Peter K Gregersen

Peter K Gregersen's AcademicInfluence.com Rankings

Peter K Gregersen

Computer Science

#4516

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#4764

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Machine Learning

#908

World Rank

#921

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Artificial Intelligence

#1125

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#1145

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Database

#1732

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#1817

Historical Rank

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Computer Science

Peter K Gregersen's Degrees

PhD Computer Science Stanford University

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Best Online PhD of Computer Science (Doctorates) 2026

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Peter K Gregersen's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

A Genome-Wide Association Study Identifies IL23R as an Inflammatory Bowel Disease Gene (2006) (2867)
Strong Association of De Novo Copy Number Mutations with Autism (2007) (2746)
The shared epitope hypothesis. An approach to understanding the molecular genetics of susceptibility to rheumatoid arthritis. (1987) (2610)
Interferon-inducible gene expression signature in peripheral blood cells of patients with severe lupus (2003) (2090)
Genetics of rheumatoid arthritis contributes to biology and drug discovery (2013) (1877)
A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis. (2004) (1570)
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci (2010) (1285)
STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus. (2007) (1041)
Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. (2008) (926)
Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis (2011) (812)
A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus (2009) (782)
TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. (2007) (711)
Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE. (2004) (689)
A common haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus (2006) (680)
Genome-wide association study in alopecia areata implicates both innate and adaptive immunity (2010) (631)
Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes. (2005) (612)
Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4. (2005) (603)
High density genetic mapping identifies new susceptibility loci for rheumatoid arthritis (2012) (595)
Refining the complex rheumatoid arthritis phenotype based on specificity of the HLA-DRB1 shared epitope for antibodies to citrullinated proteins. (2005) (594)
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis (2007) (592)
Defining inflammatory cell states in rheumatoid arthritis joint synovial tissues by integrating single-cell transcriptomics and mass cytometry (2018) (560)
Common variants at CD40 and other loci confer risk of rheumatoid arthritis (2008) (550)
Pervasive Sharing of Genetic Effects in Autoimmune Disease (2011) (537)
Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America (2009) (494)
Gene-gene and gene-environment interactions involving HLA-DRB1, PTPN22, and smoking in two subsets of rheumatoid arthritis. (2007) (477)
Three functional variants of IFN regulatory factor 5 (IRF5) define risk and protective haplotypes for human lupus (2007) (454)
Multiple polymorphisms in the TNFAIP3 region are independently associated with systemic lupus erythematosus (2008) (447)
An autoinflammatory disease with deficiency of the interleukin-1-receptor antagonist. (2009) (439)
Apoptosis of CD8+ T cells is mediated by macrophages through interaction of HIV gp120 with chemokine receptor CXCR4 (1998) (437)
Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis (2012) (411)
Shortened telomeres in clonally expanded CD28-CD8+ T cells imply a replicative history that is distinct from their CD28+CD8+ counterparts. (1996) (401)
A genomewide screen in multiplex rheumatoid arthritis families suggests genetic overlap with other autoimmune diseases. (2001) (386)
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus (2010) (377)
RAGE and arthritis: the G82S polymorphism amplifies the inflammatory response (2002) (375)
Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis (2010) (372)
Accounting for ancestry: population substructure and genome-wide association studies. (2008) (362)
A functional promoter polymorphism in the macrophage migration inhibitory factor (MIF) gene associated with disease severity in rheumatoid arthritis (2002) (358)
Meta-Analysis of Genome-Wide Association Studies in Celiac Disease and Rheumatoid Arthritis Identifies Fourteen Non-HLA Shared Loci (2011) (355)
Functional annotation of a novel NFKB1 promoter polymorphism that increases risk for ulcerative colitis. (2004) (346)
Genetic variants at CD28, PRDM1, and CD2/CD58 are associated with rheumatoid arthritis risk (2009) (343)
Human polymorphism at microRNAs and microRNA target sites. (2013) (330)
Clonal predominance of T cell receptors within the CD8+ CD45RO+ subset in normal human subjects. (1993) (329)
Recent advances in the genetics of autoimmune disease. (2009) (323)
Genomics and the multifactorial nature of human autoimmune disease. (2011) (313)
REL, a member of the NF-κB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis (2009) (310)
The genetics revolution and the assault on rheumatoid arthritis. (1999) (308)
Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population (2012) (299)
Elevated Serum Levels of Interferon-Regulated Chemokines Are Biomarkers for Active Human Systemic Lupus Erythematosus (2006) (286)
A diffuse infiltrative CD8 lymphocytosis syndrome in human immunodeficiency virus (HIV) infection: a host immune response associated with HLA-DR5. (1990) (274)
The PTPN22 allele encoding an R620W variant interferes with the removal of developing autoreactive B cells in humans. (2011) (274)
Association of a functional variant downstream of TNFAIP3 with systemic lupus erythematosus (2011) (267)
Interferon-regulated chemokines as biomarkers of systemic lupus erythematosus disease activity: a validation study. (2009) (267)
Analysis and Application of European Genetic Substructure Using 300 K SNP Information (2008) (261)
Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths (2021) (257)
Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases (2009) (256)
An Interferon Signature in the Peripheral Blood of Dermatomyositis Patients is Associated with Disease Activity (2007) (256)
PTPN22: setting thresholds for autoimmunity. (2006) (253)
Transancestral mapping and genetic load in systemic lupus erythematosus (2017) (253)
Screening the genome for rheumatoid arthritis susceptibility genes: a replication study and combined analysis of 512 multicase families. (2003) (247)
PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis. (2005) (246)
European Population Substructure: Clustering of Northern and Southern Populations (2006) (245)
Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture. (2015) (240)
International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways (2015) (233)
The emerging role of interferon in human systemic lupus erythematosus. (2004) (228)
Molecular diversity of HLA-DR4 haplotypes (1986) (225)
Regulation of anti-cyclic citrullinated peptide antibodies in rheumatoid arthritis: contrasting effects of HLA-DR3 and the shared epitope alleles. (2005) (217)
A role for noncoding variation in schizophrenia. (2014) (217)
Visualizing human leukocyte antigen class II risk haplotypes in human systemic lupus erythematosus. (2002) (216)
A novel adoptive transfer model of chronic lymphocytic leukemia suggests a key role for T lymphocytes in the disease. (2011) (211)
Porphyromonas gingivalis and disease-related autoantibodies in individuals at increased risk of rheumatoid arthritis. (2012) (210)
Specificity of the STAT4 Genetic Association for Severe Disease Manifestations of Systemic Lupus Erythematosus (2008) (207)
Differential Genetic Associations for Systemic Lupus Erythematosus Based on Anti–dsDNA Autoantibody Production (2011) (205)
Genome-Wide Association Scan Identifies Candidate Polymorphisms Associated with Differential Response to Anti-TNF Treatment in Rheumatoid Arthritis (2008) (204)
Telomere length and telomerase activity delineate distinctive replicative features of the B-CLL subgroups defined by immunoglobulin V gene mutations. (2004) (202)
