Bauer, Peter

A Revised Timescale for Human Evolution Based on Ancient Mitochondrial Genomes

Fu, Q., Mittnik, A., Johnson, P. L. F., Bos, K., Lari, M., Bollongino, R., Sun, C., Giemsch, L., Schmitz, R., Burger, J., et al. (2013) · Current Biology

Forensic and Genetic ResearchPleistocene-Era Hominins and Archaeology

Cited by 709

Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients

Schüle, R., Wiethoff, S., Martus, P., Karle, K. N., Otto, S., Klebe, S., Klimpe, S., Gallenmüller, C., Kurzwelly, D., Henkel, D., et al. (2016) · Annals of Neurology

Hereditary Neurological DisordersGenetic Neurodegenerative Diseases

Cited by 315

Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia

Schule, R., Schlipf, N., Synofzik, M., Klebe, S., Klimpe, S., Hehr, U., Winner, B., Lindig, T., Dotzer, A., Riess, O., et al. (2009) · Journal of Neurology, Neurosurgery & Psychiatry

Hereditary Neurological DisordersGenetic Neurodegenerative Diseases

Cited by 80

A comprehensive genetic study of the proteasomal subunit S6 ATPase in German Parkinson’s disease patients.

Wahl, C., Kautzmann, S., Krebiehl, G., Strauss, K., Woitalla, D., Müller, T., Bauer, P., Riess, O., & Krüger, R. (2008) · Journal of Neural Transmission

Parkinson's Disease Mechanisms and TreatmentsUbiquitin and proteasome pathways

Cited by 22

The clinical and genetic landscape of developmental and epileptic encephalopathies in Egyptian children

Elkhateeb, N., Issa, M. Y., Elbendary, H. M., Elnaggar, W., Ramadan, A., Rafat, K., Kamel, M., Abdel‐Ghafar, S. F., Amer, F., Hassaan, H. M., et al. (2024) · Clinical Genetics

Epilepsy research and treatmentGenetics and Neurodevelopmental Disorders

Cited by 7