201 related articles for article (PubMed ID: 35842840)
21. The impact of assisted reproductive technologies on genomic imprinting and imprinting disorders.
Uyar A; Seli E
Curr Opin Obstet Gynecol; 2014 Jun; 26(3):210-21. PubMed ID: 24752003
[TBL] [Abstract][Full Text] [Related]
22. Imprinting disorders and assisted reproductive technology.
Odom LN; Segars J
Curr Opin Endocrinol Diabetes Obes; 2010 Dec; 17(6):517-22. PubMed ID: 20962636
[TBL] [Abstract][Full Text] [Related]
23. Imprinting disorders and assisted reproductive technology.
Manipalviratn S; DeCherney A; Segars J
Fertil Steril; 2009 Feb; 91(2):305-15. PubMed ID: 19201275
[TBL] [Abstract][Full Text] [Related]
24. (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]
25. 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]
26. Beckwith-Wiedemann syndrome and assisted reproduction technology (ART).
Maher ER; Brueton LA; Bowdin SC; Luharia A; Cooper W; Cole TR; Macdonald F; Sampson JR; Barratt CL; Reik W; Hawkins MM
J Med Genet; 2003 Jan; 40(1):62-4. PubMed ID: 12525545
[No Abstract] [Full Text] [Related]
27. A review of known imprinting syndromes and their association with assisted reproduction technologies.
Amor DJ; Halliday J
Hum Reprod; 2008 Dec; 23(12):2826-34. PubMed ID: 18703582
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?
Pignata L; Cecere F; Acquaviva F; D'Angelo E; Cioffi D; Pellino V; Palumbo O; Palumbo P; Carella M; Sparago A; De Brasi D; Cerrato F; Riccio A
Front Cell Dev Biol; 2023; 11():1237629. PubMed ID: 37635873
[TBL] [Abstract][Full Text] [Related]
31. Risk assessment of assisted reproductive technology and parental age at childbirth for the development of uniparental disomy-mediated imprinting disorders caused by aneuploid gametes.
Hara-Isono K; Matsubara K; Nakamura A; Sano S; Inoue T; Kawashima S; Fuke T; Yamazawa K; Fukami M; Ogata T; Kagami M
Clin Epigenetics; 2023 May; 15(1):78. PubMed ID: 37147716
[TBL] [Abstract][Full Text] [Related]
32. Double paternal uniparental isodisomy 7 and 15 presenting with Beckwith-Wiedemann spectrum features.
Berland S; Rustad CF; Bentsen MHL; Wollen EJ; Turowski G; Johansson S; Houge G; Haukanes BI
Cold Spring Harb Mol Case Stud; 2021 Dec; 7(6):. PubMed ID: 34615670
[TBL] [Abstract][Full Text] [Related]
33. Maxillo-Facial Morphology in Beckwith-Wiedemann Syndrome: A Preliminary Study on (epi)Genotype-Phenotype Association in Caucasians.
Defabianis P; Mussa A; Ninivaggi R; Carli D; Romano F
Int J Environ Res Public Health; 2022 Feb; 19(4):. PubMed ID: 35206635
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith-Wiedemann locus.
Valente FM; Sparago A; Freschi A; Hill-Harfe K; Maas SM; Frints SGM; Alders M; Pignata L; Franzese M; Angelini C; Carli D; Mussa A; Gazzin A; Gabbarini F; Acurzio B; Ferrero GB; Bliek J; Williams CA; Riccio A; Cerrato F
Genet Med; 2019 Aug; 21(8):1808-1820. PubMed ID: 30635621
[TBL] [Abstract][Full Text] [Related]
36. Epigenetic risks related to assisted reproductive technologies: epigenetics, imprinting, ART and icebergs?
Maher ER; Afnan M; Barratt CL
Hum Reprod; 2003 Dec; 18(12):2508-11. PubMed ID: 14645164
[TBL] [Abstract][Full Text] [Related]
37. Genome-wide paternal uniparental disomy mosaicism in a woman with Beckwith-Wiedemann syndrome and ovarian steroid cell tumour.
Gogiel M; Begemann M; Spengler S; Soellner L; Göretzlehner U; Eggermann T; Strobl-Wildemann G
Eur J Hum Genet; 2013 Jul; 21(7):788-91. PubMed ID: 23188046
[TBL] [Abstract][Full Text] [Related]
38. Imprinting disorders and assisted reproductive technology.
Owen CM; Segars JH
Semin Reprod Med; 2009 Sep; 27(5):417-28. PubMed ID: 19711252
[TBL] [Abstract][Full Text] [Related]
39. Performance Metrics of the Scoring System for the Diagnosis of the Beckwith-Wiedemann Spectrum (BWSp) and Its Correlation with Cancer Development.
Luca M; Carli D; Cardaropoli S; Milani D; Cocchi G; Leoni C; Macchiaiolo M; Bartuli A; Tarani L; Melis D; Bontempo P; D'Elia G; Prada E; Vitale R; Grammegna A; Tannorella P; Sparago A; Pignata L; Riccio A; Russo S; Ferrero GB; Mussa A
Cancers (Basel); 2023 Jan; 15(3):. PubMed ID: 36765732
[TBL] [Abstract][Full Text] [Related]
40. Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19.
DeBaun MR; Niemitz EL; Feinberg AP
Am J Hum Genet; 2003 Jan; 72(1):156-60. PubMed ID: 12439823
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]