Variants at IRF5-TNPO3, 17q12-21 and MMEL1 are associated with primary biliary cirrhosis (2010) (202)
BLM Heterozygosity and the Risk of Colorectal Cancer (2002) (199)
Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci (2015) (199)
Ulcerative colitis loci on chromosomes 1p36 and 12q15 identified by genome-wide association study (2008) (199)
Dissecting the genetic complexity of the association between human leukocyte antigens and rheumatoid arthritis. (2002) (195)
Genetics of autoimmune diseases — disorders of immune homeostasis (2006) (193)
Fine Mapping Major Histocompatibility Complex Associations in Psoriasis and Its Clinical Subtypes (2014) (190)
Association of STAT4 with Rheumatoid Arthritis in the Korean Population (2007) (189)
Notch signaling drives synovial fibroblast identity and arthritis pathology (2020) (186)
Cholinergic Anti-Inflammatory Pathway Activity and High Mobility Group Box-1 (HMGB1) Serum Levels in Patients with Rheumatoid Arthritis (2007) (182)
Association between common variants near the melanocortin 4 receptor gene and severe antipsychotic drug-induced weight gain. (2012) (181)
Selective IgA Deficiency in Autoimmune Diseases (2011) (180)
Oligoclonal CD8+ T cells are preferentially expanded in the CD57+ subset. (1995) (179)
Circulating immune complexes contain citrullinated fibrinogen in rheumatoid arthritis (2008) (179)
T cell receptor V-segment frequencies in peripheral blood T cells correlate with human leukocyte antigen type (1991) (178)
Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis. (2014) (177)
Clonal expansion within the CD4+CD57+ and CD8+CD57+ T cell subsets in chronic lymphocytic leukemia. (1997) (173)
A genetic study on C5-TRAF1 and progression of joint damage in rheumatoid arthritis (2015) (172)
Interaction between smoking, the shared epitope, and anti-cyclic citrullinated peptide: a mixed picture in three large North American rheumatoid arthritis cohorts. (2007) (171)
An ancestry informative marker set for determining continental origin: validation and extension using human genome diversity panels (2009) (168)
Fine mapping seronegative and seropositive rheumatoid arthritis to shared and distinct HLA alleles by adjusting for the effects of heterogeneity. (2014) (167)
Risk Alleles for Systemic Lupus Erythematosus in a Large Case-Control Collection and Associations with Clinical Subphenotypes (2011) (165)
Specific combinations of HLA-DR2 and DR3 class II haplotypes contribute graded risk for disease susceptibility and autoantibodies in human SLE (2007) (164)
Molecular diversity of HLA-DR4 haplotypes. (1986) (158)
Identification of Novel Genetic Markers Associated with Clinical Phenotypes of Systemic Sclerosis through a Genome-Wide Association Strategy (2011) (158)
Functionally defective germline variants of sialic acid acetylesterase in autoimmunity (2010) (158)
Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases (2015) (156)
STAT4: Genetics, mechanisms, and implications for autoimmunity (2008) (153)
Genome-Wide Association Study and Gene Expression Analysis Identifies CD84 as a Predictor of Response to Etanercept Therapy in Rheumatoid Arthritis (2013) (152)
Role for Msh5 in the regulation of Ig class switch recombination (2007) (151)
Expression levels for many genes in human peripheral blood cells are highly sensitive to ex vivo incubation (2004) (151)
Risk for myasthenia gravis maps to a 151Pro→Ala change in TNIP1 and to human leukocyte antigen‐B*08 (2012) (149)
Early childhood music education and predisposition to absolute pitch: teasing apart genes and environment. (2001) (148)
A Genome-Wide Scan of Ashkenazi Jewish Crohn's Disease Suggests Novel Susceptibility Loci (2012) (148)
Absolute pitch: prevalence, ethnic variation, and estimation of the genetic component. (1999) (147)
Circulating biomarkers for detection of ovarian cancer and predicting cancer outcomes (2013) (147)
Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency (2010) (146)
Examination of ancestry and ethnic affiliation using highly informative diallelic DNA markers: application to diverse and admixed populations and implications for clinical epidemiology and forensic medicine (2005) (146)
Unraveling multiple MHC gene associations with systemic lupus erythematosus: model choice indicates a role for HLA alleles and non-HLA genes in Europeans. (2012) (143)
Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants. (2012) (143)
Different patterns of associations with anti-citrullinated protein antibody-positive and anti-citrullinated protein antibody-negative rheumatoid arthritis in the extended major histocompatibility complex region. (2009) (143)
A prospective approach to investigating the natural history of preclinical rheumatoid arthritis (RA) using first-degree relatives of probands with RA. (2009) (142)
Frequency of CHEK2*1100delC in New York breast cancer cases and controls (2003) (141)
Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility loci. (2011) (139)
Simultaneous detection of microsatellite repeats and SNPs in the macrophage migration inhibitory factor (MIF) gene by thin-film biosensor chips and application to rural field studies (2005) (136)
A genomewide single-nucleotide-polymorphism panel for Mexican American admixture mapping. (2007) (134)
A large-scale genetic analysis reveals a strong contribution of the HLA class II region to giant cell arteritis susceptibility. (2015) (133)
Microarray Analyses of Peripheral Blood Cells Identifies Unique Gene Expression Signature in Psoriatic Arthritis (2005) (132)
Commitment to X inactivation precedes the twinning event in monochorionic MZ twins. (1998) (131)
The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population. (2002) (129)
Integration of Sequence Data from a Consanguineous Family with Genetic Data from an Outbred Population Identifies PLB1 as a Candidate Rheumatoid Arthritis Risk Gene (2014) (128)
Quantifying Missing Heritability at Known GWAS Loci (2013) (127)
Human genetic and immunological determinants of critical COVID-19 pneumonia (2022) (126)
Multiple cytokines and chemokines are associated with rheumatoid arthritis-related autoimmunity in first-degree relatives without rheumatoid arthritis: Studies of the Aetiology of Rheumatoid Arthritis (SERA) (2012) (126)
Genetic risk factors for rheumatoid arthritis differ in Caucasian and Korean populations. (2009) (126)
Blood autoantibody and cytokine profiles predict response to anti-tumor necrosis factor therapy in rheumatoid arthritis (2009) (123)
Overlapping Probabilities of Top Ranking Gene Lists, Hypergeometric Distribution, and Stringency of Gene Selection Criterion (2006) (123)
Genome-wide association study of dermatomyositis reveals genetic overlap with other autoimmune disorders. (2013) (122)
A 15-Year Follow-up of AJCC Stage III Malignant Melanoma Patients Treated Postsurgically with Newcastle Disease Virus (NDV) Oncolysate and Determination of Alterations in the CD8 T Cell Repertoire (1998) (118)
Rheumatoid arthritis risk allele PTPRC is also associated with response to anti-tumor necrosis factor alpha therapy. (2010) (117)
Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups (2015) (116)
Kallikrein genes are associated with lupus and glomerular basement membrane-specific antibody-induced nephritis in mice and humans. (2009) (116)
Evaluation of imputation-based association in and around the integrin-alpha-M (ITGAM) gene and replication of robust association between a non-synonymous functional variant within ITGAM and systemic lupus erythematosus (SLE). (2009) (112)
Cerebral Ischemia Enhances Polyamine Oxidation: Identification of Enzymatically Formed 3-Aminopropanal as an Endogenous Mediator of Neuronal and Glial Cell Death (1998) (111)
Adrenal hyperplasia and adenomas are associated with inhibition of phosphodiesterase 11A in carriers of PDE11A sequence variants that are frequent in the population. (2006) (110)
Analysis of East Asia Genetic Substructure Using Genome-Wide SNP Arrays (2008) (108)
Oligoclonality of CD8+ T cells in health and disease: aging, infection, or immune regulation? (1996) (107)
High-density genotyping of immune loci in Koreans and Europeans identifies eight new rheumatoid arthritis risk loci. (2015) (106)
Is synaesthesia more common in autism? (2013) (106)
