Craig Blackstone

Craig Blackstone

Harvard University

H-index: 67

North America-United States

About Craig Blackstone

Craig Blackstone, With an exceptional h-index of 67 and a recent h-index of 39 (since 2020), a distinguished researcher at Harvard University, specializes in the field of Neurology, Neurogenetics, Cell Biology.

His recent articles reflect a diverse array of research interests and contributions to the field:

Motion of VAPB molecules reveals ER–mitochondria contact site subdomains

Getting to the heart of Lewy body disease

Neuropathy target esterase activity predicts retinopathy among PNPLA6 disorders

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

The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15

Chenodeoxycholic acid rescues axonal degeneration in induced pluripotent stem cell-derived neurons from spastic paraplegia type 5 and cerebrotendinous xanthomatosis patients

Ligand-free mitochondria-localized mutant AR-induced cytotoxicity in spinal bulbar muscular atrophy

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

Craig Blackstone Information

University

Position

Chief, Movement Disorders Division, Massachusetts General Hospital

Citations(all)

30185

Citations(since 2020)

10912

Cited By

21649

hIndex(all)

67

hIndex(since 2020)

39

i10Index(all)

122

i10Index(since 2020)

87

Email

University Profile Page

Harvard University

Google Scholar

View Google Scholar Profile

Craig Blackstone Skills & Research Interests

Neurology

Neurogenetics

Cell Biology

Top articles of Craig Blackstone

Title

Journal

Author(s)

Publication Date

Motion of VAPB molecules reveals ER–mitochondria contact site subdomains

Nature

Christopher J Obara

Jonathon Nixon-Abell

Andrew S Moore

Federica Riccio

David P Hoffman

...

2024/1/24

Getting to the heart of Lewy body disease

The Journal of Clinical Investigation

Anna E Goodheart

Craig Blackstone

2024/1/2

Neuropathy target esterase activity predicts retinopathy among PNPLA6 disorders

bioRxiv

James Liu

Yi He

Cara Lwin

Marina Han

Bin Guan

...

2023

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

Human Molecular Genetics

Julian E Alecu

Afshin Saffari

Catherine Jordan

Siddharth Srivastava

Craig Blackstone

...

2023/1/1

The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15

Brain

Afshin Saffari

Melanie Kellner

Catherine Jordan

Helena Rosengarten

Alisa Mo

...

2023/5/2

Chenodeoxycholic acid rescues axonal degeneration in induced pluripotent stem cell-derived neurons from spastic paraplegia type 5 and cerebrotendinous xanthomatosis patients

Orphanet Journal of Rare Diseases

Yongchao Mou

Ghata Nandi

Sukhada Mukte

Eric Chai

Zhenyu Chen

...

2023/4/6

Ligand-free mitochondria-localized mutant AR-induced cytotoxicity in spinal bulbar muscular atrophy

Brain

Xia Feng

Xiu-Tang Cheng

Pengli Zheng

Yan Li

Jill Hakim

...

2023/1/4

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

Nature Communications

Huan Yang

Caroline Sibilla

Raymond Liu

Jina Yun

Bruce A Hay

...

2022/3/24

Transverse endoplasmic reticulum expansion in hereditary spastic paraplegia corticospinal axons

Human Molecular Genetics

Peng-Peng Zhu

Hui-Fang Hung

Natalia Batchenkova

Jonathon Nixon-Abell

James Henderson

...

2022/8/15

Publisher Correction: ER proteins decipher the tubulin code to regulate organelle distribution

Nature

Pengli Zheng

Christopher J Obara

Ewa Szczesna

Jonathon Nixon-Abell

Kishore K Mahalingan

...

2022

Nonalcoholic fatty liver disease in patients with inherited and sporadic motor neuron degeneration

Djuro Macut

Jelica Bjekić-Macut

Sarantis Livadas

Olivera Stanojlović

Dragan Hrnčić

...

2018/10/1

Early‐Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST

Movement Disorders

Alisa Mo

Afshin Saffari

Melanie Kellner

Marion Döbler‐Neumann

Catherine Jordan

...

2022/12

ER proteins decipher the tubulin code to regulate organelle distribution (Mar, 10.1038/s41586-021-04204-9, 2022)

Nature

Pengli Zheng

Christopher J Obara

Ewa Szczesna

Jonathon Nixon-Abell

Kishore K Mahalingan

...

2022/1/6

Inhibiting mitochondrial fission rescues degeneration in hereditary spastic paraplegia neurons

Brain

Zhenyu Chen

Eric Chai

Yongchao Mou

Ricardo H Roda

Craig Blackstone

...

2022/1/13

Liver X receptor-agonist treatment rescues degeneration in a Drosophila model of hereditary spastic paraplegia

Acta Neuropathologica Communications

Dwayne J Byrne

M Elena Garcia-Pardo

Nelson B Cole

Belguun Batnasan

Sophia Heneghan

...

2022/3/28

Importance of genetic testing for childhood-onset hereditary spastic paraplegia.

Developmental Medicine and Child Neurology

Craig Blackstone

2022/9/27

An integrated modelling methodology for estimating global incidence and prevalence of hereditary spastic paraplegia subtypes SPG4, SPG7, SPG11, and SPG15

BMC neurology

Geert Vander Stichele

Alexandra Durr

Grace Yoon

Rebecca Schüle

Craig Blackstone

...

2022/3/24

Motion of single molecular tethers reveals dynamic subdomains at ER-mitochondria contact sites

bioRxiv

Christopher J Obara

Jonathon Nixon-Abell

Andrew S Moore

Federica Riccio

David P Hoffman

...

2022/9/3

Spastic paraplegia 15

Darius Ebrahimi-Fakhari

Julian E Alecu

Craig Blackstone

2021/6/1

Expanding the Spectrum of AP5Z1‐Related Hereditary Spastic Paraplegia (HSP‐SPG48): A Multicenter Study on a Rare Disease

Movement Disorders

Marianthi Breza

Jennifer Hirst

Viorica Chelban

Guillaume Banneau

Laurène Tissier

...

2021/4

See List of Professors in Craig Blackstone University(Harvard University)

Co-Authors

H-index: 162
Allan I Levey, MD, PhD

Allan I Levey, MD, PhD

Emory University

H-index: 152
Richard L Huganir

Richard L Huganir

Johns Hopkins University

H-index: 102
Stephen Moss

Stephen Moss

Tufts University

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