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Craig Blackstone

National Institute of Neurological Disorders and Stroke · US
Area of research
Cellular and Molecular Neuroscience · Neurology
Research interest
Research interests include Biology, Cell biology, Endoplasmic reticulum, Organelle, Hereditary spastic paraplegia, and Genetics.
h-index
citations
1,634
works
15
NIH funding
primary concept
email

Recent publications

Motion of VAPB molecules reveals ER–mitochondria contact site subdomains
Nature 2024cited by 114position: middledoi
Neuropathy target esterase activity defines phenotypes among <i>PNPLA6</i> disorders
Brain 2024cited by 8position: middledoi
Clueless/CLUH regulates mitochondrial fission by promoting recruitment of Drp1 to mitochondria
Nature Communications 2022cited by 53position: middledoi
Transverse endoplasmic reticulum expansion in hereditary spastic paraplegia corticospinal axons
Human Molecular Genetics 2022cited by 28position: lastdoi
Publisher Correction: ER proteins decipher the tubulin code to regulate organelle distribution
Nature 2022cited by 4position: lastdoi
ER proteins decipher the tubulin code to regulate organelle distribution
Nature 2021cited by 160position: lastdoi
Impaired lipid metabolism in astrocytes underlies degeneration of cortical projection neurons in hereditary spastic paraplegia
Acta Neuropathologica Communications 2020cited by 54position: middledoi
Spastin tethers lipid droplets to peroxisomes and directs fatty acid trafficking through ESCRT-III
The Journal of Cell Biology 2019cited by 200position: middledoi
Chronic Dengue Virus Panencephalitis in a Patient with Progressive Dementia with Extrapyramidal Features
Annals of Neurology 2019cited by 48position: middledoi
Impaired mitochondrial dynamics underlie axonal defects in hereditary spastic paraplegias
Human Molecular Genetics 2018cited by 50position: middledoi
Increased spatiotemporal resolution reveals highly dynamic dense tubular matrices in the peripheral ER
Science 2016cited by 485position: middledoi
Loss of AP-5 results in accumulation of aberrant endolysosomes: defining a new type of lysosomal storage disease
Human Molecular Genetics 2015cited by 94position: middledoi
Mutation in<i>CPT1C</i>Associated With Pure Autosomal Dominant Spastic Paraplegia
JAMA Neurology 2015cited by 77position: middledoi
A Conserved Role for Atlastin GTPases in Regulating Lipid Droplet Size
Cell Reports 2013cited by 166position: middledoi
Hereditary Spastic Paraplegia Type 43 (SPG43) is Caused by Mutation in<i>C19orf12</i>
Human Mutation 2013cited by 93position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Jonathon Nixon‐Abell · Wellcome/MRC Cambridge Stem Cell Institute5 papers (2016–2024)Jennifer Lippincott‐Schwartz · Northwestern University5 papers (2016–2024)Harald F. Hess · Integral Consulting (United States)4 papers (2016–2024)Christopher J. Obara · National Institute of Allergy and Infectious Diseases4 papers (2016–2024)C. Shan Xu · Howard Hughes Medical Institute4 papers (2016–2024)H. Amalia Pasolli · Rockefeller University3 papers (2016–2024)Pengli Zheng · National Institute of Neurological Disorders and Stroke3 papers (2021–2022)Kishore K. Mahalingan · National Institute of Neurological Disorders and Stroke2 papers (2021–2022)Aubrey V. Weigel · Imaging Center2 papers (2016–2019)Benoît Renvoisé · National Institute of Neurological Disorders and Stroke2 papers (2015–2022)Xue-Jun Li · University of Illinois Urbana-Champaign2 papers (2018–2020)Yongchao Mou · University of Illinois Chicago2 papers (2018–2020)Giovanni Stévanin · Centre Hospitalier Universitaire de Bordeaux2 papers (2015–2015)Antonina Roll‐Mecak · National Heart Lung and Blood Institute2 papers (2021–2022)Alexandra Dürr · Centre National de la Recherche Scientifique2 papers (2015–2015)Jaerak Chang · Center for Cancer Research2 papers (2015–2018) · 2 papers (2018–2020)Gleb Shtengel · Helix (United States)2 papers (2019–2024)Ewa Szczęsna · National Institute of Neurological Disorders and Stroke2 papers (2021–2022)Ilya Kister · Multiple Sclerosis Center Of Northeastern New York1 papers (2019–2019)