TYK2 Protein-Coding Variants Protect against Rheumatoid Arthritis and Autoimmunity, with No Evidence of Major Pleiotropic Effects on Non-Autoimmune Complex Traits (2015) (105)
Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes (2015) (105)
Gaining insight into PTPN22 and autoimmunity (2005) (105)
CSK regulatory polymorphism is associated with systemic lupus erythematosus and influences B cell signaling and activation (2012) (105)
Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritis. (2013) (104)
Influence of male sex on disease phenotype in familial rheumatoid arthritis. (2006) (102)
Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder (2013) (102)
Macrophage migration inhibitory factor promoter polymorphisms and the clinical expression of scleroderma. (2006) (102)
Analysis of the molecular specificities of anti-class II monoclonal antibodies by using L cell transfectants expressing HLA class II molecules. (1988) (101)
Genome-wide association analysis of anti-TNF drug response in patients with rheumatoid arthritis (2012) (101)
Several Regions in the Major Histocompatibility Complex Confer Risk for Anti-CCP-Antibody Positive Rheumatoid Arthritis, Independent of the DRB1 Locus (2008) (101)
Gene expression profiling in human autoimmunity (2006) (99)
Oligoclonality of V beta 3 TCR chains in the CD8+ T cell population of rheumatoid arthritis patients. (1996) (99)
MicroRNA-3148 Modulates Allelic Expression of Toll-Like Receptor 7 Variant Associated with Systemic Lupus Erythematosus (2013) (99)
Fine-mapping and functional studies highlight potential causal variants for rheumatoid arthritis and type 1 diabetes (2018) (98)
The New York cancer project: Rationale, organization, design, and baseline characteristics (2004) (97)
Effects of Serotonin Transporter Promoter Polymorphisms on Serotonin Function (2004) (97)
Macrophage migration inhibitory factor (MIF) gene polymorphisms are associated with increased prostate cancer incidence (2007) (94)
High mobility group box chromosomal protein 1 as a nuclear protein, cytokine, and potential therapeutic target in arthritis. (2003) (92)
Genetics of rheumatoid arthritis: confronting complexity (1999) (92)
European Population Genetic Substructure: Further Definition of Ancestry Informative Markers for Distinguishing among Diverse European Ethnic Groups (2009) (91)
Oligoclonality in the Human CD8+ T Cell Repertoire in Normal Subjects and Monozygotic Twins: Implications for Studies of Infectious and Autoimmune Diseases (1995) (91)
A Large-Scale Rheumatoid Arthritis Genetic Study Identifies Association at Chromosome 9q33.2 (2008) (90)
Prevention of autoimmune rheumatic disease: state of the art and future perspectives (2010) (89)
Menstruation: science and society (2020) (88)
Identification of a systemic lupus erythematosus susceptibility locus at 11p13 between PDHX and CD44 in a multiethnic study. (2011) (88)
The architecture of long-range haplotypes shared within and across populations. (2012) (86)
Association of a single-nucleotide polymorphism in CD40 with the rate of joint destruction in rheumatoid arthritis. (2009) (83)
The role of X-chromosome inactivation in female predispositionto autoimmunity (2000) (83)
A role for the polymorphism at position 247 of the beta2-glycoprotein I gene in the generation of anti-beta2-glycoprotein I antibodies in the antiphospholipid syndrome. (1999) (83)
Regulation of dendritic cell activation by microRNA let-7c and BLIMP1. (2013) (81)
Pathways to gene identification in rheumatoid arthritis: PTPN22 and beyond (2005) (80)
Fine-mapping, trans-ancestral, and genomic analyses identify causal variants, cells, genes, and drug targets for type 1 diabetes (2020) (79)
Randomized, Double‐Blind, Placebo‐Controlled Trial of the Effect of Vitamin D3 on the Interferon Signature in Patients With Systemic Lupus Erythematosus (2015) (78)
Identification of grade and origin specific cell populations in serous epithelial ovarian cancer by single cell RNA-seq (2018) (75)
Rheumatoid arthritis: a view of the current genetic landscape (2009) (75)
Use of a multiethnic approach to identify rheumatoid- arthritis-susceptibility loci, 1p36 and 17q12. (2012) (75)
Crowdsourced assessment of common genetic contribution to predicting anti-TNF treatment response in rheumatoid arthritis (2016) (74)
Beliefs and attitudes towards participating in genetic research – a population based cross-sectional study (2013) (74)
Association of K121Q polymorphism in ENPP1 (PC-1) with BMI in Caucasian and African-American adults (2006) (73)
Transancestral mapping of the MHC region in systemic lupus erythematosus identifies new independent and interacting loci at MSH5, HLA-DPB1 and HLA-G (2012) (72)
Performance of anti-cyclic citrullinated Peptide assays differs in subjects at increased risk of rheumatoid arthritis and subjects with established disease. (2013) (72)
Corrigendum: Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study (2009) (71)
Polymorphism of HLA-DR beta chains in DR4, -7, and -9 haplotypes: implications for the mechanisms of allelic variation. (1986) (71)
Macrophage migration inhibitory factor, MIF alleles, and the genetics of inflammatory disorders: incorporating disease outcome into the definition of phenotype. (2003) (71)
Genome-wide meta-analysis reveals shared new loci in systemic seropositive rheumatic diseases (2018) (70)
Omega-3 fatty acids are associated with a lower prevalence of autoantibodies in shared epitope-positive subjects at risk for rheumatoid arthritis (2016) (69)
Methods for high-dimensonal analysis of cells dissociated from cyropreserved synovial tissue (2018) (69)
Plasma carboxypeptidase B downregulates inflammatory responses in autoimmune arthritis. (2011) (69)
Classical HLA-DRB1 and DPB1 Alleles Account for HLA Associations with Primary Biliary Cirrhosis (2012) (69)
Neuroprotection in cerebral ischemia by neutralization of 3-aminopropanal (2002) (68)
Transethnic meta-analysis identifies GSDMA and PRDM1 as susceptibility genes to systemic sclerosis (2017) (68)
Correction: Identification of Novel Genetic Markers Associated with Clinical Phenotypes of Systemic Sclerosis through a Genome-Wide Association Strategy (2011) (67)
Allele-specific expression changes dynamically during T cell activation in HLA and other autoimmune loci (2019) (66)
Implication of a rare deletion at distal 16p11.2 in schizophrenia. (2013) (66)
Absolute pitch exhibits phenotypic and genetic overlap with synesthesia. (2013) (65)
Rheumatoid arthritis. The genetic components. (2002) (65)
Oligoclonal expansions in the CD8(+)CD28(-) T cells largely explain the shorter telomeres detected in this subset: analysis by flow FISH. (2000) (65)
Analysis of DR beta and DQ beta chain cDNA clones from a DR7 haplotype. (1986) (65)
Clonal expansion within CD4+ and CD8+ T cell subsets in human T lymphotropic virus type I-infected individuals. (1998) (63)
Polymorphism of the HLA-D region in American blacks. A DR3 haplotype generated by recombination. (1988) (62)
Clustering of disease features within 512 multicase rheumatoid arthritis families. (2004) (62)
Focused HLA analysis in Caucasians with myositis identifies significant associations with autoantibody subgroups (2019) (61)
A method to decipher pleiotropy by detecting underlying heterogeneity driven by hidden subgroups applied to autoimmune and neuropsychiatric diseases (2016) (59)
Clinical follow-up and immunogenetic studies of 32 patients with eosinophilia-myalgia syndrome (1991) (59)
Identification of a genetic variant for joint damage progression in autoantibody-positive rheumatoid arthritis (2013) (58)
Examples of in vivo isotype class switching in IgM+ chronic lymphocytic leukemia B cells. (1996) (58)
Data for Genetic Analysis Workshop 16 Problem 1, association analysis of rheumatoid arthritis data (2009) (58)
New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. (2015) (58)
Phase 1 double-blind randomized safety trial of the Janus kinase inhibitor tofacitinib in systemic lupus erythematosus (2021) (58)
European genetic ancestry is associated with a decreased risk of lupus nephritis. (2012) (57)
Human Genetics in Rheumatoid Arthritis Guides a High-Throughput Drug Screen of the CD40 Signaling Pathway (2013) (56)
Recombination sites in the HLA class II region are haplotype dependent. (1988) (56)
