163 related articles for article (PubMed ID: 36980758)
1. Investigation of 11p15.5 Methylation Defects Associated with Beckwith-Wiedemann Spectrum and Embryonic Tumor Risk in Lateralized Overgrowth Patients.
Tüysüz B; Bozlak S; Uludağ Alkaya D; Ocak S; Kasap B; Sunamak Çifçi E; Seker A; Bayhan IA; Apak H
Cancers (Basel); 2023 Mar; 15(6):. PubMed ID: 36980758
[TBL] [Abstract][Full Text] [Related]
2. Investigation of (epi)genotype causes and follow-up manifestations in the patients with classical and atypical phenotype of Beckwith-Wiedemann spectrum.
Tüysüz B; Güneş N; Geyik F; Yeşil G; Celkan T; Vural M
Am J Med Genet A; 2021 Jun; 185(6):1721-1731. PubMed ID: 33704912
[TBL] [Abstract][Full Text] [Related]
3. Characterization of the Beckwith-Wiedemann spectrum: Diagnosis and management.
Duffy KA; Cielo CM; Cohen JL; Gonzalez-Gandolfi CX; Griff JR; Hathaway ER; Kupa J; Taylor JA; Wang KH; Ganguly A; Deardorff MA; Kalish JM
Am J Med Genet C Semin Med Genet; 2019 Dec; 181(4):693-708. PubMed ID: 31469230
[TBL] [Abstract][Full Text] [Related]
4. Isolated- and Beckwith-Wiedemann syndrome related- lateralised overgrowth (hemihypertrophy): Clinical and molecular correlations in 94 individuals.
Radley JA; Connolly M; Sabir A; Kanani F; Carley H; Jones RL; Hyder Z; Gompertz L; Reardon W; Richardson R; McClelland L; Maher ER
Clin Genet; 2021 Sep; 100(3):292-297. PubMed ID: 33993487
[TBL] [Abstract][Full Text] [Related]
5. Molecular Basis of Beckwith-Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice.
Eggermann T; Maher ER; Kratz CP; Prawitt D
Cancers (Basel); 2022 Jun; 14(13):. PubMed ID: 35804856
[TBL] [Abstract][Full Text] [Related]
6. Characterization and Childhood Tumor Risk Assessment of Genetic and Epigenetic Syndromes Associated With Lateralized Overgrowth.
Griff JR; Duffy KA; Kalish JM
Front Pediatr; 2020; 8():613260. PubMed ID: 33392121
[TBL] [Abstract][Full Text] [Related]
7. Lateralized and Segmental Overgrowth in Children.
Mussa A; Carli D; Cardaropoli S; Ferrero GB; Resta N
Cancers (Basel); 2021 Dec; 13(24):. PubMed ID: 34944785
[TBL] [Abstract][Full Text] [Related]
8. Whole-exome sequencing reveals causative genetic variants for several overgrowth syndromes in molecularly negative Beckwith-Wiedemann spectrum.
Higashimoto K; Sun F; Imagawa E; Saida K; Miyake N; Hara S; Yatsuki H; Kubiura-Ichimaru M; Fujita A; Mizuguchi T; Matsumoto N; Soejima H
J Med Genet; 2024 Jan; ():. PubMed ID: 38228391
[No Abstract] [Full Text] [Related]
9. High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith-Wiedemann syndrome.
Baskin B; Choufani S; Chen YA; Shuman C; Parkinson N; Lemyre E; Micheil Innes A; Stavropoulos DJ; Ray PN; Weksberg R
Hum Genet; 2014 Mar; 133(3):321-30. PubMed ID: 24154661
[TBL] [Abstract][Full Text] [Related]
10. Clinical and molecular features of children with Beckwith-Wiedemann syndrome in China: a single-center retrospective cohort study.
Wang R; Xiao Y; Li D; Hu H; Li X; Ge T; Yu R; Wang Y; Zhang T
Ital J Pediatr; 2020 Apr; 46(1):55. PubMed ID: 32349794
[TBL] [Abstract][Full Text] [Related]
11. Deciphering Epigenetic Backgrounds in a Korean Cohort with Beckwith-Wiedemann Syndrome.
Kim HY; Shin CH; Lee YA; Shin CH; Kim GH; Ko JM
Ann Lab Med; 2022 Nov; 42(6):668-677. PubMed ID: 35765875
[TBL] [Abstract][Full Text] [Related]
12. (Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome.
