Wilms tumour surveillance in at-risk children: Literature review and recommendations from the SIOP-Europe Host Genome Working Group and SIOP Renal Tumour Study Group

Cancer incidence and spectrum among children with genetically confirmed Beckwith-Wiedemann spectrum in Germany: a retrospective cohort study

(2020) Sümeyye Cöktü et al.   BRITISH JOURNAL OF CANCER

Results of treatment for patients with multicentric or bilaterally predisposed unilateral Wilms tumor (AREN0534): A report from the Children's Oncology Group

(2020) Peter F. Ehrlich et al.   CANCER

Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome

(2020) Marc Tischkowitz et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Recent advances in Wilms’ tumor predisposition

(2020) Jamie L Maciaszek et al.   HUMAN MOLECULAR GENETICS

Bilateral Tumors — Inherited or Acquired?

(2020) William D. Foulkes et al.   NEW ENGLAND JOURNAL OF MEDICINE

Wilms tumor in patients with osteopathia striata with cranial sclerosis

(2020) Alicia Bach et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

The Natural History of Wilms Tumor–A Case Comparison of Two Different Tumors

(2019) Jonathan P. Walker et al.   UROLOGY

The genetic changes of Wilms tumour

(2019) Taryn Dora Treger et al.   Nature Reviews Nephrology

Overgrowth syndromes — clinical and molecular aspects and tumour risk

(2019) Frédéric Brioude et al.   Nature Reviews Endocrinology

TRIM28 haploinsufficiency predisposes to Wilms tumor

(2019) Illja J. Diets et al.   INTERNATIONAL JOURNAL OF CANCER

LMO2 gene deletions significantly worsen the prognosis of Wilms’ tumor development in patients with WAGR syndrome

(2019) Andrey V Marakhonov et al.   HUMAN MOLECULAR GENETICS

An eHealth decision‐support tool to prioritize referral practices for genetic evaluation of patients with Wilms tumor

(2019) Noelle Cullinan et al.   INTERNATIONAL JOURNAL OF CANCER

The effectiveness of Wilms tumor screening in Beckwith–Wiedemann spectrum

(2019) Alessandro Mussa et al.   JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY

Embryonal precursors of Wilms tumor

(2019) Tim H. H. Coorens et al.   SCIENCE

Identification of a novel CTR9 germline mutation in a family with Wilms tumor

(2018) António G. Martins et al.   European Journal of Medical Genetics

Loss ofDis3l2partially phenocopies Perlman syndrome in mice and results in up-regulation ofIgf2in nephron progenitor cells

(2018) Ryan W. Hunter et al.   GENES & DEVELOPMENT

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

Normal pelvic ultrasound or MRI does not rule out neoplasm in patients with gonadal dysgenesis and Y chromosome material

(2018) Kristin M. Ebert et al.   Journal of Pediatric Urology

Germline mutations and somatic inactivation of TRIM28 in Wilms tumour

(2018) Benjamin J. Halliday et al.   PLoS Genetics

Mutation update for the GPC3 gene involved in Simpson-Golabi-Behmel syndrome and review of the literature

(2018) Marie-Laure Vuillaume et al.   HUMAN MUTATION

Wilms Tumor Associated With the 9q22.3 Microdeletion Syndrome

(2018) Julie Cayrol et al.   JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY

A unique subset of low-risk Wilms tumors is characterized by loss of function of TRIM28 (KAP1), a gene critical in early renal development: A Children’s Oncology Group study

(2018) Amy E. Armstrong et al.   PLoS One

Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregation

(2017) Shawn Yost et al.   NATURE GENETICS

Position paper: Rationale for the treatment of Wilms tumour in the UMBRELLA SIOP–RTSG 2016 protocol

(2017) Marry M. van den Heuvel-Eibrink et al.   Nature Reviews Urology

Sonographic screening for Wilms tumor in children with CLOVES syndrome

(2017) Caitlin M. Peterman et al.   PEDIATRIC BLOOD & CANCER

Renal findings in patients with Mulibrey nanism

(2017) Johanna Sivunen et al.   PEDIATRIC NEPHROLOGY

Nephroblastomatosis or Wilms tumor in a fourth patient with a somaticPIK3CAmutation

(2016) Karen W. Gripp et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

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

Constitutional 560.49 kb chromosome 2p24.3 duplication including the MYCN gene identified by SNP chromosome microarray analysis in a child with multiple congenital anomalies and bilateral Wilms tumor

(2016) Mark A. Micale et al.   European Journal of Medical Genetics

Is Nephron Sparing Surgery Justified in Wilms Tumor With Beckwith-Wiedemann Syndrome or Isolated Hemihypertrophy?

