Simon Schnaiter

Low‐level mosaicism in tuberous sclerosis complex in four unrelated patients: Comparison of clinical characteristics and diagnostic pathways

S. Rudnik-Schöneborn, H. Manzanilla-Romero, Denisa Weis, 2021, American journal of medical genetics. Part A.

Oncotyrol--Center for Personalized Cancer Medicine: Methods and Applications of Health Technology Assessment and Outcomes Research.

U. Siebert, N. Mühlberger, B. Jahn, 2015, Zeitschrift fur Evidenz, Fortbildung und Qualitat im Gesundheitswesen.

Ca2+/Calmodulin-dependent kinase II signaling causes skeletal overgrowth and premature chondrocyte maturation.

C. Hartmann, M. Taschner, Simon Schnaiter, 2008, Developmental biology.

Array genotyping as diagnostic approach in medical genetics

J. Zschocke, M. Witsch-Baumgartner, P. Kirchmeier, 2022, Molecular genetics & genomic medicine.

Teenage-Onset Colorectal Cancers in a Digenic Cancer Predisposition Syndrome Provide Clues for the Interaction between Mismatch Repair and Polymerase δ Proofreading Deficiency in Tumorigenesis

K. Wimmer, N. Friedrichs, J. Zschocke, 2022, Biomolecules.

Genotype-phenotype associations in a large PTEN Hamartoma Tumor Syndrome (PHTS) patient cohort.

J. Schuurs-Hoeijmakers, M. Genuardi, T. Kleefstra, 2022, European journal of medical genetics.