: 25351781
[TBL] [Abstract][Full Text] [Related]
16. Exploration of hydroxymethylation in Kagami-Ogata syndrome caused by hypermethylation of imprinting control regions.
Matsubara K; Kagami M; Nakabayashi K; Hata K; Fukami M; Ogata T; Yamazawa K
Clin Epigenetics; 2015; 7(1):90. PubMed ID: 26322139
[TBL] [Abstract][Full Text] [Related]
17. Temple syndrome and Kagami-Ogata syndrome: clinical presentations, genotypes, models and mechanisms.
Prasasya R; Grotheer KV; Siracusa LD; Bartolomei MS
Hum Mol Genet; 2020 Sep; 29(R1):R107-R116. PubMed ID: 32592473
[TBL] [Abstract][Full Text] [Related]
18. Novel microdeletions on chromosome 14q32.2 suggest a potential role for non-coding RNAs in Kagami-Ogata syndrome.
van der Werf IM; Buiting K; Czeschik C; Reyniers E; Vandeweyer G; Vanhaesebrouck P; Lüdecke HJ; Wieczorek D; Horsthemke B; Mortier G; Leroy JG; Kooy RF
Eur J Hum Genet; 2016 Dec; 24(12):1724-1729. PubMed ID: 27406249
[TBL] [Abstract][Full Text] [Related]
19. The IG-DMR and the MEG3-DMR at human chromosome 14q32.2: hierarchical interaction and distinct functional properties as imprinting control centers.
Kagami M; O'Sullivan MJ; Green AJ; Watabe Y; Arisaka O; Masawa N; Matsuoka K; Fukami M; Matsubara K; Kato F; Ferguson-Smith AC; Ogata T
PLoS Genet; 2010 Jun; 6(6):e1000992. PubMed ID: 20585555
[TBL] [Abstract][Full Text] [Related]
20. Kagami-Ogata syndrome: a case report.
Suriapperuma T; Randeny S; Mettananda S
J Med Case Rep; 2022 Jul; 16(1):284. PubMed ID: 35864517
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]