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 *

225 related articles for article (PubMed ID: 34828445)

  • 1. 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]  

  • 2. 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]  

  • 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. Expanded phenotype and cancer risk in patients with Beckwith-Wiedemann spectrum caused by CDKN1C variants.
    George AM; Viswanathan A; Best LG; Monahan C; Limmina M; Ganguly A; Kalish JM
    Am J Med Genet A; 2024 Oct; 194(10):e63777. PubMed ID: 38822599
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. (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]  

  • 9. Epigenotype and phenotype correlations in patients with Beckwith-Wiedemann syndrome.
    Bilgin B; Kabaçam S; Taşkıran E; Şimşek-Kiper PÖ; Alanay Y; Boduroğlu K; Utine GE
    Turk J Pediatr; 2018; 60(5):506-513. PubMed ID: 30968633
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular Basis of Beckwith-Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice.
    Eggermann T; Maher ER; Kratz CP; Prawitt D
    Cancers (Basel); 2022 Jun; 14(13):. PubMed ID: 35804856
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Pediatric Cushing syndrome: An early sign of an underling cancer predisposition syndrome.
    Schweiger BM; Esakhan CL; Frishberg D; Grand K; Garg R; Sanchez-Lara PA
    Am J Med Genet A; 2021 Sep; 185(9):2824-2828. PubMed ID: 33960620
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Occurrence of Hepatoblastomas in Patients with Beckwith-Wiedemann Spectrum (BWSp).
    Klein SD; DeMarchis M; Linn RL; MacFarland SP; Kalish JM
    Cancers (Basel); 2023 Apr; 15(9):. PubMed ID: 37174013
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques.
    Carli D; Operti M; Russo S; Cocchi G; Milani D; Leoni C; Prada E; Melis D; Falco M; Spina J; Uliana V; Sara O; Sirchia F; Tarani L; Macchiaiolo M; Cerrato F; Sparago A; Pignata L; Tannorella P; Cardaropoli S; Bartuli A; Riccio A; Ferrero GB; Mussa A
    Clin Genet; 2022 Oct; 102(4):314-323. PubMed ID: 35842840
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.