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

Alice Saparov

Showing results (1-10 of 11) with videos related to

Pageof 2
Sort By:
Parkinsonism & Related Disorders|February 9, 2025
Big data and transformative bioinformatics in genomic diagnostics and beyondAlice Saparov, Michael Zech
Medrxiv : the Preprint Server for Health Sciences|January 13, 2025
From Text to Translation: Using Language Models to Prioritize Variants for Clinical ReviewWeijiang Li, Xiaomin Li, Ethan Lavallee, et al.
Genome Medicine|May 20, 2026
From text to translation: using language models to prioritize variants for clinical reviewWeijiang Li, Xiaomin Li, Ethan Lavallee, et al.
Population Health Management|August 5, 2024
Social Determinants of Hepatitis C Virus Infection in the United States, 2016-2021Justin K Niles, Alexandra Panov, Alice Saparov, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 25, 2025
Expanding the Allelic and Clinical Heterogeneity of Movement Disorders Linked to Defects of Mitochondrial Adenosine Triphosphate SynthasePhilip Harrer, Magdalena Krygier, Martin Krenn, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 9, 2026
Resolving Complex Structural Variants in Undiagnosed Rare Movement Disorders via Multimodal Genomics and Multi-omicsUgo Sorrentino, Melanie Brugger, Alice Saparov, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 10, 2026
Neurodevelopmental Disorder with Dystonia and Chorea Linked to De Novo Variants in the Splicing Regulator SRRM4Philip Harrer, Volker Kittke, Alice Saparov, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 1, 2025
Integrating Long-Read Nanopore Sequencing for Precision Resolution of Genomic Variants in DystoniaUgo Sorrentino, Martin Pavlov, Nazanin Mirza-Schreiber, et al.
Annals of Neurology|February 2, 2026
Fibroblast Transcriptomics in Molecular Diagnostics of a Comprehensive Dystonia CohortAlice Saparov, Ivana Dzinovic, Theresa Brunet, et al.
Brain : a Journal of Neurology|June 11, 2025
Deciphering DST-associated disorders: biallelic variants affecting DST-b cause a congenital myopathyMaureen Jacob, Heike Kölbel, Philip Harrer, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Parkinsonism & Related Disorders|February 9, 2025
Big data and transformative bioinformatics in genomic diagnostics and beyondAlice Saparov, Michael Zech
Medrxiv : the Preprint Server for Health Sciences|January 13, 2025
From Text to Translation: Using Language Models to Prioritize Variants for Clinical ReviewWeijiang Li, Xiaomin Li, Ethan Lavallee, et al.
Genome Medicine|May 20, 2026
From text to translation: using language models to prioritize variants for clinical reviewWeijiang Li, Xiaomin Li, Ethan Lavallee, et al.
Population Health Management|August 5, 2024
Social Determinants of Hepatitis C Virus Infection in the United States, 2016-2021Justin K Niles, Alexandra Panov, Alice Saparov, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 25, 2025
Expanding the Allelic and Clinical Heterogeneity of Movement Disorders Linked to Defects of Mitochondrial Adenosine Triphosphate SynthasePhilip Harrer, Magdalena Krygier, Martin Krenn, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 9, 2026
Resolving Complex Structural Variants in Undiagnosed Rare Movement Disorders via Multimodal Genomics and Multi-omicsUgo Sorrentino, Melanie Brugger, Alice Saparov, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 10, 2026
Neurodevelopmental Disorder with Dystonia and Chorea Linked to De Novo Variants in the Splicing Regulator SRRM4Philip Harrer, Volker Kittke, Alice Saparov, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 1, 2025
Integrating Long-Read Nanopore Sequencing for Precision Resolution of Genomic Variants in DystoniaUgo Sorrentino, Martin Pavlov, Nazanin Mirza-Schreiber, et al.
Annals of Neurology|February 2, 2026
Fibroblast Transcriptomics in Molecular Diagnostics of a Comprehensive Dystonia CohortAlice Saparov, Ivana Dzinovic, Theresa Brunet, et al.
Brain : a Journal of Neurology|June 11, 2025
Deciphering DST-associated disorders: biallelic variants affecting DST-b cause a congenital myopathyMaureen Jacob, Heike Kölbel, Philip Harrer, et al.
Pageof 2