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The Lancet. Neurology
|
May 5, 2018
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study
Cyril Pottier, Xiaolai Zhou, Ralph B Perkerson, et al.
Nature Communications
|
April 25, 2025
Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing
Cyril Pottier, Fahri Küçükali, Matt Baker, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 9, 2024
Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome Sequencing
Cyril Pottier, Fahri Küçükali, Matt Baker, et al.
Nature Genetics
|
April 5, 2011
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
Adam C Naj, Gyungah Jun, Gary W Beecham, et al.
JAMA Neurology
|
January 31, 2022
Prevalence Estimates of Amyloid Abnormality Across the Alzheimer Disease Clinical Spectrum
Willemijn J Jansen, Olin Janssen, Betty M Tijms, et al.
JAMA
|
June 6, 2023
Development of a Definition of Postacute Sequelae of SARS-CoV-2 Infection
Tanayott Thaweethai, Sarah E Jolley, Elizabeth W Karlson, et al.
JAMA Neurology
|
September 10, 2014
Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study
Adam C Naj, Gyungah Jun, Christiane Reitz, et al.
Neurology
|
June 23, 2012
Novel late-onset Alzheimer disease loci variants associate with brain gene expression
Mariet Allen, Fanggeng Zou, High Seng Chai, et al.
JAMA Neurology
|
December 23, 2014
Rarity of the Alzheimer disease-protective APP A673T variant in the United States
Li-San Wang, Adam C Naj, Robert R Graham, et al.
Geroscience
|
January 31, 2025
Dynamic proportional loss of functional connectivity revealed change of left superior frontal gyrus in subjective cognitive decline: an explanatory study based on Chinese and Western cohorts
Luyao Wang, Wenjing Hu, Fan Dong, et al.
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of 44
Search research articles
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Showing results (421-430 of 436) with videos related to
Sort By:
Page
of 44
The Lancet. Neurology
|
May 5, 2018
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study
Cyril Pottier, Xiaolai Zhou, Ralph B Perkerson, et al.
Nature Communications
|
April 25, 2025
Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing
Cyril Pottier, Fahri Küçükali, Matt Baker, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 9, 2024
Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome Sequencing
Cyril Pottier, Fahri Küçükali, Matt Baker, et al.
Nature Genetics
|
April 5, 2011
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
Adam C Naj, Gyungah Jun, Gary W Beecham, et al.
JAMA Neurology
|
January 31, 2022
Prevalence Estimates of Amyloid Abnormality Across the Alzheimer Disease Clinical Spectrum
Willemijn J Jansen, Olin Janssen, Betty M Tijms, et al.
JAMA
|
June 6, 2023
Development of a Definition of Postacute Sequelae of SARS-CoV-2 Infection
Tanayott Thaweethai, Sarah E Jolley, Elizabeth W Karlson, et al.
JAMA Neurology
|
September 10, 2014
Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study
Adam C Naj, Gyungah Jun, Christiane Reitz, et al.
Neurology
|
June 23, 2012
Novel late-onset Alzheimer disease loci variants associate with brain gene expression
Mariet Allen, Fanggeng Zou, High Seng Chai, et al.
JAMA Neurology
|
December 23, 2014
Rarity of the Alzheimer disease-protective APP A673T variant in the United States
Li-San Wang, Adam C Naj, Robert R Graham, et al.
Geroscience
|
January 31, 2025
Dynamic proportional loss of functional connectivity revealed change of left superior frontal gyrus in subjective cognitive decline: an explanatory study based on Chinese and Western cohorts
Luyao Wang, Wenjing Hu, Fan Dong, et al.
Page
of 44