Mussa A; Russo S; De Crescenzo A; Freschi A; Calzari L; Maitz S; Macchiaiolo M; Molinatto C; Baldassarre G; Mariani M; Tarani L; Bedeschi MF; Milani D; Melis D; Bartuli A; Cubellis MV; Selicorni A; Cirillo Silengo M; Larizza L; Riccio A; Ferrero GB
Eur J Hum Genet; 2016 Feb; 24(2):183-90. PubMed ID: 25898929
[TBL] [Abstract][Full Text] [Related]
13. Characteristics Associated with Tumor Development in Individuals Diagnosed with Beckwith-Wiedemann Spectrum: Novel Tumor-(epi)Genotype-Phenotype Associations in the BWSp Population.
Duffy KA; Getz KD; Hathaway ER; Byrne ME; MacFarland SP; Kalish JM
Genes (Basel); 2021 Nov; 12(11):. PubMed ID: 34828445
[TBL] [Abstract][Full Text] [Related]
14. Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.
Weksberg R; Nishikawa J; Caluseriu O; Fei YL; Shuman C; Wei C; Steele L; Cameron J; Smith A; Ambus I; Li M; Ray PN; Sadowski P; Squire J
Hum Mol Genet; 2001 Dec; 10(26):2989-3000. PubMed ID: 11751681
[TBL] [Abstract][Full Text] [Related]
15. SNP arrays in Beckwith-Wiedemann syndrome: an improved diagnostic strategy.
Keren B; Chantot-Bastaraud S; Brioude F; Mach C; Fonteneau E; Azzi S; Depienne C; Brice A; Netchine I; Le Bouc Y; Siffroi JP; Rossignol S
Eur J Med Genet; 2013 Oct; 56(10):546-50. PubMed ID: 23892181
[TBL] [Abstract][Full Text] [Related]
16. Performance Metrics of the Scoring System for the Diagnosis of the Beckwith-Wiedemann Spectrum (BWSp) and Its Correlation with Cancer Development.
Luca M; Carli D; Cardaropoli S; Milani D; Cocchi G; Leoni C; Macchiaiolo M; Bartuli A; Tarani L; Melis D; Bontempo P; D'Elia G; Prada E; Vitale R; Grammegna A; Tannorella P; Sparago A; Pignata L; Riccio A; Russo S; Ferrero GB; Mussa A
Cancers (Basel); 2023 Jan; 15(3):. PubMed ID: 36765732
[TBL] [Abstract][Full Text] [Related]
17. Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome.
Gaston V; Le Bouc Y; Soupre V; Burglen L; Donadieu J; Oro H; Audry G; Vazquez MP; Gicquel C
Eur J Hum Genet; 2001 Jun; 9(6):409-18. PubMed ID: 11436121
[TBL] [Abstract][Full Text] [Related]
18. Improved molecular detection of mosaicism in Beckwith-Wiedemann Syndrome.
Baker SW; Duffy KA; Richards-Yutz J; Deardorff MA; Kalish JM; Ganguly A
J Med Genet; 2021 Mar; 58(3):178-184. PubMed ID: 32430359
[TBL] [Abstract][Full Text] [Related]
19. Prospective study of epigenetic alterations responsible for isolated hemihyperplasia/hemihypoplasia and their association with leg length discrepancy.
Shin CH; Lim C; Kim HY; Yoo WJ; Cho TJ; Choi IH; Ko JM
Orphanet J Rare Dis; 2021 Oct; 16(1):418. PubMed ID: 34627330
[TBL] [Abstract][Full Text] [Related]
20. Evolution over Time of Leg Length Discrepancy in Patients with Syndromic and Isolated Lateralized Overgrowth.
Carli D; De Pellegrin M; Franceschi L; Zinali F; Paonessa M; Spolaore S; Cardaropoli S; Cravino M; Marcucci L; Andreacchio A; Resta N; Ferrero GB; Mussa A
J Pediatr; 2021 Jul; 234():123-127. PubMed ID: 33465347
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
