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DNA Methylation Analysis in Nonalcoholic Fatty Liver Disease Suggests Distinct Disease-Specific and Remodeling Signatures after Bariatric Surgery

Cell metabolism, 2013-08, Vol.18 (2), p.296-302

2013

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The curious case of Merkel cell carcinoma: epigenetic youth and lack of pluripotency

Epigenetics, 2020-12, Vol.15 (12), p.1319-1324

2020

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Aberrant DNA methylation of ADAMTS16 in colorectal and other epithelial cancers

BMC cancer, 2018-08, Vol.18 (1), p.796-10, Article 796

2018

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A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndrome

European journal of human genetics : EJHG, 2016-08, Vol.24 (9), p.1280-1286

2016

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The DNA methylation status of the TERT promoter differs between subtypes of mature B-cell lymphomas

Blood cancer journal (New York), 2023-06, Vol.13 (1), p.98-98, Article 98

2023

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DNA-methylation profiling of fetal tissues reveals marked epigenetic differences between chorionic and amniotic samples

PloS one, 2012-06, Vol.7 (6), p.e39014-e39014

2012

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PLAGL1 epimutation and bladder exstrophy: Coincidence or concurrent etiology?

Birth defects research. A Clinical and molecular teratology, 2016-08, Vol.106 (8), p.724-728

2016

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In vivo investigations of the effect of short- and long-term recombinant growth hormone treatment on DNA-methylation in humans

PloS one, 2015-03, Vol.10 (3), p.e0120463

2015

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Mosaic genome-wide maternal isodiploidy: an extreme form of imprinting disorder presenting as prenatal diagnostic challenge

Clinical epigenetics, 2017-10, Vol.9 (1), p.111-111, Article 111

2017

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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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Charakterisierung der dna-methylierung geprägter gene im kontext physiologischer und gestörter entwicklung und somatischer differenzierung

Kolarova, Julia

2018

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Genome‑wide expression and methylation analyses reveal aberrant cell adhesion signaling in tyrosine kinase inhibitor‑resistant CML cells

Oncology reports, 2022-08, Vol.48 (2), p.144, Article 144

2022

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DNA methylome analysis in Burkitt and follicular lymphomas identifies differentially methylated regions linked to somatic mutation and transcriptional control

Nature genetics, 2015-11, Vol.47 (11), p.1316-1325

2015

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Quantitative DNA Methylation Profiling in Cancer

Methods in molecular biology (Clifton, N.J.), 2016, Vol.1381, p.75

2016

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DNA methylation profiling of pediatric B‐cell lymphoblastic leukemia with KMT2A rearrangement identifies hypomethylation at enhancer sites

Pediatric blood & cancer, 2017-03, Vol.64 (3), p.np-n/a

2017

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Genome-wide methylation analysis of retrocopy-associated CpG islands and their genomic environment

Epigenetics, 2016-03, Vol.11 (3), p.216-226

2016

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Molecular characterization of an embryonal rhabdomyosarcoma occurring in a patient with Kabuki syndrome: report and literature review in the light of tumor predisposition syndromes

Familial cancer, 2023-01, Vol.22 (1), p.103-118

2023

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Array-based DNA methylation analysis in individuals with developmental delay/intellectual disability and normal molecular karyotype

European journal of medical genetics, 2015-08, Vol.58 (8), p.419-425

2015

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The tissue is the issue: improved methylome analysis from paraffin-embedded tissues by application of the HOPE technique

Laboratory investigation, 2014-08, Vol.94 (8), p.927-933

2014

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The differentially methylated region of MEG8 is hypermethylated in patients with Temple syndrome

Epigenomics, 2015-10, Vol.7 (7), p.1089-1097

2015

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Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbances

Epigenomics, 2016-06, Vol.8 (6), p.801-816

2016

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The differentially methylated region of

Epigenomics, 2015-10, Vol.7 (7), p.1089-1097

2015

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DNA Methylation Analysis in Nonalcoholic Fatty Liver Disease Suggests Distinct Disease-Specific and Remodeling Signatures after Bariatric Surgery

The curious case of Merkel cell carcinoma: epigenetic youth and lack of pluripotency

Aberrant DNA methylation of ADAMTS16 in colorectal and other epithelial cancers

A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndrome

The DNA methylation status of the TERT promoter differs between subtypes of mature B-cell lymphomas

DNA-methylation profiling of fetal tissues reveals marked epigenetic differences between chorionic and amniotic samples

PLAGL1 epimutation and bladder exstrophy: Coincidence or concurrent etiology?

In vivo investigations of the effect of short- and long-term recombinant growth hormone treatment on DNA-methylation in humans

Mosaic genome-wide maternal isodiploidy: an extreme form of imprinting disorder presenting as prenatal diagnostic challenge

Frequency and characterization of DNA methylation defects in children born SGA

Charakterisierung der dna-methylierung geprägter gene im kontext physiologischer und gestörter entwicklung und somatischer differenzierung

Genome‑wide expression and methylation analyses reveal aberrant cell adhesion signaling in tyrosine kinase inhibitor‑resistant CML cells

Maternal variants in NLRP and other maternal effect proteins are associated with multilocus imprinting disturbance in offspring

DNA methylome analysis in Burkitt and follicular lymphomas identifies differentially methylated regions linked to somatic mutation and transcriptional control

Quantitative DNA Methylation Profiling in Cancer

Rhabdoid tumors in patients conceived following ART: is there an association?

DNA methylation profiling of pediatric B‐cell lymphoblastic leukemia with KMT2A rearrangement identifies hypomethylation at enhancer sites

Genome-wide methylation analysis of retrocopy-associated CpG islands and their genomic environment

Molecular characterization of an embryonal rhabdomyosarcoma occurring in a patient with Kabuki syndrome: report and literature review in the light of tumor predisposition syndromes

Array-based DNA methylation analysis in individuals with developmental delay/intellectual disability and normal molecular karyotype

IG-MYC+ neoplasms with precursor B-cell phenotype are molecularly distinct from Burkitt lymphomas

The tissue is the issue: improved methylome analysis from paraffin-embedded tissues by application of the HOPE technique

The differentially methylated region of MEG8 is hypermethylated in patients with Temple syndrome

Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbances

The differentially methylated region of

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