Area of research
Genetics · Endocrinology, Diabetes and Metabolism
Research interest
Research interests include Genetic Associations and Epidemiology, Hormonal Regulation and Hypertension, Ion Transport and Channel Regulation, and Parathyroid Disorders and Treatments.
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy
Dissecting the genetic heterogeneity of gastric cancer
Corrigendum to “Dissecting the genetic heterogeneity of gastric cancer”
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies
Identification of risk loci for primary aldosteronism in genome-wide association studies
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
The copy number variation landscape of congenital anomalies of the kidney and urinary tract
Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk
Genetic evidence of assortative mating in humans
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome
CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function
Identification of NF-κB and PLCL2 as new susceptibility genes and highlights on a potential role of IRF8 through interferon signature modulation in systemic sclerosis
TET2 and CSMD1 genes affect SBP response to hydrochlorothiazide in never-treated essential hypertensives
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens
Genome-wide association study of kidney function decline in individuals of European descent
Inactive Matrix Gla Protein Is Causally Related to Adverse Health Outcomes
Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index
Genome-Wide Association Study Identifies CAMKID Variants Involved in Blood Pressure Response to Losartan: The Sophia Study
Brief Report: A Regulatory Variant in <i>CCR6</i> Is Associated With Susceptibility to Antitopoisomerase‐Positive Systemic Sclerosis
Genome-wide association study of obsessive-compulsive disorder
Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk Analysis
Human serum albumin cysteinylation is increased in end stage renal disease patients and reduced by hemodialysis: mass spectrometry studies