Item Type | Name |
Concept
|
ADAM17 Protein
|
Concept
|
Tumor Necrosis Factor alpha-Induced Protein 3
|
Concept
|
Animals
|
Concept
|
Apolipoprotein L1
|
Concept
|
Olfaction Disorders
|
Concept
|
Age Factors
|
Concept
|
Antibodies, Bacterial
|
Concept
|
c-Mer Tyrosine Kinase
|
Concept
|
Histocompatibility Antigens Class II
|
Concept
|
Algorithms
|
Concept
|
Antibodies, Antinuclear
|
Concept
|
Alleles
|
Concept
|
Alzheimer Disease
|
Concept
|
African Americans
|
Concept
|
Carcinoma, Renal Cell
|
Concept
|
B-Lymphocytes
|
Concept
|
Basal Ganglia Diseases
|
Concept
|
Base Sequence
|
Concept
|
Bayes Theorem
|
Concept
|
Cell Line
|
Concept
|
Cell Movement
|
Concept
|
Biopsy
|
Concept
|
Chromosomes, Human, Pair 10
|
Concept
|
Chromosomes, Human, Pair 3
|
Concept
|
Chromosomes, Human, Pair 6
|
Concept
|
Craniosynostoses
|
Concept
|
Cross-Sectional Studies
|
Concept
|
Cross-Cultural Comparison
|
Concept
|
Clinical Trials as Topic
|
Concept
|
Cryoglobulins
|
Concept
|
Europe
|
Concept
|
Exons
|
Concept
|
Eye
|
Concept
|
Complement C3
|
Concept
|
Complement C4
|
Concept
|
Enzyme-Linked Immunosorbent Assay
|
Concept
|
Epilepsy
|
Concept
|
Epilepsies, Myoclonic
|
Concept
|
Epistaxis
|
Concept
|
Fibrosis
|
Concept
|
Genetic Carrier Screening
|
Concept
|
von Hippel-Lindau Disease
|
Concept
|
Histological Techniques
|
Concept
|
HLA-DQ Antigens
|
Concept
|
Humans
|
Concept
|
Huntington Disease
|
Concept
|
Hydrocephalus
|
Concept
|
Genes, Dominant
|
Concept
|
Genes, Recessive
|
Concept
|
Genetic Counseling
|
Concept
|
Genetic Testing
|
Concept
|
Genetics, Population
|
Concept
|
HeLa Cells
|
Concept
|
Hydroxychloroquine
|
Concept
|
Lip
|
Concept
|
Lipoproteins, HDL
|
Concept
|
Liver Cirrhosis, Biliary
|
Concept
|
Keratoconjunctivitis Sicca
|
Concept
|
Kidney Neoplasms
|
Concept
|
Klinefelter Syndrome
|
Concept
|
Lupus Nephritis
|
Concept
|
Lymphocyte Activation
|
Concept
|
Lymphocytes
|
Concept
|
Macrophages
|
Concept
|
Magnetic Resonance Imaging
|
Concept
|
Granuloma
|
Concept
|
Leukocytes
|
Concept
|
Interferon Type I
|
Concept
|
Interferons
|
Concept
|
Mycobacterium tuberculosis
|
Concept
|
Terminology as Topic
|
Concept
|
Japan
|
Concept
|
Mexico
|
Concept
|
Mice, Inbred C57BL
|
Concept
|
Models, Biological
|
Concept
|
Models, Molecular
|
Concept
|
Molecular Sequence Data
|
Concept
|
Monocytes
|
Concept
|
Morbidity
|
Concept
|
Mosaicism
|
Concept
|
Predictive Value of Tests
|
Concept
|
Mouth Mucosa
|
Concept
|
Registries
|
Concept
|
Saliva
|
Concept
|
Salivary Glands
|
Concept
|
Salivary Glands, Minor
|
Concept
|
Parkinson Disease
|
Concept
|
Sarcoidosis
|
Concept
|
Repetitive Sequences, Nucleic Acid
|
Concept
|
Parotid Gland
|
Concept
|
Polymorphism, Restriction Fragment Length
|
Concept
