Results 101 to 110 of about 10,755 (158)
Large-scale cross-ancestry genome-wide meta-analysis of serum urate
Hyperuricemia is an essential causal risk factor for gout and is associated with cardiometabolic diseases. Given the limited contribution of East Asian ancestry to genome-wide association studies of serum urate, the genetic architecture of serum urate ...
Chamlee Cho +16 more
doaj +1 more source
Using phenome-wide association studies and the SF-12 quality of life metric to identify profound consequences of adverse childhood experiences on adult mental and physical health in a Northern Nevadan population. [PDF]
Schlauch KA +4 more
europepmc +1 more source
Background: At present, there are still limitations and challenges in the treatment of hyperuricemia (HUA). Mendelian randomization (MR) has been widely used to identify new therapeutic targets.
Na Chen +6 more
doaj +1 more source
BackgroundPrevious studies have explored the role of plasma proteins on osteonecrosis. This Mendelian randomization (MR) study further assessed plasma proteins on osteonecrosis whether a causal relationship exists and provides some evidence of causality ...
Chen Meng +12 more
doaj +1 more source
A phenome-wide association study of uterine fibroids reveals a marked burden of comorbidities
Abstract Background The burden of comorbidities in those with uterine fibroids compared to those without fibroids is understudied. We performed a phenome-wide association study to systematically assess the association between fibroids and other conditions.
Elizabeth A. Jasper +10 more
openaire +3 more sources
Phenome-wide association studies go large [PDF]
openaire +1 more source
Depression is associated with increased risk for a variety of medical conditions. However, the extent to which these associations reflect a causal impact of depression on medical conditions, or vice-versa, remains unresolved.
Yu Fang +4 more
doaj +1 more source
Leveraging Genome and Phenome-Wide Association Studies to Investigate Genetic Risk of Acute Lymphoblastic Leukemia. [PDF]
Semmes EC +5 more
europepmc +1 more source
Central serous chorioretinopathy (CSC) is a major cause of vision loss, especially in middle-aged men, and its chronic subtype can lead to legal blindness. Despite its clinical importance, the underlying mechanisms of CSC need further clarification.
Yuki Mori +30 more
doaj +1 more source
Background The progression of type 2 diabetes (T2D) is driven by pancreatic β-cell dysfunction and loss, yet current therapies fail to address this core pathophysiology. Methods We implemented an integrative pipeline combining genetic and functional data
Ming Yi +5 more
doaj +1 more source

