Area of research
Physiology · Rheumatology
Research interest
Research interests include Biology, Immunology, Medicine, Genome-wide association study, Genetics, and Internal medicine.
Transcriptomic profiling of Sjögren’s disease salivary glands identifies signatures associated with both follicular and extrafollicular responses linked to rheumatoid factor and anti-La/SSB seropositivity
Genome-wide association study identifies Sjögren’s risk loci with functional implications in immune and glandular cells
Addressing the clinical unmet needs in primary Sjögren’s Syndrome through the sharing, harmonization and federated analysis of 21 European cohorts
Epidemiological profile and north–south gradient driving baseline systemic involvement of primary Sjögren’s syndrome
Unique Sjögren’s syndrome patient subsets defined by molecular features
Novel genetic associations with interferon in systemic lupus erythematosus identified by replication and fine-mapping of trait-stratified genome-wide screen
Genetic fine mapping of systemic lupus erythematosus MHC associations in Europeans and African Americans
A plausibly causal functional lupus-associated risk variant in the STAT1–STAT4 locus
Transancestral mapping and genetic load in systemic lupus erythematosus
A missense variant in NCF1 is associated with susceptibility to multiple autoimmune diseases
Identification of a Sjögren's syndrome susceptibility locus at OAS1 that influences isoform switching, protein expression, and responsiveness to type I interferons
Brief Report: Rare X Chromosome Abnormalities in Systemic Lupus Erythematosus and Sjögren's Syndrome
Klinefelter's syndrome (47,XXY) is in excess among men with Sjögren's syndrome
X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome
Genome‐Wide Association Study in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture
Identification of a Systemic Lupus Erythematosus Risk Locus Spanning <i>ATG16L2, FCHSD2</i>, and <i>P2RY2</i> in Koreans
Germline variation of TNFAIP3 in primary Sjögren's syndrome-associated lymphoma
Lupus Risk Variant Increases pSTAT1 Binding and Decreases ETS1 Expression
GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region
The IRF5–TNPO3 association with systemic lupus erythematosus has two components that other autoimmune disorders variably share
Genetic analysis of the pathogenic molecular sub-phenotype interferon-alpha identifies multiple novel loci involved in systemic lupus erythematosus
Two Functional Lupus-Associated BLK Promoter Variants Control Cell-Type- and Developmental-Stage-Specific Transcription
End‐Stage Renal Disease in African Americans With Lupus Nephritis Is Associated With <i>APOL1</i>
Germline and somatic genetic variations of TNFAIP3 in lymphoma complicating primary Sjögren’s syndrome
PTPN22 Association in Systemic Lupus Erythematosus (SLE) with Respect to Individual Ancestry and Clinical Sub-Phenotypes