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Bernhard Horsthemke (1953-)

Biochemiker

Name	Bernhard Horsthemke
Time	1953- (Date of birth and death)
Place	Ahlen (Kreis Warendorf) (Geburtsort) Deutschland
Gender	männlich
Academic degree	Prof. Dr. rer. nat.
Profession	Biochemiker (characteristic profession)
Related	Universitätsklinikum Essen. Institut für Humangenetik Zentrum für Medizinische Biotechnologie (Essen)
Further information	1972-1978: Studium der Chemie an der Technischen Universität Berlin 1989: Habilitation für das Fach Humangenetik an der Universität Essen seit 2001: Direktor des Instituts für Humangenetik am Universitätsklinikum Essen Forschungsschwerpunkte: Bedeutung genetischer und epigenetischer Variation für die Entstehung von Krankheiten, Genexpressionsunterschiede, Genomisches Imprinting Diss. Fachbereich für Phys. u. Angew. Chemie der Tejchn. Univ. Berlin 1982
Source	Homepage: https://www.uni-due.de/zmb/members/horsthemke/overview.shtml (Stand: 23.06.2020) Homepage: https://www.leopoldina.org/fileadmin/redaktion/Mitglieder/CV_Horsthemke_Bernhard_D.pdf (Stand: 05.02.2021)
Record type	Person
GND-Identifier	172144035
Record ID	172144035
Involved in show all Pancreatic cancer acquires resistance to MAPK pathway inhibition by clonal expansion and adaptive DNA hypermethylation The role of epigenetics in rare diseases Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome X No evidence for intervention-associated DNA methylation changes in monocytes of patients with posttraumatic stress disorder Evidence for correlations between BMI-associated SNPs and circRNAs No evidence for intervention-associated DNA methylation changes in monocytes of patients with posttraumatic stress disorder The adult phenotype of Schaaf-Yang syndrome wg-blimp: an end-to-end analysis pipeline for whole genome bisulfite sequencing data Artifizielle humane Imprints Genome-Wide Analysis of the Nucleosome Landscape in Individuals with Coffin-Siris Syndrome Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3 A critical view on transgenerational epigenetic inheritance in humans Regions of common inter-individual DNA methylation differences in human monocytes: genetic basis and potential function Epigenetic dynamics of monocyte-to-macrophage differentiation The imprinted NPAP1 gene in the Prader-Willi syndrome region belongs to a POM121-related family of retrogenes Newly established human retinoblastoma cell lines exhibit an "immortalized" but not an invasive phenotype in vitro Charakterisierung einer Luliberin spaltenden Endopeptidase

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Katalog der Deutschen Nationalbibliothek

Bernhard Horsthemke (1953-)

Pancreatic cancer acquires resistance to MAPK pathway inhibition by clonal expansion and adaptive DNA hypermethylation

The role of epigenetics in rare diseases

Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome X

No evidence for intervention-associated DNA methylation changes in monocytes of patients with posttraumatic stress disorder

Evidence for correlations between BMI-associated SNPs and circRNAs

No evidence for intervention-associated DNA methylation changes in monocytes of patients with posttraumatic stress disorder

The adult phenotype of Schaaf-Yang syndrome

wg-blimp: an end-to-end analysis pipeline for whole genome bisulfite sequencing data

Artifizielle humane Imprints

Genome-Wide Analysis of the Nucleosome Landscape in Individuals with Coffin-Siris Syndrome

Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3

A critical view on transgenerational epigenetic inheritance in humans

Regions of common inter-individual DNA methylation differences in human monocytes: genetic basis and potential function

Epigenetic dynamics of monocyte-to-macrophage differentiation

The imprinted NPAP1 gene in the Prader-Willi syndrome region belongs to a POM121-related family of retrogenes

Newly established human retinoblastoma cell lines exhibit an "immortalized" but not an invasive phenotype in vitro

Charakterisierung einer Luliberin spaltenden Endopeptidase