The molecular pathogenesis of schwannomatosis, a paradigm for the co-involvement of multiple tumour suppressor genes in tumorigenesis
2016 · Human Genetics · 152 citations
https://doi.org/10.1007/s00439-016-1753-8
S
Said Farschtschi
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Said Farschtschi is an academic researcher from Universität Hamburg. The author has contributed to research in topics: Neurofibromatosis and Schwannoma Cases & Meningioma and schwannoma management & Sarcoma Diagnosis and Treatment. The author has an h-index of 24, co-authored 74 publications.
ORCID: 0000-0002-3596-5932Papers by this author
worksERN GENTURIS tumour surveillance guidelines for individuals with neurofibromatosis type 1
2023 · EClinicalMedicine · 105 citations
https://doi.org/10.1016/j.eclinm.2022.101818
Non-optic glioma in adults and children with neurofibromatosis 1
2017 · Orphanet Journal of Rare Diseases · 47 citations
https://doi.org/10.1186/s13023-017-0588-2
Clinical characterization of children and adolescents with NF1 microdeletions
2020 · Child s Nervous System · 30 citations
https://doi.org/10.1007/s00381-020-04717-0
Keratinocytic epidermal nevus syndrome with Schwann cell proliferation, lipomatous tumour and mosaic KRAS mutation
2015 · BMC Medical Genetics · 29 citations
https://doi.org/10.1186/s12881-015-0146-5
Long-term Follow-up and Histological Correlation of Peripheral Nervous System Alterations in Neurofibromatosis Type 2
2021 · Clinical Neuroradiology · 7 citations
https://doi.org/10.1007/s00062-021-01102-5
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