Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Ruth Chia

Showing results (51-60 of 69) with videos related to

Pageof 7
Sort By:
Communications Biology|January 5, 2024
Differential methylation analysis in neuropathologically confirmed dementia with Lewy bodiesPaolo Reho, Sara Saez-Atienzar, Paola Ruffo, et al.
Brain : a Journal of Neurology|March 30, 2026
Clinical and biochemical characterization of amyotrophic lateral sclerosis in a CHCHD10 R15L familyJustin Y Kwan, Christian I Lantz, Vlad A Korobeynikov, et al.
Neurology. Genetics|June 9, 2023
Cumulative Genetic Score and John Dou, Kelly Bakulski, Kai Guo, et al.
Neurology. Genetics|July 31, 2023
Erratum: Cumulative Genetic Score and C9orf72 Repeat Status Independently Contribute to Amyotrophic Lateral Sclerosis Risk in 2 Case-Control StudiesJohn Dou, Kelly Bakulski, Kai Guo, et al.
Brain : a Journal of Neurology|April 22, 2026
Machine learning model based on plasma proteomics for the identification of Parkinson's diseaseBoluwatife Adewale, Ruth Chia, Ruin Moaddel, et al.
Nature Medicine|August 19, 2025
A plasma proteomics-based candidate biomarker panel predictive of amyotrophic lateral sclerosisRuth Chia, Ruin Moaddel, Justin Y Kwan, et al.
Nature Neuroscience|April 2, 2014
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosisJanel O Johnson, Erik P Pioro, Ashley Boehringer, et al.
Medrxiv : the Preprint Server for Health Sciences|February 13, 2023
<i>HLA</i> in isolated REM sleep behavior disorder and Lewy body dementiaEric Yu, Lynne Krohn, Jennifer A Ruskey, et al.
Neurobiology of Aging|June 13, 2017
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseasesCornelis Blauwendraat, Faraz Faghri, Lasse Pihlstrom, et al.
Annals of Neurology|January 25, 2023
Genome-Wide Analysis of Structural Variants in Parkinson DiseaseKimberley J Billingsley, Jinhui Ding, Pilar Alvarez Jerez, et al.
Pageof 7

Showing results (51-60 of 69) with videos related to

Sort By:
Pageof 7
Communications Biology|January 5, 2024
Differential methylation analysis in neuropathologically confirmed dementia with Lewy bodiesPaolo Reho, Sara Saez-Atienzar, Paola Ruffo, et al.
Brain : a Journal of Neurology|March 30, 2026
Clinical and biochemical characterization of amyotrophic lateral sclerosis in a CHCHD10 R15L familyJustin Y Kwan, Christian I Lantz, Vlad A Korobeynikov, et al.
Neurology. Genetics|June 9, 2023
Cumulative Genetic Score and John Dou, Kelly Bakulski, Kai Guo, et al.
Neurology. Genetics|July 31, 2023
Erratum: Cumulative Genetic Score and C9orf72 Repeat Status Independently Contribute to Amyotrophic Lateral Sclerosis Risk in 2 Case-Control StudiesJohn Dou, Kelly Bakulski, Kai Guo, et al.
Brain : a Journal of Neurology|April 22, 2026
Machine learning model based on plasma proteomics for the identification of Parkinson's diseaseBoluwatife Adewale, Ruth Chia, Ruin Moaddel, et al.
Nature Medicine|August 19, 2025
A plasma proteomics-based candidate biomarker panel predictive of amyotrophic lateral sclerosisRuth Chia, Ruin Moaddel, Justin Y Kwan, et al.
Nature Neuroscience|April 2, 2014
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosisJanel O Johnson, Erik P Pioro, Ashley Boehringer, et al.
Medrxiv : the Preprint Server for Health Sciences|February 13, 2023
<i>HLA</i> in isolated REM sleep behavior disorder and Lewy body dementiaEric Yu, Lynne Krohn, Jennifer A Ruskey, et al.
Neurobiology of Aging|June 13, 2017
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseasesCornelis Blauwendraat, Faraz Faghri, Lasse Pihlstrom, et al.
Annals of Neurology|January 25, 2023
Genome-Wide Analysis of Structural Variants in Parkinson DiseaseKimberley J Billingsley, Jinhui Ding, Pilar Alvarez Jerez, et al.
Pageof 7