|
Retrospective Studies
|
Concept
|
Rheumatoid Factor
|
Concept
|
Sensitivity and Specificity
|
Concept
|
Ribonucleoproteins
|
Concept
|
Serologic Tests
|
Concept
|
Severity of Illness Index
|
Concept
|
Sex Chromosome Aberrations
|
Concept
|
Risk
|
Concept
|
Risk Factors
|
Concept
|
ROC Curve
|
Concept
|
Periodontitis
|
Concept
|
Putamen
|
Concept
|
Quality of Life
|
Concept
|
Surveys and Questionnaires
|
Concept
|
Thalamus
|
Concept
|
Receptors, Antigen, T-Cell
|
Concept
|
CD4-Positive T-Lymphocytes
|
Concept
|
Spinocerebellar Degenerations
|
Concept
|
2',5'-Oligoadenylate Synthetase
|
Concept
|
Blotting, Western
|
Concept
|
Reproducibility of Results
|
Concept
|
Statistics as Topic
|
Concept
|
Calcium Channels
|
Concept
|
Antibodies, Anticardiolipin
|
Concept
|
Cohort Studies
|
Concept
|
Submandibular Gland
|
Concept
|
Sulfur Radioisotopes
|
Concept
|
In Situ Hybridization, Fluorescence
|
Concept
|
Porphyromonas gingivalis
|
Concept
|
Protein Tyrosine Phosphatases
|
Concept
|
Vimentin
|
Concept
|
Disease Progression
|
Concept
|
Microsatellite Repeats
|
Concept
|
CpG Islands
|
Concept
|
Trinucleotide Repeats
|
Concept
|
Antirheumatic Agents
|
Concept
|
Patient Selection
|
Concept
|
Myosin Heavy Chains
|
Concept
|
Founder Effect
|
Concept
|
Fluorescent Antibody Technique, Indirect
|
Concept
|
DNA Methylation
|
Concept
|
Central Nervous System Neoplasms
|
Concept
|
Mutation, Missense
|
Concept
|
Anticipation, Genetic
|
Concept
|
Reverse Transcriptase Polymerase Chain Reaction
|
Concept
|
Myoclonic Epilepsy, Juvenile
|
Concept
|
Lafora Disease
|
Concept
|
Mice, Inbred NOD
|
Concept
|
Polymorphism, Single Nucleotide
|
Concept
|
RNA, Small Cytoplasmic
|
Concept
|
Spinocerebellar Ataxias
|
Concept
|
Germ-Line Mutation
|
Concept
|
Molecular Motor Proteins
|
Concept
|
beta Karyopherins
|
Concept
|
Hemangioblastoma
|
Concept
|
Mice, Knockout
|
Concept
|
Trinucleotide Repeat Expansion
|
Concept
|
Amino Acid Substitution
|
Concept
|
Genomic Instability
|
Concept
|
Promoter Regions, Genetic
|
Concept
|
Genetic Predisposition to Disease
|
Concept
|
Mitochondrial Proton-Translocating ATPases
|
Concept
|
Principal Component Analysis
|
Concept
|
American Native Continental Ancestry Group
|
Concept
|
Psychiatric Status Rating Scales
|
Concept
|
Ubiquitin-Protein Ligases
|
Concept
|
Somatic Hypermutation, Immunoglobulin
|
Concept
|
Sjogren's Syndrome
|
Concept
|
Smell
|
Concept
|
Mice
|
Concept
|
Receptor, Fibroblast Growth Factor, Type 3
|
Concept
|
Genome-Wide Association Study
|
Concept
|
Trisomy
|
Concept
|
Tuberculosis
|
Concept
|
Turner Syndrome
|
Concept
|
United States
|
Concept
|
Single-Cell Analysis
|
Concept
|
White Matter
|
Concept
|
Gray Matter
|
Concept
|
Iron-Binding Proteins
|
