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

British journal of cancer, 2020-08, Vol.123 (4), p.619-623

2020

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Molecular Basis of Beckwith–Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice

Cancers, 2022-06, Vol.14 (13), p.3083

2022

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Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domains

Epigenetics, 2018-02, Vol.13 (2), p.117-121

2018

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CDKN1C mutations: two sides of the same coin

Trends in molecular medicine, 2014-11, Vol.20 (11), p.614-622

2014

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High calcium concentration in bones promotes bone metastasis in renal cell carcinomas expressing calcium-sensing receptor

Molecular cancer, 2014-02, Vol.13 (1), p.42-42, Article 42

2014

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EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome

European journal of human genetics : EJHG, 2016-10, Vol.24 (10), p.1377-1387

2016

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The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites

Human molecular genetics, 2013-02, Vol.22 (3), p.544-557

2013

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Clinical utility gene card for: Beckwith-Wiedemann Syndrome

European journal of human genetics : EJHG, 2014-03, Vol.22 (3), p.435-435

2014

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Correction to: Molecular karyotyping and gene expression analysis in childhood cancer patients

Journal of molecular medicine (Berlin, Germany), 2020-11, Vol.98 (11), p.1657-1657

2020

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TRPM5 Is a Transient Ca2+-Activated Cation Channel Responding to Rapid Changes in [ Ca2+]i

Proceedings of the National Academy of Sciences - PNAS, 2003-12, Vol.100 (25), p.15166-15171

2003

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Prenatal molecular testing for Beckwith-Wiedemann and Silver-Russell syndromes: a challenge for molecular analysis and genetic counseling

European journal of human genetics : EJHG, 2016-06, Vol.24 (6), p.784-793

2016

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Molecular karyotyping and gene expression analysis in childhood cancer patients

Journal of molecular medicine (Berlin, Germany), 2020-08, Vol.98 (8), p.1107-1123

2020

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TRPM5 regulates glucose-stimulated insulin secretion

Pflügers Archiv, 2010-06, Vol.460 (1), p.69-76

2010

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A Unified Nomenclature for the Superfamily of TRP Cation Channels

Molecular cell, 2002-02, Vol.9 (2), p.229-231

2002

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Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)

Orphanet journal of rare diseases, 2020-06, Vol.15 (1), p.1-144, Article 144

2020

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In renal cell carcinoma the PTEN splice variant PTEN-Δ shows similar function as the tumor suppressor PTEN itself

Cell communication and signaling, 2018-06, Vol.16 (1), p.35-35, Article 35

2018

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Comprehensive genetic testing approaches as the basis for personalized management of growth disturbances: current status and perspectives

Endocrine Connections, 2022-11, Vol.11 (11), p.1-14

2022

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Microdeletion of Target Sites for Insulator Protein CTCF in a Chromosome 11p15 Imprinting Center in Beckwith-Wiedemann Syndrome and Wilms' Tumor

Proceedings of the National Academy of Sciences - PNAS, 2005-03, Vol.102 (11), p.4085-4090

2005

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Hypermethylation of RAD9A intron 2 in childhood cancer patients, leukemia and tumor cell lines suggest a role for oncogenic transformation

EXCLI journal, 2022-01, Vol.21, p.117-143

2022

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Further understanding of paternal uniparental disomy in Beckwith-Wiedemann syndrome

Expert review of endocrinology & metabolism, 2022-11, Vol.17 (6), p.513-521

2022

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Frequency and characterization of DNA methylation defects in children born SGA

European journal of human genetics : EJHG, 2013-08, Vol.21 (8), p.838-843

2013

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Hyperuricemia Drives Pancreatic β‐cell Death Facilitated by DEPTOR uratylation

The FASEB journal, 2021-05, Vol.35 (S1), p.n/a, Article fasebj.2021.35.S1.02240

2021

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Basics and disturbances of genomic imprinting

Medizinische Genetik, 2020-12, Vol.32 (4), p.297-304

2020

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Kaiso mediates human ICR1 methylation maintenance and H19 transcriptional fine regulation

Clinical epigenetics, 2016-05, Vol.8 (47), p.47-47, Article 47

2016

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ERBB2-mediated transcriptional up-regulation of the α5β1 integrin fibronectin receptor promotes tumor cell survival under adverse conditions

Cancer research (Chicago, Ill.), 2006-04, Vol.66 (7), p.3715-3725

2006

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

Molecular Basis of Beckwith–Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice

Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domains

CDKN1C mutations: two sides of the same coin

High calcium concentration in bones promotes bone metastasis in renal cell carcinomas expressing calcium-sensing receptor

EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome

The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites

Clinical utility gene card for: Beckwith-Wiedemann Syndrome

Correction to: Molecular karyotyping and gene expression analysis in childhood cancer patients

TRPM5 Is a Transient Ca2+-Activated Cation Channel Responding to Rapid Changes in [ Ca2+]i

Prenatal molecular testing for Beckwith-Wiedemann and Silver-Russell syndromes: a challenge for molecular analysis and genetic counseling

Molecular karyotyping and gene expression analysis in childhood cancer patients

TRPM5 regulates glucose-stimulated insulin secretion

A Unified Nomenclature for the Superfamily of TRP Cation Channels

Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)

In renal cell carcinoma the PTEN splice variant PTEN-Δ shows similar function as the tumor suppressor PTEN itself

Comprehensive genetic testing approaches as the basis for personalized management of growth disturbances: current status and perspectives

Microdeletion of Target Sites for Insulator Protein CTCF in a Chromosome 11p15 Imprinting Center in Beckwith-Wiedemann Syndrome and Wilms' Tumor

Hypermethylation of RAD9A intron 2 in childhood cancer patients, leukemia and tumor cell lines suggest a role for oncogenic transformation

Further understanding of paternal uniparental disomy in Beckwith-Wiedemann syndrome

Frequency and characterization of DNA methylation defects in children born SGA

Hyperuricemia Drives Pancreatic β‐cell Death Facilitated by DEPTOR uratylation

Basics and disturbances of genomic imprinting

Kaiso mediates human ICR1 methylation maintenance and H19 transcriptional fine regulation

ERBB2-mediated transcriptional up-regulation of the α5β1 integrin fibronectin receptor promotes tumor cell survival under adverse conditions

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