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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.
Brain : a Journal of Neurology
|
March 20, 2025
Novel modelling approaches to elucidate the genetic architecture of resilience to Alzheimer's disease
Jared M Phillips, Logan C Dumitrescu, Derek B Archer, 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.
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.
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.
JAMA Neurology
|
October 19, 2020
Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis
Brian W Kunkle, Michael Schmidt, Hans-Ulrich Klein, et al.
Nature
|
November 4, 2014
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis, Xin He, Arthur P Goldberg, et al.
Molecular Psychiatry
|
October 23, 2019
Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation
Joshua C Bis, Xueqiu Jian, Brian W Kunkle, et al.
Molecular Psychiatry
|
August 16, 2018
Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation
Joshua C Bis, Xueqiu Jian, Brian W Kunkle, et al.
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of 47
Search research articles
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Showing results (431-440 of 467) with videos related to
Sort By:
Page
of 47
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.
Brain : a Journal of Neurology
|
March 20, 2025
Novel modelling approaches to elucidate the genetic architecture of resilience to Alzheimer's disease
Jared M Phillips, Logan C Dumitrescu, Derek B Archer, 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.
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.
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.
JAMA Neurology
|
October 19, 2020
Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis
Brian W Kunkle, Michael Schmidt, Hans-Ulrich Klein, et al.
Nature
|
November 4, 2014
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis, Xin He, Arthur P Goldberg, et al.
Molecular Psychiatry
|
October 23, 2019
Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation
Joshua C Bis, Xueqiu Jian, Brian W Kunkle, et al.
Molecular Psychiatry
|
August 16, 2018
Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation
Joshua C Bis, Xueqiu Jian, Brian W Kunkle, et al.
Page
of 47