BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

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]
    of 11.