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Anke Katharina Bergmann

Ärztin

Name	Anke Katharina Bergmann
Place	Kiel (Wirkungsort) Würzburg (Wirkungsort) Deutschland
Academic degree	Prof. Dr. med.
Profession	Ärztin (characteristic profession) Genetikerin
Variant	Anke K. Bergmann Anke Bergmann
Further information	Wissenschaftliche Mitarbeiterin, Klinik für Allgemeine Pädiatrie, Universitätsklinikum Schleswig-Holstein (UK-SH), Campus Kiel, Habilitation 2017, seit 2024 Professorin für klinische Genetik und Genommedizin am Uniklinikum der Univ. Würzburg
Record type	Person
GND-Identifier	1069177504
Record ID	1069177504
Involved in show all SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation Epigenomische Analyse von Kandidatengenen in der großgranulären T-Lymphozyten Leukämie : mittels Methylierungs-Microarray-Analyse und Pyrosequenzierung Recurrent DNMT3B rearrangements are associated with unfavorable outcome in dicentric (9;20)-positive pediatric BCP-ALL Molecular complete remission following combination treatment of daratumumab and venetoclax in an adolescent with relapsed mixed phenotype acute leukemia Systematic genetic analysis of pediatric patients with autoinflammatory diseases Graph4Med: a web application and a graph database for visualizing and analyzing medical databases Graph4Med: a web application and a graph database for visualizing and analyzing medical databases Genetic Variation in ABCC4 and CFTR and Acute Pancreatitis during Treatment of Pediatric Acute Lymphoblastic Leukemia Identifizierung und Charakterisierung genomischer, epigenomischer und transkriptomischer Veränderungen in reifen T- und B-Zell-Neoplasien Changes of bivalent chromatin coincide with increased expression of developmental genes in cancer Changes of bivalent chromatin coincide with increased expression of developmental genes in cancer

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Anke Katharina Bergmann

SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation

Epigenomische Analyse von Kandidatengenen in der großgranulären T-Lymphozyten Leukämie : mittels Methylierungs-Microarray-Analyse und Pyrosequenzierung

Recurrent DNMT3B rearrangements are associated with unfavorable outcome in dicentric (9;20)-positive pediatric BCP-ALL

Molecular complete remission following combination treatment of daratumumab and venetoclax in an adolescent with relapsed mixed phenotype acute leukemia

Systematic genetic analysis of pediatric patients with autoinflammatory diseases

Graph4Med: a web application and a graph database for visualizing and analyzing medical databases

Graph4Med: a web application and a graph database for visualizing and analyzing medical databases

Genetic Variation in ABCC4 and CFTR and Acute Pancreatitis during Treatment of Pediatric Acute Lymphoblastic Leukemia

Identifizierung und Charakterisierung genomischer, epigenomischer und transkriptomischer Veränderungen in reifen T- und B-Zell-Neoplasien

Changes of bivalent chromatin coincide with increased expression of developmental genes in cancer

Changes of bivalent chromatin coincide with increased expression of developmental genes in cancer