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Nature Genetics
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March 13, 2026
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions
Wouter De Coster, Marleen Van den Broeck, 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.
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.
American Journal of Human Genetics
|
June 18, 2024
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia
Claudia Manzoni, Demis A Kia, Raffaele Ferrari, et al.
The Lancet. Neurology
|
June 20, 2014
Frontotemporal dementia and its subtypes: a genome-wide association study
Raffaele Ferrari, Dena G Hernandez, Michael A Nalls, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 10, 2023
Creating the Pick's disease International Consortium: Association study of <i>MAPT</i> H2 haplotype with risk of Pick's disease
Rebecca R Valentino, William J Scotton, Shanu F Roemer, et al.
Nature Genetics
|
February 16, 2021
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
Ruth Chia, Marya S Sabir, Sara Bandres-Ciga, 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
|
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.
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of 96
Search research articles
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Showing results (941-950 of 957) with videos related to
Sort By:
Page
of 96
Nature Genetics
|
March 13, 2026
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions
Wouter De Coster, Marleen Van den Broeck, 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.
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.
American Journal of Human Genetics
|
June 18, 2024
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia
Claudia Manzoni, Demis A Kia, Raffaele Ferrari, et al.
The Lancet. Neurology
|
June 20, 2014
Frontotemporal dementia and its subtypes: a genome-wide association study
Raffaele Ferrari, Dena G Hernandez, Michael A Nalls, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 10, 2023
Creating the Pick's disease International Consortium: Association study of <i>MAPT</i> H2 haplotype with risk of Pick's disease
Rebecca R Valentino, William J Scotton, Shanu F Roemer, et al.
Nature Genetics
|
February 16, 2021
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
Ruth Chia, Marya S Sabir, Sara Bandres-Ciga, 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
|
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.
Page
of 96