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Prof. Dr. med. Martin Zenker working place, University Hospital Otto-von-Guericke Magdeburg
Prof. Dr. med. Martin Zenker
Excellent
AiroScore
9.90

Prof. Dr. med. Martin Zenker

pediatrics, neonatology, and human genetics
pediatrics, neonatology, and human genetics
User ScoreExperienceRatingPrice RangePublicationsOnline Consultations
95%32 years9.9/10$$$531No

Overview

Country, City
Germany, Magdeburg
Health facility
University Hospital Otto-von-Guericke Magdeburg
Medical unit
Department of human genetics

About the doctor

Prof. Dr. med. Martin Zenker is a highly experienced and accomplished doctor in Germany, specializing in pediatrics, neonatology, and human genetics. With an impressive 31 years of experience, Dr. Zenker has dedicated his career to providing exceptional medical care and advancing the field through his research. Dr. Zenker obtained his medical degree from the Friedrich-Alexander University in Erlangen-Nuremberg, followed by a residency at the prestigious university. He later obtained additional qualifications in neonatology and specialization in human genetics. Throughout his career, Dr. Zenker has held various positions at renowned institutions, including the Institute for Human Genetics at the Friedrich-Alexander University and the University Hospital Otto-von-Guericke Magdeburg, where he currently serves as the Director of the Department of Human Genetics. In addition to his clinical work, Dr. Zenker is a prolific researcher with over 500 scientific publications to his name. His research focuses on genetic testing and inherited disorders, including endocrine conditions and pancreatic dysfunction. He has received recognition for his work, including the Hans Krebs Prize. With his vast knowledge and expertise, Prof. Dr. med. Martin Zenker is regarded as a top expert in his field. He is highly regarded for his contributions to pediatrics, neonatology, and human genetics, making him a valuable asset to the medical community and a trusted doctor for his patients.

Skills & Expertise

mutation
noonan syndrome
gene
phenotype
children
nephrotic syndrome
cardiomyopathy
genetics
ubr1
johansonblizzard syndrome
hypertrophic cardiomyopathy
cancer
leukemia
kras mutations
fraser syndrome
neurofibromatosis
anomalies
phenotypic spectrum
ptpn11
pierson syndrome
adamsoliver syndrome
nephrosis
eye
deficiency
mental retardation
plasminogen
steroidresistant nephrotic syndrome
germline kras mutations
neonatology
juvenile myelomonocytic leukemia
congenital hyperinsulinism
myelomonocytic leukemia
raf1
costello syndrome
cardiofaciocutaneous syndrome
gallowaymowat syndrome
deletion syndrome
happletinschert syndrome
congenital nephrosis
marshallsmith syndrome
mota syndrome
eye abnormalities
mesangial sclerosis
giant cell
lymphoblastic leukemia
dopamine d2 receptor
congenital inherited anomalies
congenital nephrotic syndrome
pediatrics
rasopathyassociated hypertrophic cardiomyopathy

Resume

CV (Curriculum Vitae)

Education
  • 1985-1992 Studied human medicine at the Friedrich-Alexander University in Erlangen-Nuremberg
  • 1993 Obtaining a license for medical practice
  • 1993-2001 Residency at the Department for children and adolescents at the Friedrich-Alexander University in Erlangen-Nuremberg
  • 1995 Defense of the dissertation at the Friedrich-Alexander University in Erlangen-Nuremberg
  • 2000 Obtaining specialization in pediatrics
  • 2001 Received additional qualifications in the field of neonatology
  • 2005 Obtaining further specialization in human genetics
  • 2006 Habilitation and a teaching license for human genetics
Experience
  • 1992-1993 Physician in an internship at the Children's Clinic of the Central Clinic Augsburg
  • 2000-2001 Senior Physician at the Department of neonatology at the Friedrich-Alexander University in Erlangen-Nuremberg
  • 2001-2009 Research Associate at the Institute for Human Genetics of the Friedrich-Alexander University in Erlangen-Nuremberg
  • 2006-2009 Senior Physician at the Institute for Human Genetics in Erlangen
  • 2009 Professor of human genetics at the medical faculty of the Otto von Guericke University in Magdeburg
  • 2009 Director of the Department of human genetics at the University Hospital Otto-von-Guericke Magdeburg
Awards & Memberships
  • 2006 Hans Krebs Prize by the Hannover Medical School
  • 2006-2009 Group Leader at the Institute for Human Genetics in Erlangen

Languages

English flag
English
German flag
German

Publications

Epilepsy in cardiofaciocutaneous syndrome: Clinical burden and response to anti‐seizure medication

October, 2023

C-terminal variants in CDC42 drive type I interferon-dependent autoinflammation in NOCARH syndrome reversible by ruxolitinib.

22 September, 2023

Bifidobacteria shape antimicrobial T-helper cell responses during infancy and adulthood

September, 2023

Location

Leipziger Str., 44, 39120 Magdeburg, Germany

FAQ

What is the specialization of Prof. Dr. med. Martin Zenker?

The primary specialization of the doctor is pediatrics, neonatology, and human genetics.

What is the experience of the specialist?

Prof. Dr. med. Martin Zenker has been practicing for more than 32 years.

What is the rating of the doctor?

What topics does Prof. Dr. med. Martin Zenker expert at?

The doctor has excellent knowledge in mutation, noonan syndrome, gene, phenotype, children.

Is the specialist involved in the research?

Does the specialist offer online consultations?

No, Prof. Dr. med. Martin Zenker doesn’t perform virtual appointments.

Prof. Dr. med. Martin Zenker
Prof. Dr. med. Martin Zenker

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