Emeline Crutcher

The expanding clinical phenotype of germline ABL1‐associated congenital heart defects and skeletal malformations syndrome

R. Pfundt, D. Misceo, Yaping Yang, 2020, Human mutation.

Brain Network Analysis of EEG Recordings Can Be Used to Assess Cognitive Function in Teenagers With 15q13.3 Microdeletion Syndrome

A. Geva, C. Schaaf, Z. Peremen, 2021, Frontiers in Neuroscience.

mTOR and autophagy pathways are dysregulated in murine and human models of Schaaf-Yang syndrome

C. Schaaf, M. Laugsch, A. Bajić, 2019, Scientific Reports.

Inactivating histone deacetylase HDA promotes longevity by mobilizing trehalose metabolism

M. C. Jo, M. Kaeberlein, Luyang Sun, 2021, Nature Communications.

Assessment of Cognitive Outcome Measures in Teenagers with 15q13.3 Microdeletion Syndrome

C. Schaaf, B. Gomez-Mancilla, J. Sóvágó, 2016, Journal of autism and developmental disorders.