(2016) Aurélien Scalabre et al.   PEDIATRIC BLOOD & CANCER

Clinical management of patients withASXL1mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance

(2015) Bianca Russell et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A high incidence of WT1 abnormality in bilateral Wilms tumours in Japan and the penetrance rates in children with WT1 germline mutation

(2015) Y Kaneko et al.   BRITISH JOURNAL OF CANCER

Clinical and Molecular Characterization of Patients with Heterozygous Mutations in Wilms Tumor Suppressor Gene 1

(2015) A. Lehnhardt et al.   Clinical Journal of the American Society of Nephrology

Advances in Wilms Tumor Treatment and Biology: Progress Through International Collaboration

(2015) Jeffrey S. Dome et al.   JOURNAL OF CLINICAL ONCOLOGY

Mutations in the transcriptional repressor REST predispose to Wilms tumor

(2015) Shazia S Mahamdallie et al.   NATURE GENETICS

Multiple mechanisms of MYCN dysregulation in Wilms tumour

(2015) Richard D. Williams et al.   Oncotarget

Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors

(2015) Gaia Roversi et al.   Scientific Reports

Genotype–phenotype associations in WT1 glomerulopathy

(2014) Beata S. Lipska et al.   KIDNEY INTERNATIONAL

Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumour

(2014) Sandra Hanks et al.   Nature Communications

Involvement of germline DDX1–MYCN duplication in inherited nephroblastoma

(2013) Alice Fievet et al.   European Journal of Medical Genetics

Frequency of WT1 and 11p15 constitutional aberrations and phenotypic correlation in childhood Wilms tumour patients

(2012) H. Segers et al.   EUROPEAN JOURNAL OF CANCER

Nephron Sparing Surgery for Unilateral Wilms Tumor in Children with Predisposing Syndromes: Single Center Experience Over 10 Years

(2012) Rodrigo L.P. Romão et al.   JOURNAL OF UROLOGY

Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility

(2012) Dewi Astuti et al.   NATURE GENETICS

Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay

(2011) Eric A. Muller et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Analysis of the Wilms' Tumor Suppressor Gene (WT1) in Patients 46,XY Disorders of Sex Development

(2011) B. Köhler et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Mutations in CEP57 cause mosaic variegated aneuploidy syndrome

(2011) Katie Snape et al.   NATURE GENETICS

De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome

(2011) Alexander Hoischen et al.   NATURE GENETICS

Haploinsufficiency of HDAC4 Causes Brachydactyly Mental Retardation Syndrome, with Brachydactyly Type E, Developmental Delays, and Behavioral Problems

(2010) Stephen R. Williams et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Novel duplication in glypican-4 as an apparent cause of Simpson-Golabi-Behmel syndrome

(2010) John Waterson et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations

(2010) G. Chernin et al.   Clinical Journal of the American Society of Nephrology

WTX mutations can occur both early and late in the pathogenesis of Wilms tumour

(2010) R. Fukuzawa et al.   JOURNAL OF MEDICAL GENETICS

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

(2009) Helen V. Firth et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Experience with hemihyperplasia and Beckwith-Wiedemann syndrome surveillance protocol

(2009) Yuri A. Zarate et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Diagnostic criteria and tumor screening for individuals with isolated hemihyperplasia

(2009) Carol L Clericuzio et al.   GENETICS IN MEDICINE

Osteopathia striata with cranial sclerosis owing to WTX gene defect

(2009) Bram Perdu et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene

(2009) I. Slade et al.   JOURNAL OF MEDICAL GENETICS

High frequency of tumours in Mulibrey nanism

(2009) Niklas Karlberg et al.   JOURNAL OF PATHOLOGY

Perlman syndrome: Report, prenatal findings and review

(2008) Jean-Luc Alessandri et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Clinical relevance of mutations in the Wilms tumor suppressor 1 geneWT1and the cadherin-associated protein β1 geneCTNNB1for patients with Wilms tumors

(2008) Brigitte Royer-Pokora et al.   CANCER

Epigenotype, Phenotype, and Tumors in Patients with Isolated Hemihyperplasia

(2008) Jet Bliek et al.   JOURNAL OF PEDIATRICS

Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis

(2008) Zandra A Jenkins et al.   NATURE GENETICS

Management of Wilms tumors in Drash and Frasier syndromes

(2008) F. Auber et al.   PEDIATRIC BLOOD & CANCER