189 related articles for article (PubMed ID: 15580204)
1. Epigenotyping as a tool for the prediction of tumor risk and tumor type in patients with Beckwith-Wiedemann syndrome (BWS).
Bliek J; Gicquel C; Maas S; Gaston V; Le Bouc Y; Mannens M
J Pediatr; 2004 Dec; 145(6):796-9. PubMed ID: 15580204
[TBL] [Abstract][Full Text] [Related]
2. Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS.
Bliek J; Maas SM; Ruijter JM; Hennekam RC; Alders M; Westerveld A; Mannens MM
Hum Mol Genet; 2001 Mar; 10(5):467-76. PubMed ID: 11181570
[TBL] [Abstract][Full Text] [Related]
3. Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.
Engel JR; Smallwood A; Harper A; Higgins MJ; Oshimura M; Reik W; Schofield PN; Maher ER
J Med Genet; 2000 Dec; 37(12):921-6. PubMed ID: 11106355
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour.
Sparago A; Russo S; Cerrato F; Ferraiuolo S; Castorina P; Selicorni A; Schwienbacher C; Negrini M; Ferrero GB; Silengo MC; Anichini C; Larizza L; Riccio A
Hum Mol Genet; 2007 Feb; 16(3):254-64. PubMed ID: 17158821
[TBL] [Abstract][Full Text] [Related]
7. Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroups.
Maas SM; Vansenne F; Kadouch DJ; Ibrahim A; Bliek J; Hopman S; Mannens MM; Merks JH; Maher ER; Hennekam RC
Am J Med Genet A; 2016 Sep; 170(9):2248-60. PubMed ID: 27419809
[TBL] [Abstract][Full Text] [Related]
8. Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome.
Cooper WN; Luharia A; Evans GA; Raza H; Haire AC; Grundy R; Bowdin SC; Riccio A; Sebastio G; Bliek J; Schofield PN; Reik W; Macdonald F; Maher ER
Eur J Hum Genet; 2005 Sep; 13(9):1025-32. PubMed ID: 15999116
[TBL] [Abstract][Full Text] [Related]
9. Diagnosis of Beckwith-Wiedemann syndrome in children presenting with Wilms tumor.
MacFarland SP; Duffy KA; Bhatti TR; Bagatell R; Balamuth NJ; Brodeur GM; Ganguly A; Mattei PA; Surrey LF; Balis FM; Kalish JM
Pediatr Blood Cancer; 2018 Oct; 65(10):e27296. PubMed ID: 29932284
[TBL] [Abstract][Full Text] [Related]
10. A constitutional BWS-related t(11;16) chromosome translocation occurring in the same region of chromosome 16 implicated in Wilms' tumors.
Newsham I; Kindler-Röhrborn A; Daub D; Cavenee W
Genes Chromosomes Cancer; 1995 Jan; 12(1):1-7. PubMed ID: 7534105
[TBL] [Abstract][Full Text] [Related]
11. Children with idiopathic hemihypertrophy and beckwith-wiedemann syndrome have different constitutional epigenotypes associated with wilms tumor.
Niemitz EL; Feinberg AP; Brandenburg SA; Grundy PE; DeBaun MR
Am J Hum Genet; 2005 Nov; 77(5):887-91. PubMed ID: 16252245
[TBL] [Abstract][Full Text] [Related]
12. Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors.
O'Keefe D; Dao D; Zhao L; Sanderson R; Warburton D; Weiss L; Anyane-Yeboa K; Tycko B
Am J Hum Genet; 1997 Aug; 61(2):295-303. PubMed ID: 9311733
[TBL] [Abstract][Full Text] [Related]
13. Wilms tumour in Beckwith-Wiedemann Syndrome and loss of methylation at imprinting centre 2: revisiting tumour surveillance guidelines.
Brzezinski J; Shuman C; Choufani S; Ray P; Stavropoulos DJ; Basran R; Steele L; Parkinson N; Grant R; Thorner P; Lorenzo A; Weksberg R
Eur J Hum Genet; 2017 Sep; 25(9):1031-1039. PubMed ID: 28699632
[TBL] [Abstract][Full Text] [Related]
14. Characteristics and outcome of children with Beckwith-Wiedemann syndrome and Wilms' tumor: a report from the National Wilms Tumor Study Group.
Porteus MH; Narkool P; Neuberg D; Guthrie K; Breslow N; Green DM; Diller L
J Clin Oncol; 2000 May; 18(10):2026-31. PubMed ID: 10811666
[TBL] [Abstract][Full Text] [Related]
15. The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region.
Rossignol S; Steunou V; Chalas C; Kerjean A; Rigolet M; Viegas-Pequignot E; Jouannet P; Le Bouc Y; Gicquel C
J Med Genet; 2006 Dec; 43(12):902-7. PubMed ID: 16825435
[TBL] [Abstract][Full Text] [Related]
16. Concurrent Hepatoblastoma and Wilms Tumor Leading to Diagnosis of Beckwith-Wiedemann Syndrome.
Wolfe DM; Webster Carrion A; Masukhani MM; Oberg JA; Pavisic J; El-Ali A; Gupta M; Weng K; Glasser CL
J Pediatr Hematol Oncol; 2023 May; 45(4):e525-e529. PubMed ID: 36730589
[TBL] [Abstract][Full Text] [Related]
17. Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith-Wiedemann syndrome.
Lin HY; Chuang CK; Tu RY; Fang YY; Su YN; Chen CP; Chang CY; Liu HC; Chu TH; Niu DM; Lin SP
Mol Genet Metab; 2016 Sep; 119(1-2):8-13. PubMed ID: 27436784
[TBL] [Abstract][Full Text] [Related]
18. Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor.
Riccio A; Sparago A; Verde G; De Crescenzo A; Citro V; Cubellis MV; Ferrero GB; Silengo MC; Russo S; Larizza L; Cerrato F
Endocr Dev; 2009; 14():1-9. PubMed ID: 19293570
[TBL] [Abstract][Full Text] [Related]
19. Beck-Wiedemann syndrome and Wilms' tumour.
Ward A
Mol Hum Reprod; 1997 Feb; 3(2):157-68. PubMed ID: 9239720
[TBL] [Abstract][Full Text] [Related]
20. Tumor risk in Beckwith-Wiedemann syndrome: A review and meta-analysis.
Rump P; Zeegers MP; van Essen AJ
Am J Med Genet A; 2005 Jul; 136(1):95-104. PubMed ID: 15887271
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
