Peter Krawitz    

Biosketch

I was trained as a physicist and physician in Munich (Germany) and continued with a residency in Medical Genetics and a postdoc in Bioformatics in Berlin (Germany). As a clinician scientist, I was able to identify the disease-causing variants in the gene PIGV in patients with Hyperphosphatasia with Mental Retardation (aka Mabry syndrome) by exome sequencing in 2009. Since that year, I am interested in the molecular pathway disease of glycosylphosphatidylinositol biosynthesis defects, of which PIGV is just one out of 30 genes involved. I contributed to establishing next-generation sequencing protocols in routine health care and soon realized that the large number of variants that these tests yield will require better and faster phenotyping. I therefore focused my research on deep learning methods to analyze medical imaging data.
After establishing the Institute for Genomic Statistics and Bioinformatics (IGSB) in 2017, I started collaborative research projects with groups at University Bonn but also internationally. One project that involves groups from all continents and that I enjoy very much is GestaltMatcher and its associated FAIR database. If you are interested in joining, please reach out!

Avatar Krawitz

Prof. Dr. med. Dipl. Phys. Peter Krawitz

2G/620

Venusberg Campus 1

53127 Bonn

IGSB
Immunosensation
TRA1 Modelling

 Scientific Vitae  

  • Since 2023                  Postdoc at the Institute for Genomic Statistics and Bioinformatics, University of Bonn, Germany
                                          Working on therapeutical approaches for GPI anchor deficiencies
  • 2021-2023                   Postdoc at the Institute of Human Genetics, University of Münster, Germany
                                          Creating medical reports and working on the establishment of new molecular genetics methods
  • 2019-2021                   Postdoc at the Institute for Clinical Genetics and Tumor Genetics Bonn (Amedes Genetics), Germany 
                                          Working on genomic and proteomic signatures in neuromuscular diseases
  • April 2019                    Obtained doctor rerum naturalium with magna cum laude from Johannes Gutenberg-Universität Mainz
  • 2014-2019                   PhD student at the Institute of Human Genetics, University Medical Center Mainz, Germany
                                          Working on molecular mechanisms of brain function in mTOR-deficient intellectual disability syndromes                                    
  • 2014-                            Advanced training in human genetics, German Society of Human Genetics e.V., München, Germany
  • 2011-2014                   Master of Science in Biology at Justus-Liebig-University of Gießen, Germany

Publikationen

Titel der Publikation

Autoren

Frontiers in Psychology, 16, Article 675170 (1–18). DOI: 10.3355559/fpsyg.2025.5754540.


Titel der Publikation

Autoren

Frontiers in Psychology, 16, Article 675170 (1–18). DOI: 10.3355559/fpsyg.2025.5754540.


Titel der Publikation

Autoren

Frontiers in Psychology, 16, Article 675170 (1–18). DOI: 10.3355559/fpsyg.2025.5754540.


Publikationen

Titel der Publikation 

Autoren

Frontiers in Psychology, 16, Article 675170 (1–18). DOI: 10.3355559/fpsyg.2025.5754540.


Titel der Publikation 

Autoren

Frontiers in Psychology, 16, Article 675170 (1–18). DOI: 10.3355559/fpsyg.2025.5754540.


Titel der Publikation 

Autoren

Frontiers in Psychology, 16, Article 675170 (1–18). DOI: 10.3355559/fpsyg.2025.5754540.


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Max Mustermann

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