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List of works by Craig Blackstone

<i>De novo</i> variants cause complex symptoms in HSP-<i>ATL1</i> (SPG3A) and uncover genotype–phenotype correlations

scientific article published in 2022

Clueless/CLUH regulates mitochondrial fission by promoting recruitment of Drp1 to mitochondria

scientific article published on 24 March 2022

Early-onset hereditary spastic paraplegia: the possibility of a genetic diagnosis

scientific article published on 18 May 2020

Hereditary spastic paraplegia SPG8 mutations impair CAV1-dependent, integrin-mediated cell adhesion

scientific article published on 07 January 2020

Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12

scientific article

Loss of AP-5 results in accumulation of aberrant endolysosomes: defining a new type of lysosomal storage disease

scientific article published on 17 June 2015

Loss of the Mitochondrial Fission GTPase Drp1 Contributes to Neurodegeneration in a Drosophila Model of Hereditary Spastic Paraplegia

scientific article published on 17 September 2020

Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia

scientific article

Spastin tethers lipid droplets to peroxisomes and directs fatty acid trafficking through ESCRT-III

scientific article published on 21 June 2019

Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases

scientific article

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