Area of research
Nephrology · Molecular Biology
Research interest
Research interests include Biology, Genetics, Medicine, Genome-wide association study, Nephropathy, and Allele.
Loss of GalNAc-T14 links O-glycosylation defects to alterations in B cell homing in IgA nephropathy
Exome analysis links kidney malformations to developmental disorders and reveals causal genes
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease
De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis
The copy number variation landscape of congenital anomalies of the kidney and urinary tract
Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in Children
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations
Rituximab in Children with Steroid-Dependent Nephrotic Syndrome
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens
Phenotypic Expansion of DGKE-Associated Diseases
Rituximab is a safe and effective long-term treatment for children with steroid and calcineurin inhibitor–dependent idiopathic nephrotic syndrome