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

James Snyder

Showing results (71-80 of 90) with videos related to

Pageof 9
Sort By:
BMC Musculoskeletal Disorders|November 11, 2016
Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing studyChristopher J Cardinale, Dong Li, Lifeng Tian, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
Single-nucleus multiomics unveils malignant cellular states, regulatory architectures and microenvironmental reorganization across the G-CIMP epigenomic transition in IDH-mutant gliomaGrayson A Herrgott, Luciano Garofano, Natalia Silva Morosini, et al.
Ophthalmic Genetics|February 20, 2014
Advantage of Whole Exome Sequencing over Allele-Specific and Targeted Segment Sequencing in Detection of Novel TULP1 Mutation in Leber Congenital AmaurosisYiran Guo, Ivan Prokudin, Cong Yu, et al.
The Oncologist|March 31, 2025
A pilot survey into the landscape of neuro-oncology care in the communityChristine Lu-Emerson, Sajeel Chowdhary, Rupesh Kotecha, et al.
Neuro-Oncology|February 25, 2021
DNA methylation-based signatures classify sporadic pituitary tumors according to clinicopathological featuresMaritza S Mosella, Thais S Sabedot, Tiago C Silva, et al.
Neuro-Oncology|February 9, 2021
A serum-based DNA methylation assay provides accurate detection of gliomaThais S Sabedot, Tathiane M Malta, James Snyder, et al.
Neuro-Oncology|January 17, 2019
Advances in multidisciplinary therapy for meningiomasPriscilla K Brastianos, Evanthia Galanis, Nicholas Butowski, et al.
Genetics in Medicine Open|March 5, 2026
Single vs dual genetic disease in children with congenital anomalies and solid tumorsDeborah J Watson, Amir Hossein Saeidian, Xiang Wang, et al.
Cell Reports|April 12, 2018
A Distinct DNA Methylation Shift in a Subset of Glioma CpG Island Methylator Phenotypes during Tumor RecurrenceCamila Ferreira de Souza, Thais S Sabedot, Tathiane M Malta, et al.
Scientific Reports|June 21, 2017
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signalingDong Li, Xiao Chang, John J Connolly, et al.
Pageof 9

Showing results (71-80 of 90) with videos related to

Sort By:
Pageof 9
BMC Musculoskeletal Disorders|November 11, 2016
Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing studyChristopher J Cardinale, Dong Li, Lifeng Tian, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
Single-nucleus multiomics unveils malignant cellular states, regulatory architectures and microenvironmental reorganization across the G-CIMP epigenomic transition in IDH-mutant gliomaGrayson A Herrgott, Luciano Garofano, Natalia Silva Morosini, et al.
Ophthalmic Genetics|February 20, 2014
Advantage of Whole Exome Sequencing over Allele-Specific and Targeted Segment Sequencing in Detection of Novel TULP1 Mutation in Leber Congenital AmaurosisYiran Guo, Ivan Prokudin, Cong Yu, et al.
The Oncologist|March 31, 2025
A pilot survey into the landscape of neuro-oncology care in the communityChristine Lu-Emerson, Sajeel Chowdhary, Rupesh Kotecha, et al.
Neuro-Oncology|February 25, 2021
DNA methylation-based signatures classify sporadic pituitary tumors according to clinicopathological featuresMaritza S Mosella, Thais S Sabedot, Tiago C Silva, et al.
Neuro-Oncology|February 9, 2021
A serum-based DNA methylation assay provides accurate detection of gliomaThais S Sabedot, Tathiane M Malta, James Snyder, et al.
Neuro-Oncology|January 17, 2019
Advances in multidisciplinary therapy for meningiomasPriscilla K Brastianos, Evanthia Galanis, Nicholas Butowski, et al.
Genetics in Medicine Open|March 5, 2026
Single vs dual genetic disease in children with congenital anomalies and solid tumorsDeborah J Watson, Amir Hossein Saeidian, Xiang Wang, et al.
Cell Reports|April 12, 2018
A Distinct DNA Methylation Shift in a Subset of Glioma CpG Island Methylator Phenotypes during Tumor RecurrenceCamila Ferreira de Souza, Thais S Sabedot, Tathiane M Malta, et al.
Scientific Reports|June 21, 2017
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signalingDong Li, Xiao Chang, John J Connolly, et al.
Pageof 9