Results 161 to 170 of about 6,140 (191)
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Nucleic Acids Research
Transcriptome-wide association study (TWAS) has successfully identified numerous complex disease susceptibility genes in the post-genome-wide association study (GWAS) era.
Chen Cao +8 more
semanticscholar +1 more source
Transcriptome-wide association study (TWAS) has successfully identified numerous complex disease susceptibility genes in the post-genome-wide association study (GWAS) era.
Chen Cao +8 more
semanticscholar +1 more source
European Heart Journal
Genetically regulated long non-coding RNAs (lncRNAs) in coronary artery disease (CAD) have not been investigated. To discover CAD-relevant lncRNAs, we performed the transcriptome-wide association study (TWAS) using a subset genomic data of ...
S. Li +4 more
semanticscholar +1 more source
Genetically regulated long non-coding RNAs (lncRNAs) in coronary artery disease (CAD) have not been investigated. To discover CAD-relevant lncRNAs, we performed the transcriptome-wide association study (TWAS) using a subset genomic data of ...
S. Li +4 more
semanticscholar +1 more source
Scientific Reports
Age-related macular degeneration (AMD) is a complex multifactorial disease with a significant genetic component. Despite extensive research efforts, the underlying molecular mechanisms remain elusive, necessitating innovative approaches to identify ...
Hongfan Yang, Haofei Huang, Kunlin Pu
semanticscholar +1 more source
Age-related macular degeneration (AMD) is a complex multifactorial disease with a significant genetic component. Despite extensive research efforts, the underlying molecular mechanisms remain elusive, necessitating innovative approaches to identify ...
Hongfan Yang, Haofei Huang, Kunlin Pu
semanticscholar +1 more source
Journal of Neurophysiology
Background: Despite a significant genetic component to insomnia (heritability: 22-25%), the genetic loci that modulate insomnia risk remain limited. Methods: We employed the Unified Test for Molecular Markers (UTMOST) for transcriptome-wide association ...
Li Li +6 more
semanticscholar +1 more source
Background: Despite a significant genetic component to insomnia (heritability: 22-25%), the genetic loci that modulate insomnia risk remain limited. Methods: We employed the Unified Test for Molecular Markers (UTMOST) for transcriptome-wide association ...
Li Li +6 more
semanticscholar +1 more source
Andrology
BACKGROUND Erectile dysfunction (ED) is a common condition affecting millions of men worldwide. While genome-wide association studies (GWAS) have identified genetic loci associated with ED risk, the potential causative genes and their biological ...
Tianle Zhu +8 more
semanticscholar +1 more source
BACKGROUND Erectile dysfunction (ED) is a common condition affecting millions of men worldwide. While genome-wide association studies (GWAS) have identified genetic loci associated with ED risk, the potential causative genes and their biological ...
Tianle Zhu +8 more
semanticscholar +1 more source
Scientific Reports
Benign prostatic hyperplasia (BPH) is a prevalent urinary system disorder. Despite evidence of a significant genetic component from previous studies, the specific pathogenic genes and biological mechanisms are still largely unknown.
Li Wang +7 more
semanticscholar +1 more source
Benign prostatic hyperplasia (BPH) is a prevalent urinary system disorder. Despite evidence of a significant genetic component from previous studies, the specific pathogenic genes and biological mechanisms are still largely unknown.
Li Wang +7 more
semanticscholar +1 more source
Intermittent fasting in the prevention and treatment of cancer
Ca-A Cancer Journal for Clinicians, 2021Katherine Clifton +2 more
exaly
An overview of real‐world data sources for oncology and considerations for research
Ca-A Cancer Journal for Clinicians, 2022Lynne Penberthy +2 more
exaly
Social determinants of health and US cancer screening interventions: A systematic review
Ca-A Cancer Journal for Clinicians, 2023Ariella R Korn
exaly