Concept
|
Gene Expression
|
Concept
|
Prevalence
|
Concept
|
Cluster Analysis
|
Concept
|
Linear Models
|
Concept
|
Logistic Models
|
Concept
|
Odds Ratio
|
Concept
|
Case-Control Studies
|
Concept
|
Transcriptome
|
Concept
|
TATA-Box Binding Protein
|
Concept
|
Immunophenotyping
|
Concept
|
T-Lymphocyte Subsets
|
Concept
|
HLA-DRB1 Chains
|
Concept
|
HLA-DQ beta-Chains
|
Concept
|
Thymocytes
|
Concept
|
Embryonic Development
|
Concept
|
Clonal Anergy
|
Concept
|
Age of Onset
|
Concept
|
Datasets as Topic
|
Concept
|
Treponema denticola
|
Concept
|
Age Distribution
|
Concept
|
Sex Distribution
|
Concept
|
Adaptor Proteins, Signal Transducing
|
Concept
|
Cell Proliferation
|
Concept
|
CD11b Antigen
|
Concept
|
B-Cell Activating Factor
|
Concept
|
OX40 Ligand
|
Concept
|
Apolipoprotein E4
|
Concept
|
Quantitative Trait Loci
|
Concept
|
Chromosomes, Human, X
|
Concept
|
Chromosomes, Human, Y
|
Concept
|
Interleukin-1 Receptor-Associated Kinases
|
Concept
|
Presenilin-1
|
Concept
|
NADPH Oxidases
|
Concept
|
Histone Code
|
Concept
|
Computational Biology
|
Concept
|
DNA Repeat Expansion
|
Concept
|
Microsatellite Instability
|
Concept
|
Republic of Korea
|
Concept
|
Area Under Curve
|
Concept
|
Mannose-Binding Protein-Associated Serine Proteases
|
Concept
|
STAT4 Transcription Factor
|
Concept
|
Interferon Regulatory Factors
|
Concept
|
Protein Tyrosine Phosphatases, Non-Receptor
|
Concept
|
Receptors, Purinergic P2Y2
|
Concept
|
Sex Chromosome Disorders of Sex Development
|
Concept
|
Ikaros Transcription Factor
|
Concept
|
Genetic Loci
|
Concept
|
Spatial Analysis
|
Concept
|
Apolipoproteins
|
Concept
|
Apolipoproteins E
|
Concept
|
Arthritis, Rheumatoid
|
Concept
|
Asian Americans
|
Concept
|
Autoantibodies
|
Concept
|
Autoantigens
|
Concept
|
Cells, Cultured
|
Concept
|
Central Nervous System Diseases
|
Concept
|
Cerebellar Ataxia
|
Concept
|
Cerebellar Neoplasms
|
Concept
|
Cerebellum
|
Concept
|
Chile
|
Concept
|
Diagnostic Errors
|
Concept
|
Disease Models, Animal
|
Concept
|
Follow-Up Studies
|
Concept
|
Friedreich Ataxia
|
Concept
|
Hypergammaglobulinemia
|
Concept
|
Ichthyosis
|
Concept
|
Immunoglobulin G
|
Concept
|
Immunization, Passive
|
Concept
|
Indians, North American
|
Concept
|
Indians, South American
|
Concept
|
Intellectual Disability
|
Concept
|
Methionine
|
Concept
|
Oklahoma
|
Academic Article
|
Interaction between innate immunity and Ro52-induced antibody causes Sjögren's syndrome-like disorder in mice.
|
Academic Article
|
Antibodies to periodontogenic bacteria are associated with higher disease activity in lupus patients.
|
Academic Article
|
Anti-La positive, anti-Ro negative subset of primary Sjögren's syndrome: anti-La is a reality but is the disease?
