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Mojca Strazisar

Showing results (31-40 of 41) with videos related to

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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 11, 2012
Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage-dependent calcium channels in psychiatric disordersMaarten J Van Den Bossche, Mojca Strazisar, Stephan De Bruyne, et al.
BMC Ecology and Evolution|October 7, 2025
Genomic insights into the population structure and adaptive variation of Mullus barbatus in the Mediterranean SeaPiergiorgio Massa, Henrique G Leitão, Tereza Manousaki, et al.
Frontiers in Cell and Developmental Biology|May 10, 2021
Long-Read Sequencing to Unravel Complex Structural Variants of <i>CEP78</i> Leading to Cone-Rod Dystrophy and Hearing LossGiulia Ascari, Nanna D Rendtorff, Marieke De Bruyne, et al.
Acta Neuropathologica|June 6, 2025
Analysis of the splicing landscape of the frontal cortex in FTLD-TDP reveals subtype specific patterns and cryptic splicingJúlia Faura, Bavo Heeman, Cyril Pottier, et al.
Acta Neuropathologica|March 16, 2019
Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitabilityRita Cacace, Bavo Heeman, Sara Van Mossevelde, et al.
Molecular Psychiatry|February 17, 2022
Rare variants in IFFO1, DTNB, NLRC3 and SLC22A10 associate with Alzheimer's disease CSF profile of neuronal injury and inflammationAlexander Neumann, Fahri Küçükali, Isabelle Bos, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 5, 2022
Whole-exome rare-variant analysis of Alzheimer's disease and related biomarker traitsFahri Küçükali, Alexander Neumann, Jasper Van Dongen, et al.
Molecular Neurodegeneration|July 6, 2025
Methylome analysis of FTLD patients with TDP-43 pathology identifies epigenetic signatures specific to pathological subtypesCristina T Vicente, Tejasvi Niranjan, Elise Coopman, et al.
Nature Genetics|March 13, 2026
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusionsWouter De Coster, Marleen Van den Broeck, Matt Baker, et al.
Npj Biodiversity|October 15, 2024
Author Correction: The European Reference Genome Atlas: piloting a decentralised approach to equitable biodiversity genomicsAnn M Mc Cartney, Giulio Formenti, Alice Mouton, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 11, 2012
Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage-dependent calcium channels in psychiatric disordersMaarten J Van Den Bossche, Mojca Strazisar, Stephan De Bruyne, et al.
BMC Ecology and Evolution|October 7, 2025
Genomic insights into the population structure and adaptive variation of Mullus barbatus in the Mediterranean SeaPiergiorgio Massa, Henrique G Leitão, Tereza Manousaki, et al.
Frontiers in Cell and Developmental Biology|May 10, 2021
Long-Read Sequencing to Unravel Complex Structural Variants of <i>CEP78</i> Leading to Cone-Rod Dystrophy and Hearing LossGiulia Ascari, Nanna D Rendtorff, Marieke De Bruyne, et al.
Acta Neuropathologica|June 6, 2025
Analysis of the splicing landscape of the frontal cortex in FTLD-TDP reveals subtype specific patterns and cryptic splicingJúlia Faura, Bavo Heeman, Cyril Pottier, et al.
Acta Neuropathologica|March 16, 2019
Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitabilityRita Cacace, Bavo Heeman, Sara Van Mossevelde, et al.
Molecular Psychiatry|February 17, 2022
Rare variants in IFFO1, DTNB, NLRC3 and SLC22A10 associate with Alzheimer's disease CSF profile of neuronal injury and inflammationAlexander Neumann, Fahri Küçükali, Isabelle Bos, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 5, 2022
Whole-exome rare-variant analysis of Alzheimer's disease and related biomarker traitsFahri Küçükali, Alexander Neumann, Jasper Van Dongen, et al.
Molecular Neurodegeneration|July 6, 2025
Methylome analysis of FTLD patients with TDP-43 pathology identifies epigenetic signatures specific to pathological subtypesCristina T Vicente, Tejasvi Niranjan, Elise Coopman, et al.
Nature Genetics|March 13, 2026
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusionsWouter De Coster, Marleen Van den Broeck, Matt Baker, et al.
Npj Biodiversity|October 15, 2024
Author Correction: The European Reference Genome Atlas: piloting a decentralised approach to equitable biodiversity genomicsAnn M Mc Cartney, Giulio Formenti, Alice Mouton, et al.
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