C. Rohr

Serum aminotransferases in nonalcoholic fatty liver disease are a signature of liver metabolic perturbations at the amino acid and Krebs cycle level.

H. Dopazo, S. Sookoian, G. Castaño, 2016, The American journal of clinical nutrition.

Mitochondrial genome architecture in non‐alcoholic fatty liver disease

H. Dopazo, S. Sookoian, T. Gianotti, 2016, The Journal of pathology.

Exome-first approach identified novel INDELs and gene deletions in Mowat-Wilson Syndrome patients

F. Fay, G. Méjico, Bianca Brun, 2018, Human Genome Variation.