Concepedia
Statistics
Publications
3
Citations
249
H-Index
Active since
2010
Affiliations
Helmholtz Zentrum München(Current)
Radboud University Nijmegen
Technical University of Munich
Newcastle University
Paracelsus Medical University
Martina Herzer is an author at Helmholtz Zentrum München specializing in molecular genetics, genetics, and mitochondrial genetics.
Publications per year
2010–2011
Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy
John F. O’Toole, Yangjian Liu, Erica E. Davis et al. · Journal of Clinical Investigation · 2010 · 118 citations · Full text
Medicine, Genetics, Molecular Genetics +16
Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including <i>NDUFB9</i>
Tobias B. Haack, Florence Madignier, Martina Herzer et al. · Journal of Medical Genetics · 2011 · 93 citations
Life Sciences, Genetics, Molecular Genetics +15
Leigh Disease with Brainstem Involvement in Complex I Deficiency due to Assembly Factor NDUFAF2 Defect
Martina Herzer, Johannes Koch, Holger Prokisch et al. · Neuropediatrics · 2010 · 38 citations
Medicine, Genetics, Molecular Genetics +7
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