Merle Hillebrand

Cathepsin D Deficiency Is Associated with a Human Neurodegenerative Disorder

Robert Steinfeld, K Reinhardt, Kathrin Schreiber et al. · The American Journal of Human Genetics · 2006 · 299 citations · Full text

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Degenerative Diseases +8

Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin

Peter Huppke, Cornelia Brendel, Vera M. Kalscheuer et al. · The American Journal of Human Genetics · 2012 · 101 citations · Full text

Mendelian Disorder, Ophthalmology, Genetic Disorder +8

Live Cell FRET Microscopy

Merle Hillebrand, Sophie Verrier, Andreas Ohlenbusch et al. · Journal of Biological Chemistry · 2007 · 54 citations · Full text

Microscopy, Cellular Physiology, Microscopy Method +17

Identification of a New Fatty Acid Synthesis-Transport Machinery at the Peroxisomal Membrane

Merle Hillebrand, Søren W. Gersting, Amelie S. Lotz‐Havla et al. · Journal of Biological Chemistry · 2011 · 38 citations · Full text

Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severity

Elinor Lazarov, Merle Hillebrand, Simone Schröder et al. · Neurobiology of Disease · 2020 · 22 citations · Full text