A Major Histocompatibility Class I Locus Contributes to Multiple Sclerosis Susceptibility Independently from HLA-DRB1*15:01 (2010) (56)
Common variants at CD 40 and other loci confer risk of rheumatoid arthritis (2008) (56)
IgA Deficiency and the MHC: Assessment of Relative Risk and Microheterogeneity Within the HLA A1 B8, DR3 (8.1) Haplotype (2009) (56)
Blood pressure regulation by CD4+ lymphocytes expressing choline acetyltransferase (2016) (55)
Lower omega-3 fatty acids are associated with the presence of anti-cyclic citrullinated peptide autoantibodies in a population at risk for future rheumatoid arthritis: a nested case-control study. (2016) (55)
High-Density SNP Mapping of the HLA Region Identifies Multiple Independent Susceptibility Loci Associated with Selective IgA Deficiency (2012) (54)
Plasma 25,OH Vitamin D Concentrations Are Not Associated with Rheumatoid Arthritis (RA)-related Autoantibodies in Individuals at Elevated Risk for RA (2009) (54)
X chromosome-inactivation patterns confirm the late timing of monoamniotic-MZ twinning. (1999) (52)
Genome‐wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation (2012) (52)
Oligoclonality of CD8+ T cells in multiple sclerosis. (1996) (51)
Discordance for autoimmunity in monozygotic twins. Are "identical" twins really identical? (1993) (51)
Identical MHC markers in non-Jewish Iranian and Ashkenazi Jewish patients with pemphigus vulgaris: possible common central Asian ancestral origin. (1997) (51)
The serotonin transporter gene and disease modification in psychosis: Evidence for systematic differences in allelic directionality at the 5-HTTLPR locus (2009) (51)
Checkpoints for Autoreactive B Cells in the Peripheral Blood of Lupus Patients Assessed by Flow Cytometry (2016) (51)
Microheterogeneity of HLA-DR4 haplotypes: DNA sequence analysis of LD"KT2" and LD"TAS" haplotypes. (1987) (50)
Evidence for progenitors of chronic lymphocytic leukemia B cells that undergo intraclonal differentiation and diversification. (1996) (50)
Increased Cathepsin S in Prdm1−/− dendritic cells alters TFH repertoire and contributes to lupus (2017) (50)
Implications for health and disease in the genetic signature of the Ashkenazi Jewish population (2012) (49)
Genome-wide meta-analysis for rheumatoid arthritis (2006) (48)
Relatives without rheumatoid arthritis show reactivity to anti-citrullinated protein/peptide antibodies that are associated with arthritis-related traits: studies of the etiology of rheumatoid arthritis. (2013) (48)
Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A and Identification of ZBTB10 and Three Distinct HLA Associations (2015) (47)
Characterization of the human homolog of the IL-4 induced gene-1 (Fig1). (2002) (47)
Nucleotide sequence of a DRw10 beta chain cDNA clone. Identity of the third D region with that of the DRw53 allele of the beta 2 locus and as the probable site encoding a polymorphic MHC class II epitope. (1988) (47)
Genome-wide association study reveals novel genetic determinants of DNA repair capacity in lung cancer. (2013) (46)
Modular Analysis of Peripheral Blood Gene Expression in Rheumatoid Arthritis Captures Reproducible Gene Expression Changes in Tumor Necrosis Factor Responders (2015) (46)
Associations of Smoking and Age With Inflammatory Joint Signs Among Unaffected First‐Degree Relatives of Rheumatoid Arthritis Patients: Results From Studies of the Etiology of Rheumatoid Arthritis (2016) (46)
Genetic Variants of TSLP and Asthma in an Admixed Urban Population (2011) (45)
The inflammatory disease-associated variants in IL12B and IL23R are not associated with rheumatoid arthritis. (2008) (45)
Genome-Wide Methylation Analyses in Glioblastoma Multiforme (2014) (45)
X Chromosome Inactivation Patterns Correlate with Fetal-Placental Anatomy in Monozygotic Twin Pairs: Implications for Immune Relatedness and Concordance for Autoimmunity (1994) (45)
Type 1 Diabetes Risk in African-Ancestry Participants and Utility of an Ancestry-Specific Genetic Risk Score (2019) (45)
Analysis of menstrual effluent: diagnostic potential for endometriosis (2018) (44)
The functional -169T-->C single-nucleotide polymorphism in FCRL3 is not associated with rheumatoid arthritis in white North Americans. (2006) (44)
Convergent Random Forest predictor: methodology for predicting drug response from genome-scale data applied to anti-TNF response. (2009) (44)
The RAGE Gly82Ser polymorphism is not associated with cardiovascular disease in the Framingham offspring study. (2005) (44)
The DR3(w18),DQw4 haplotype differs from DR3(w17),DQw2 haplotypes at multiple class II loci. (1989) (44)
HLA class II polymorphism: implications for genetic susceptibility to autoimmune disease. (1989) (43)
PTPN22 and rheumatoid arthritis: gratifying replication. (2005) (43)
Recent Advances in Defining the Genetic Basis of Rheumatoid Arthritis. (2016) (43)
Relationship between air pollution and positivity of RA-related autoantibodies in individuals without established RA: a report on SERA (2013) (43)
Genetic influences on susceptibility to rheumatoid arthritis in African‐Americans (2018) (42)
Simultaneous flow cytometric analysis of cell surface markers and telomere length: analysis of human tonsilar B cells. (2001) (41)
Increased pretreatment serum IFN-β/α ratio predicts non-response to tumour necrosis factor α inhibition in rheumatoid arthritis. (2016) (41)
Anticitrullinated protein antibody (ACPA) in rheumatoid arthritis: influence of an interaction between HLA-DRB1 shared epitope and a deletion polymorphism in glutathione s-transferase in a cross-sectional study (2010) (41)
First Domain Sequence Diversity of DR and DQ Subregion Alleles (1989) (41)
The autoimmunity-associated BLK haplotype exhibits cis-regulatory effects on mRNA and protein expression that are prominently observed in B cells early in development. (2012) (40)
Alternative splicing of CD79a (Ig-alpha/mb-1) and CD79b (Ig-beta/B29) RNA transcripts in human B cells. (1995) (40)
Brief Report: Identification of BACH2 and RAD51B as Rheumatoid Arthritis Susceptibility Loci in a Meta-Analysis of Genome-Wide Data (2013) (40)
Studying severe long COVID to understand post-infectious disorders beyond COVID-19 (2022) (40)
Data for Genetic Analysis Workshop (GAW) 15 Problem 2, genetic causes of rheumatoid arthritis and associated traits (2007) (38)
Autoimmune Disease–Associated Haplotypes of BLK Exhibit Lowered Thresholds for B Cell Activation and Expansion of Ig Class‐Switched B Cells (2015) (38)
A broad analysis of IL1 polymorphism and rheumatoid arthritis. (2008) (38)
Refining the association of MHC with multiple sclerosis in African Americans. (2010) (38)
Supervised machine learning and logistic regression identifies novel epistatic risk factors with PTPN22 for rheumatoid arthritis (2010) (37)
The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies (2022) (37)
Metabolism and biochemical effects of nicotine for primary care providers. (2004) (36)
Immune‐Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA–DRB1 Amino Acid Heterogeneity Across the Myositis Spectrum (2017) (35)
Variation in radiologic joint destruction in rheumatoid arthritis differs between monozygotic and dizygotic twins and pairs of unrelated patients. (2006) (35)
Teasing apart the complex genetics of human autoimmunity: lessons from rheumatoid arthritis. (2003) (34)
Modern genetics, ancient defenses, and potential therapies. (2007) (34)
Persistent alterations in the T-cell repertoires of HIV-1-infected and at-risk uninfected men (2004) (33)
Clonal dominance patterns of CD8 T cells in relation to disease progression in HIV-infected children. (1999) (33)
HLA–DRB1–Associated Rheumatoid Arthritis Risk at Multiple Levels in African Americans: Hierarchical Classification Systems, Amino Acid Positions, and Residues (2014) (32)
Extended haplotype association study in Crohn’s disease identifies a novel, Ashkenazi Jewish-specific missense mutation in the NF-κB pathway gene, HEATR3 (2013) (32)
Association of a single-nucleotide polymorphism in CD 40 with the rate of joint destruction in rheumatoid arthritis (2011) (31)
Susceptibility genes for rheumatoid arthritis - a rapidly expanding harvest. (2010) (31)
DNA sequence analysis of the HLA-DRw12 allele. (1989) (31)
Instant recognition: the genetics of pitch perception. (1998) (30)
