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Brain : a Journal of Neurology
|
August 14, 2025
Connectivity as a universal predictor of tau progression in atypical Alzheimer's disease
Hannah de Bruin, Colin Groot, Henryk Barthel, et al.
Brain : a Journal of Neurology
|
September 26, 2018
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers
Ming Zhang, Raffaele Ferrari, Maria Carmela Tartaglia, et al.
Annals of Neurology
|
January 29, 2026
Individualized Atrophy-Based Prediction of Dementia Progression in Familial Frontotemporal Lobar Degeneration With Bayesian Linear Mixed-Effects Modeling
Shubir Dutt, Dana Leichter, Yann Cobigo, et al.
Acta Neuropathologica
|
February 11, 2019
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD
Cyril Pottier, Yingxue Ren, Ralph B Perkerson, 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.
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.
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.
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of 45
Search research articles
Search
Showing results (431-440 of 448) with videos related to
Sort By:
Page
of 45
Brain : a Journal of Neurology
|
August 14, 2025
Connectivity as a universal predictor of tau progression in atypical Alzheimer's disease
Hannah de Bruin, Colin Groot, Henryk Barthel, et al.
Brain : a Journal of Neurology
|
September 26, 2018
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers
Ming Zhang, Raffaele Ferrari, Maria Carmela Tartaglia, et al.
Annals of Neurology
|
January 29, 2026
Individualized Atrophy-Based Prediction of Dementia Progression in Familial Frontotemporal Lobar Degeneration With Bayesian Linear Mixed-Effects Modeling
Shubir Dutt, Dana Leichter, Yann Cobigo, et al.
Acta Neuropathologica
|
February 11, 2019
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD
Cyril Pottier, Yingxue Ren, Ralph B Perkerson, 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.
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.
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.
Page
of 45