221 related articles for article (PubMed ID: 35230882)
1. Prevalence of (Epi)genetic Predisposing Factors in a 5-Year Unselected National Wilms Tumor Cohort: A Comprehensive Clinical and Genomic Characterization.
Hol JA; Kuiper RP; van Dijk F; Waanders E; van Peer SE; Koudijs MJ; Bladergroen R; van Reijmersdal SV; Morgado LM; Bliek J; Lombardi MP; Hopman S; Drost J; de Krijger RR; van den Heuvel-Eibrink MM; Jongmans MCJ
J Clin Oncol; 2022 Jun; 40(17):1892-1902. PubMed ID: 35230882
[TBL] [Abstract][Full Text] [Related]
2. Germline (epi)genetics reveals high predisposition in females: a 5-year, nationwide, prospective Wilms tumour cohort.
Stoltze UK; Hildonen M; Hansen TVO; Foss-Skiftesvik J; Byrjalsen A; Lundsgaard M; Pignata L; Grønskov K; Tumer Z; Schmiegelow K; Brok JS; Wadt KAW
J Med Genet; 2023 Sep; 60(9):842-849. PubMed ID: 37019617
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Frequency of WT1 and 11p15 constitutional aberrations and phenotypic correlation in childhood Wilms tumour patients.
Segers H; Kersseboom R; Alders M; Pieters R; Wagner A; van den Heuvel-Eibrink MM
Eur J Cancer; 2012 Nov; 48(17):3249-56. PubMed ID: 22796116
[TBL] [Abstract][Full Text] [Related]
5. 11p15.5 epimutations in children with Wilms tumor and hepatoblastoma detected in peripheral blood.
Fiala EM; Ortiz MV; Kennedy JA; Glodzik D; Fleischut MH; Duffy KA; Hathaway ER; Heaton T; Gerstle JT; Steinherz P; Shukla N; McNeer N; Tkachuk K; Bouvier N; Cadoo K; Carlo MI; Latham A; Dubard Gault M; Joseph V; Kemel Y; Kentsis A; Stadler Z; La Quaglia M; Papaemmanuil E; Friedman D; Ganguly A; Kung A; Offit K; Kalish JM; Walsh MF
Cancer; 2020 Jul; 126(13):3114-3121. PubMed ID: 32320050
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Familial Beckwith-Wiedemann syndrome in a multigenerational family: Forty years of careful phenotyping.
Best LG; Duffy KA; George AM; Ganguly A; Kalish JM
Am J Med Genet A; 2023 Feb; 191(2):348-356. PubMed ID: 36322462
[TBL] [Abstract][Full Text] [Related]
8. Cancer predisposition signaling in Beckwith-Wiedemann Syndrome drives Wilms tumor development.
Nirgude S; Naveh NSS; Kavari SL; Traxler EM; Kalish JM
Br J Cancer; 2024 Mar; 130(4):638-650. PubMed ID: 38142265
[TBL] [Abstract][Full Text] [Related]
9. Recent advances in Wilms' tumor predisposition.
Maciaszek JL; Oak N; Nichols KE
Hum Mol Genet; 2020 Oct; 29(R2):R138-R149. PubMed ID: 32412586
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Wilms tumor genes.
Huff V; Saunders GF
Biochim Biophys Acta; 1993 Dec; 1155(3):295-306. PubMed ID: 8268188
[TBL] [Abstract][Full Text] [Related]
12. Genetic and epigenetic features of bilateral Wilms tumor predisposition in patients from the Children's Oncology Group AREN18B5-Q.
Murphy AJ; Cheng C; Williams J; Shaw TI; Pinto EM; Dieseldorff-Jones K; Brzezinski J; Renfro LA; Tornwall B; Huff V; Hong AL; Mullen EA; Crompton B; Dome JS; Fernandez CV; Geller JI; Ehrlich PF; Mulder H; Oak N; Maciezsek J; Jablonowski CM; Fleming AM; Pichavaram P; Morton CL; Easton J; Nichols KE; Clay MR; Santiago T; Zhang J; Yang J; Zambetti GP; Wang Z; Davidoff AM; Chen X
Nat Commun; 2023 Dec; 14(1):8006. PubMed ID: 38110397
[TBL] [Abstract][Full Text] [Related]
13. Cytogenetics and molecular genetics of Wilms' tumor of childhood.
Slater RM; Mannens MM
Cancer Genet Cytogenet; 1992 Jul; 61(2):111-21. PubMed ID: 1322233
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. The pathophysiology of bilateral and multifocal Wilms tumors: What we can learn from the study of predisposition syndromes.
Welter N; Brzezinski J; Treece A; Chintagumpala M; Young MD; Perotti D; Kieran K; Jongmans MCJ; Murphy AJ
Pediatr Blood Cancer; 2023 May; 70 Suppl 2():e29984. PubMed ID: 36094328
[TBL] [Abstract][Full Text] [Related]
18. Wilms' tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomas.
Isidor B; Bourdeaut F; Lafon D; Plessis G; Lacaze E; Kannengiesser C; Rossignol S; Pichon O; Briand A; Martin-Coignard D; Piccione M; David A; Delattre O; Jeanpierre C; Sévenet N; Le Caignec C
Eur J Hum Genet; 2013 Jul; 21(7):784-7. PubMed ID: 23169491
[TBL] [Abstract][Full Text] [Related]
19. Confirmation of Xp22.11 Duplication as a Germline Susceptibility Alteration in a Wilms Tumor Arising in Horseshoe Kidney.
Zhou HF; Amarillo IE; Snyder S; Granadillo JL; O'Conor CJ; Dillon P; Wilson D; Huang FS; Dehner LP; He M
Fetal Pediatr Pathol; 2022 Aug; 41(4):682-688. PubMed ID: 33960268
[No Abstract] [Full Text] [Related]
20. 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 May; 61(6):590-594. PubMed ID: 38228391
[No Abstract] [Full Text] [Related]
[Next] [New Search]
