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Prof. Dr. med. Dagmar Wieczorek working place, University Hospital Dusseldorf
Prof. Dr. med. Dagmar Wieczorek
Excellent
AiroScore
9.70

Prof. Dr. med. Dagmar Wieczorek

human genetics, rare diseases
human genetics, rare diseases
User ScoreExperienceRatingPrice RangePublicationsOnline Consultations
93%31 years9.7/10$$$$546No

Overview

Country, City
Germany, Dusseldorf
Health facility
University Hospital Dusseldorf
Medical unit
Department of human genetics with the center for rare diseases

About the doctor

Prof. Dr. Dagmar Wieczorek is an experienced doctor specializing in human genetics and rare diseases. With over 30 years of experience, she has made significant contributions to the field through her research and publications, totaling 546 scientific articles. She works at the Department of Human Genetics with the Center for Rare Diseases at the University Hospital Dusseldorf in Germany. One of the most notable aspects of Dr. Wieczorek's career is her role as the Site Spokeswoman of the West German Genome Center and the spokesperson for the Center for Rare Diseases in Dusseldorf. Her expertise in rare diseases and genetics allows her to provide specialized care to patients with complex medical conditions. Additionally, she serves as the Healthcare Professionals Representative for the European Reference Network for Rare Malformation Syndromes and Intellectual and Other Neurodevelopmental Disorders, further highlighting her commitment to advancing knowledge and collaboration in the medical community. Dr. Wieczorek's extensive experience and numerous roles in the medical field make her a highly respected and sought-after doctor. Her dedication to research, teaching, and clinical practice demonstrates her passion for helping patients with rare diseases. With her expertise and leadership in human genetics, Dr. Wieczorek is well-equipped to provide exceptional care and contribute to advancements in rare diseases.

Skills & Expertise

syndrome
mutation
tropomyosin
phenotype
intellectual disability
gene
cardiomyopathy
genetics
hypertrophic cardiomyopathy
microcephaly
familial hypertrophic cardiomyopathy
mental retardation
coffinsiris syndrome
treacher collins syndrome
anomalies
children
dilated cardiomyopathy
noonan syndrome
kabuki syndrome
craniofacial disorders
mandibulofacial dysostosis
neurodevelopmental disorder
cardiac hypertrophy
dysmorphic faces
cognitive impairment
nonsyndromic intellectual disability
children cancer
pluripotent stem
heart defect
congenital heart defect
charcotmarietooth neuropathies
costello syndrome
alphatropomyosin mutation
floatingharbor syndrome
earlyonset dystonia
rubinsteintaybi syndrome
burnmckeown syndrome
esophageal atresia
face
cleft palate
rare malformation syndromes
osteodysplastic primordial dwarfism
wolfhirschhorn syndrome
choanal atresia
abnormal gait
frontometaphyseal dysplasia
anophthalmia syndrome
spliceosomal defects
borjesonforssmanlehmann syndrome
craniofacial dysmorphism

Resume

CV (Curriculum Vitae)

Education
  • 1987-1993 Study of human medicine at the Ruhr University Bochum
  • Obtaining a license for medical practice
  • 1994-1998 Specialist training in human genetics at the Institute for Human Genetics, University Hospital Essen
  • 1994 Promotion Dr. med. at the Ruhr University Bochum
  • 1998-1999 Specialist training in pediatrics at the University Children's Hospital Munster
  • 2000 Specialist examination in human genetics
  • 2005 Habilitation and teaching license in human genetics, University of Essen
Experience
  • 2000-2005 Research Assistant (C1), Department of human genetics at the University Hospital Essen
  • 2006-2015 Senior Physician and Head, Center of genetic counseling and Leader of the working group at the Institute for Human Genetics, University Hospital Essen
  • 2010-2015 Associate Professor, University of Duisburg-Essen
  • 2015 W3 Professorship and Director, Department of human genetics with the center for rare diseases at the University Hospital Dusseldorf
Awards & Memberships
  • 2010-2015 Mentor in the MediMent project at the University of Duisburg-Essen
  • 2015 Examiner at the Institute for Medical and Pharmaceutical Examination Questions
  • 2016 Healthcare Professionals Representative European Reference Network for Rare Malformation Syndromes, Intellectual and Other Neurodevelopmental Disorders
  • 2016 Editor-in-Chief of medical genetics
  • 2017 Member of the scientific advisory board, Alliance of Chronic Rare Diseases
  • 2017 Expert of the German Academy for Rare Neurological Diseases
  • 2019 Site Spokeswoman of the West German Genome Center in Dusseldorf
  • 2020 Spokesperson for the Center for Rare Diseases in Dusseldorf

Languages

English flag
English
German flag
German

Publications

Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals.

4 August, 2023

Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals

August, 2023

A study on inter-planner plan quality variability using a manual planning- or Lightning dose optimizer-approach for single brain lesions treated with the Gamma Knife® Icon™.

6 July, 2023

FAQ

Where does the doctor practice?

What is the specialization of Prof. Dr. med. Dagmar Wieczorek?

The primary specialization of the doctor is human genetics, rare diseases.

What is the experience of the specialist?

Prof. Dr. med. Dagmar Wieczorek has been practicing for more than 31 years.

What is the rating of the doctor?

What topics does Prof. Dr. med. Dagmar Wieczorek expert at?

The doctor has excellent knowledge in syndrome, mutation, tropomyosin, phenotype, intellectual disability.

Is the specialist involved in the research?

Does the specialist offer online consultations?

No, Prof. Dr. med. Dagmar Wieczorek doesn’t perform virtual appointments.

Prof. Dr. med. Dagmar Wieczorek
Prof. Dr. med. Dagmar Wieczorek

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