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Publications by Stefan Vollmar

A Model for Ageing With Hereditary Mutations

Journal de Physique I

English

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Hereditary Breast Cancer: Mutations Within BRCA1 and BRCA2 With Phenotypic Responses

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Hereditary Spastic Paraplegia-Causing Mutations in Atlastin-1 Interfere With BMPRII Trafficking

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Dynein Mutations Associated With Hereditary Motor Neuropathies Impair Mitochondrial Morphology and Function With Age

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Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia

American Journal of Human Genetics

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Existence and Stability Estimate for the Solution of the Ageing Hereditary Linear Viscoelasticity Problem

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Truncating Mutations inSPASTpatients Are Associated With a High Rate of Psychiatric Comorbidities in Hereditary Spastic Paraplegia

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Explanations of Risk in Families Without Identified Mutations for Hereditary Nonpolyposis Colorectal Cancer

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Beneficial Effects of Rapamycin in a Drosophila Model for Hereditary Spastic Paraplegia

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Olaparib Significantly Delays Photoreceptor Loss in a Model for Hereditary Retinal Degeneration

Scientific Reports

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