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1. OP0113 GENOME-WIDE ASSOCIATION STUDY OF Ro/SSA+ AND Ro/SSA-SJÖGREN’S CASES IN THE SJÖGREN’S GENETIC NETWORK (SGENE) DEMONSTRATES DIVERGENT GENETIC ARCHITECTURE IN PATIENT SUBPHENOTYPES

3. POS0240 SINGLE-CELL TRANSCRIPTOMICS OFFERS NEW INSIGHTS INTO SJÖGREN’S DISEASE PATHOGENESIS IN THE SALIVARY GLAND

4. OP0128 SPATIAL TRANSCRIPTOMICS IMPLICATES GLANDULAR CELL INVOLVEMENT IN PATHOPHYSIOLOGY OF SJÖGREN’S DISEASE

5. POS1130 DESIGNING OF A PHASE 2, MULTICENTER, RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-BLIND STUDY TO ASSESS THE EFFICACY AND SAFETY OF NIPOCALIMAB, AN FCRN INHIBITOR, IN ADULTS WITH PRIMARY SJÖGREN’S SYNDROME

6. POS0096 SJÖGREN’S DISEASE AND SYSTEMIC LUPUS ERYTHEMATOSUS DDX6-CXCR5 RISK INTERVALS REVEAL COMMON SNPS WITH FUNCTIONAL SIGNIFICANCE IN IMMUNE AND SALIVARY GLAND CELLS

7. POS0098 LINC01871, IMPLICATED IN SJÖGREN’S DISEASE PATHOGENESIS, IS REGULATED BY INTERFERON-G AND CALCINEURIN SIGNALING

8. OP0111 INTEGRATION OF GWAS AND EPIGENETIC STUDIES IDENTIFIES NOVEL GENES THAT ALTER EXPRESSION IN THE MINOR SALIVARY GLAND IN SJÖGREN’S DISEASE

12. Two Be or Not Two Be: The Nuclear Autoantigen La/SS-B Is Able to Form Dimers and Oligomers in a Redox Dependent Manner

13. A functional haplotype of UBE2L3 confers risk for systemic lupus erythematosus

14. Role of MYH9 and APOL1 in African and non-African populations with lupus nephritis

15. Evaluation of the TREX1 gene in a large multi-ancestral lupus cohort

17. Replication of the BANK1 genetic association with systemic lupus erythematosus in a European-derived population

18. Two Be or Not Two Be: The Nuclear Autoantigen La/SS-B Is able to form Dimers and Oligomers in a Redox Dependent Manner

19. T Cell Mediated Conversion of a Non-anti-La Reactive B cell to an Autoreactive anti-La B Cell by Somatic Hypermutation

21. OP0047 GENOME-WIDE ASSOCIATION STUDY OF SJÖGREN’S SYNDROME IDENTIFIES TEN NEW RISK LOCI

22. OP0139 FUNCTIONAL EVALUATION OF THE SJÖGREN’S SYNDROME AND SYSTEMIC LUPUS ERYTHEMATOSUS DDX6-CXCR5 RISK INTERVAL

34. Identification of Sjögren's Syndrome Risk Loci near TNFAIP3 and PRDM1

36. Identification of Multiple Sjogren'S Syndrome Susceptibility Loci

37. Preferential Binding to Elk-1 by SLE-Associated IL10 Risk Allele Upregulates IL10 Expression

38. Analysis of autosomal genes reveals gene-sex interactions and higher total genetic risk in men with systemic lupus erythematosus

39. A functional haplotype of UBE2L3 confers risk for systemic lupus erythematosus

40. Role of MYH9 and APOL1 in African and non-African populations with lupus nephritis

41. Evaluation of the TREX1 gene in a large multi-ancestral lupus cohort

42. Identification of a systemic lupus erythematosus susceptibility locus at 11p13 between PDHX and CD44 in a multiethnic study

43. Evaluation of the TREX1 gene in a large multi-ancestral lupus cohort.

44. OP0020 Identification of Multiple Sjögren’s Syndrome Susceptibility Loci

45. THU0292 Comparison of the Aecg Sjogren’s Syndrome Classification Criteria to the Newly Proposed ACR Criteria in a Large, Carefully Characterized Sicca Cohort.

47. Vitamin D deficiency is associated with an increased autoimmune response in healthy individuals and in patients with systemic lupus erythematosus

48. The Lupus Family Registry and Repository

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