Area of research
Genetics · Sensory Systems
Research interest
Research focused on Haploinsufficiency and Autism spectrum disorder, with related work in Phenotype, Hearing loss, p38 mitogen-activated protein kinases. Notable publications include 'Haploinsufficiency of the Notch Ligand DLL1 Causes Variable Neurodevelopmental Disorders', 'Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases', and 'Variability in Cochlear Implantation Outcomes in a Large German Cohort With a Genetic Etiology of Hearing Loss'.
Variability in Cochlear Implantation Outcomes in a Large German Cohort With a Genetic Etiology of Hearing Loss
Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases
Haploinsufficiency of the Notch Ligand DLL1 Causes Variable Neurodevelopmental Disorders
Selective p38α MAP kinase/MAPK14 inhibition in enzymatically modified LDL‐stimulated human monocytes: implications for atherosclerosis