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Introduction to the Beckwith–Wiedemann Syndrome and Cancer Special Issue

Cancers, 2023-10, Vol.15 (20), p.4939

2023

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Characterization of the Beckwith‐Wiedemann spectrum: Diagnosis and management

American journal of medical genetics. Part C, Seminars in medical genetics, 2019-12, Vol.181 (4), p.693-708

2019

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Allele-specific RNA imaging shows that allelic imbalances can arise in tissues through transcriptional bursting

PLoS genetics, 2019-01, Vol.15 (1), p.e1007874-e1007874

2019

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Diagnosis and Management of Beckwith-Wiedemann Syndrome

Frontiers in pediatrics, 2020-01, Vol.7, p.562-562

2020

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Molecular networks of hepatoblastoma predisposition and oncogenesis in Beckwith‐Wiedemann syndrome

Hepatology communications, 2022-08, Vol.6 (8), p.2132-2146

2022

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Altered microRNA expression profiles in large offspring syndrome and Beckwith-Wiedemann syndrome

Epigenetics, 2019-09, Vol.14 (9), p.850-876

2019

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The effectiveness of Wilms tumor screening in Beckwith–Wiedemann spectrum

Journal of cancer research and clinical oncology, 2019-12, Vol.145 (12), p.3115-3123

2019

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Occurrence of Hepatoblastomas in Patients with Beckwith-Wiedemann Spectrum (BWSp)

Cancers, 2023-04, Vol.15 (9), p.2548

2023

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Visualizing allele-specific expression in single cells reveals epigenetic mosaicism in an H19 loss-of-imprinting mutant

Genes & development, 2016-03, Vol.30 (5), p.567-578

2016

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Characterization and Childhood Tumor Risk Assessment of Genetic and Epigenetic Syndromes Associated With Lateralized Overgrowth

Frontiers in pediatrics, 2020-12, Vol.8, p.613260-613260

2020

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Androgenetic chimerism as an etiology for Beckwith-Wiedemann syndrome: diagnosis and management

Genetics in medicine, 2019-11, Vol.21 (11), p.2644-2649

2019

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Derivation and investigation of the first human cell-based model of Beckwith-Wiedemann syndrome

Epigenetics, 2021-12, Vol.16 (12), p.1295-1305

2021

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Characteristics Associated with Tumor Development in Individuals Diagnosed with Beckwith-Wiedemann Spectrum: Novel Tumor-(epi)Genotype-Phenotype Associations in the BWSp Population

Genes, 2021-11, Vol.12 (11), p.1839

2021

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Nomenclature and definition in asymmetric regional body overgrowth

American journal of medical genetics. Part A, 2017-07, Vol.173 (7), p.1735-1738

2017

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Results From the WAGR Syndrome Patient Registry: Characterization of WAGR Spectrum and Recommendations for Care Management

Frontiers in pediatrics, 2021-12, Vol.9, p.733018-733018

2021

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Epigenetic mosaicism and cell burden in Beckwith-Wiedemann syndrome due to loss of methylation at imprinting control region 2

Cold Spring Harbor molecular case studies, 2021-12, Vol.7 (6), p.a006115

2021

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Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients

American journal of medical genetics. Part A, 2018-08, Vol.176 (8), p.1711-1722

2018

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Urological Findings in Beckwith-Wiedemann Syndrome with Chromosomal Duplications of 11P15.5: Evaluation and Management

Urology (Ridgewood, N.J.), 2017-02, Vol.100, p.224-227

2017

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Longitudinal Monitoring of Alpha-Fetoprotein by Dried Blood Spot for Hepatoblastoma Screening in Beckwith⁻Wiedemann Syndrome

Cancers, 2019-01, Vol.11 (1), p.86

2019

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Epigenetics and imprinting in human disease

The International journal of developmental biology, 2014, Vol.58 (2-4), p.291

2014

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Overgrowth syndromes, diagnosis and management

Current opinion in pediatrics, 2023-12, Vol.35 (6), p.620

2023

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Recommendations for Cancer Surveillance in Individuals with RASopathies and Other Rare Genetic Conditions with Increased Cancer Risk

Clinical cancer research, 2017-06, Vol.23 (12), p.e83-e90

2017

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Prenatal molecular testing and diagnosis of Beckwith‐Wiedemann syndrome

Prenatal diagnosis, 2021-06, Vol.41 (7), p.817-822

2021

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Case Report: Two Distinct Focal Congenital Hyperinsulinism Lesions Resulting From Separate Genetic Events

Frontiers in pediatrics, 2021-07, Vol.9, p.699129

2021

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Surveillance Recommendations for Children with Overgrowth Syndromes and Predisposition to Wilms Tumors and Hepatoblastoma

Clinical cancer research, 2017-07, Vol.23 (13), p.e115-e122

2017

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Introduction to the Beckwith–Wiedemann Syndrome and Cancer Special Issue

Characterization of the Beckwith‐Wiedemann spectrum: Diagnosis and management

Allele-specific RNA imaging shows that allelic imbalances can arise in tissues through transcriptional bursting

Diagnosis and Management of Beckwith-Wiedemann Syndrome

Molecular networks of hepatoblastoma predisposition and oncogenesis in Beckwith‐Wiedemann syndrome

Altered microRNA expression profiles in large offspring syndrome and Beckwith-Wiedemann syndrome

The effectiveness of Wilms tumor screening in Beckwith–Wiedemann spectrum

Occurrence of Hepatoblastomas in Patients with Beckwith-Wiedemann Spectrum (BWSp)

Visualizing allele-specific expression in single cells reveals epigenetic mosaicism in an H19 loss-of-imprinting mutant

Characterization and Childhood Tumor Risk Assessment of Genetic and Epigenetic Syndromes Associated With Lateralized Overgrowth

Androgenetic chimerism as an etiology for Beckwith-Wiedemann syndrome: diagnosis and management

Derivation and investigation of the first human cell-based model of Beckwith-Wiedemann syndrome

Characteristics Associated with Tumor Development in Individuals Diagnosed with Beckwith-Wiedemann Spectrum: Novel Tumor-(epi)Genotype-Phenotype Associations in the BWSp Population

Nomenclature and definition in asymmetric regional body overgrowth

Results From the WAGR Syndrome Patient Registry: Characterization of WAGR Spectrum and Recommendations for Care Management

Epigenetic mosaicism and cell burden in Beckwith-Wiedemann syndrome due to loss of methylation at imprinting control region 2

Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients

Urological Findings in Beckwith-Wiedemann Syndrome with Chromosomal Duplications of 11P15.5: Evaluation and Management

Longitudinal Monitoring of Alpha-Fetoprotein by Dried Blood Spot for Hepatoblastoma Screening in Beckwith⁻Wiedemann Syndrome

Epigenetics and imprinting in human disease

Overgrowth syndromes, diagnosis and management

Recommendations for Cancer Surveillance in Individuals with RASopathies and Other Rare Genetic Conditions with Increased Cancer Risk

Prenatal molecular testing and diagnosis of Beckwith‐Wiedemann syndrome

Case Report: Two Distinct Focal Congenital Hyperinsulinism Lesions Resulting From Separate Genetic Events

Surveillance Recommendations for Children with Overgrowth Syndromes and Predisposition to Wilms Tumors and Hepatoblastoma

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