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Medrxiv : the Preprint Server for Health Sciences
|
February 6, 2026
Evidence for reduced somatic T-cell receptor sequence diversity profiles among Midwestern Amish in an aging cohort study
Lauren A Cruz, Shiying Liu, Kristy L Miskimen, et al.
International Journal of Geriatric Psychiatry
|
September 1, 2023
Neuropsychiatric features in a multi-ethnic population with Alzheimer disease and mild cognitive impairment
Katrina Celis, Andrew Zaman, Larry Deon Adams, et al.
Human Molecular Genetics
|
May 1, 2012
Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways
Anthony J Griswold, Deqiong Ma, Holly N Cukier, et al.
JAMA Neurology
|
July 25, 2017
Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport
Brian W Kunkle, Badri N Vardarajan, Adam C Naj, et al.
Biorxiv : the Preprint Server for Biology
|
November 24, 2025
Multi-ancestry Transcriptome-Wide Association Study Reveals Shared and Population-Specific Genetic Effects in Alzheimer's Disease
Xinyu Sun, Makaela Mews, Nicholas R Wheeler, et al.
The Journal of Prevention of Alzheimer'S Disease
|
July 10, 2026
Can we identify people with Alzheimer's disease from examination of the eye? A bidirectional Mendelian randomization (MR) study
Humayun Kiser, Ashley Budu-Aggrey, Jessica N Cooke Bailey, et al.
American Journal of Human Genetics
|
January 14, 2003
Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1)
Kirk Mykytyn, Darryl Y Nishimura, Charles C Searby, et al.
Neurology. Genetics
|
December 21, 2018
Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease
Gary W Beecham, Badri Vardarajan, Elizabeth Blue, et al.
The New England Journal of Medicine
|
July 31, 2007
Risk alleles for multiple sclerosis identified by a genomewide study
, David A Hafler, Alastair Compston, et al.
Human Molecular Genetics
|
July 9, 2004
Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping
Stephen J Sawcer, Mel Maranian, Sara Singlehurst, et al.
Page
of 91
Search research articles
Search
Showing results (671-680 of 908) with videos related to
Sort By:
Page
of 91
Medrxiv : the Preprint Server for Health Sciences
|
February 6, 2026
Evidence for reduced somatic T-cell receptor sequence diversity profiles among Midwestern Amish in an aging cohort study
Lauren A Cruz, Shiying Liu, Kristy L Miskimen, et al.
International Journal of Geriatric Psychiatry
|
September 1, 2023
Neuropsychiatric features in a multi-ethnic population with Alzheimer disease and mild cognitive impairment
Katrina Celis, Andrew Zaman, Larry Deon Adams, et al.
Human Molecular Genetics
|
May 1, 2012
Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways
Anthony J Griswold, Deqiong Ma, Holly N Cukier, et al.
JAMA Neurology
|
July 25, 2017
Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport
Brian W Kunkle, Badri N Vardarajan, Adam C Naj, et al.
Biorxiv : the Preprint Server for Biology
|
November 24, 2025
Multi-ancestry Transcriptome-Wide Association Study Reveals Shared and Population-Specific Genetic Effects in Alzheimer's Disease
Xinyu Sun, Makaela Mews, Nicholas R Wheeler, et al.
The Journal of Prevention of Alzheimer'S Disease
|
July 10, 2026
Can we identify people with Alzheimer's disease from examination of the eye? A bidirectional Mendelian randomization (MR) study
Humayun Kiser, Ashley Budu-Aggrey, Jessica N Cooke Bailey, et al.
American Journal of Human Genetics
|
January 14, 2003
Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1)
Kirk Mykytyn, Darryl Y Nishimura, Charles C Searby, et al.
Neurology. Genetics
|
December 21, 2018
Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease
Gary W Beecham, Badri Vardarajan, Elizabeth Blue, et al.
The New England Journal of Medicine
|
July 31, 2007
Risk alleles for multiple sclerosis identified by a genomewide study
, David A Hafler, Alastair Compston, et al.
Human Molecular Genetics
|
July 9, 2004
Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping
Stephen J Sawcer, Mel Maranian, Sara Singlehurst, et al.
Page
of 91