Search research articles
Contact Us
Filters
Showing results (241-250 of 299) with videos related to
Page
of 30
Sort By:
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 23, 2025
Public Health
Pei-Chuan Ho, Boon Lead Tee, Clara Li, et al.
Genomics
|
June 2, 2018
Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project
Adam C Naj, Honghuang Lin, Badri N Vardarajan, et al.
Journal of Alzheimer'S Disease : JAD
|
August 8, 2022
The Advisory Group on Risk Evidence Education for Dementia: Multidisciplinary and Open to All
Allyson C Rosen, Jalayne J Arias, J Wesson Ashford, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 11, 2023
Association of Common and Rare Variants with Alzheimer's Disease in over 13,000 Diverse Individuals with Whole-Genome Sequencing from the Alzheimer's Disease Sequencing Project
Wan-Ping Lee, Seung Hoan Choi, Margaret G Shea, et al.
Dementia and Geriatric Cognitive Disorders
|
February 28, 2018
Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project
Elizabeth E Blue, Joshua C Bis, Michael O Dorschner, et al.
Medrxiv : the Preprint Server for Health Sciences
|
October 3, 2025
A multi-ancestry polygenic risk score for Alzheimer disease is associated with cognitive decline, hippocampal atrophy and neuropathological hallmarks in diverse populations
Nuzulul Kurniansyah, Shinya Tasaki, Habbibur Rehman, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 25, 2025
Basic Science and Pathogenesis
Alaina Durant, Shubhabrata Mukherjee, Michael L Lee, et al.
Archives of Neurology
|
August 11, 2010
Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes
Gyungah Jun, Adam C Naj, Gary W Beecham, et al.
Neuron
|
January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders
Elaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
Nature Genetics
|
June 21, 2011
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
Günter U Höglinger, Nadine M Melhem, Dennis W Dickson, et al.
Page
of 30
Search research articles
Search
Showing results (241-250 of 299) with videos related to
Sort By:
Page
of 30
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 23, 2025
Public Health
Pei-Chuan Ho, Boon Lead Tee, Clara Li, et al.
Genomics
|
June 2, 2018
Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project
Adam C Naj, Honghuang Lin, Badri N Vardarajan, et al.
Journal of Alzheimer'S Disease : JAD
|
August 8, 2022
The Advisory Group on Risk Evidence Education for Dementia: Multidisciplinary and Open to All
Allyson C Rosen, Jalayne J Arias, J Wesson Ashford, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 11, 2023
Association of Common and Rare Variants with Alzheimer's Disease in over 13,000 Diverse Individuals with Whole-Genome Sequencing from the Alzheimer's Disease Sequencing Project
Wan-Ping Lee, Seung Hoan Choi, Margaret G Shea, et al.
Dementia and Geriatric Cognitive Disorders
|
February 28, 2018
Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project
Elizabeth E Blue, Joshua C Bis, Michael O Dorschner, et al.
Medrxiv : the Preprint Server for Health Sciences
|
October 3, 2025
A multi-ancestry polygenic risk score for Alzheimer disease is associated with cognitive decline, hippocampal atrophy and neuropathological hallmarks in diverse populations
Nuzulul Kurniansyah, Shinya Tasaki, Habbibur Rehman, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 25, 2025
Basic Science and Pathogenesis
Alaina Durant, Shubhabrata Mukherjee, Michael L Lee, et al.
Archives of Neurology
|
August 11, 2010
Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes
Gyungah Jun, Adam C Naj, Gary W Beecham, et al.
Neuron
|
January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders
Elaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
Nature Genetics
|
June 21, 2011
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
Günter U Höglinger, Nadine M Melhem, Dennis W Dickson, et al.
Page
of 30