Results 181 to 190 of about 8,166 (222)
Multivariate genome-wide analysis reveals shared genetic architecture and brain structural correlates of human cognitive abilities. [PDF]
Chen H +5 more
europepmc +1 more source
Genetic insights into alcohol-associated liver disease: integrative transcriptome-wide analysis identifies novel susceptibility genes. [PDF]
Wang Q, Wang Z, Hu M, Liu F, Wang Z.
europepmc +1 more source
Multitrait transcriptome‐wide association study (TWAS) tests
AbstractMultitrait tests can improve power to detect associations between individual single‐nucleotide polymorphisms (SNPs) and several related traits. Here, we develop methods for multi‐SNP transcriptome‐wide association (TWAS) tests to test the association between predicted gene expression levels and multiple phenotypes.
Helian Feng +3 more
semanticscholar +4 more sources
Abstract Pancreatic Ductal Adenocarcinoma (PDAC) is the third leading cause of cancer-related deaths in United States with a 5-year survival rate of only 8%. Inherited predisposition plays an important role in PDAC risk. Rare, moderately to highly penetrant mutations in hereditary cancer and pancreatitis genes, identified in families ...
Jun Zhong +22 more
semanticscholar +4 more sources
AbstractMotivationTranscriptome-wide association study (TWAS) is a significant methodology utilized for identifying associations between genes and diseases by integrating transcriptome and genome-wide association studies (GWAS) data. The approach has been successful in pinpointing risk genes for various diseases, including Alzheimer’s disease ...
Yong Liang, Handong Wang, Yan Zhang
semanticscholar +3 more sources
Transcriptome-wide association study (TWAS) of nasal respiratory epithelium and childhood asthma
Erick Forno +9 more
semanticscholar +3 more sources
Some of the next articles are maybe not open access.
Related searches:
Related searches:
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
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
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

