204 related articles for article (PubMed ID: 22615066)
21. Wilms tumour in Beckwith-Wiedemann Syndrome and loss of methylation at imprinting centre 2: revisiting tumour surveillance guidelines.
Brzezinski J; Shuman C; Choufani S; Ray P; Stavropoulos DJ; Basran R; Steele L; Parkinson N; Grant R; Thorner P; Lorenzo A; Weksberg R
Eur J Hum Genet; 2017 Sep; 25(9):1031-1039. PubMed ID: 28699632
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Molecular and genomic characterisation of cryptic chromosomal alterations leading to paternal duplication of the 11p15.5 Beckwith-Wiedemann region.
Russo S; Finelli P; Recalcati MP; Ferraiuolo S; Cogliati F; Dalla Bernardina B; Tibiletti MG; Agosti M; Sala M; Bonati MT; Larizza L
J Med Genet; 2006 Aug; 43(8):e39. PubMed ID: 16882733
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. A 4-Year-Old Boy with Beckwith Wiedemann Syndrome (BWS).
Janchevska A; Tasic V; Laban N; Polenakovic M; Gucev Z; Bachmann N; Bergmann C
Pril (Makedon Akad Nauk Umet Odd Med Nauki); 2018 Dec; 39(2-3):131-135. PubMed ID: 30864369
[TBL] [Abstract][Full Text] [Related]
26. Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells.
Bliek J; Alders M; Maas SM; Oostra RJ; Mackay DM; van der Lip K; Callaway JL; Brooks A; van 't Padje S; Westerveld A; Leschot NJ; Mannens MM
Eur J Hum Genet; 2009 Dec; 17(12):1625-34. PubMed ID: 19513094
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Brain abnormalities in patients with Beckwith-Wiedemann syndrome.
Gardiner K; Chitayat D; Choufani S; Shuman C; Blaser S; Terespolsky D; Farrell S; Reiss R; Wodak S; Pu S; Ray PN; Baskin B; Weksberg R
Am J Med Genet A; 2012 Jun; 158A(6):1388-94. PubMed ID: 22585446
[TBL] [Abstract][Full Text] [Related]
29. (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]
30. 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]
31. 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]
32. The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases.
Chiesa N; De Crescenzo A; Mishra K; Perone L; Carella M; Palumbo O; Mussa A; Sparago A; Cerrato F; Russo S; Lapi E; Cubellis MV; Kanduri C; Cirillo Silengo M; Riccio A; Ferrero GB
Hum Mol Genet; 2012 Jan; 21(1):10-25. PubMed ID: 21920939
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. An 11p15 imprinting centre region 2 deletion in a family with Beckwith Wiedemann syndrome provides insights into imprinting control at CDKN1C.
Algar E; Dagar V; Sebaj M; Pachter N
PLoS One; 2011; 6(12):e29034. PubMed ID: 22205991
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. 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]
37. 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]
38. 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]
39. Genetic variation affecting DNA methylation and the human imprinting disorder, Beckwith-Wiedemann syndrome.
Dagar V; Hutchison W; Muscat A; Krishnan A; Hoke D; Buckle A; Siswara P; Amor DJ; Mann J; Pinner J; Colley A; Wilson M; Sachdev R; McGillivray G; Edwards M; Kirk E; Collins F; Jones K; Taylor J; Hayes I; Thompson E; Barnett C; Haan E; Freckmann ML; Turner A; White S; Kamien B; Ma A; Mackenzie F; Baynam G; Kiraly-Borri C; Field M; Dudding-Byth T; Algar EM
Clin Epigenetics; 2018 Aug; 10(1):114. PubMed ID: 30165906
[TBL] [Abstract][Full Text] [Related]
40. [Genetic analysis of two pediatric patients with Beckwith-Wiedemann syndrome].
Li X; Lyu Y; Gao M; Yan X; Meng C; Zhang K; Liu Y; Gai Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Dec; 34(6):831-834. PubMed ID: 29188610
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]