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Sebastian Guelfi

Showing results (11-20 of 22) with videos related to

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Molecular Neurodegeneration|January 20, 2024
Unravelling cell type-specific responses to Parkinson's Disease at single cell resolutionAraks Martirosyan, Rizwan Ansari, Francisco Pestana, et al.
Brain Communications|April 11, 2020
Genetic variability in response to amyloid beta deposition influences Alzheimer's disease riskDervis A Salih, Sevinc Bayram, Sebastian Guelfi, et al.
Nature Communications|February 27, 2020
Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant informationSebastian Guelfi, Karishma D'Sa, Juan A Botía, et al.
Cell Reports|January 27, 2015
A genome-wide gene-expression analysis and database in transgenic mice during development of amyloid or tau pathologyMar Matarin, Dervis A Salih, Marina Yasvoina, et al.
Plos Genetics|September 18, 2023
eQTL Catalogue 2023: New datasets, X chromosome QTLs, and improved detection and visualisation of transcript-level QTLsNurlan Kerimov, Ralf Tambets, James D Hayhurst, et al.
Biorxiv : the Preprint Server for Biology|April 17, 2023
Systematic visualisation of molecular QTLs reveals variant mechanisms at GWAS lociNurlan Kerimov, Ralf Tambets, James D Hayhurst, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 2016
Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseasesRaffaele Ferrari, Yunpeng Wang, Jana Vandrovcova, et al.
European Heart Journal. Quality of Care & Clinical Outcomes|March 4, 2026
Integrating genetic and imaging information to enhance cardiovascular risk stratification: rationale and design of the CVRISK-IT randomised controlled trialEmanuele Di Angelantonio, Massimo Piepoli, Serenella Castelvecchio, et al.
Brain : a Journal of Neurology|September 8, 2022
Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson's disease at 16q11.2 and MAPT H1 lociMarc P M Soutar, Daniela Melandri, Benjamin O'Callaghan, et al.
Nature|January 22, 2015
Common genetic variants influence human subcortical brain structuresDerrek P Hibar, Jason L Stein, Miguel E Renteria, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Molecular Neurodegeneration|January 20, 2024
Unravelling cell type-specific responses to Parkinson's Disease at single cell resolutionAraks Martirosyan, Rizwan Ansari, Francisco Pestana, et al.
Brain Communications|April 11, 2020
Genetic variability in response to amyloid beta deposition influences Alzheimer's disease riskDervis A Salih, Sevinc Bayram, Sebastian Guelfi, et al.
Nature Communications|February 27, 2020
Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant informationSebastian Guelfi, Karishma D'Sa, Juan A Botía, et al.
Cell Reports|January 27, 2015
A genome-wide gene-expression analysis and database in transgenic mice during development of amyloid or tau pathologyMar Matarin, Dervis A Salih, Marina Yasvoina, et al.
Plos Genetics|September 18, 2023
eQTL Catalogue 2023: New datasets, X chromosome QTLs, and improved detection and visualisation of transcript-level QTLsNurlan Kerimov, Ralf Tambets, James D Hayhurst, et al.
Biorxiv : the Preprint Server for Biology|April 17, 2023
Systematic visualisation of molecular QTLs reveals variant mechanisms at GWAS lociNurlan Kerimov, Ralf Tambets, James D Hayhurst, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 2016
Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseasesRaffaele Ferrari, Yunpeng Wang, Jana Vandrovcova, et al.
European Heart Journal. Quality of Care & Clinical Outcomes|March 4, 2026
Integrating genetic and imaging information to enhance cardiovascular risk stratification: rationale and design of the CVRISK-IT randomised controlled trialEmanuele Di Angelantonio, Massimo Piepoli, Serenella Castelvecchio, et al.
Brain : a Journal of Neurology|September 8, 2022
Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson's disease at 16q11.2 and MAPT H1 lociMarc P M Soutar, Daniela Melandri, Benjamin O'Callaghan, et al.
Nature|January 22, 2015
Common genetic variants influence human subcortical brain structuresDerrek P Hibar, Jason L Stein, Miguel E Renteria, et al.
Pageof 3