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

Matthew B Harms

Showing results (11-20 of 68) with videos related to

Pageof 7
Sort By:
Genetic Epidemiology|February 12, 2020
Incorporating external information to improve sparse signal detection in rare-variant gene-set-based analysesMengqi Zhang, Sahar Gelfman, Janice McCarthy, et al.
Briefings in Bioinformatics|December 1, 2021
Focused goodness of fit tests for gene set analysesMengqi Zhang, Sahar Gelfman, Cristiane Araujo Martins Moreno, et al.
Neuromuscular Disorders : NMD|January 6, 2015
Autophagic vacuolar pathology in desminopathiesConrad C Weihl, Stanley Iyadurai, Robert H Baloh, et al.
Neurobiology of Aging|November 3, 2012
Parkinson disease is not associated with C9ORF72 repeat expansionsMatthew B Harms, Drexel Neumann, Bruno A Benitez, et al.
Muscle & Nerve|March 1, 2013
Multifocal radiculoneuropathy during ipilimumab treatment of melanomaGeorgios Manousakis, James Koch, R Brian Sommerville, et al.
Annals of Neurology|November 11, 2014
Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genesJanet Cady, Peggy Allred, Taha Bali, et al.
Annals of Neurology|February 16, 2012
Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathyMatthew B Harms, R Brian Sommerville, Peggy Allred, et al.
Neuromuscular Disorders : NMD|January 25, 2015
Targeted sequencing and identification of genetic variants in sporadic inclusion body myositisConrad C Weihl, Robert H Baloh, Youjin Lee, et al.
Neurology|July 26, 2015
SQSTM1 splice site mutation in distal myopathy with rimmed vacuolesRobert C Bucelli, Khalid Arhzaouy, Alan Pestronk, et al.
Cell Death & Disease|August 6, 2021
Precision genetic cellular models identify therapies protective against ER stressIrina V Lebedeva, Michelle V Wagner, Sunil Sahdeo, et al.
Pageof 7

Showing results (11-20 of 68) with videos related to

Sort By:
Pageof 7
Genetic Epidemiology|February 12, 2020
Incorporating external information to improve sparse signal detection in rare-variant gene-set-based analysesMengqi Zhang, Sahar Gelfman, Janice McCarthy, et al.
Briefings in Bioinformatics|December 1, 2021
Focused goodness of fit tests for gene set analysesMengqi Zhang, Sahar Gelfman, Cristiane Araujo Martins Moreno, et al.
Neuromuscular Disorders : NMD|January 6, 2015
Autophagic vacuolar pathology in desminopathiesConrad C Weihl, Stanley Iyadurai, Robert H Baloh, et al.
Neurobiology of Aging|November 3, 2012
Parkinson disease is not associated with C9ORF72 repeat expansionsMatthew B Harms, Drexel Neumann, Bruno A Benitez, et al.
Muscle & Nerve|March 1, 2013
Multifocal radiculoneuropathy during ipilimumab treatment of melanomaGeorgios Manousakis, James Koch, R Brian Sommerville, et al.
Annals of Neurology|November 11, 2014
Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genesJanet Cady, Peggy Allred, Taha Bali, et al.
Annals of Neurology|February 16, 2012
Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathyMatthew B Harms, R Brian Sommerville, Peggy Allred, et al.
Neuromuscular Disorders : NMD|January 25, 2015
Targeted sequencing and identification of genetic variants in sporadic inclusion body myositisConrad C Weihl, Robert H Baloh, Youjin Lee, et al.
Neurology|July 26, 2015
SQSTM1 splice site mutation in distal myopathy with rimmed vacuolesRobert C Bucelli, Khalid Arhzaouy, Alan Pestronk, et al.
Cell Death & Disease|August 6, 2021
Precision genetic cellular models identify therapies protective against ER stressIrina V Lebedeva, Michelle V Wagner, Sunil Sahdeo, et al.
Pageof 7