173 results on '"Marion, Miranda C."'
Search Results
2. Molecular pathways identified from single nucleotide polymorphisms demonstrate mechanistic differences in systemic lupus erythematosus patients of Asian and European ancestry.
3. Identification of a regulatory pathway governing TRAF1 via an arthritis-associated non-coding variant
4. Mendelian randomization and pathway analysis demonstrate shared genetic associations between lupus and coronary artery disease
5. Transancestral mapping and genetic load in systemic lupus erythematosus.
6. Lupus Risk Variant Increases pSTAT1 Binding and Decreases ETS1 Expression
7. Effects of Intensive Systolic Blood Pressure Control on All-Cause Hospitalizations
8. Fine mapping of Xq28: both MECP2 and IRAK1 contribute to risk for systemic lupus erythematosus in multiple ancestral groups
9. Association of two independent functional risk haplotypes in TNIP1 with systemic lupus erythematosus
10. Impact of genetic ancestry and sociodemographic status on the clinical expression of systemic lupus erythematosus in American Indian–European populations
11. Identification of a regulatory pathway governing TRAF1 via an arthritis-associated non-coding variant
12. The modifying influence of HLA class II DQB1∗06:02 on the Streptococcus and clinical phenotype correlation among anti-Ro+ mothers of children with neonatal lupus
13. Identification of a regulatory pathway governing TRAF1 via an arthritis-associated non-coding variant
14. 1401 A Genome Wide Association Scan of SLE genetic risk in a cohort of African-American persons
15. The modifying influence of HLA class II DQB1∗06:02 on the Streptococcus and clinical phenotype correlation among anti-Ro+ mothers of children with neonatal lupus
16. Genome‐Wide Association Meta‐Analysis Reveals Novel Juvenile Idiopathic Arthritis Susceptibility Loci
17. Brief Report: Association of Natural Killer Cell Ligand Polymorphism HLA–C Asn80Lys With the Development of Anti‐SSA/Ro–Associated Congenital Heart Block
18. Gut dysbiosis and the clinical spectrum in anti-Ro positive mothers of children with neonatal lupus
19. Nucleic Acid-Sensing and Interferon-Inducible Pathways Show Differential Methylation in MZ Twins Discordant for Lupus and Overexpression in Independent Lupus Samples: Implications for Pathogenic Mechanism and Drug Targeting
20. Genetic Variation in the Peroxisome Proliferator Activated Receptor-Gamma Gene Is Associated with Histologically Advanced NAFLD
21. Bitableau bases for Garsia–Haiman modules of hollow type
22. A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis
23. Platelet Glycoprotein Ib α‐Chain as a Putative Therapeutic Target for Juvenile Idiopathic Arthritis: A Mendelian Randomization Study
24. Analysis of Trans-Ancestral SLE Risk Loci Identifies Unique Biologic Networks and Drug Targets in African and European Ancestries
25. Combined genetic analysis of juvenile idiopathic arthritis clinical subtypes identifies novel risk loci, target genes and key regulatory mechanisms
26. Enrichment of associations in genes with fibrosis, apoptosis, and innate immunity functions with cardiac manifestations of neonatal lupus
27. Genome-wide association analysis of juvenile idiopathic arthritis identifies a new susceptibility locus at chromosomal region 3q13
28. Preferential transmission of genetic risk variants of candidate loci at 6p21 from asymptomatic grandparents to mothers of children with neonatal lupus
29. Association of PPP2CA polymorphisms with systemic lupus erythematosus susceptibility in multiple ethnic groups
30. P20 The identification of novel genetic susceptibility loci for juvenile idiopathic arthritis by analysis across clinical subgroups
31. Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus
32. The susceptibility loci juvenile idiopathic arthritis shares with other autoimmune diseases extend to PTPN2, COG6, and ANGPT1
33. Features Associated With, and the Impact of, Hemolytic Anemia in Patients With Systemic Lupus Erythematosus: LX, Results From a Multiethnic Cohort
34. Genetic variation in the CRP promoter: association with systemic lupus erythematosus
35. Morphometric Analysis of Arteriolar Tortuosity in Human Cerebral White Matter of Preterm, Young, and Aged Subjects
36. The genetic profile of RF-positive polyarticular juvenile idiopathic arthritis (JIA) resembles adult rheumatoid arthritis (RA)
37. Association ofSLCO 1B1*14 Allele with Poor Response to Methotrexate in Juvenile Idiopathic Arthritis Patients
38. Combined genetic analysis of juvenile idiopathic arthritis clinical subtypes identifies novel risk loci, target genes and key regulatory mechanisms.
39. Brief Report: The Genetic Profile of Rheumatoid Factor-Positive Polyarticular Juvenile Idiopathic Arthritis Resembles That of Adult Rheumatoid Arthritis
40. Association of Natural Killer Cell Ligand Polymorphism, HLAC Asn80Lys, with the Development of Anti-SSA/Ro Associated Congenital Heart Block
41. GG-05 Predictive ability of SLE genetic risk factors varies across ethnicities
42. BD-01 E-genes identified via transancestral SNP mapping and gene expression analysis reveal novel targeted therapies for african-american and european-american SLE patients
43. Novel targeted therapies for African-American and European-American SLE patients identified from E-Genes elucidated by transancestral SNP mapping
44. A plausibly causal functional lupus-associated risk variant in the STAT1–STAT4 locus
45. O35. THE AUTOIMMUNE GENETIC ARCHITECTURE OF CHILDHOOD-ONSET RHEUMATOID ARTHRITIS
46. Association of SLCO1B1 *14 Allele with Poor Response to Methotrexate in Juvenile Idiopathic Arthritis Patients.
47. Brief Report: The Genetic Profile of Rheumatoid Factor–Positive Polyarticular Juvenile Idiopathic Arthritis Resembles That of Adult Rheumatoid Arthritis.
48. Association of Natural Killer Cell Ligand Polymorphism HLA-C Asn80Lys With the Development of Anti- SSA/Ro-Associated Congenital Heart Block.
49. Two Independent Functional Risk Haplotypes in TNIP1 are Associated with Systemic Lupus Erythematosus
50. Association of PPP2CA polymorphisms with SLE susceptibility in multiple ethnic groups
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