These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

213 related articles for article (PubMed ID: 36428656)

  • 1. Placental Mesenchymal Dysplasia and Beckwith-Wiedemann Syndrome.
    Soejima H; Hara S; Ohba T; Higashimoto K
    Cancers (Basel); 2022 Nov; 14(22):. PubMed ID: 36428656
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasia.
    Aoki S; Higashimoto K; Hidaka H; Ohtsuka Y; Aoki S; Mishima H; Yoshiura KI; Nakabayashi K; Hata K; Yatsuki H; Hara S; Ohba T; Katabuchi H; Soejima H
    Clin Epigenetics; 2022 May; 14(1):64. PubMed ID: 35581658
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi.
    Paganini L; Carlessi N; Fontana L; Silipigni R; Motta S; Fiori S; Guerneri S; Lalatta F; Cereda A; Sirchia S; Miozzo M; Tabano S
    Epigenetics; 2015; 10(7):643-9. PubMed ID: 26061650
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Beckwith-Wiedemann syndrome with long QT caused by a deletion involving KCNQ1 but not KCNQ1OT1:TSS-DMR.
    Urakawa T; Ozawa J; Tanaka M; Narusawa H; Matsuoka K; Fukami M; Nagasaki K; Kagami M
    Eur J Med Genet; 2023 Jan; 66(1):104671. PubMed ID: 36402267
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders.
    Soejima H; Higashimoto K
    J Hum Genet; 2013 Jul; 58(7):402-9. PubMed ID: 23719190
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. The clinical phenotype of mosaicism for genome-wide paternal uniparental disomy: two new reports.
    Wilson M; Peters G; Bennetts B; McGillivray G; Wu ZH; Poon C; Algar E
    Am J Med Genet A; 2008 Jan; 146A(2):137-48. PubMed ID: 18033734
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol.
    Mussa A; Molinatto C; Baldassarre G; Riberi E; Russo S; Larizza L; Riccio A; Ferrero GB
    J Pediatr; 2016 Sep; 176():142-149.e1. PubMed ID: 27372391
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes.
    Russo S; Calzari L; Mussa A; Mainini E; Cassina M; Di Candia S; Clementi M; Guzzetti S; Tabano S; Miozzo M; Sirchia S; Finelli P; Prontera P; Maitz S; Sorge G; Calcagno A; Maghnie M; Divizia MT; Melis D; Manfredini E; Ferrero GB; Pecile V; Larizza L
    Clin Epigenetics; 2016; 8():23. PubMed ID: 26933465
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The placenta in Beckwith-Wiedemann syndrome: genotype-phenotype associations, excessive extravillous trophoblast and placental mesenchymal dysplasia.
    Armes JE; McGown I; Williams M; Broomfield A; Gough K; Lehane F; Lourie R
    Pathology; 2012 Oct; 44(6):519-27. PubMed ID: 22772341
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.
    Catchpoole D; Lam WW; Valler D; Temple IK; Joyce JA; Reik W; Schofield PN; Maher ER
    J Med Genet; 1997 May; 34(5):353-9. PubMed ID: 9152830
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal presentation in two fetuses with features of Beckwith Wiedemann syndrome-An unexpected diagnosis of androgenetic chimera and its clinical implications.
    Yu PT; Shu W; Mok SL; Hui PW; Chan LW; Kwok KY; Chan KYK; Lo TK; Chung BHY; Luk HM; Kan ASY
    Am J Med Genet A; 2022 May; 188(5):1562-1567. PubMed ID: 35179302
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci.
    Azzi S; Rossignol S; Steunou V; Sas T; Thibaud N; Danton F; Le Jule M; Heinrichs C; Cabrol S; Gicquel C; Le Bouc Y; Netchine I
    Hum Mol Genet; 2009 Dec; 18(24):4724-33. PubMed ID: 19755383
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Androgenetic chimerism as an etiology for Beckwith-Wiedemann syndrome: diagnosis and management.
    Sheppard SE; Lalonde E; Adzick NS; Beck AE; Bhatti T; De Leon DD; Duffy KA; Ganguly A; Hathaway E; Ji J; Linn R; Lord K; Randolph LM; Sajorda B; States L; Conlin LK; Kalish JM
    Genet Med; 2019 Nov; 21(11):2644-2649. PubMed ID: 31147633
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 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. Mosaic genome-wide paternal uniparental disomy after discordant results from primary fetal samples and cultured cells.
    Mastromoro G; Guadagnolo D; Marchionni E; Torres B; Goldoni M; Onori A; Bernardini L; De Luca A; Torrente I; Pizzuti A
    Am J Med Genet A; 2023 Apr; 191(4):1101-1106. PubMed ID: 36598152
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Somatic Mosaicism for Paternal Uniparental Disomy of 11p15.5 Region in Adrenal and Liver Tissues in a Newborn with Atypical Beckwith-Wiedemann Syndrome.
    Urzua A; Burattini S; Pinochet C; Benavides F; Repetto GM
    J Pediatr Genet; 2019 Dec; 8(4):226-230. PubMed ID: 31687262
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Quantitative analysis of methylation status at 11p15 and 7q21 for the genetic diagnosis of Beckwith-Wiedemann syndrome and Silver-Russell syndrome.
    Lee BH; Kim GH; Oh TJ; Kim JH; Lee JJ; Choi SH; Lee JY; Kim JM; Choi IH; Kim YM; Choi JH; Yoo HW
    J Hum Genet; 2013 Sep; 58(9):604-10. PubMed ID: 23803580
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.