Holger Prokisch 

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    'Dr. Holger Prokisch' (19 chars)
    
                                
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    'TUM Klinikum' (12 chars)
    
                                
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    'Dr. Holger Prokisch is the head of the research group “Genetics of  Mitochon
     drial Diseases” at the Institute of Human Genetics, School of  Medicine, TUM
      Klinikum, and the Institute of Neurogenomics, Department  of Computational 
     Health, Helmholtz Munich, Germany <br />&nbsp;<br />Holger  Prokisch explore
     s genetic variation in both rare and common diseases  with a functional focu
     s on mitochondria-related disease mechanisms. His  group was successful in i
     ntegrating genomic approaches with detailed  functional biochemical investig
     ations. Holger Prokisch contributed to  the discovery of more than 80 novel 
     disease genes, by applying whole  exome and genome sequencing. He extended t
     he diagnostic toolbox by  establishing RNA-sequencing and proteomics pipelin
     es for the diagnosis  of Mendelian diseases. Much of his work is focused on 
     advanced  diagnostics by multi-omics integration. He coordinates the German 
      network for mitochondrial disorders and two Eurasian networks, the  GENOMIT
      network for mitochondrial disorders (EJP RD), and the  Personalized Mitocho
     ndrial Medicine network, PerMiM (ERA PerMed). In  2024 the German Society of
      Human Genetics honored Holger Prokisch with  its most prestigious award, th
     e GfH Medal of Honour.
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