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Molecular Neurodegeneration
|
August 16, 2024
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 18, 2024
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
Journal of Neuropathology and Experimental Neurology
|
June 8, 2017
Multisite Assessment of Aging-Related Tau Astrogliopathy (ARTAG)
Gabor G Kovacs, Sharon X Xie, Edward B Lee, et al.
Acta Neuropathologica
|
December 15, 2015
Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy
Gabor G Kovacs, Isidro Ferrer, Lea T Grinberg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 8, 2025
Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 23, 2022
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System Atrophy
Franziska Hopfner, Anja K Tietz, Viktoria C Ruf, et al.
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.
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.
Acta Neuropathologica
|
November 1, 2021
Genome-wide association study and functional validation implicates JADE1 in tauopathy
Kurt Farrell, SoongHo Kim, Natalia Han, 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.
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of 30
Search research articles
Search
Showing results (281-290 of 296) with videos related to
Sort By:
Page
of 30
Molecular Neurodegeneration
|
August 16, 2024
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 18, 2024
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
Journal of Neuropathology and Experimental Neurology
|
June 8, 2017
Multisite Assessment of Aging-Related Tau Astrogliopathy (ARTAG)
Gabor G Kovacs, Sharon X Xie, Edward B Lee, et al.
Acta Neuropathologica
|
December 15, 2015
Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy
Gabor G Kovacs, Isidro Ferrer, Lea T Grinberg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 8, 2025
Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 23, 2022
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System Atrophy
Franziska Hopfner, Anja K Tietz, Viktoria C Ruf, et al.
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.
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.
Acta Neuropathologica
|
November 1, 2021
Genome-wide association study and functional validation implicates JADE1 in tauopathy
Kurt Farrell, SoongHo Kim, Natalia Han, 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.
Page
of 30