|
Academic Article
|
Single Cell Transcriptomics Implicate Novel Monocyte and T Cell Immune Dysregulation in Sarcoidosis.
|
Academic Article
|
Brief Report: Patients With Primary Sjögren's Syndrome Who Are Positive for Autoantibodies to Tripartite Motif-Containing Protein 38 Show Greater Disease Severity.
|
Academic Article
|
Recent developments in the quest for myoclonic epilepsy genes.
|
Academic Article
|
Mutations in EFHC1 cause juvenile myoclonic epilepsy.
|
Academic Article
|
Clinical heterogeneity of recessive ataxia in the Mexican population.
|
Academic Article
|
DNA variants in coding region of EFHC1: SNPs do not associate with juvenile myoclonic epilepsy.
|
Academic Article
|
Clinical and molecular features of familial and sporadic cases of von Hippel-Lindau disease from Mexico.
|
Academic Article
|
Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome.
|
Academic Article
|
X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome.
|
Academic Article
|
Klinefelter's syndrome (47,XXY) is in excess among men with Sjögren's syndrome.
|
Academic Article
|
Expansion of the variable expression of Muenke syndrome: Hydrocephalus without craniosynostosis.
|
Academic Article
|
Clinical and Serologic Features in Patients With Incomplete Lupus Classification Versus Systemic Lupus Erythematosus Patients and Controls.
|
Academic Article
|
A missense variant in NCF1 is associated with susceptibility to multiple autoimmune diseases.
|
Academic Article
|
Effect of Tobacco Smoking on The Clinical, Histopathological, and Serological Manifestations of Sjögren's Syndrome.
|
Academic Article
|
Fatty infiltration of the minor salivary glands is a selective feature of aging but not Sjögren's syndrome.
|
Academic Article
|
Genetics and epigenetics in primary Sjögren's syndrome.
|
Academic Article
|
American Indians Have a Higher Risk of Sjögren's Syndrome and More Disease Activity Than European Americans and African Americans.
|
Academic Article
|
Drs. Rasmussen and Scofield reply.
|
Academic Article
|
Drs. Rasmussen and Scofield reply.
|
Academic Article
|
Genotype-phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotype.
|
Academic Article
|
Von Hippel-Lindau disease germline mutations in Mexican patients with cerebellar hemangioblastoma.
|
Academic Article
|
Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer's disease in Mexican families.
|
Academic Article
|
Apolipoprotein E epsilon4 allele is associated with Parkinson disease risk in a Mexican Mestizo population.
|
Academic Article
|
Uptake of genetic testing and long-term tumor surveillance in von Hippel-Lindau disease.
|
Academic Article
|
Impact of genetic ancestry and sociodemographic status on the clinical expression of systemic lupus erythematosus in American Indian-European populations.
|
Academic Article
|
Allelic heterogeneity in NCF2 associated with systemic lupus erythematosus (SLE) susceptibility across four ethnic populations.
|
Academic Article
|
Genome-wide DNA methylation patterns in naive CD4+ T cells from patients with primary Sjögren's syndrome.
|
Academic Article
|
2016 American College of Rheumatology/European League Against Rheumatism Classification Criteria for Primary Sjögren's Syndrome: A Consensus and Data-Driven Methodology Involving Three International Patient Cohorts.
|
Academic Article
|
2016 American College of Rheumatology/European League Against Rheumatism classification criteria for primary Sjögren's syndrome: A consensus and data-driven methodology involving three international patient cohorts.
|
Academic Article
|
Reply.
|
Academic Article
|
Identification of a Sjögren's syndrome susceptibility locus at OAS1 that influences isoform switching, protein expression, and responsiveness to type I interferons.
|
Academic Article
|
Evidence of Alternative Modes of B Cell Activation Involving Acquired Fab Regions of N-Glycosylation in Antibody-Secreting Cells Infiltrating the Labial Salivary Glands of Patients With Sjögren's Syndrome.
