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Craig Blackstone

ORCID

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 9

Top Venues

Developmental medicine and child neurology

Human molecular genetics

Science signaling

Brain sciences

National Institutes of Health

Johns Hopkins School of Medicine (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

National Institutes of Health Sep 1o 2001

United States

Senior Investigator :: NINDS

Education History

Johns Hopkins School of Medicine

United States

PHD :: Neuroscience

Publications

Craig Blackstone
Importance of genetic testing for childhood-onset hereditary spastic paraplegia. Developmental medicine and child neurology (2022)
Julian Emanuel Alecu, Afshin Saffari, Catherine Jordan, Siddharth Srivastava, Craig Blackstone, Darius Ebrahimi-Fakhari
De novo variants cause complex symptoms in HSP-ATL1 (SPG3A) and uncover genotype-phenotype correlations. Human molecular genetics (2022)
Huan Yang, Caroline Sibilla, Raymond Liu, Jina Yun, Bruce A Hay, Craig Blackstone, David C Chan, Robert J Harvey, Ming Guo
Clueless/CLUH regulates mitochondrial fission by promoting recruitment of Drp1 to mitochondria. Nature communications 13 (1) (2022)
Peng-Peng Zhu, Hui-Fang Hung, Natalia Batchenkova, Jonathon Nixon-Abell, James Henderson, Pengli Zheng, Benoit Renvoisé, Song Pang, C Shan Xu, Stephan Saalfeld, Jan Funke, Yuxiang Xie, Fabian Svara, Harald F Hess, Craig Blackstone
Transverse endoplasmic reticulum expansion in hereditary spastic paraplegia corticospinal axons. Human molecular genetics 31 (16) (2022)
Pengli Zheng, Christopher J Obara, Ewa Szczesna, Jonathon Nixon-Abell, Kishore K Mahalingan, Antonina Roll-Mecak, Jennifer Lippincott-Schwartz, Craig Blackstone
ER proteins decipher the tubulin code to regulate organelle distribution. Nature 601 (7891) (2021)
Philippa C Fowler, Dwayne J Byrne, Craig Blackstone, Niamh C O'Sullivan
Loss of the Mitochondrial Fission GTPase Drp1 Contributes to Neurodegeneration in a Drosophila Model of Hereditary Spastic Paraplegia. Brain sciences 10 (9) (2020)
Craig Blackstone
Early-onset hereditary spastic paraplegia: the possibility of a genetic diagnosis. Developmental medicine and child neurology 62 (9) (2020)
Seongju Lee, Hyungsun Park, Peng-Peng Zhu, Soon-Young Jung, Craig Blackstone, Jaerak Chang
Hereditary spastic paraplegia SPG8 mutations impair CAV1-dependent, integrin-mediated cell adhesion. Science signaling 13 (613) (2020)
Chi-Lun Chang, Aubrey V Weigel, Maria S Ioannou, H Amalia Pasolli, C Shan Xu, David R Peale, Gleb Shtengel, Melanie Freeman, Harald F Hess, Craig Blackstone, Jennifer Lippincott-Schwartz
Spastin tethers lipid droplets to peroxisomes and directs fatty acid trafficking through ESCRT-III. The Journal of cell biology 218 (8) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Craig Blackstone