Bernd Rautenstrauß
Medical Genetics Center(DE)Bayer (Germany)(DE)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Genetic Neurodegenerative Diseases, Neurological diseases and metabolism, Glaucoma and retinal disorders, Cellular Mechanics and Interactions
Most-Cited Works
- → Mutations in a Gene Encoding a Novel SH3/TPR Domain Protein Cause Autosomal Recessive Charcot-Marie-Tooth Type 4C Neuropathy(2003)210 cited
- → Transcriptional regulator PRDM12 is essential for human pain perception(2015)171 cited
- → Mechanisms for Nonrecurrent Genomic Rearrangements Associated with CMT1A or HNPP: Rare CNVs as a Cause for Missing Heritability(2010)161 cited
- → Heterozygous NTF4 Mutations Impairing Neurotrophin-4 Signaling in Patients with Primary Open-Angle Glaucoma(2009)143 cited
- → An Organismal CNV Mutator Phenotype Restricted to Early Human Development(2017)112 cited
- → Widespread expression of the peripheral myelin protein‐22 gene (pmp22) in neural and non‐neural tissues during murine development(1995)106 cited