Valentina Strecker

Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency

Tobias B. Haack, Katharina Danhauser, Birgit Haberberger et al. · Nature Genetics · 2010 · 252 citations

Life Sciences, Genetics, Molecular Genetics +9

Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing

Tobias B. Haack, Birgit Haberberger, Eva-Maria Frisch et al. · Journal of Medical Genetics · 2012 · 185 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Homozygous missense mutation in <i>BOLA3</i> causes multiple mitochondrial dysfunctions syndrome in two siblings

Tobias B. Haack, Boris Rolinski, Birgit Haberberger et al. · Journal of Inherited Metabolic Disease · 2012 · 94 citations

Life Sciences, Genetics, Molecular Genetics +14

Mic13 Is Essential for Formation of Crista Junctions in Mammalian Cells

Ruchika Anand, Valentina Strecker, Jennifer Urbach et al. · PLoS ONE · 2016 · 90 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +17

Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency: is riboflavin supplementation effective?

Birgit Repp, Elisa Mastantuono, Charlotte L. Alston et al. · Orphanet Journal of Rare Diseases · 2018 · 87 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17