11p15.5 epimutations in children with Wilms tumor and hepatoblastoma detected in peripheral blood

Molecular diagnosis of somatic overgrowth conditions: A single‐center experience

(2019) Emilie Lalonde et al.   Molecular Genetics & Genomic Medicine

Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement

(2018) Frédéric Brioude et al.   Nature Reviews Endocrinology

Diagnosis of Beckwith-Wiedemann syndrome in children presenting with Wilms tumor

(2018) Suzanne P. MacFarland et al.   PEDIATRIC BLOOD & CANCER

Clinical cancer genomic profiling by three-platform sequencing of whole genome, whole exome and transcriptome

(2018) Michael Rusch et al.   Nature Communications

Evidence of predisposing epimutation in retinoblastoma

(2018) Elisa Gelli et al.   HUMAN MUTATION

Bilateral Wilms tumour: a review of clinical and molecular features

(2017) Jocelyn Charlton et al.   EXPERT REVIEWS IN MOLECULAR MEDICINE

Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroups

(2016) Saskia M. Maas et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol

(2016) Alessandro Mussa et al.   JOURNAL OF PEDIATRICS

Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors

(2016) D. Williams Parsons et al.   JAMA Oncology

Integrative Clinical Sequencing in the Management of Refractory or Relapsed Cancer in Youth

(2015) Rajen J. Mody et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Germline Mutations in Predisposition Genes in Pediatric Cancer

(2015) Jinghui Zhang et al.   NEW ENGLAND JOURNAL OF MEDICINE

Stratification of Wilms tumor by genetic and epigenetic analysis

(2015) Richard H. Scott et al.   Oncotarget

The IGF signalling pathway in Wilms tumours - A report from the ENCCA Renal Tumours Biology-driven drug development workshop

(2015) Mariana Maschietto et al.   Oncotarget

Prenatal diagnosis in haemophilia A: experience of the genetic diagnostic laboratory

(2014) L. Kessler et al.   HAEMOPHILIA

Recurrent epimutation of SDHC in gastrointestinal stromal tumors

(2014) J. K. Killian et al.   Science Translational Medicine

Beckwith-Wiedemann Syndrome: Growth Pattern and Tumor Risk according to Molecular Mechanism, and Guidelines for Tumor Surveillance

(2013) F. Brioude et al.   Hormone Research in Paediatrics

Signatures of mutational processes in human cancer

(2013) Ludmil B. Alexandrov et al.   NATURE

Targeting the Insulin Growth Factor Receptor 1

(2012) Fernanda I. Arnaldez et al.   HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA

Constitutive promoter methylation of BRCA1 and RAD51C in patients with familial ovarian cancer and early-onset sporadic breast cancer

(2012) T. Hansmann et al.   HUMAN MOLECULAR GENETICS

The Pediatric Cancer Genome Project

(2012) James R Downing et al.   NATURE GENETICS

DNA methylation signatures for breast cancer classification and prognosis

(2012) Moshe Szyf   Genome Medicine

Allele-specific methylated multiplex real-time quantitative PCR (ASMM RTQ-PCR), a powerful method for diagnosing loss of imprinting of the 11p15 region in Russell Silver and Beckwith Wiedemann syndromes

(2010) Salah Azzi et al.   HUMAN MUTATION

Whole-genome profiling of chromosomal aberrations in hepatoblastoma using high-density single-nucleotide polymorphism genotyping microarrays

(2008) Makoto Suzuki et al.   CANCER SCIENCE

Further evidence for heritability of an epimutation in one of 12 cases with MLH1 promoter methylation in blood cells clinically displaying HNPCC

(2008) Monika Morak et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor

(2008) Richard H Scott et al.   NATURE GENETICS