|
Academic Article
|
Transcriptomic and Network Analysis of Minor Salivary Glands of Patients With Primary Sjögren's Syndrome.
|
Academic Article
|
Childhood-onset of primary Sjögren's syndrome: phenotypic characterization at diagnosis of 158 children.
|
Academic Article
|
Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11-p12: LRRC1, GCLC, KIAA0057 and CLIC5.
|
Academic Article
|
Olfactory dysfunction in hereditary ataxia and basal ganglia disorders.
|
Academic Article
|
Huntington's Disease-like 2 (HDL2) in North America and Japan.
|
Academic Article
|
Genetic admixture of European FRDA genes is the cause of Friedreich ataxia in the Mexican population.
|
Academic Article
|
Progressive GAA expansions in dorsal root ganglia of Friedreich's ataxia patients.
|
Academic Article
|
Clinical and genetic characteristics of Mexican Huntington's disease patients.
|
Academic Article
|
Identification of IRF8, TMEM39A, and IKZF3-ZPBP2 as susceptibility loci for systemic lupus erythematosus in a large-scale multiracial replication study.
|
Academic Article
|
Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instability.
|
Academic Article
|
Expansion of the Spinocerebellar ataxia type 10 (SCA10) repeat in a patient with Sioux Native American ancestry.
|
Academic Article
|
Repeat interruptions in spinocerebellar ataxia type 10 expansions are strongly associated with epileptic seizures.
|
Academic Article
|
Single-cell analysis of glandular T cell receptors in Sjögren's syndrome.
|
Academic Article
|
Influence of geolocation and ethnicity on the phenotypic expression of primary Sjögren's syndrome at diagnosis in 8310 patients: a cross-sectional study from the Big Data Sjögren Project Consortium.
|
Academic Article
|
Rare X Chromosome Abnormalities in Systemic Lupus Erythematosus and Sjögren's Syndrome.
|
Academic Article
|
Minor salivary gland fibrosis in Sjögren's syndrome is elevated, associated with focus score and not solely a consequence of aging.
|
Academic Article
|
Corrigendum to "Klinefelter's syndrome (47,XXY) is in excess among men with Sjögren's syndrome" [Clin. Immunol. 168 (2016) 25-29].
|
Academic Article
|
Unique clinical characteristics, autoantibodies and medication use in Native American patients with systemic lupus erythematosus.
|
Academic Article
|
Extensive cerebellar and thalamic degeneration in spinocerebellar ataxia type 10.
|
Academic Article
|
Sjögren's Syndrome Minor Salivary Gland CD4+ Memory T Cells Associate with Glandular Disease Features and have a Germinal Center T Follicular Helper Transcriptional Profile.
|
Academic Article
|
Systemic phenotype related to primary Sjögren's syndrome in 279 patients carrying isolated anti-La/SSB antibodies.
|
Academic Article
|
Juvenile myoclonic epilepsy: linkage to chromosome 6p12 in Mexico families.
|
Academic Article
|
Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10.
|
Academic Article
|
Mutation analyses of genes on 6p12-p11 in patients with juvenile myoclonic epilepsy.
|
Academic Article
|
Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population.
|
Academic Article
|
Anticipation and intergenerational repeat instability in spinocerebellar ataxia type 17.
|
Academic Article
|
Somatic instability of the expanded GAA triplet-repeat sequence in Friedreich ataxia progresses throughout life.
|
Academic Article
|
Presymptomatic diagnosis in Huntington's disease: the Mexican experience.
|
Academic Article
|
Genetically determined Amerindian ancestry correlates with increased frequency of risk alleles for systemic lupus erythematosus.
|
Academic Article
|
The lupus family registry and repository.
|
Academic Article
|
Role of MYH9 and APOL1 in African and non-African populations with lupus nephritis.
|
Academic Article
|
Comparison of the American-European Consensus Group Sjogren's syndrome classification criteria to newly proposed American College of Rheumatology criteria in a large, carefully characterised sicca cohort.
