Search research articles
Contact Us
Filters
Showing results (601-610 of 621) with videos related to
Page
of 63
Sort By:
Medrxiv : the Preprint Server for Health Sciences
|
March 11, 2024
Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and <i>MAPT</i> Sub-haplotypes
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
Neurobiology of Disease
|
April 7, 2019
Heritability and genetic variance of dementia with Lewy bodies
Rita Guerreiro, Valentina Escott-Price, Dena G Hernandez, et al.
Human Molecular Genetics
|
May 5, 2012
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
Giovanni Coppola, Subashchandrabose Chinnathambi, Jason JiYong Lee, et al.
Acta Neuropathologica
|
November 1, 2021
Genome-wide association study and functional validation implicates JADE1 in tauopathy
Kurt Farrell, SoongHo Kim, Natalia Han, et al.
Neuron
|
May 3, 2024
Genome sequence analyses identify novel risk loci for multiple system atrophy
Ruth Chia, Anindita Ray, Zalak Shah, et al.
Nature Neuroscience
|
July 16, 2025
Tau PET positivity in individuals with and without cognitive impairment varies with age, amyloid-β status, APOE genotype and sex
Rik Ossenkoppele, Emma M Coomans, Liana G Apostolova, 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.
Nature Genetics
|
February 16, 2010
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
Vivianna M Van Deerlin, Patrick M A Sleiman, Maria Martinez-Lage, 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.
Page
of 63
Search research articles
Search
Showing results (601-610 of 621) with videos related to
Sort By:
Page
of 63
Medrxiv : the Preprint Server for Health Sciences
|
March 11, 2024
Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and <i>MAPT</i> Sub-haplotypes
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
Neurobiology of Disease
|
April 7, 2019
Heritability and genetic variance of dementia with Lewy bodies
Rita Guerreiro, Valentina Escott-Price, Dena G Hernandez, et al.
Human Molecular Genetics
|
May 5, 2012
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
Giovanni Coppola, Subashchandrabose Chinnathambi, Jason JiYong Lee, et al.
Acta Neuropathologica
|
November 1, 2021
Genome-wide association study and functional validation implicates JADE1 in tauopathy
Kurt Farrell, SoongHo Kim, Natalia Han, et al.
Neuron
|
May 3, 2024
Genome sequence analyses identify novel risk loci for multiple system atrophy
Ruth Chia, Anindita Ray, Zalak Shah, et al.
Nature Neuroscience
|
July 16, 2025
Tau PET positivity in individuals with and without cognitive impairment varies with age, amyloid-β status, APOE genotype and sex
Rik Ossenkoppele, Emma M Coomans, Liana G Apostolova, 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.
Nature Genetics
|
February 16, 2010
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
Vivianna M Van Deerlin, Patrick M A Sleiman, Maria Martinez-Lage, 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.
Page
of 63