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Schizophrenia (Heidelberg, Germany)
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May 21, 2025
Body fluid biomarkers and psychosis risk in The Accelerating Medicines Partnership® Schizophrenia Program: design considerations
Diana O Perkins, Clark D Jeffries, Scott R Clark, et al.
Stroke
|
January 24, 2015
Genetic overlap between diagnostic subtypes of ischemic stroke
Elizabeth G Holliday, Matthew Traylor, Rainer Malik, et al.
Biological Psychiatry
|
February 4, 2017
Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder
Yanni Zeng, Pau Navarro, Masoud Shirali, et al.
NPJ Genomic Medicine
|
March 7, 2020
Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosis
Marta F Nabais, Tian Lin, Beben Benyamin, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 15, 2024
Antidepressant Exposure and DNA Methylation: Insights from a Methylome-Wide Association Study
E Davyson, X Shen, F Huider, et al.
Nature Neuroscience
|
February 6, 2019
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions
David M Howard, Mark J Adams, Toni-Kim Clarke, et al.
BMJ Open
|
June 18, 2026
Strategic Amyotrophic Lateral Sclerosis Australia-Systems Genomics Consortium (SALSA-SGC): cohort profile
Anjali K Henders, Laura Ziser, Fleur C Garton, et al.
Nature Communications
|
January 28, 2018
GWAS of epigenetic aging rates in blood reveals a critical role for TERT
Ake T Lu, Luting Xue, Elias L Salfati, et al.
Science (New York, N.Y.)
|
April 27, 2023
Leveraging base-pair mammalian constraint to understand genetic variation and human disease
Patrick F Sullivan, Jennifer R S Meadows, Steven Gazal, et al.
Biorxiv : the Preprint Server for Biology
|
March 22, 2023
Leveraging Base Pair Mammalian Constraint to Understand Genetic Variation and Human Disease
Patrick F Sullivan, Jennifer R S Meadows, Steven Gazal, et al.
Page
of 55
Search research articles
Search
Showing results (471-480 of 544) with videos related to
Sort By:
Page
of 55
Schizophrenia (Heidelberg, Germany)
|
May 21, 2025
Body fluid biomarkers and psychosis risk in The Accelerating Medicines Partnership® Schizophrenia Program: design considerations
Diana O Perkins, Clark D Jeffries, Scott R Clark, et al.
Stroke
|
January 24, 2015
Genetic overlap between diagnostic subtypes of ischemic stroke
Elizabeth G Holliday, Matthew Traylor, Rainer Malik, et al.
Biological Psychiatry
|
February 4, 2017
Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder
Yanni Zeng, Pau Navarro, Masoud Shirali, et al.
NPJ Genomic Medicine
|
March 7, 2020
Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosis
Marta F Nabais, Tian Lin, Beben Benyamin, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 15, 2024
Antidepressant Exposure and DNA Methylation: Insights from a Methylome-Wide Association Study
E Davyson, X Shen, F Huider, et al.
Nature Neuroscience
|
February 6, 2019
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions
David M Howard, Mark J Adams, Toni-Kim Clarke, et al.
BMJ Open
|
June 18, 2026
Strategic Amyotrophic Lateral Sclerosis Australia-Systems Genomics Consortium (SALSA-SGC): cohort profile
Anjali K Henders, Laura Ziser, Fleur C Garton, et al.
Nature Communications
|
January 28, 2018
GWAS of epigenetic aging rates in blood reveals a critical role for TERT
Ake T Lu, Luting Xue, Elias L Salfati, et al.
Science (New York, N.Y.)
|
April 27, 2023
Leveraging base-pair mammalian constraint to understand genetic variation and human disease
Patrick F Sullivan, Jennifer R S Meadows, Steven Gazal, et al.
Biorxiv : the Preprint Server for Biology
|
March 22, 2023
Leveraging Base Pair Mammalian Constraint to Understand Genetic Variation and Human Disease
Patrick F Sullivan, Jennifer R S Meadows, Steven Gazal, et al.
Page
of 55