A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response (2021) (30)
Evidence for the separate molecular expression of four distinct polymorphic Ia epitopes on cells of DR4 homozygous individuals. (1984) (30)
European population substructure is associated with mucocutaneous manifestations and autoantibody production in systemic lupus erythematosus. (2009) (30)
Further DNA sequence microheterogeneity of the HLA-DR4/Dw13 haplotype group: importance of amino acid position 86 of the DR beta 1 chain for T-cell recognition. (1990) (29)
Concomitant autoimmunity in myasthenia gravis — Lack of association with IgA deficiency (2011) (28)
Oligoclonality in the CD8+ T‐Cell Population (1995) (28)
The North American Rheumatoid Arthritis Consortium--bringing genetic analysis to bear on disease susceptibility, severity, and outcome. (1998) (27)
The 6q22.33 Locus and Breast Cancer Susceptibility (2009) (27)
Molecular signatures in systemic lupus erythematosus: distinction between disease flare and infection (2016) (27)
The human Ig-beta cDNA sequence, a homologue of murine B29, is identical in B cell and plasma cell lines producing all the human Ig isotypes. (1993) (27)
Polymorphism of the HLA-DR1 haplotype in American blacks. Identification of a DR1 beta-chain determinant recognized in the mixed lymphocyte reaction. (1988) (27)
Studies on ageing and the severity of radiographic joint damage in rheumatoid arthritis (2015) (27)
Recombination between DQ alpha and DQ beta genes generates human histocompatibility leukocyte antigen class II haplotype diversity. (1987) (26)
Identification of novel genetic markers associated with the clinical phenotypes of systemic sclerosis through a genome wide association strategy (2010) (26)
Inferring causal relationships among intermediate phenotypes and biomarkers: a case study of rheumatoid arthritis (2006) (25)
The PRL -1149 G/T polymorphism and rheumatoid arthritis susceptibility. (2009) (25)
Harnessing Type I IFN Immunity Against SARS-CoV-2 with Early Administration of IFN-β (2021) (24)
Hypogalactosylation of serum N-glycans fails to predict clinical response to methotrexate and TNF inhibition in rheumatoid arthritis (2012) (24)
Crowdsourcing genetic prediction of clinical utility in the Rheumatoid Arthritis Responder Challenge (2013) (24)
Association analysis of copy numbers of FC-gamma receptor genes for rheumatoid arthritis and other immune-mediated phenotypes (2015) (24)
A 129-kb Deletion on Chromosome 12 Confers Substantial Protection Against Rheumatoid Arthritis, Implicating the Gene SLC2A3 (2013) (24)
Genotyping of immune-related genetic variants identifies TYK2 as a novel associated locus for idiopathic inflammatory myopathies (2014) (23)
Clonal Dominance of CD8+ T‐Cells in Multiple Sclerosis (1995) (23)
The molecular basis of susceptibility to rheumatoid arthritis: The conformational equivalence hypothesis (2005) (23)
Notch signalling drives synovial fibroblast identity and arthritis pathology (2020) (22)
GWAS implicates a role for quantitative immune traits and threshold effects in risk for human autoimmune disorders. (2012) (22)
Copy-number-variation and copy-number-alteration region detection by cumulative plots (2009) (22)
Studying associations between variants in TRAF1-C5 and TNFAIP3-OLIG3 and the progression of joint destruction in rheumatoid arthritis in multiple cohorts (2012) (22)
Distinct HLA Associations with Rheumatoid Arthritis Subsets Defined by Serological Subphenotype (2019) (22)
The search for rheumatoid arthritis susceptibility genes: a call for global collaboration. (2002) (22)
IRF5 genetic risk variants drive myeloid-specific IRF5 hyper-activation and pre-symptomatic SLE. (2019) (22)
Association of genetic variants in the IL4 and IL4R genes with the severity of joint damage in rheumatoid arthritis: a study in seven cohorts. (2013) (21)
Genome-Wide Association Study and Gene Expression Analysis Identifies CD 84 as a Predictor of Response to Etanercept Therapy in Rheumatoid Arthritis (2013) (21)
Genome-wide linkage scan for spontaneous DZ twinning (2006) (21)
Dissecting the heterogeneity of rheumatoid arthritis through linkage analysis of quantitative traits. (2007) (21)
Oligoclonality in the CD8+ T-cell population. Analysis using a multiplex PCR assay for CDR3 length. (1995) (21)
Recommendations for publication of genetic association studies in Arthritis & Rheumatism. (2011) (20)
Association of single-nucleotide polymorphisms in CCR6, TAGAP, and TNFAIP3 with rheumatoid arthritis in African Americans. (2012) (20)
Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations (2018) (20)
European population substructure correlates with systemic lupus erythematosus endophenotypes in North Americans of European descent (2010) (20)
Closing the gap between genotype and phenotype (2009) (20)
Linkage analysis of rheumatoid arthritis in US and UK families reveals interactions between HLA-DRB1 and loci on chromosomes 6q and 16p. (2006) (19)
The role of X-chromosome inactivation in female predisposition to autoimmunity (2000) (19)
Analysis of 30 Genes (355 SNPS) Related to Energy Homeostasis for Association with Adiposity in European-American and Yup’ik Eskimo Populations (2008) (19)
Immunochip Identifies Novel, and Replicates Known, Genetic Risk Loci for Rheumatoid Arthritis in Black South Africans (2014) (19)
Current understanding of the genetic aetiology of rheumatoid arthritis and likely future developments. (2005) (18)
Association of Valine and Leucine at HLA–DRB1 Position 11 With Radiographic Progression in Rheumatoid Arthritis, Independent of the Shared Epitope Alleles but Not Independent of Anti–Citrullinated Protein Antibodies (2015) (18)
Vaccine breakthrough hypoxemic COVID-19 pneumonia in patients with auto-Abs neutralizing type I IFNs (2022) (18)
Genetic susceptibility to rheumatoid arthritis and human leukocyte antigen class II polymorphism. The role of shared conformational determinants. (1988) (18)
Evidence for malaria selection of a CR1 haplotype in Sardinia (2011) (17)
Loci associated with N-glycosylation of human IgG are not associated with rheumatoid arthritis: a Mendelian randomisation study (2015) (17)
Specificity of the STAT 4 Genetic Association for Severe Disease Manifestations of Systemic Lupus Erythematosus (2008) (17)
REL, encoding a member of the NF-kB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis (2020) (16)
Effective sample size: Quick estimation of the effect of related samples in genetic case-control association analyses (2006) (16)
Expression of Blimp-1 in Dendritic Cells Modulates the Innate Inflammatory Response in Dextran Sodium Sulfate-Induced Colitis (2014) (16)
Progress towards understanding the genetic pathogenesis of systemic lupus erythematosus. (2005) (16)
Reply to Henthorn and Deutsch: Ethnicity versus early environment: Comment on ‘Early Childhood Music Education and Predisposition to Absolute Pitch: Teasing Apart Genes and Environment’ by Peter K. Gregersen, Elena Kowalsky, Nina Kohn, and Elizabeth West Marvin [2000] (2007) (16)
Locus category based analysis of a large genome-wide association study of rheumatoid arthritis. (2010) (16)
Factors associated with progression to inflammatory arthritis in first-degree relatives of individuals with RA following autoantibody positive screening in a non-clinical setting (2020) (16)
Molecular analysis of the HLA class II genes in two DRw6-related haplotypes, DRw13 DQw1 and DRw14 DQw3. (1989) (15)
Gene expression patterns in peripheral blood cells associated with radiographic severity in African Americans with early rheumatoid arthritis (2011) (15)
Kruppel-like factor4 regulates PRDM1 expression through binding to an autoimmune risk allele. (2017) (15)
Dense Genotyping of Immune-Related Regions Identifies Loci for Rheumatoid Arthritis Risk and Damage in African Americans (2017) (15)
Genome-Wide Association Study of Dermatomyositis Reveals Shared Genetic Risk Factors with Other Autoimmune Diseases (2011) (14)
Arg206Cys substitution in DNASE1L3 causes a defect in DNASE1L3 protein secretion that confers risk of systemic lupus erythematosus (2021) (14)
Unexpected HLA haplotype sharing in dizygotic twin pairs discordant for rheumatoid arthritis. (1996) (14)
Randomized , Double-Blind , Placebo-Controlled Trial of the Effect of Vitamin D 3 on the Interferon Signature in Patients With Systemic Lupus Erythematosus (2018) (14)
