Johanna Sandling
Projektkoordinator vid Institutionen för medicinska vetenskaper; Reumatologi
- Telefon:
- 018-471 47 29
- Mobiltelefon:
- 070-425 06 25
- E-post:
- johanna.sandling@medsci.uu.se
- Besöksadress:
- Rudbecklaboratoriet, R3, vån 2
751 85 Uppsala - Postadress:
- Rudbecklaboratoriet, C11
751 85 Uppsala
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Publikationer
Senaste publikationer
- A survey of ficolin-3 activity in Systemic Lupus Erythematosus reveals a link to hematological disease manifestations and autoantibody profile (2024)
- B cell polygenic risk scores associate with anti-dsDNA antibodies and nephritis in systemic lupus erythematosus (2023)
- Distinct HLA associations with autoantibody-defined subgroups in idiopathic inflammatory myopathies (2023)
- Contribution of rare genetic variation to disease susceptibility in a large Scandinavian myositis cohort (2022)
- Complement C4 Copy Number Variation is Linked to SSA/Ro and SSB/La Autoantibodies in Systemic Inflammatory Autoimmune Diseases (2022)
Alla publikationer
Artiklar
- A survey of ficolin-3 activity in Systemic Lupus Erythematosus reveals a link to hematological disease manifestations and autoantibody profile (2024)
- B cell polygenic risk scores associate with anti-dsDNA antibodies and nephritis in systemic lupus erythematosus (2023)
- Distinct HLA associations with autoantibody-defined subgroups in idiopathic inflammatory myopathies (2023)
- Contribution of rare genetic variation to disease susceptibility in a large Scandinavian myositis cohort (2022)
- Complement C4 Copy Number Variation is Linked to SSA/Ro and SSB/La Autoantibodies in Systemic Inflammatory Autoimmune Diseases (2022)
- Strong Association of Combined Genetic Deficiencies in the Classical Complement Pathway With Risk of Systemic Lupus Erythematosus and Primary Sjögren's Syndrome (2022)
- Mer-tyrosine kinase (2022)
- Variants in BANK1 are associated with lupus nephritis of European ancestry. (2021)
- Contributions of de novo variants to systemic lupus erythematosus (2021)
- DNA Methylation-Based Interferon Scores Associate With Sub-Phenotypes in Primary Sjögren's Syndrome (2021)
- Interaction between the STAT4rs11889341(T) risk allele and smoking confers increased risk of myocardial infarction and nephritis in patients with systemic lupus erythematosus (2021)
- Molecular pathways in patients with systemic lupus erythematosus revealed by gene-centred DNA sequencing (2021)
- Genetic and clinical basis for two distinct subtypes of primary Sjögren's syndrome (2021)
- Toll-like receptors revisited (2021)
- Function of multiple sclerosis-protective HLA class I alleles revealed by genome-wide protein-quantitative trait loci mapping of interferon signalling (2020)
- High genetic risk score is associated with early disease onset, damage accrual and decreased survival in systemic lupus erythematosus (2020)
- Whole-genome sequencing identifies complex contributions to genetic risk by variants in genes causing monogenic systemic lupus erythematosus (2019)
- A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts (2019)
- Circulating Levels of Interferon Regulatory Factor-5 Associates With Subgroups of Systemic Lupus Erythematosus Patients. (2019)
- Shared and Unique Patterns of DNA Methylation in Systemic Lupus Erythematosus and Primary Sjogren's Syndrome (2019)
- Genetic variations in A20 DUB domain provide a genetic link to citrullination and neutrophil extracellular traps in systemic lupus erythematosus (2019)
- Cytokine production by activated plasmacytoid dendritic cells and NK cells is suppressed by an IRAK4 inhibitor (2018)
- Cytokine production by activated plasmacytoid dendritic cells and natural killer cells is suppressed by an IRAK4 inhibitor (2018)
- DNA methylation mapping identifies gene regulatory effects in patients with systemic lupus erythematosus (2018)
- Shared and unique patterns of DNA methylation in primary Sjogren's syndrome and systemic lupus erythematosus (2018)
- Transcription profiling of peripheral B cells in antibody-positive primary Sjogren's syndrome reveals upregulated expression of CX3CR1 and a type I and type II interferon signature (2018)
- Epigenetic alterations in primary Sjogren's syndrome (2018)
- Novel gene variants associated with cardiovascular disease in systemic lupus erythematosus and rheumatoid arthritis (2018)
- A DNA methylation biomarker of alcohol consumption. (2018)
- Genetic basis and clinical evidence for two variants of primary Sjögren's syndrome with distinct outcomes (2018)
