Wilms tumour in Beckwith–Wiedemann Syndrome and loss of methylation at imprinting centre 2: revisiting tumour surveillance guidelines

[1]  Saskia M. J. Hopman,et al.  Phenotype, cancer risk, and surveillance in Beckwith–Wiedemann syndrome depending on molecular genetic subgroups , 2016, American journal of medical genetics. Part A.

[2]  G. Ferrero,et al.  Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol. , 2016, The Journal of pediatrics.

[3]  M. Maghnie,et al.  A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes , 2016, Clinical Epigenetics.

[4]  M. Cubellis,et al.  (Epi)genotype–phenotype correlations in Beckwith–Wiedemann syndrome , 2015, European Journal of Human Genetics.

[5]  A. Lorenzo,et al.  Renal function in patients with Wilms tumor. , 2016, Urologic oncology.

[6]  R. Brusati,et al.  Recommendations of the Scientific Committee of the Italian Beckwith-Wiedemann Syndrome Association on the diagnosis, management and follow-up of the syndrome. , 2016, European journal of medical genetics.

[7]  P. Ostrosky-Wegman,et al.  “Monoallelic germline methylation and sequence variant in the promoter of the RB1 gene: a possible constitutive epimutation in hereditary retinoblastoma” , 2016, Clinical Epigenetics.

[8]  P. Joly,et al.  A late onset sickle cell disease reveals a mosaic segmental uniparental isodisomy of chromosome 11p15. , 2015, Blood cells, molecules & diseases.

[9]  Nardin Samuel,et al.  Management of familial cancer: sequencing, surveillance and society , 2014, Nature Reviews Clinical Oncology.

[10]  L. Tee,et al.  Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjects , 2014, Clinical Epigenetics.

[11]  L. Tee,et al.  Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjects , 2014, Clinical Epigenetics.

[12]  C. M. van der Horst,et al.  Methylation analysis in tongue tissue of BWS patients identifies the (EPI)genetic cause in 3 patients with normal methylation levels in blood. , 2014, European journal of medical genetics.

[13]  N. Breslow,et al.  Outcome of patients with stage II/favorable histology wilms tumor with and without local tumor spill: A report from the National Wilms Tumor Study Group , 2014, Pediatric blood & cancer.

[14]  M. Vazquez,et al.  Beckwith-Wiedemann Syndrome: Growth Pattern and Tumor Risk according to Molecular Mechanism, and Guidelines for Tumor Surveillance , 2013, Hormone Research in Paediatrics.

[15]  L. Richiardi,et al.  Prevalence of beckwith–wiedemann syndrome in North West of Italy , 2013, American journal of medical genetics. Part A.

[16]  J. Mill,et al.  A data-driven approach to preprocessing Illumina 450K methylation array data , 2013, BMC Genomics.

[17]  R. Weksberg,et al.  Molecular Findings in Beckwith–Wiedemann Syndrome , 2013, American journal of medical genetics. Part C, Seminars in medical genetics.

[18]  Ruth Pidsley,et al.  A data-driven approach to preprocessing Illumina 450K methylation array data , 2013, BMC Genomics.

[19]  L. Robison,et al.  Childhood cancer survivorship: an update on evolving paradigms for understanding pathogenesis and screening for therapy-related late effects , 2013, Current opinion in pediatrics.

[20]  C. Cytrynbaum,et al.  Mosaicism for genome‐wide paternal uniparental disomy with features of multiple imprinting disorders: Diagnostic and management issues , 2013, American journal of medical genetics. Part A.

[21]  R. Weksberg,et al.  Nephron sparing surgery for unilateral Wilms tumor in children with predisposing syndromes: single center experience over 10 years. , 2012, The Journal of urology.

[22]  D. Pinto,et al.  A novel approach identifies new differentially methylated regions (DMRs) associated with imprinted genes. , 2011, Genome research.

[23]  R. Weksberg,et al.  Beckwith–Wiedemann syndrome , 2010, European Journal of Human Genetics.

[24]  T. Eggermann,et al.  Use of multiplex ligation‐dependent probe amplification increases the detection rate for 11p15 epigenetic alterations in Silver–Russell syndrome , 2007, Clinical genetics.

[25]  D. Amor,et al.  Tumour surveillance in Beckwith–Wiedemann syndrome and hemihyperplasia: A critical review of the evidence and suggested guidelines for local practice , 2006, Journal of paediatrics and child health.

[26]  N. Rahman,et al.  Surveillance for Wilms tumour in at-risk children: pragmatic recommendations for best practice , 2006, Archives of Disease in Childhood.

[27]  A. Feinberg,et al.  Children with idiopathic hemihypertrophy and beckwith-wiedemann syndrome have different constitutional epigenotypes associated with wilms tumor. , 2005, American journal of human genetics.

[28]  R. Weksberg,et al.  Renal abnormalities in beckwith-wiedemann syndrome are associated with 11p15.5 uniparental disomy. , 2002, Journal of the American Society of Nephrology : JASN.

[29]  R. Weksberg,et al.  Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1. , 2001, Human molecular genetics.

[30]  M. DeBaun,et al.  Screening for Wilms tumor and hepatoblastoma in children with Beckwith-Wiedemann syndromes: a cost-effective model. , 2001, Medical and pediatric oncology.

[31]  J. Ruijter,et al.  Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS. , 2001, Human molecular genetics.

[32]  N. Breslow,et al.  Characteristics and outcome of children with Beckwith-Wiedemann syndrome and Wilms' tumor: a report from the National Wilms Tumor Study Group. , 2000, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[33]  D. Barton,et al.  Mosaic uniparental disomy in Beckwith-Wiedemann syndrome. , 1994, Journal of medical genetics.

[34]  N. Kiviat,et al.  Nephrogenic rests, nephroblastomatosis, and the pathogenesis of Wilms' tumor. , 1990, Pediatric pathology.

[35]  Nan Faion T. Wu,et al.  The Beckwith-Wiedemann Syndrome , 1974, Clinical pediatrics.