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

Manu Sharma

Showing results (261-270 of 325) with videos related to

Pageof 33
Sort By:
European Journal of Human Genetics : EJHG|November 4, 2004
PARK11 is not linked with Parkinson's disease in European familiesJürgen Prestel, Manu Sharma, Petra Leitner, et al.
Lancet (London, England)|February 5, 2011
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies, Michael A Nalls, Vincent Plagnol, et al.
Neurobiology of Aging|September 5, 2017
Establishing the role of rare coding variants in known Parkinson's disease risk lociIris E Jansen, J Raphael Gibbs, Mike A Nalls, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 29, 2018
Understanding the role of genetic variability in LRRK2 in Indian populationAsha Kishore, Ashwin Ashok Kumar Sreelatha, Marc Sturm, et al.
Antioxidants & Redox Signaling|July 16, 2019
Mutations in <i>RHOT1</i> Disrupt Endoplasmic Reticulum-Mitochondria Contact Sites Interfering with Calcium Homeostasis and Mitochondrial Dynamics in Parkinson's DiseaseDajana Grossmann, Clara Berenguer-Escuder, Marie Estelle Bellet, et al.
American Journal of Human Genetics|December 24, 2003
The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing intervalAlexander Zimprich, Bertram Müller-Myhsok, Matthew Farrer, et al.
NPJ Parkinson'S Disease|September 22, 2021
Fine mapping of the HLA locus in Parkinson's disease in EuropeansEric Yu, Aditya Ambati, Maren Stolp Andersen, et al.
Human Mutation|July 11, 2012
Use of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunitiesFlorian Mittag, Finja Büchel, Mohamad Saad, et al.
Biological Psychiatry. Cognitive Neuroscience and Neuroimaging|February 28, 2026
Threading the needle: Practical considerations for merging theory-driven computational psychiatry with data-driven analytics to enhance precision health at scaleAnnie Cheng, Anna Konova, Albert Powers, et al.
Annals of Neurology|May 20, 2024
Polygenic Risk Scores Validated in Patient-Derived Cells Stratify for Mitochondrial Subtypes of Parkinson's DiseaseGiuseppe Arena, Zied Landoulsi, Dajana Grossmann, et al.
Pageof 33

Showing results (261-270 of 325) with videos related to

Sort By:
Pageof 33
European Journal of Human Genetics : EJHG|November 4, 2004
PARK11 is not linked with Parkinson's disease in European familiesJürgen Prestel, Manu Sharma, Petra Leitner, et al.
Lancet (London, England)|February 5, 2011
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies, Michael A Nalls, Vincent Plagnol, et al.
Neurobiology of Aging|September 5, 2017
Establishing the role of rare coding variants in known Parkinson's disease risk lociIris E Jansen, J Raphael Gibbs, Mike A Nalls, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 29, 2018
Understanding the role of genetic variability in LRRK2 in Indian populationAsha Kishore, Ashwin Ashok Kumar Sreelatha, Marc Sturm, et al.
Antioxidants & Redox Signaling|July 16, 2019
Mutations in <i>RHOT1</i> Disrupt Endoplasmic Reticulum-Mitochondria Contact Sites Interfering with Calcium Homeostasis and Mitochondrial Dynamics in Parkinson's DiseaseDajana Grossmann, Clara Berenguer-Escuder, Marie Estelle Bellet, et al.
American Journal of Human Genetics|December 24, 2003
The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing intervalAlexander Zimprich, Bertram Müller-Myhsok, Matthew Farrer, et al.
NPJ Parkinson'S Disease|September 22, 2021
Fine mapping of the HLA locus in Parkinson's disease in EuropeansEric Yu, Aditya Ambati, Maren Stolp Andersen, et al.
Human Mutation|July 11, 2012
Use of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunitiesFlorian Mittag, Finja Büchel, Mohamad Saad, et al.
Biological Psychiatry. Cognitive Neuroscience and Neuroimaging|February 28, 2026
Threading the needle: Practical considerations for merging theory-driven computational psychiatry with data-driven analytics to enhance precision health at scaleAnnie Cheng, Anna Konova, Albert Powers, et al.
Annals of Neurology|May 20, 2024
Polygenic Risk Scores Validated in Patient-Derived Cells Stratify for Mitochondrial Subtypes of Parkinson's DiseaseGiuseppe Arena, Zied Landoulsi, Dajana Grossmann, et al.
Pageof 33