- Novel risk genes for systemic lupus erythematosus predicted by random forest classification (2017)
- SLE Comprises Four Immune-Phenotypes, Which Differ Regarding HLA-DRB1 and Clinical Associations (2017)
- Epigenetic Patterns in Blood Associated With Lipid Traits Predict Incident Coronary Heart Disease Events and Are Enriched for Results From Genome-Wide Association Studies (2017)
- Treatment-Associated DNA Methylation Patterns in Systemic Lupus Erythematosus (2017)
- Transancestral mapping and genetic load in systemic lupus erythematosus (2017)
- High Genetic Risk Score Is Associated with Increased Organ Damage in SLE (2017)
- Higher Nevus Count Exhibits a Distinct DNA Methylation Signature in Healthy Human Skin (2017)
- Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity (2017)
- The Effect of Hydroxychloroquine and IRAK4 Inhibition on The IFN-A and TNF-A Production Induced by Sle Related Immune Complexes (2016)
- Genome-wide DNA methylation analysis in multiple tissues in primary Sjögren's syndrome reveals regulatory effects at interferon-induced genes (2016)
- Immunoseq (2016)
- Epigenome-wide DNA methylation patterns associated with fatigue in primary Sjogren's syndrome (2016)
- Epigenome-wide association study (EWAS) of BMI, BMI change and waist circumference in African American adults identifies multiple replicated loci (2015)
- Hypomethylation in Enhancer and Promoter Regions of Interferon Regulated Genes in Multiple Tissues Is Associated with Primary Sjogren's Syndrome (2015)
- Genome-Wide Analysis of DNA Methylation Profiles in Multiple Tissues in Primary Sjogren's Syndrome (2015)
- Epigenome-Wide DNA Methylation Patterns Associated with Fatigue in Primary Sjogren's Syndrome (2015)
- Genome-Wide DNA Methylation Patterns Associated with Fatigue in Primary Sjogren's Syndrome (2015)
- DNA methylation of lipid-related genes affects blood lipid levels. (2015)
- Genome-wide analysis of DNA methylation in systemic lupus erythematosus (2015)
- DNA methylation and body-mass index (2014)
- Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12 (2014)
- Genome-Wide DNA Methylation Analysis of CD19+B Cells in Primary Sjogren's Syndrome (2014)
- Association of STAT4 Polymorphism with Severe Renal Insufficiency in Lupus Nephritis (2013)
- Global Analysis of DNA Methylation Variation in Adipose Tissue from Twins Reveals Links to Disease-Associated Variants in Distal Regulatory Elements (2013)
- Coronary heart disease in systemic lupus erythematosus is associated with interferon regulatory factor-8 gene variants (2013)
- HLA-DRB1*04/*13 alleles are associated with vascular disease and antiphospholipid antibodies in systemic lupus erythematosus (2013)
- Genes identified in Asian SLE GWASs are also associated with SLE in Caucasian populations (2013)
- Contribution of IKBKE and IFIH1 gene variants to SLE susceptibility (2013)
- Genome-wide profiling of target genes for the systemic lupus erythematosus-associated transcription factors IRF5 and STAT4 (2013)
- Evidence of association between interferon regulatory factor 5 gene polymorphisms and asthma (2012)
- Fetal, Developmental, and Parental Influences on Cystatin C in Childhood (2011)
- A candidate gene study of the type I interferon pathway implicates IKBKE and IL8 as risk loci for SLE (2011)
- Association between Common Variation at the FTO Locus and Changes in Body Mass Index from Infancy to Late Childhood (2011)
- Preferential Association of Interferon Regulatory Factor 5 Gene Variants with Seronegative Rheumatoid Arthritis in 2 Swedish Case-Control Studies (2011)
- Variation in STAT4 is associated with systemic lupus erythematosus in a Finnish family cohort (2010)
- A STAT4 risk allele is associated with ischaemic cerebrovascular events and anti-phospholipid antibodies in systemic lupus erythematosus (2010)
- A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus (2009)
- Interferon Regulatory Factor 5 (IRF5) Gene Variants are Associated with Multiple Sclerosis in Three Distinct Populations (2008)
- Comprehensive evaluation of the genetic variants of interferon regulatory factor 5 (IRF5) reveals a novel 5 bp length polymorphism as strong risk factor for systemic lupus erythematosus (2008)
- Variants in BANK1 are associated with lupus nephritis
- From genetic predisposition to clinical outcome in systemic lupus erythematosus
- Dissection of genes in the type I interferon pathway reveals two novel risk loci for SLE