A cross-disease meta-GWAS identifies four new susceptibility loci shared between systemic sclerosis and Crohn’s disease (2020) (14)
Enrichment of Genetic Variants for Rheumatoid Arthritis within T-Cell and NK-Cell Enhancer Regions (2015) (14)
Lineage-Specific Functionality of an Interferon Regulatory Factor 5 Lupus Risk Haplotype: Lack of B Cell Intrinsic Effects (2018) (13)
Persons with Chronic Spinal Cord Injury Have Decreased Natural Killer Cell and Increased Toll-Like Receptor/Inflammatory Gene Expression (2018) (13)
Strong association of rheumatoid arthritis with the presence of a polymorphic Ia epitope defined by a monoclonal antibody: comparison with the allodeterminant DR4 (2004) (13)
Molecular analysis of HLA-DR beta and DQ beta polymorphism in Chinese with rheumatoid arthritis. (1993) (13)
Cellular deconstruction of inflamed synovium defines diverse inflammatory phenotypes in rheumatoid arthritis (2022) (12)
Bimodal distribution of performance in discriminating major/minor modes. (2013) (12)
Rheumatoid Arthritis: Genetics (2006) (12)
Correspondence Reply to Henthorn and Deutsch: Ethnicity Versus Early Environment: Comment on 'Early Childhood Music Education and Predisposition to Absolute Pitch: Teasing Apart Genes and Environment' (2007) (12)
A novel association of DQ alpha and DQ beta genes in the DRw10 haplotype. Determination of a DQw1 specificity by the DQ beta-chain. (1989) (12)
The Genotype and Phenotype (GaP) registry: a living biobank for the analysis of quantitative traits (2015) (12)
Serologic features of cohorts with variable genetic risk for systemic lupus erythematosus (2018) (11)
A high-resolution HLA reference panel capturing global population diversity enables multi-ethnic fine-mapping in HIV host response (2020) (11)
HLA associations with rheumatoid arthritis: a piece of the puzzle. (1992) (11)
Perceived Stress and Inflammatory Arthritis: A Prospective Investigation in the Studies of the Etiologies of Rheumatoid Arthritis Cohort (2020) (11)
Chronic lymphocytic leukemia: a proliferation of B cells at two distinct stages of differentiation. (2000) (11)
Two microRNA signatures for malignancy and immune infiltration predict overall survival in advanced epithelial ovarian cancer (2017) (11)
CIITA is not associated with risk of developing rheumatoid arthritis (2011) (11)
FOXO in the Hole: Leveraging GWAS for Outcome and Function (2013) (11)
183 A phase 1B/2A trial of tofacitinib, an oral janus kinase inhibitor, in systemic lupus erythematosus (2019) (10)
The complete sequence of the human CD79b (lgβ/B29) gene: identification of a conserved exon/intron organization, immunoglobulin-like regulatory regions, and allelic polymorphism (2004) (10)
The Influence of Polygenic Risk Scores on Heritability of Anti-CCP Level in RA (2014) (10)
Brief Report: The Role of Rare Protein‐Coding Variants in Anti–Tumor Necrosis Factor Treatment Response in Rheumatoid Arthritis (2017) (10)
Genome-wide association study implicates NDST 3 in schizophrenia and bipolar disorder (2013) (10)
Trans-ancestry genome-wide association study identifies novel genetic mechanisms in rheumatoid arthritis (2021) (10)
Diminished cytokine-induced Jak/STAT signaling is associated with rheumatoid arthritis and disease activity (2021) (10)
Coronary Artery Calcification and Rheumatoid Arthritis: Lack of Relationship to Risk Alleles for Coronary Artery Disease in the General Population (2017) (10)
Genetic associations with radiological damage in rheumatoid arthritis: Meta-analysis of seven genome-wide association studies of 2,775 cases (2019) (9)
Anti-Cyclic Citrullinated Peptide Assays Differ in Subjects at Elevated Risk for Rheumatoid Arthritis and Subjects with Established Disease (2013) (9)
Variability in CD8 + T‐Cell Oligoclonality Patterns in Monozygotic Twins (1995) (9)
Cell type–specific eQTLs in the human immune system (2012) (9)
Fine mapping the phenotype in autoimmune disease: the promise and pitfalls of DNA microarray technologies (2003) (9)
Correction: Identification of grade and origin specific cell populations in serous epithelial ovarian cancer by single cell RNA-seq (2018) (9)
Functional polymorphisms among HLA-DR4+ DR beta chains associated with limited peptide diversity. (1987) (9)
Genetic Variation : Evidence for Multiple Variants Associated with Rheumatoid Arthritis (2005) (8)
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis (2022) (8)
Fine-mapping identifies causal variants for RA and T1D in DNASE1L3, SIRPG, MEG3, TNFAIP3 and CD28/CTLA4 loci (2017) (8)
Detection of disease-associated deletions in case–control studies using SNP genotypes with application to rheumatoid arthritis (2009) (8)
The PTPN22 susceptibility risk variant is not associated with the rate of joint destruction in anti-citrullinated protein antibody-positive rheumatoid arthritis (2010) (8)
Hypotheses on the molecular basis of susceptibility to rheumatoid arthritis. (1988) (7)
Association of Lipid Mediators With Development of Future Incident Inflammatory Arthritis in an Anti–Citrullinated Protein Antibody–Positive Population (2020) (7)
Chromosomal localization, genomic structure, and allelic polymorphism of the human CD79a (lg-αmb-1) gene (2004) (7)
Pancreatic Cancer Patient-derived Organoids Can Predict Response to Neoadjuvant Chemotherapy (2022) (7)
PTPN 22 genetic variation : evidence for multiple variants associated with rheumatoid arthritis (2016) (7)
Single-cell analysis of menstrual endometrial tissues defines phenotypes associated with endometriosis (2022) (7)
Defining inflammatory cell states in rheumatoid arthritis joint synovial tissues by integrating single-cell transcriptomics and mass cytometry (2019) (7)
Functional analysis of MHC class II-restricted T cells derived from a Caucasian with a DR4, Dw15, DQw8 haplotype. (1990) (7)
Corrigendum: Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus (2011) (7)
Increased X-inactivation skewing in SLE? (1999) (7)
Deep sequencing reveals a DAP1 regulatory haplotype that potentiates autoimmunity in systemic lupus erythematosus (2020) (6)
Identification of the NF-κB activating protein-like locus as a risk locus for rheumatoid arthritis (2012) (6)
A Broad Analysis of IL 1 Polymorphism and Rheumatoid Arthritis (2008) (6)
Letter to the Editor Early Childhood Music Education and Predisposition to Absolute Pitch: Teasing Apart Genes and Environment (2001) (6)
Using genotype data to distinguish pleiotropy from heterogeneity: deciphering coheritability in autoimmune and neuropsychiatric diseases (2015) (6)
The chromosome 7q region association with rheumatoid arthritis in females in a British population is not replicated in a North American case-control series. (2009) (6)
Does a Genetic Variant in FOXO3A Predict a Milder Course of Rheumatoid Arthritis? (2014) (6)
DR and DQ beta cDNA sequences associated with a DR2 haplotype. (1988) (5)
Molecular Definition of the DRW10 Haplotype (1989) (5)
Editorial: The Power of a Modular Approach to Transcriptional Analysis (2014) (5)
Response: CALHM1 Association with Alzheimer's Disease Risk (2008) (5)
Anticyclic Citrullinated Peptide Antibodies 3.1 and Anti-CCP-IgA Are Associated with Increasing Age in Individuals Without Rheumatoid Arthritis (2019) (5)
Distinct HLA Associations with Rheumatoid Arthritis Subsets Defined by Serological Subphenotype (2019) (5)
A Simple Method for Analyzing Exome Sequencing Data Shows Distinct Levels of Nonsynonymous Variation for Human Immune and Nervous System Genes (2012) (5)
Genome-Wide SNP Scan Identifies Polymorphisms Associated with Differential Response to Anti-TNF Treatment Among Rheumatoid Arthritis Patients in the ABCoN Cohort (2007) (4)
High dimensional analyses of cells dissociated from cryopreserved synovial tissue (2018) (4)
Localization of Type 1 Diabetes susceptibility in the ancestral haplotype 18.2 by high density SNP mapping. (2009) (4)
T-cell receptor-major histocompatibility complex genetic interactions in rheumatoid arthritis. (1992) (4)
Proteomic and Single-Cell Transcriptomic Dissection of Human Plasmacytoid Dendritic Cell Response to Influenza Virus (2021) (4)
Corrigendum: Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants (2009) (4)
A NOVEL ASSOCIATION OF DQa AND DQ@ GENES IN THE DRwlO HAPLOTYPE Determination of a DQwl Specificity by the DQ &Chain1 (1989) (4)
