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J Raphael Gibbs

Showing results (11-20 of 140) with videos related to

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Neurobiology of Aging|December 14, 2020
Replication assessment of NUS1 variants in Parkinson's diseaseBernabe I Bustos, Sara Bandres-Ciga, J Raphael Gibbs, et al.
Science Translational Medicine|July 27, 2022
Association of a common genetic variant with Parkinson's disease is mediated by microgliaRebekah G Langston, Alexandra Beilina, Xylena Reed, et al.
Brain : a Journal of Neurology|November 8, 2022
Genome-wide contribution of common short-tandem repeats to Parkinson's disease genetic riskBernabe I Bustos, Kimberley Billingsley, Cornelis Blauwendraat, et al.
Biorxiv : the Preprint Server for Biology|October 3, 2025
Integrative analysis reveals generalizable human neurodegenerative disease-associated glial statesLiam Horan-Portelance, Dominic J Acri, Alexandra Mann, et al.
NPJ Parkinson'S Disease|February 20, 2024
Genetic analysis of the X chromosome in people with Lewy body dementia nominates new risk lociEce Bayram, Paolo Reho, Irene Litvan, et al.
Nature Neuroscience|February 19, 2013
mRNA expression, splicing and editing in the embryonic and adult mouse cerebral cortexAllissa A Dillman, David N Hauser, J Raphael Gibbs, et al.
Human Mutation|November 13, 2007
Genomewide SNP assay reveals mutations underlying Parkinson diseaseJavier Simon-Sanchez, Sonja Scholz, Maria del Mar Matarin, et al.
Muscle & Nerve|January 1, 2017
Exome sequencing establishes a gelsolin mutation as the cause of inherited bulbar-onset neuropathyJames B Caress, Janel O Johnson, Yevgeniya A Abramzon, et al.
Scientific Reports|March 19, 2021
Exploring dementia and neuronal ceroid lipofuscinosis genes in 100 FTD-like patients from 6 towns and rural villages on the Adriatic Sea cost of ApuliaCeleste Sassi, Rosa Capozzo, Monia Hammer, et al.
Scientific Reports|December 6, 2017
Transcriptomic profiling of the human brain reveals that altered synaptic gene expression is associated with chronological agingAllissa A Dillman, Elisa Majounie, Jinhui Ding, et al.
Pageof 14

Showing results (11-20 of 140) with videos related to

Sort By:
Pageof 14
Neurobiology of Aging|December 14, 2020
Replication assessment of NUS1 variants in Parkinson's diseaseBernabe I Bustos, Sara Bandres-Ciga, J Raphael Gibbs, et al.
Science Translational Medicine|July 27, 2022
Association of a common genetic variant with Parkinson's disease is mediated by microgliaRebekah G Langston, Alexandra Beilina, Xylena Reed, et al.
Brain : a Journal of Neurology|November 8, 2022
Genome-wide contribution of common short-tandem repeats to Parkinson's disease genetic riskBernabe I Bustos, Kimberley Billingsley, Cornelis Blauwendraat, et al.
Biorxiv : the Preprint Server for Biology|October 3, 2025
Integrative analysis reveals generalizable human neurodegenerative disease-associated glial statesLiam Horan-Portelance, Dominic J Acri, Alexandra Mann, et al.
NPJ Parkinson'S Disease|February 20, 2024
Genetic analysis of the X chromosome in people with Lewy body dementia nominates new risk lociEce Bayram, Paolo Reho, Irene Litvan, et al.
Nature Neuroscience|February 19, 2013
mRNA expression, splicing and editing in the embryonic and adult mouse cerebral cortexAllissa A Dillman, David N Hauser, J Raphael Gibbs, et al.
Human Mutation|November 13, 2007
Genomewide SNP assay reveals mutations underlying Parkinson diseaseJavier Simon-Sanchez, Sonja Scholz, Maria del Mar Matarin, et al.
Muscle & Nerve|January 1, 2017
Exome sequencing establishes a gelsolin mutation as the cause of inherited bulbar-onset neuropathyJames B Caress, Janel O Johnson, Yevgeniya A Abramzon, et al.
Scientific Reports|March 19, 2021
Exploring dementia and neuronal ceroid lipofuscinosis genes in 100 FTD-like patients from 6 towns and rural villages on the Adriatic Sea cost of ApuliaCeleste Sassi, Rosa Capozzo, Monia Hammer, et al.
Scientific Reports|December 6, 2017
Transcriptomic profiling of the human brain reveals that altered synaptic gene expression is associated with chronological agingAllissa A Dillman, Elisa Majounie, Jinhui Ding, et al.
Pageof 14