BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

170 related articles for article (PubMed ID: 36730589)

  • 21. The utility of alpha-fetoprotein screening in Beckwith-Wiedemann syndrome.
    Duffy KA; Deardorff MA; Kalish JM
    Am J Med Genet A; 2017 Mar; 173(3):581-584. PubMed ID: 28160403
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Molecular networks of hepatoblastoma predisposition and oncogenesis in Beckwith-Wiedemann syndrome.
    Sobel Naveh NS; Traxler EM; Duffy KA; Kalish JM
    Hepatol Commun; 2022 Aug; 6(8):2132-2146. PubMed ID: 35507738
    [TBL] [Abstract][Full Text] [Related]  

  • 23. (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]  

  • 24. Paternal Uniparental Disomy of the Entire Chromosome 20 in a Child with Beckwith-Wiedemann Syndrome.
    Choufani S; Ko JM; Lou Y; Shuman C; Fishman L; Weksberg R
    Genes (Basel); 2021 Jan; 12(2):. PubMed ID: 33513760
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Metastatic Phyllodes Tumor in a Patient With Beckwith-Wiedemann Syndrome.
    Saini A; Gupte T; Choudhury MSR; Jacques SM; Roxas R
    J Investig Med High Impact Case Rep; 2022; 10():23247096221133197. PubMed ID: 36314358
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. 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]  

  • 28. The significance of molecular studies in the long-term follow-up of children with beckwith- wiedemann syndrome.
    Gizewska M; Wilk M; Patalan M; Mackay D; Peregud-Pegorzelski J; Gawrych E; Walczak M; Petriczko E; Brodkiewicz A
    Turk J Pediatr; 2014; 56(2):177-82. PubMed ID: 24911853
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.
    Calvello M; Tabano S; Colapietro P; Maitz S; Pansa A; Augello C; Lalatta F; Gentilin B; Spreafico F; Calzari L; Perotti D; Larizza L; Russo S; Selicorni A; Sirchia SM; Miozzo M
    Epigenetics; 2013 Oct; 8(10):1053-60. PubMed ID: 23917791
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. 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]  

  • 33. Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects.
    DeBaun MR; Niemitz EL; McNeil DE; Brandenburg SA; Lee MP; Feinberg AP
    Am J Hum Genet; 2002 Mar; 70(3):604-11. PubMed ID: 11813134
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Beckwith-Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature.
    Sassi H; Elaribi Y; Jilani H; Rejeb I; Hizem S; Sebai M; Kasdallah N; Bouthour H; Hannachi S; Beygo J; Saad A; Buiting K; H'mida Ben-Brahim D; BenJemaa L
    Mol Genet Genomic Med; 2021 Oct; 9(10):e1796. PubMed ID: 34510813
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. 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]  

  • 37. Usefulness of the MS-MLPA technique in the diagnosis of Beckwith-Wiedemann syndrome and Silver-Russell syndrome.
    Acosta-Fernández E; Corona-Rivera JR; Ríos-Flores IM; Torres-Anguiano E; Corona-Rivera A; Peña-Padilla C; Bobadilla-Morales L
    Gac Med Mex; 2022; 158(4):202-209. PubMed ID: 36256576
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. 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]  

  • 40. Genomic profiles of a hepatoblastoma from a patient with Beckwith-Wiedemann syndrome with uniparental disomy on chromosome 11p15 and germline mutation of APC and PALB2.
    Kim SY; Jung SH; Kim MS; Han MR; Park HC; Jung ES; Lee SH; Lee SH; Chung YJ
    Oncotarget; 2017 Nov; 8(54):91950-91957. PubMed ID: 29190888
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.