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V Harris

Showing results (301-310 of 309) with videos related to

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Ebiomedicine|May 31, 2022
Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discoveryKaren L Oliver, Colin A Ellis, Ingrid E Scheffer, et al.
Annals of Neurology|August 19, 2023
Familial Mesial Temporal Lobe Epilepsy: Clinical Spectrum and Genetic Evidence for a Polygenic ArchitectureRebekah V Harris, Karen L Oliver, Piero Perucca, et al.
Nature Communications|January 23, 2015
Structure and boosting activity of a starch-degrading lytic polysaccharide monooxygenaseLeila Lo Leggio, Thomas J Simmons, Jens-Christian N Poulsen, et al.
Bioorganic & Medicinal Chemistry Letters|December 20, 2011
Novel heterocyclic DPP-4 inhibitors for the treatment of type 2 diabetesJon M Sutton, David E Clark, Stephen J Dunsdon, et al.
Neurology|May 26, 2021
Association of <i>SLC32A1</i> Missense Variants With Genetic Epilepsy With Febrile Seizures PlusSarah E Heron, Brigid M Regan, Rebekah V Harris, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2026
Genome sequencing boosts diagnostic yield for the developmental and epileptic encephalopathiesJacob E Munro, Harshini Thiyagarajah, Mark F Bennett, et al.
Ebiomedicine|July 30, 2025
SUDEP risk is influenced by longevity genomics: a polygenic risk score studyHelena Martins, James D Mills, Susanna Pagni, et al.
Journal of Medical Genetics|July 5, 2022
Clinical, biochemical and genetic characteristics of MOGS-CDG: a rare congenital disorder of glycosylationShino Shimada, Bobby G Ng, Amy L White, et al.
Epilepsia|January 28, 2026
Predictive value of seizure onset for gross motor dysfunction in individuals with pathogenic GABRB2 and GABRB3 variantsSebastian Ortiz, Leonardo Affronte, Chiara Bagliani, et al.
Pageof 31

Showing results (301-310 of 309) with videos related to

Sort By:
Pageof 31
You have reached the last page of results.This site can display upto 309 results.
Ebiomedicine|May 31, 2022
Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discoveryKaren L Oliver, Colin A Ellis, Ingrid E Scheffer, et al.
Annals of Neurology|August 19, 2023
Familial Mesial Temporal Lobe Epilepsy: Clinical Spectrum and Genetic Evidence for a Polygenic ArchitectureRebekah V Harris, Karen L Oliver, Piero Perucca, et al.
Nature Communications|January 23, 2015
Structure and boosting activity of a starch-degrading lytic polysaccharide monooxygenaseLeila Lo Leggio, Thomas J Simmons, Jens-Christian N Poulsen, et al.
Bioorganic & Medicinal Chemistry Letters|December 20, 2011
Novel heterocyclic DPP-4 inhibitors for the treatment of type 2 diabetesJon M Sutton, David E Clark, Stephen J Dunsdon, et al.
Neurology|May 26, 2021
Association of <i>SLC32A1</i> Missense Variants With Genetic Epilepsy With Febrile Seizures PlusSarah E Heron, Brigid M Regan, Rebekah V Harris, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2026
Genome sequencing boosts diagnostic yield for the developmental and epileptic encephalopathiesJacob E Munro, Harshini Thiyagarajah, Mark F Bennett, et al.
Ebiomedicine|July 30, 2025
SUDEP risk is influenced by longevity genomics: a polygenic risk score studyHelena Martins, James D Mills, Susanna Pagni, et al.
Journal of Medical Genetics|July 5, 2022
Clinical, biochemical and genetic characteristics of MOGS-CDG: a rare congenital disorder of glycosylationShino Shimada, Bobby G Ng, Amy L White, et al.
Epilepsia|January 28, 2026
Predictive value of seizure onset for gross motor dysfunction in individuals with pathogenic GABRB2 and GABRB3 variantsSebastian Ortiz, Leonardo Affronte, Chiara Bagliani, et al.
Pageof 31