Birgitt Schule, MD
Affiliations: | 2019- | Pathology | Stanford University Medical School |
Area:
Parkinson's disease; neurodegeneration; stem cell modeling; human geneticsGoogle:
"Birgitt Schule"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Christine Klein | post-doc | 2001-2002 | Medical School Lubeck |
| Uta Francke | post-doc | 2003-2005 | Stanford University Medical School (GenetiTree) |
| J. William Langston | research scientist | 2005-2019 | The Parkinson's Institute |
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Publications
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| Sastre D, Zafar F, Torres CAM, et al. (2023) Inactive S. aureus Cas9 downregulates alpha-synuclein and reduces mtDNA damage and oxidative stress levels in human stem cell model of Parkinson's disease. Scientific Reports. 13: 17796 |
| Sastre D, Zafar F, Torres CAM, et al. (2023) Nuclease-dead S. Cas9 downregulates alpha-synuclein and reduces mtDNA damage and oxidative stress levels in patient-derived stem cell model of Parkinson's disease. Biorxiv : the Preprint Server For Biology |
| Zafar F, Nallur Srinivasaraghavan V, Yang Chen M, et al. (2022) Isogenic human SNCA gene dosage induced pluripotent stem cells to model Parkinson's disease. Stem Cell Research. 60: 102733 |
| Napolioni V, Fredericks CA, Kim Y, et al. (2022) Phenotypic Heterogeneity among p.R202X Carriers in Lewy Body Spectrum Disorders. Biomedicines. 10 |
| Lai D, Alipanahi B, Fontanillas P, et al. (2021) Genome-wide association studies of LRRK2 modifiers of Parkinson's disease. Annals of Neurology |
| Eis PS, Huang N, Langston JW, et al. (2020) Loss-of-Function Mutation May Link Parkinson's Disease to Recessive Complex I Deficiency. Frontiers in Neurology. 11: 555961 |
| Morato Torres CA, Wassouf Z, Zafar F, et al. (2020) The Role of Alpha-Synuclein and Other Parkinson's Genes in Neurodevelopmental and Neurodegenerative Disorders. International Journal of Molecular Sciences. 21 |
| San Luciano M, Tanner CM, Meng C, et al. (2020) Nonsteroidal Anti-Inflammatory Use and LRRK2 Parkinson's Disease Penetrance. Movement Disorders : Official Journal of the Movement Disorder Society |
| da Costa Almeida CB, Welter AT, Abech GD, et al. (2020) Report of the Phenotype of a Patient with Roberts Syndrome and a Rare Variant. Journal of Pediatric Genetics. 9: 58-62 |
| Candelario KM, Balaj L, Zheng T, et al. (2019) Exosome/Microvesicle Content is Altered in LRRK2 Mutant iPSC-derived Neural Cells. The Journal of Comparative Neurology |