Area of research
Genetics · Cancer Research
Research interest
Research interests include Genetic Associations and Epidemiology, Cancer Genomics and Diagnostics, Genomics and Rare Diseases, and BRCA gene mutations in cancer.
Refining breast cancer genetic risk and biology through multi-ancestry fine-mapping analyses of 192 risk regions
Impact of common variants on brain gene expression from RNA to protein to schizophrenia risk
Leveraging generative AI to prioritize drug repurposing candidates for Alzheimer’s disease with real-world clinical validation
Genome-wide association analyses of breast cancer in women of African ancestry identify new susceptibility loci and improve risk prediction
Drug repurposing for Alzheimer’s disease from 2012–2022—a 10-year literature review
A novel enzymatic biosensor for CIP in food based on UCNPs and colorimetric strategy of potassium titanium oxalate
The impact of common variants on gene expression in the human brain: from RNA to protein to schizophrenia risk
Genome- and transcriptome-wide association studies of 386,000 Asian and European-ancestry women provide new insights into breast cancer genetics
Risperidone-induced changes in DNA methylation in peripheral blood from first-episode schizophrenia patients parallel changes in neuroimaging and cognitive phenotypes
Integrating Genome and Methylome Data to Identify Candidate DNA Methylation Biomarkers for Pancreatic Cancer Risk
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
An integrative multi-omics analysis to identify candidate DNA methylation biomarkers related to prostate cancer risk
Identification of novel breast cancer susceptibility loci in meta-analyses conducted among Asian and European descendants
Phenome-based approach identifies RIC1-linked Mendelian syndrome through zebrafish models, biobank associations and clinical studies
DRAMS: A tool to detect and re-align mixed-up samples for integrative studies of multi-omics data
A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data
Genetically Predicted Levels of DNA Methylation Biomarkers and Breast Cancer Risk: Data From 228 951 Women of European Descent
Re-evaluating genetic variants identified in candidate gene studies of breast cancer risk using data from nearly 280,000 women of Asian and European ancestry
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer
Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer
A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk
Genetic Data from Nearly 63,000 Women of European Descent Predicts DNA Methylation Biomarkers and Epithelial Ovarian Cancer Risk
Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling
Site-specific selection reveals selective constraints and functionality of tumor somatic mtDNA mutations
Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk
Cell-free circulating mitochondrial DNA content and risk of hepatocellular carcinoma in patients with chronic HBV infection
The impact of genotype calling errors on family-based studies
Prospective evidence of a circulating microRNA signature as a non-invasive marker of hepatocellular carcinoma in HBV patients
Genetic and chromosomal alterations in <scp>K</scp>enyan <scp>W</scp>ilms <scp>T</scp>umor