Results 101 to 110 of about 10,755 (158)

Large-scale cross-ancestry genome-wide meta-analysis of serum urate

open access: yesNature Communications
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

Identification of Therapeutic Targets for Hyperuricemia: Systematic Genome-Wide Mendelian Randomization and Colocalization Analysis

open access: yesBiomedicines
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

Association between genetically plasma proteins and osteonecrosis: a proteome-wide Mendelian randomization analysis

open access: yesFrontiers in Genetics
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

open access: yesCommunications Medicine
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

Testing bidirectional associations of major depressive disorder with medical conditions: two-sample Mendelian randomization study

open access: yesnpj Mental Health Research
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]

open access: yesCancer Epidemiol Biomarkers Prev, 2020
Semmes EC   +5 more
europepmc   +1 more source

Genome-wide association and multi-omics analyses provide insights into the disease mechanisms of central serous chorioretinopathy

open access: yesScientific Reports
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

A multi-omics Mendelian randomization study reveals PAM as a potential therapeutic target for type 2 diabetes

open access: yesJournal of Translational Medicine
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

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