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Prof. Dr. rer. nat. Brunhilde Wirth working place, University Hospital Cologne
Prof. Dr. rer. nat. Brunhilde Wirth
Excellent
AiroScore
9.70

Prof. Dr. rer. nat. Brunhilde Wirth

human genetics
human genetics
User ScoreExperienceRatingPrice RangePublicationsOnline Consultations
90%35 years9.7/10$$$$435No

Overview

Country, City
Germany, Cologne
Health facility
University Hospital Cologne
Medical unit
Department of human genetics

About the doctor

Prof. Dr. rer. nat. Brunhilde Wirth is a highly experienced doctor specializing in human genetics with over 34 years of experience. She currently works at the Department of Human Genetics in the University Hospital Cologne in Germany. Dr. Wirth has an impressive academic background, with a diploma in biology from the University of Bucharest and further studies in genetics at the Institute of Human Genetics in Bonn. She obtained her medical practice license and defended her dissertation in Bonn. Dr. Wirth's expertise and dedication are evident from her numerous achievements and contributions to the field. She has published 434 scientific papers on various topics, including spinal muscular atrophy, motor neuron diseases, and rare diseases. Her research has been highly regarded, earning her several prestigious awards and recognition. Dr. Wirth's commitment to advancing genetic knowledge and her contributions to medical genetics make her an exceptional doctor.

Skills & Expertise

atrophy
muscular atrophy
spinal muscular atrophy
gene
sma
genetics
muscle
neuropathy
spinal cord
kidney
mutation
low back pain
neck
injury
polycystic kidney
spinal cord injury
shoulder
osteoporosis
chromosome
smn gene
valproic acid
ataxia
osteoporosis fractures
neck pain
fractures
bone
axonal neuropathy
motor neuropathy
smooth muscle
xlinked osteoporosis
cell carcinoma
motor neurons
skeletal muscle
neurodegeneration
spine
joint
respiratory distress
pls3 mutations
osteogenesis
neurological phenotypes
neuromuscular defects
atp7a mutation
smn1 mutations
cathepsin d
bicd2 mutations
embryonic lethality
atrophy mutations
chp1 mutation
congenital myasthenic syndrome
epileptic ataxia syndrome

Resume

CV (Curriculum Vitae)

Education
  • 1982 Diploma in biology at the faculty of biology of the University of Bucharest
  • 1983 Specialist in applied genetics at the faculty of biology of the University of Bucharest
  • 1986-1989 Studied genetics at the Institute of Human Genetics in Bonn
  • Obtaining a license for medical practice
  • 1989 Defense of the dissertation at the Institute of Human Genetics in Bonn
  • 1989-1990 International postdoctoral scholarship of the German Research Foundation at the Imperial Cancer Research Fund Laboratories in London
  • 1990-1996 Residency at the Institute of Human Genetics at the University of Bonn
  • Obtaining specialization in human genetics from the German Society of Human Genetics
  • 1996 Habilitation and a teaching license at the Institute of Human Genetics at the University of Bonn
  • 1996-2003 Senior Research Assistant at the Institute of Human Genetics at the University of Bonn
Experience
  • 1983-1985 Biology teacher in Turnu Rosu
  • 2003 C4 Full Professor and Director of the Department of human genetics at the University Hospital Cologne
  • 2015 European Clinical Laboratory Geneticists
Awards & Memberships
  • 1996 Sanofi-Winthrop Myopathy Award from the German Society for Materials Science
  • 2001 Scientific Award for motor neuron diseases from the German Society for Materials Science
  • 2002-2006 Vice-President of the German Society of Human Genetics
  • 2003 Head of the neuromuscular and skeletal diseases research group at the University Hospital Cologne
  • 2005-2017 Member of the scientific program committee of the European Society of Human Genetics
  • 2008 Co-Director of the European School of Medical Genetics
  • 2009-2016 Chair of the scientific program committee of the European Society of Human Genetics
  • 2009-2016 Member of the scientific program committee of the International Congress of Human
  • 2010 Member of the internal scientific review board of the Cybersecurity Maturity Model Certification
  • 2010-2022 Member of the scientific review board of Spinal Muscular Atrophy-Europe
  • 2016-2018 Vice-Chair of the scientific review board of the Max-Delbrueck Award
  • 2016-2022 Chair of the scientific review board of Spinal Muscular Atrophy-Europe
  • 2019 Innovation North Rhine-Westphalia Award
  • 2019-2021 Chair of the scientific review board of the Max-Delbrueck Award
  • 2023 Duchenne-Erb Award from the German Society for Materials Science

Languages

English flag
English
German flag
German

Publications

Proteomic Investigation of Differential Interactomes of Glypican 1 and a Putative Disease-Modifying Variant of Ataxia.

1 September, 2023

Feature intertrial priming biases attentional priority: Evidence from the capture-probe paradigm.

August, 2023

To sleep or not to sleep, that is the question: A systematic review and meta-analysis on the effect of post-trauma sleep on intrusive memories of analog trauma.

August, 2023

Location

Kerpener Str., 62, 50937 Cologne, Germany

FAQ

Where does the doctor practice?

What is the specialization of Prof. Dr. rer. nat. Brunhilde Wirth?

The primary specialization of the doctor is human genetics.

What is the experience of the specialist?

Prof. Dr. rer. nat. Brunhilde Wirth has been practicing for more than 35 years.

What is the rating of the doctor?

What topics does Prof. Dr. rer. nat. Brunhilde Wirth expert at?

The doctor has excellent knowledge in atrophy, muscular atrophy, spinal muscular atrophy, gene, sma.

Is the specialist involved in the research?

Does the specialist offer online consultations?

No, Prof. Dr. rer. nat. Brunhilde Wirth doesn’t perform virtual appointments.

Prof. Dr. rer. nat. Brunhilde Wirth
Prof. Dr. rer. nat. Brunhilde Wirth

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