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Nature Communications
|
November 13, 2024
Author Correction: Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes
Kurt Farrell, Jack Humphrey, Timothy Chang, et al.
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.
Molecular Neurodegeneration
|
October 14, 2024
Correction: 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.
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.
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.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
January 12, 2024
Asian Cohort for Alzheimer's Disease (ACAD) pilot study on genetic and non-genetic risk factors for Alzheimer's disease among Asian Americans and Canadians
Pei-Chuan Ho, Wai Haung Yu, Boon Lead Tee, et al.
Nature Communications
|
April 18, 2019
Multi-platform discovery of haplotype-resolved structural variation in human genomes
Mark J P Chaisson, Ashley D Sanders, Xuefang Zhao, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 18, 2023
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies <i>LRRC4C, LHX5-AS1</i> and nominates ancestry-specific loci <i>PTPRK</i> , <i>GRB14</i> , and <i>KIAA0825</i> as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium
Farid Rajabli, Penelope Benchek, Giuseppe Tosto, et al.
Genome Biology
|
July 17, 2025
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies known and novel cross-population and ancestry-specific associations as novel risk loci for Alzheimer's disease
Farid Rajabli, Penelope Benchek, Giuseppe Tosto, et al.
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Search research articles
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Showing results (71-80 of 80) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 80 results.
Nature Communications
|
November 13, 2024
Author Correction: Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes
Kurt Farrell, Jack Humphrey, Timothy Chang, et al.
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.
Molecular Neurodegeneration
|
October 14, 2024
Correction: 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.
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.
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.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
January 12, 2024
Asian Cohort for Alzheimer's Disease (ACAD) pilot study on genetic and non-genetic risk factors for Alzheimer's disease among Asian Americans and Canadians
Pei-Chuan Ho, Wai Haung Yu, Boon Lead Tee, et al.
Nature Communications
|
April 18, 2019
Multi-platform discovery of haplotype-resolved structural variation in human genomes
Mark J P Chaisson, Ashley D Sanders, Xuefang Zhao, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 18, 2023
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies <i>LRRC4C, LHX5-AS1</i> and nominates ancestry-specific loci <i>PTPRK</i> , <i>GRB14</i> , and <i>KIAA0825</i> as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium
Farid Rajabli, Penelope Benchek, Giuseppe Tosto, et al.
Genome Biology
|
July 17, 2025
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies known and novel cross-population and ancestry-specific associations as novel risk loci for Alzheimer's disease
Farid Rajabli, Penelope Benchek, Giuseppe Tosto, et al.
Page
of 8