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Jason A Chen

Showing results (41-50 of 48) with videos related to

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Molecular Neurodegeneration|August 10, 2018
Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseasesJason A Chen, Zhongbo Chen, Hyejung Won, et al.
Alzheimer Disease and Associated Disorders|September 13, 2019
Frequency of the TREM2 R47H Variant in Various Neurodegenerative DisordersAriane H Ayer, Kevin Wojta, Eliana Marisa Ramos, et al.
JAMA Neurology|February 24, 2015
A multiancestral genome-wide exome array study of Alzheimer disease, frontotemporal dementia, and progressive supranuclear palsyJason A Chen, Qing Wang, Jeremy Davis-Turak, et al.
Nature Communications|May 15, 2025
Gabapentinoids confer survival benefit in human glioblastomaJoshua D Bernstock, Mulki Mehari, Jakob V E Gerstl, et al.
Nature Medicine|February 6, 2018
Haploinsufficiency leads to neurodegeneration in C9ORF72 ALS/FTD human induced motor neuronsYingxiao Shi, Shaoyu Lin, Kim A Staats, et al.
Neuron|June 23, 2017
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette SyndromeAlden Y Huang, Dongmei Yu, Lea K Davis, et al.
Acta Neuropathologica|January 20, 2020
Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevitySven J van der Lee, Olivia J Conway, Iris Jansen, et al.
Acta Neuropathologica|May 28, 2019
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevitySven J van der Lee, Olivia J Conway, Iris Jansen, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Molecular Neurodegeneration|August 10, 2018
Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseasesJason A Chen, Zhongbo Chen, Hyejung Won, et al.
Alzheimer Disease and Associated Disorders|September 13, 2019
Frequency of the TREM2 R47H Variant in Various Neurodegenerative DisordersAriane H Ayer, Kevin Wojta, Eliana Marisa Ramos, et al.
JAMA Neurology|February 24, 2015
A multiancestral genome-wide exome array study of Alzheimer disease, frontotemporal dementia, and progressive supranuclear palsyJason A Chen, Qing Wang, Jeremy Davis-Turak, et al.
Nature Communications|May 15, 2025
Gabapentinoids confer survival benefit in human glioblastomaJoshua D Bernstock, Mulki Mehari, Jakob V E Gerstl, et al.
Nature Medicine|February 6, 2018
Haploinsufficiency leads to neurodegeneration in C9ORF72 ALS/FTD human induced motor neuronsYingxiao Shi, Shaoyu Lin, Kim A Staats, et al.
Neuron|June 23, 2017
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette SyndromeAlden Y Huang, Dongmei Yu, Lea K Davis, et al.
Acta Neuropathologica|January 20, 2020
Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevitySven J van der Lee, Olivia J Conway, Iris Jansen, et al.
Acta Neuropathologica|May 28, 2019
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevitySven J van der Lee, Olivia J Conway, Iris Jansen, et al.
Pageof 5