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Cyril Pottier

Showing results (21-30 of 50) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|December 17, 2025
<i>APOE</i> *4 Risk-Modifying Genes and Drug Targets in Alzheimer's Disease through Cell-Type Specific Genomic AnalysesYoujie Zeng, Noah Cook, Chenyu Yang, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|June 22, 2026
APOE*4 risk-modifying genes and drug targets in Alzheimer's disease through cell-type-specific genomic analysesYoujie Zeng, Noah Cook, Chenyu Yang, et al.
Research Square|July 18, 2025
High-sensitivity plasma proteomics reveals disease-specific signatures and predictive biomarkers of Alzheimer's disease phenotypes in a large mixed dementia cohortKatherine Gong, Jigyasha Timsina, Muhammad Ali, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
Haploinsufficiency of lysosomal enzyme genes in Alzheimer's diseaseBruno A Benitez, Clare E Wallace, Maulikkumar Patel, et al.
Acta Neuropathologica Communications|December 9, 2017
Clinical and neuropathological features of ALS/FTD with TIA1 mutationsVeronica Hirsch-Reinshagen, Cyril Pottier, Alexandra M Nicholson, et al.
European Journal of Human Genetics : EJHG|April 2, 2015
Mutation in the 3'untranslated region of APP as a genetic determinant of cerebral amyloid angiopathyGaël Nicolas, David Wallon, Claudia Goupil, et al.
Acta Neuropathologica|April 19, 2024
Abundant transcriptomic alterations in the human cerebellum of patients with a C9orf72 repeat expansionEvan Udine, Mariely DeJesus-Hernandez, Shulan Tian, et al.
Brain : a Journal of Neurology|December 17, 2021
Shared brain transcriptomic signature in TDP-43 type A FTLD patients with or without GRN mutationsCyril Pottier, Ligia Mateiu, Matthew C Baker, et al.
Medrxiv : the Preprint Server for Health Sciences|May 18, 2026
An <i>APOE</i> *4-Informed Genomic Atlas of the X Chromosome in Alzheimer's DiseaseNoah Cook, Youjie Zeng, Chenyu Yang, et al.
Acta Neuropathologica|May 7, 2015
Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron diseaseCyril Pottier, Kevin F Bieniek, NiCole Finch, et al.
Pageof 5

Showing results (21-30 of 50) with videos related to

Sort By:
Pageof 5
Medrxiv : the Preprint Server for Health Sciences|December 17, 2025
<i>APOE</i> *4 Risk-Modifying Genes and Drug Targets in Alzheimer's Disease through Cell-Type Specific Genomic AnalysesYoujie Zeng, Noah Cook, Chenyu Yang, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|June 22, 2026
APOE*4 risk-modifying genes and drug targets in Alzheimer's disease through cell-type-specific genomic analysesYoujie Zeng, Noah Cook, Chenyu Yang, et al.
Research Square|July 18, 2025
High-sensitivity plasma proteomics reveals disease-specific signatures and predictive biomarkers of Alzheimer's disease phenotypes in a large mixed dementia cohortKatherine Gong, Jigyasha Timsina, Muhammad Ali, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
Haploinsufficiency of lysosomal enzyme genes in Alzheimer's diseaseBruno A Benitez, Clare E Wallace, Maulikkumar Patel, et al.
Acta Neuropathologica Communications|December 9, 2017
Clinical and neuropathological features of ALS/FTD with TIA1 mutationsVeronica Hirsch-Reinshagen, Cyril Pottier, Alexandra M Nicholson, et al.
European Journal of Human Genetics : EJHG|April 2, 2015
Mutation in the 3'untranslated region of APP as a genetic determinant of cerebral amyloid angiopathyGaël Nicolas, David Wallon, Claudia Goupil, et al.
Acta Neuropathologica|April 19, 2024
Abundant transcriptomic alterations in the human cerebellum of patients with a C9orf72 repeat expansionEvan Udine, Mariely DeJesus-Hernandez, Shulan Tian, et al.
Brain : a Journal of Neurology|December 17, 2021
Shared brain transcriptomic signature in TDP-43 type A FTLD patients with or without GRN mutationsCyril Pottier, Ligia Mateiu, Matthew C Baker, et al.
Medrxiv : the Preprint Server for Health Sciences|May 18, 2026
An <i>APOE</i> *4-Informed Genomic Atlas of the X Chromosome in Alzheimer's DiseaseNoah Cook, Youjie Zeng, Chenyu Yang, et al.
Acta Neuropathologica|May 7, 2015
Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron diseaseCyril Pottier, Kevin F Bieniek, NiCole Finch, et al.
Pageof 5