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 *

179 related articles for article (PubMed ID: 30898153)

  • 1. Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics.
    Krzyzewska IM; Alders M; Maas SM; Bliek J; Venema A; Henneman P; Rezwan FI; Lip KVD; Mul AN; Mackay DJG; Mannens MMAM
    Clin Epigenetics; 2019 Mar; 11(1):53. PubMed ID: 30898153
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Clinical and Molecular Diagnosis of Beckwith-Wiedemann Syndrome with Single- or Multi-Locus Imprinting Disturbance.
    Fontana L; Tabano S; Maitz S; Colapietro P; Garzia E; Gerli AG; Sirchia SM; Miozzo M
    Int J Mol Sci; 2021 Mar; 22(7):. PubMed ID: 33810554
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders.
    Fontana L; Bedeschi MF; Maitz S; Cereda A; Faré C; Motta S; Seresini A; D'Ursi P; Orro A; Pecile V; Calvello M; Selicorni A; Lalatta F; Milani D; Sirchia SM; Miozzo M; Tabano S
    Epigenetics; 2018; 13(9):897-909. PubMed ID: 30221575
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes.
    Sperandeo MP; Ungaro P; Vernucci M; Pedone PV; Cerrato F; Perone L; Casola S; Cubellis MV; Bruni CB; Andria G; Sebastio G; Riccio A
    Am J Hum Genet; 2000 Mar; 66(3):841-7. PubMed ID: 10712200
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance.
    Urakawa T; Soejima H; Yamoto K; Hara-Isono K; Nakamura A; Kawashima S; Narusawa H; Kosaki R; Nishimura Y; Yamazawa K; Hattori T; Muramatsu Y; Inoue T; Matsubara K; Fukami M; Saitoh S; Ogata T; Kagami M
    Clin Epigenetics; 2024 Oct; 16(1):138. PubMed ID: 39369220
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 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. 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. 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]  

  • 16. Uncovering the phenotypic consequences of multi-locus imprinting disturbances using genome-wide methylation analysis in genomic imprinting disorders.
    Kim HY; Shin CH; Shin CH; Ko JM
    PLoS One; 2023; 18(8):e0290450. PubMed ID: 37594968
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. New insights into the pathogenesis of Beckwith-Wiedemann and Silver-Russell syndromes: contribution of small copy number variations to 11p15 imprinting defects.
    Demars J; Rossignol S; Netchine I; Lee KS; Shmela M; Faivre L; Weill J; Odent S; Azzi S; Callier P; Lucas J; Dubourg C; Andrieux J; Le Bouc Y; El-Osta A; Gicquel C
    Hum Mutat; 2011 Oct; 32(10):1171-82. PubMed ID: 21780245
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical and molecular analyses of Beckwith-Wiedemann syndrome: Comparison between spontaneous conception and assisted reproduction techniques.
    Tenorio J; Romanelli V; Martin-Trujillo A; Fernández GM; Segovia M; Perandones C; Pérez Jurado LA; Esteller M; Fraga M; Arias P; Gordo G; Dapía I; Mena R; Palomares M; Pérez de Nanclares G; Nevado J; García-Miñaur S; Santos-Simarro F; Martinez-Glez V; Vallespín E; ; Monk D; Lapunzina P
    Am J Med Genet A; 2016 Oct; 170(10):2740-9. PubMed ID: 27480579
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndrome.
    Reik W; Brown KW; Slatter RE; Sartori P; Elliott M; Maher ER
    Hum Mol Genet; 1994 Aug; 3(8):1297-301. PubMed ID: 7987305
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.