A Genomic Road Map for Complex Human Disease (2014) (4)
A candidate gene study of CLEC16A does not provide evidence of association with risk for anti-CCP-positive rheumatoid arthritis (2010) (4)
Comparison of genome-wide single-nucleotide polymorphism linkage analyses in Caucasian and Hispanic NARAC families (2007) (4)
Breathing New Life into Interstitial Lung Disease in Rheumatoid Arthritis. (2018) (4)
The 6 q 22 . 33 Locus and Breast Cancer Susceptibility (2009) (4)
Title Anti-citrullinated protein antibody ( ACPA ) in rheumatoid arthritis : influence of an interaction between HLA-DRB 1 shared epitope and a deletion polymorphism in glutathione S-transferase in a cross-sectional study (2011) (3)
Polymorphism of the DR1 Haplotype: Structural and Functional Analysis (1989) (3)
Influence of genetic copy number variants of the human GLUT3 glucose transporter gene SLC2A3 on protein expression, glycolysis and rheumatoid arthritis risk: A genetic replication study (2019) (3)
Correction: Identification of Novel Genetic Markers Associated with Clinical Phenotypes of Systemic Sclerosis through a Genome-Wide Association Strategy (2011) (3)
FRI0035 Prediction of TNF Inhibitor Response in Rheumatoid Arthritis Patients Using Single Cell Network Profiling of Intracellular Immune Signaling (2014) (3)
FRI0271 Modular Analysis of Peripheral Blood Gene Expression in Rheumatoid Arthritis Captures Reproducible Gene Expression Changes in TNF Responders (2014) (3)
Mission, Organization, and Future Direction of the Serological Sciences Network for COVID-19 (SeroNet) Epidemiologic Cohort Studies (2022) (3)
Chromosomal localization, genomic structure, and allelic polymorphism of the human CD79 alpha (Ig-alpha/mb-1) gene. (1994) (3)
Circulating TNF-like protein 1A (TL1A) is elevated early in rheumatoid arthritis and depends on TNF (2020) (3)
Genetics and rheumatic diseases: rheumatoid arthritis and ankylosing spondylitis. The genetics of rheumatoid arthritis. (2001) (3)
What Clinicians Should Know about Genetics (2008) (3)
Antinuclear antibodies in general population: what does that mean? (P4535) (2013) (3)
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 (2023) (3)
The Effective Sample Size of Relative Pairs in Genetic Case-Control Association Analysis (2006) (3)
Genetic Analysis Workshop 16: introduction to workshop summaries (2009) (3)
Common Variants near the Melanocortin 4 Receptor Gene are Associated with Severe Antipsychotic Drug-induced Weight Gain (2014) (3)
STAT4: Genetics, Mechanisms, and Implications for Autoimmunity Review for Current Allergy and Asthma Reports (2008) (2)
The Role of Shared Conformational Determinants (1988) (2)
Molecular analysis of HLA-DR , B and DQI 3 polymorphism in Chinese with rheumatoid arthritis (2004) (2)
GWAS defines pathogenic signaling pathways and prioritizes drug targets for IgA nephropathy (2021) (2)
Dense Genotyping of Immune-Related Loci in the Idiopathic Inflammatory Myopathies Confirms HLA alleles as strongest genetic risk factor and suggests different genetic background for major clinical subgroups. Annals of the Rheumatic Diseases. (2015) (2)
T helper 17 axis and endometrial macrophage disruption in menstrual effluent provides potential insights into the pathogenesis of endometriosis. (2022) (2)
Evaluating associations of joint swelling, joint stiffness and joint pain with physical activity in first-degree relatives of patients with rheumatoid arthritis: Studies of the Aetiology of Rheumatoid Arthritis (SERA), a prospective cohort study (2021) (2)
Searching for Gene-Environment Interactions in Cancer: Biorepository Support for the New York Cancer Project (2000) (2)
Decoding the Human Genetic and Immunological Basis of COVID-19 mRNA Vaccine-Induced Myocarditis (2022) (2)
Evidence for B Cell Oligoclonality in the Blood and Joints of Patients with Rheumatoid Arthritisa (1997) (2)
Reconstructing haplotypes in pedigrees: Importance of parental information (2004) (2)
Chapter 21 – Genetics of Rheumatic Diseases (2017) (2)
Association of Antibodies to Prevotella copri in Anti–Cyclic Citrullinated Peptide‐Positive Individuals At Risk of Developing Rheumatoid Arthritis and in Patients With Early or Established Rheumatoid Arthritis (2022) (2)
DR3 Heterogeneity in American Blacks (1989) (2)
Genome-Wide Association Analysis of Rheumatoid Arthritis Patients Treated with Anti-TNF Medication (2011) (1)
Investigations into SCAMP5, a candidate lupus risk gene expressed in plasmacytoid dendritic cells (2021) (1)
GG-08 Immune repertoire and genetic risk alleles in healthy pediatric populations with autoimmune indicators (2018) (1)
Erratum: Unraveling Multiple MHC Gene Associations with Systemic Lupus Erythematosus: Model Choice Indicates a Role for HLA Alleles and Non-HLA Genes in Europeans (The American Journal of Human Genetics (2012) 91 (778-793)) (2015) (1)
Oligoclonality in the Human CD 8 + T Cell Repertoire in Normal Subjects and Monozygotic Twins : Implications for Studies of Infectious and Autoimmune Diseases (2007) (1)
2.3-02 MHC-restriction analysis of antigen-specific helper T-cells derived from a caucasian individual with a DR4 (Dw15); DQw3 haplotype (1989) (1)
Menstrual Effluent Provides a Novel Diagnostic Window on the Pathogenesis of Endometriosis (2020) (1)
Reply: To PMID 25371395. (2015) (1)
Implications for health and disease in the genetic signature of the Ashkenazi Jewish population (2012) (1)
Diagnostic yield : the rate at which a particular diagnostic test establishes a molecular diagnosis in a population of patients INTRODUCTION (2016) (1)
O28 Largest Genetic Study to Date in Sporadic Inclusion Body Myositis Confirms the Human Leukocyte Antigen as the Most Associated Region and Suggests a Role for C-C Chemokine Receptor Type 5 (2016) (1)
A Large-Scale Rheumatoid Arthritis Genetic Study Identifies TRAF1 Variants on Chr 9q33.2 (2007) (1)
Myositis Genetics Consortium. Genome-Wide Association Study of Dermatomyositis Reveals Shared Genetic Risk Factors with Other Autoimmune Diseases (2011) (1)
Untargeted metabolomics reveals that multiple reproductive toxicants are present at the endometrium. (2021) (1)
Fine mapping in over 14,000 rheumatoid arthritis cases and 18,500 controls refines associations to known loci, indicates multiple independent affects and reveals novel associations (2012) (1)
Concurrent Oral 3 – Genetics and Epidemiology [OP16–OP23] OP16. Genetic Variation in the Dream Pain Modulation Pathway is Associated with the Extent of Musculoskeletal Pain (2010) (1)
Proteomic Signatures of Secreted Proteins for the Prediction of Treatment Response to TNF Blockers in RA (2007) (1)
Absolute Pitch: Genetics (2013) (1)
Autologous Human T Cells and Allogeneic Antigen-Presenting Cells Permit Effective Adoptive Transfer of B-CLL Cells Into Immune Deficient Mice. (2009) (1)
FRI0356 Studies on Ageing and the Severity of Radiographic Joint Damage in Rheumatoid Arthritis (2015) (1)
OR.103. Combined Analysis of Three Genome-wide Scans Reveals Additional Loci Associated with Rheumatoid Arthritis (2008) (1)
Genome-Wide Association Study On the Severity of Joint Destruction in Autoantibody Positive Rheumatoid Arthritis Identifies a Role for Sperm Associated Antigen 16 (2012) (1)
A novel NFKB1 promoter polymorphism shows altered binding to nuclear proteins and increases risk for ulcerative colitis (2003) (1)
Replication Study of Association of IL13 Pathway Polymorphisms and Asthma Using an Admixed Urban Population. (2009) (1)
Validation of differential expression of microRNA profiles in prostate cancer specimens. (2014) (1)
Genome-wide imputation identifies novel associations and localises signals in idiopathic inflammatory myopathies. (2022) (1)
Biological Significance of AntiCyclic Citrullinated Peptide Antibody in Rheumatoid Arthritis (2008) (1)
Evolution of DQw2-Related Haplotypes (1989) (1)
Cardiovascular Risk Factors Are Increased in People Reporting Chronic Pain Symptoms (2010) (1)
The Role of Rare Protein-Coding Variants in Anti–Tumor Necrosis Factor Treatment Response in Rheumatoid Arthritis (2017) (1)
A Novel DR5 B1 (DRw11) Chain with a Distinctive Third Diversity Region (1989) (0)
21 – Genetics of Rheumatic Diseases (2013) (0)
Genome Analysis of CLL by Representational Oligonucleotide Microarray Analysis (ROMA) (2006) (0)
