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Human Molecular Genetics
|
April 6, 2022
Genetic architecture of RNA editing regulation in Alzheimer's disease across diverse ancestral populations
Olivia K Gardner, Derek Van Booven, Lily Wang, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 24, 2025
Basic Science and Pathogenesis
Abel Belachew, Sarah Biber, Walter W Kukull, et al.
JAMA Network Open
|
March 30, 2019
Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry
Devanshi Patel, Jesse Mez, Badri N Vardarajan, et al.
Trauma Surgery & Acute Care Open
|
March 27, 2023
Screening and intervention for intimate partner violence at trauma centers and emergency departments: an evidence-based systematic review from the Eastern Association for the Surgery of Trauma
Amanda L Teichman, Stephanie Bonne, Rishi Rattan, et al.
Biorxiv : the Preprint Server for Biology
|
November 1, 2024
African origin haplotype protective for Alzheimer's disease in <i>APOE</i>ε4 carriers: exploring potential mechanisms
Luciana Bertholim-Nasciben, Karen Nuytemans, Derek Van Booven, et al.
American Journal of Pharmaceutical Education
|
October 6, 2022
Well-being Content Inclusion in Pharmacy Education Across the United States and Canada
Elizabeth Buckley, Simi Gunaseelan, Benjamin D Aronson, et al.
Neurology
|
June 9, 2004
Apolipoprotein E controls the risk and age at onset of Parkinson disease
Y J Li, M A Hauser, W K Scott, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
September 15, 2015
Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease
Brian W Kunkle, James Jaworski, Sandra Barral, et al.
Translational Psychiatry
|
July 27, 2012
Genome-wide association study of Alzheimer's disease
M I Kamboh, F Y Demirci, X Wang, et al.
Neurogenetics
|
December 14, 1999
Linkage analysis of candidate myelin genes in familial multiple sclerosis
E Seboun, J R Oksenberg, A Rombos, et al.
Page
of 91
Search research articles
Search
Showing results (681-690 of 908) with videos related to
Sort By:
Page
of 91
Human Molecular Genetics
|
April 6, 2022
Genetic architecture of RNA editing regulation in Alzheimer's disease across diverse ancestral populations
Olivia K Gardner, Derek Van Booven, Lily Wang, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 24, 2025
Basic Science and Pathogenesis
Abel Belachew, Sarah Biber, Walter W Kukull, et al.
JAMA Network Open
|
March 30, 2019
Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry
Devanshi Patel, Jesse Mez, Badri N Vardarajan, et al.
Trauma Surgery & Acute Care Open
|
March 27, 2023
Screening and intervention for intimate partner violence at trauma centers and emergency departments: an evidence-based systematic review from the Eastern Association for the Surgery of Trauma
Amanda L Teichman, Stephanie Bonne, Rishi Rattan, et al.
Biorxiv : the Preprint Server for Biology
|
November 1, 2024
African origin haplotype protective for Alzheimer's disease in <i>APOE</i>ε4 carriers: exploring potential mechanisms
Luciana Bertholim-Nasciben, Karen Nuytemans, Derek Van Booven, et al.
American Journal of Pharmaceutical Education
|
October 6, 2022
Well-being Content Inclusion in Pharmacy Education Across the United States and Canada
Elizabeth Buckley, Simi Gunaseelan, Benjamin D Aronson, et al.
Neurology
|
June 9, 2004
Apolipoprotein E controls the risk and age at onset of Parkinson disease
Y J Li, M A Hauser, W K Scott, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
September 15, 2015
Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease
Brian W Kunkle, James Jaworski, Sandra Barral, et al.
Translational Psychiatry
|
July 27, 2012
Genome-wide association study of Alzheimer's disease
M I Kamboh, F Y Demirci, X Wang, et al.
Neurogenetics
|
December 14, 1999
Linkage analysis of candidate myelin genes in familial multiple sclerosis
E Seboun, J R Oksenberg, A Rombos, et al.
Page
of 91