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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.
The Lancet. Neurology
|
December 22, 2017
Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study
Rita Guerreiro, Owen A Ross, Celia Kun-Rodrigues, et al.
Neurobiology of Aging
|
September 27, 2016
Analysis of C9orf72 repeat expansions in a large international cohort of dementia with Lewy bodies
Celia Kun-Rodrigues, Owen A Ross, Tatiana Orme, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
November 13, 2025
The Neighborhoods Study: Examining the social exposome in Alzheimer's disease and related dementias
Grace C George, Sarah A Keller, Erin Abner, 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.
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.
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.
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.
Neuron
|
May 3, 2024
Genome sequence analyses identify novel risk loci for multiple system atrophy
Ruth Chia, Anindita Ray, Zalak Shah, 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.
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Search research articles
Search
Showing results (231-240 of 243) with videos related to
Sort By:
Page
of 25
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.
The Lancet. Neurology
|
December 22, 2017
Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study
Rita Guerreiro, Owen A Ross, Celia Kun-Rodrigues, et al.
Neurobiology of Aging
|
September 27, 2016
Analysis of C9orf72 repeat expansions in a large international cohort of dementia with Lewy bodies
Celia Kun-Rodrigues, Owen A Ross, Tatiana Orme, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
November 13, 2025
The Neighborhoods Study: Examining the social exposome in Alzheimer's disease and related dementias
Grace C George, Sarah A Keller, Erin Abner, 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.
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.
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.
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.
Neuron
|
May 3, 2024
Genome sequence analyses identify novel risk loci for multiple system atrophy
Ruth Chia, Anindita Ray, Zalak Shah, 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.
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of 25