Area of research
Genetics · Molecular Biology
Research interest
Research interests include Genetic Associations and Epidemiology, Epigenetics and DNA Methylation, Metabolomics and Mass Spectrometry Studies, and Bioinformatics and Genomic Networks.
Common variation at 1q23.3, 2p23.3, 2q33.3, and 2p21 influences the risk of acute myeloid leukemia.
DNA methylation of genes involved in lipid metabolism drives adiponectin levels and metabolic disease.
Epigenome-wide association study of circulating interleukin-6 connects DNA methylation to immunometabolic and inflammatory health.
A genome-wide association meta-analysis of cholesterol synthesis intermediates identifies three associations for lanosterol
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
LEOPARD: missing view completion for multi-timepoint omics data via representation disentanglement and temporal knowledge transfer.
Metabolomics Reveals Reasons for the Efficacy of Acupuncture in Migraine Patients: The Role of Anaerobic Glycolysis and Mitochondrial Citrate in Migraine Relief.
Multi-ancestry genome-wide association analyses incorporating SNP-by-psychosocial interactions identify novel loci for serum lipids
Novel and Known Genetic Players in Hypertension: From Gene Expression to Striking Insights
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
Genome-wide characterization of circulating metabolic biomarkers
Genome-wide characterization of circulating metabolic biomarkers
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction
Understanding the genetic complexity of puberty timing across the allele frequency spectrum
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction.
Loss of atrial natriuretic peptide signaling causes insulin resistance, mitochondrial dysfunction, and low endurance capacity.
Analyzing longitudinal trait trajectories using GWAS identifies genetic variants for kidney function decline.
Analyzing longitudinal trait trajectories using GWAS identifies genetic variants for kidney function decline
Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum
Interpretable multimodal machine learning (IMML) framework reveals pathological signatures of distal sensorimotor polyneuropathy.
Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets
Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets.
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification