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Carol Dobson

Showing results (71-80 of 81) with videos related to

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International Journal of Molecular Sciences|October 14, 2023
Blood-Based Transcriptomic Biomarkers Are Predictive of Neurodegeneration Rather Than Alzheimer's DiseaseArtur Shvetcov, Shannon Thomson, Jessica Spathos, et al.
Science Advances|May 5, 2023
Short tandem repeat expansions in sporadic amyotrophic lateral sclerosis and frontotemporal dementiaLyndal Henden, Liam G Fearnley, Natalie Grima, et al.
Journal of Integrative Neuroscience|May 3, 2007
Integrating objective gene-brain-behavior markers of psychiatric disordersEvian Gordon, Belinda J Liddell, Kerri J Brown, et al.
Human Molecular Genetics|May 21, 2026
Ultra-rare variants in LAMA2 are risk factors for frontotemporal dementia and motor neuron diseaseHiu Chuen Lok, Carol Dobson-Stone, Marianne Hallupp, et al.
Brain : a Journal of Neurology|March 19, 2020
CYLD is a causative gene for frontotemporal dementia - amyotrophic lateral sclerosisCarol Dobson-Stone, Marianne Hallupp, Hamideh Shahheydari, et al.
Nature Communications|April 16, 2016
CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementiaKelly L Williams, Simon Topp, Shu Yang, et al.
Acta Neuropathologica|January 21, 2014
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansionsMichael D Gallagher, Eunran Suh, Murray Grossman, et al.
Brain : a Journal of Neurology|September 26, 2018
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriersMing Zhang, Raffaele Ferrari, Maria Carmela Tartaglia, et al.
American Journal of Human Genetics|June 18, 2024
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementiaClaudia Manzoni, Demis A Kia, Raffaele Ferrari, et al.
The Lancet. Neurology|June 20, 2014
Frontotemporal dementia and its subtypes: a genome-wide association studyRaffaele Ferrari, Dena G Hernandez, Michael A Nalls, et al.
Pageof 9

Showing results (71-80 of 81) with videos related to

Sort By:
Pageof 9
International Journal of Molecular Sciences|October 14, 2023
Blood-Based Transcriptomic Biomarkers Are Predictive of Neurodegeneration Rather Than Alzheimer's DiseaseArtur Shvetcov, Shannon Thomson, Jessica Spathos, et al.
Science Advances|May 5, 2023
Short tandem repeat expansions in sporadic amyotrophic lateral sclerosis and frontotemporal dementiaLyndal Henden, Liam G Fearnley, Natalie Grima, et al.
Journal of Integrative Neuroscience|May 3, 2007
Integrating objective gene-brain-behavior markers of psychiatric disordersEvian Gordon, Belinda J Liddell, Kerri J Brown, et al.
Human Molecular Genetics|May 21, 2026
Ultra-rare variants in LAMA2 are risk factors for frontotemporal dementia and motor neuron diseaseHiu Chuen Lok, Carol Dobson-Stone, Marianne Hallupp, et al.
Brain : a Journal of Neurology|March 19, 2020
CYLD is a causative gene for frontotemporal dementia - amyotrophic lateral sclerosisCarol Dobson-Stone, Marianne Hallupp, Hamideh Shahheydari, et al.
Nature Communications|April 16, 2016
CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementiaKelly L Williams, Simon Topp, Shu Yang, et al.
Acta Neuropathologica|January 21, 2014
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansionsMichael D Gallagher, Eunran Suh, Murray Grossman, et al.
Brain : a Journal of Neurology|September 26, 2018
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriersMing Zhang, Raffaele Ferrari, Maria Carmela Tartaglia, et al.
American Journal of Human Genetics|June 18, 2024
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementiaClaudia Manzoni, Demis A Kia, Raffaele Ferrari, et al.
The Lancet. Neurology|June 20, 2014
Frontotemporal dementia and its subtypes: a genome-wide association studyRaffaele Ferrari, Dena G Hernandez, Michael A Nalls, et al.
Pageof 9