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

Jamil Ahmad

Showing results (241-250 of 260) with videos related to

Pageof 26
Sort By:
Genome Research|January 13, 2016
Exome sequencing and CRISPR/Cas genome editing identify mutations of ZAK as a cause of limb defects in humans and miceMalte Spielmann, Naseebullah Kakar, Naeimeh Tayebi, et al.
Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
Association of rare variants in <i>ARSA</i> with Parkinson's diseaseKonstantin Senkevich, Mariia Beletskaia, Aliza Dworkind, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 29, 2023
Association of Rare Variants in ARSA with Parkinson's DiseaseKonstantin Senkevich, Mariia Beletskaia, Aliza Dworkind, et al.
HGG Advances|December 11, 2025
Lack of association between G6PD variants and Parkinson diseaseLeah V Chifamba, Sitki Cem Parlar, Lang Liu, et al.
Human Genetics|April 15, 2019
Variants in KIAA0825 underlie autosomal recessive postaxial polydactylyIrfan Ullah, Naseebullah Kakar, Isabelle Schrauwen, et al.
Facial Plastic Surgery & Aesthetic Medicine|April 17, 2026
Features of Importance in the Nasal Exam in RhinoplastyElizabeth S Longino, Cherian K Kandathil, Jamil Ahmad, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 23, 2026
The GBA1 p.E427K (p.E388K) Variant Is a Risk Factor for Synucleinopathies: A Meta-AnalysisLeah V Chifamba, Sitki Cem Parlar, Emma N Somerville, et al.
Medrxiv : the Preprint Server for Health Sciences|March 27, 2026
The <i>GBA1</i> p.E427K (p.E388K) Variant is a Risk Factor for Synucleinopathies: A Meta-AnalysisLeah V Chifamba, Sitki Cem Parlar, Emma N Somerville, et al.
Brain : a Journal of Neurology|November 12, 2022
GALC variants affect galactosylceramidase enzymatic activity and risk of Parkinson's diseaseKonstantin Senkevich, Cornelia E Zorca, Aliza Dworkind, et al.
Research Square|April 2, 2024
The Parkinson's disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neuronsJace Jones-Tabah, Kathy He, Konstantin Senkevich, et al.
Pageof 26

Showing results (241-250 of 260) with videos related to

Sort By:
Pageof 26
Genome Research|January 13, 2016
Exome sequencing and CRISPR/Cas genome editing identify mutations of ZAK as a cause of limb defects in humans and miceMalte Spielmann, Naseebullah Kakar, Naeimeh Tayebi, et al.
Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
Association of rare variants in <i>ARSA</i> with Parkinson's diseaseKonstantin Senkevich, Mariia Beletskaia, Aliza Dworkind, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 29, 2023
Association of Rare Variants in ARSA with Parkinson's DiseaseKonstantin Senkevich, Mariia Beletskaia, Aliza Dworkind, et al.
HGG Advances|December 11, 2025
Lack of association between G6PD variants and Parkinson diseaseLeah V Chifamba, Sitki Cem Parlar, Lang Liu, et al.
Human Genetics|April 15, 2019
Variants in KIAA0825 underlie autosomal recessive postaxial polydactylyIrfan Ullah, Naseebullah Kakar, Isabelle Schrauwen, et al.
Facial Plastic Surgery & Aesthetic Medicine|April 17, 2026
Features of Importance in the Nasal Exam in RhinoplastyElizabeth S Longino, Cherian K Kandathil, Jamil Ahmad, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 23, 2026
The GBA1 p.E427K (p.E388K) Variant Is a Risk Factor for Synucleinopathies: A Meta-AnalysisLeah V Chifamba, Sitki Cem Parlar, Emma N Somerville, et al.
Medrxiv : the Preprint Server for Health Sciences|March 27, 2026
The <i>GBA1</i> p.E427K (p.E388K) Variant is a Risk Factor for Synucleinopathies: A Meta-AnalysisLeah V Chifamba, Sitki Cem Parlar, Emma N Somerville, et al.
Brain : a Journal of Neurology|November 12, 2022
GALC variants affect galactosylceramidase enzymatic activity and risk of Parkinson's diseaseKonstantin Senkevich, Cornelia E Zorca, Aliza Dworkind, et al.
Research Square|April 2, 2024
The Parkinson's disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neuronsJace Jones-Tabah, Kathy He, Konstantin Senkevich, et al.
Pageof 26