|
Academic Article
|
Antibody-secreting cell specificity in labial salivary glands reflects the clinical presentation and serology in patients with Sjögren's syndrome.
|
Academic Article
|
The IRF5-TNPO3 association with systemic lupus erythematosus has two components that other autoimmune disorders variably share.
|
Academic Article
|
Genome-Wide Association Study in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture.
|
Academic Article
|
Identification of a Systemic Lupus Erythematosus Risk Locus Spanning ATG16L2, FCHSD2, and P2RY2 in Koreans.
|
Academic Article
|
Previous diagnosis of Sjögren's Syndrome as rheumatoid arthritis or systemic lupus erythematosus.
|
Academic Article
|
Use of SLICC criteria in a large, diverse lupus registry enables SLE classification of a subset of ACR-designated subjects with incomplete lupus.
|
Academic Article
|
How immunological profile drives clinical phenotype of primary Sjögren's syndrome at diagnosis: analysis of 10,500 patients (Sjögren Big Data Project).
|
Academic Article
|
Sjogren's syndrome: An update on disease pathogenesis, clinical manifestations and treatment.
|
Academic Article
|
Sjögren Syndrome without Focal Lymphocytic Infiltration of the Salivary Glands.
|
Academic Article
|
Reproducibility of Ocular Surface Staining in the Assessment of Sjögren Syndrome-Related Keratoconjunctivitis Sicca: Implications on Disease Classification.
|
Academic Article
|
Systemic manifestations of primary Sjögren's syndrome out of the ESSDAI classification: prevalence and clinical relevance in a large international, multi-ethnic cohort of patients.
|
Academic Article
|
Epidemiological profile and north-south gradient driving baseline systemic involvement of primary Sjögren's syndrome.
|
Academic Article
|
Defective Efferocytosis in a Murine Model of Sjögren's Syndrome Is Mediated by Dysfunctional Mer Tyrosine Kinase Receptor.
|
Academic Article
|
Genetic variants at the RTP4/MASP1 locus are associated with fatigue in Scandinavian patients with primary Sjögren's syndrome.
|
Academic Article
|
Influence of the age at diagnosis in the disease expression of primary Sjögren syndrome. Analysis of 12,753 patients from the Sjögren Big Data Consortium.
|
Academic Article
|
Characterization and outcomes of 414 patients with primary SS who developed hematological malignancies.
|
Academic Article
|
Genome-wide association study identifies Sjögren's risk loci with functional implications in immune and glandular cells.
|
Academic Article
|
Novel HLA associations with outcomes of Mycobacterium tuberculosis exposure and sarcoidosis in individuals of African ancestry using nearest-neighbor feature selection.
|
Academic Article
|
Dysregulated long non-coding RNA in Sjögren's disease impacts both interferon and adaptive immune responses.
|
Academic Article
|
Author Correction: Genome-wide association study identifies Sjögren's risk loci with functional implications in immune and glandular cells.
|
Academic Article
|
Author Correction: Genome-wide association study identifies Sj?gren's risk loci with functional implications in immune and glandular cells.
|
Academic Article
|
Genetics of neurosarcoidosis.
|
Academic Article
|
Anti-vimentin antibodies are associated with higher severity of Sj?gren's disease.
|
Academic Article
|
Autoantibodies identify primary Sj?gren's syndrome in patients lacking serum IgG specific for Ro/SS-A and La/SS-B.
|
Academic Article
|
Multiple Correspondence Analysis and HLA-Associations of Organ Involvement in a Large Cohort of African-American and European-American Patients with Sarcoidosis.
|
Academic Article
|
Inclusivity in Research Matters: Variants in PVT1 Specific to People of African Descent Are Associated with Pulmonary Fibrosis.
|
Academic Article
|
Rewriting the rule book for Sj?gren's syndrome? The promise of new approaches to old treatments.
|