Association of MiR-26b mediated doxorubicin resistance signature with poor prognosis in epithelial ovarian cancer (EOC). (2016) (0)
MP49-10 DIFFERENTIAL EXPRESSION OF MICRORNA PROFILES IN PROSTATE CANCER SPECIMENS: A VALIDATION STUDY (2014) (0)
Type I-Infected Individuals VirusCell Subsets in Human T Lymphotropic T + and CD 8 + Clonal Expansion Within CD 4 (1998) (0)
Molecular diversity of HLA-DR4 haplotypes (major histocompatibility complex/cDNA dones/DR and DQ/gene conversion) (2016) (0)
Replication Of An Association Of The Interleukin-1 Receptor Antagonist Gene With Asthma In An Adult Urban Admixed Population (2010) (0)
Serologic features of cohorts with variable genetic risk for systemic lupus erythematosus (2018) (0)
Genetic risk alleles associated with serologic autoimmunity in normal individuals (BA3P.113) (2015) (0)
050. International Immunochip Study in the Idiopathic Inflammatory Myopathies Identifies Genetic Differences Between Clinical Subgroups, and Confirms HLA Alleles as Strongest Genetic Risk Factor (2015) (0)
Choline acetyltransferase+ T cells represent a discrete lymphocyte subset that regulates innate immunity. (P1008) (2013) (0)
GG-07 SLE risk haplotypes are associated with development of serologic autoimmunity in healthy individuals (2016) (0)
DRβ Chain Polymorphism in Pemphigus Vulgaris (1989) (0)
Molecular analysis ofHLA-DR,B andDQI3 polymorphism inChinese withrheumatoid arthritis (1993) (0)
Differential Expression Genes of CLL Subgroups Defined by Ki67 Expression Level Which Correlated with Clinical Outcome (2010) (0)
Integrated analysis reveals microRNA mediated immune system regulation in advanced epithelial ovarian cancer associated with clinical prognosis (2017) (0)
Oral abstracts 7: Molecular mechanisms of disease—osteoarthritisS1. Identification of novel osteoarthritis genes using zebrafish (2012) (0)
Is Elevated Serum IL-10 in B-CLL Associated with IL-10 Promoter Polymorphisms?. (2005) (0)
Combining Expression of Hypervariably Expressed Genes with IGHV Mutation Status Is a More Robust Prognostic Indicator Than Mutation Status Alone in Chronic Lymphocytic Leukemia (2011) (0)
The Journal of Rheumatology Without Rheumatoid Arthritis Anti-CCP3.1 and Anti-CCP-IgA Are Associated with Increasing Age in Individuals (2019) (0)
Oligoclonality of CDC8+ T cells is common in normal subjects, enriched in the CD57+ subset, and altered in autoimmune diseases (1995) (0)
Research Highlights (2007) (0)
The Genotype and Phenotype (GAP) Registry: A National Resource for Studying Genetic Regulation of Immune Function in Normal Populations (2010) (0)
GG-07 Regulatory polymorphisms in EMSY gene are associated with autoantibodies in healthy individuals (2018) (0)
45 – The Major Histocompatibility Complex (2012) (0)
2.2-03 The DRw11/w13 family: A continuum of diversity (1989) (0)
Reply (2015) (0)
GG-03 IRF5 genetic risk variants drive an SLE immune-phenotype in healthy donors (2018) (0)
A genetic study on C 5-TRAF 1 and progression of joint damage in rheumatoid arthritis (2015) (0)
A cross-disease meta-GWAS identifies four new susceptibility loci shared between systemic sclerosis and Crohn’s disease (2020) (0)
OP0208 High density fine mapping in rheumatoid arthritis indentifies 14 new loci (2013) (0)
International immunochip study in the idiopathic inflammatory myopathies identifies novel susceptability loci and confirms HLA as strongest genetic risk factor (2014) (0)
Lupus Nephritis Susceptibility Markers in PDGRFA-GSX2, SLC5A11, ID4, and HAS2-SNTB1 Regions Identified From a Meta-Analysis of Genome Wide Association Studies of Women with Systemic Lupus Erythematosus (2011) (0)
The most significant canonical pathways represented in our validated gene list. (2014) (0)
Additional file 1: of Studies on ageing and the severity of radiographic joint damage in rheumatoid arthritis (2015) (0)
From the Editorial Board (2022) (0)
Choline acetyltransferase+ lymphocytes regulate endothelial nitric oxide synthase (MUC2P.939) (2015) (0)
Biological Significance of Anti-Cyclic Citrullinated Peptide Antibody in Rheumatoid Arthritis. Authors' reply (2008) (0)
Pediatric Leukemia-Specific miRNA Expression Profiles Induced by the Leukemic Stem Cell Niche (2010) (0)
Abstract P2-07-09: Integrative analysis of miRNA and mRNA expression in metastatic versus non-metastatic triple negative breast cancer (2018) (0)
Immunochip Analysis Identifies New Susceptibility Loci For Systemic Sclerosis: Implications For Pathogenesis (2013) (0)
Association of CSK Variants with Systemic Lupus Erythematosus (2010) (0)
Risk of progression from UA to RA 81 Chapter 6 A single nucleotide polymorphism in CD 40 associates with the rate of joint destruction in Rheumatoid Arthritis (2010) (0)
A Systems Immunology Approach Identifies Cytokine-Induced STAT Signaling Pathways Critical to Rheumatoid Arthritis Disease Activity and Treatment Response (2019) (0)
393 Rare genetic mutations identify extracellular matrix genes as a contributing factor in alopecia areata etiology (2019) (0)
Polymorphism of HLA-DR f 8 chains in DR 4 ,7 , and-9 haplotypes : Implications for the mechanisms of allelic variation ( cDNA clones / major histocompatibility complex / selection ) (0)
alpha7 nicotinic acetylcholine receptor and cAMP response element binding protein are essential for prolonged monocyte deactivation by vagus nerve signaling (116.37) (2011) (0)
Author Correction: A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response (2021) (0)
Deep sequencing reveals a DAP1 regulatory haplotype that potentiates autoimmunity in systemic lupus erythematosus (2020) (0)
Expansion of the IgD class switched B cell population in carriers of the autoimmune disease associated risk haplotype in BLK (HUM2P.332) (2014) (0)
A rare deletion at distal 16 p 11 . 2 is implicated in schizophrenia (2013) (0)
Allele-specific expression changes dynamically during T cell activation in HLA and other autoimmune loci (2020) (0)
1.16 Gene Set Enrichment Analysis of CLL Subgroups Defined by Ki-67 Expression (2011) (0)
Expression and Characterization of Leucocyte Antigens (1984) (0)
Analysis of menstrual effluent: diagnostic potential for endometriosis (2018) (0)
Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations (2018) (0)
BSR AND BHPR ORAL PRESENTATION OF ABSTRACTS GENETIC DIFFERENCES BETWEEN CLINICAL SUBGROUPS, AND CONFIRMS HLA ALLELES AS STRONGEST GENETIC (2015) (0)
Erratum: Crowdsourced assessment of common genetic contribution to predicting anti-TNF treatment response in rheumatoid arthritis (2016) (0)
Evolution of DQ genes (1988) (0)
Polymorphisms in Thymic Stromal Lymphopoietin (TSLP) Pathways and Asthma in an Urban Admixed Population. (2009) (0)
Biological Insights From Genetics Of Rheumatoid Arthritis Contribute To Drug Discovery (2013) (0)
Abstract P131: Associations Between Joint Symptoms and Prospective Changes in Physical Activity in First-degree Relatives of Rheumatoid Arthritis (RA) Patients (2016) (0)
Review Genetics of rheumatoid arthritis: confronting complexity (1999) (0)
Potential Of Integrating Human Genetics and Electronic Medical Records For Drug Discovery : The Example Of TYK2 and Rheumatoid Arthritis (2013) (0)
Regulation of Immunological Tolerance and Autoimmunity by the Enzyme Sialic Acid Acetylesterase (SIAE) (2010) (0)
OP0209 Genetic variance in IL2RA associates with progression of joint destruction and circulating SIL-2RA levels in rheumatoid arthritis (2013) (0)
NpgRJ_Ng_2007-27 1..6 (2007) (0)
Associations of joint swelling, joint stiffness, and joint pain with physical activity in first-degree relatives of patients with rheumatoid arthritis (2020) (0)
Integrated network analysis of miRNA–mRNA interactions in ovarian cancer outcomes (2015) (0)
Transcription Profiles of Rheumatoid Arthritis Patients Reveal Genes Characterizing Different Response to Anti-TNF Therapy (2007) (0)
Emerging relationships: rheumatoid arthritis and the PTPN22 associated autoimmune disorders (2006) (0)
Effective Sample Size of Affected Sib Pairs in Case-Control Analyses (2005) (0)
F.99. Identification of Signaling Alterations in Rheumatoid Arthritis by Phospho-specific Flow Cytometry (2009) (0)
OP0234 Rheumatoid Arthritis Subsets Defined by Sub-Specificities of Anti-Citrullinated Antibodies (ACPAS) Have Unique HLA Associations (2016) (0)
Intracellular signaling as measured by single cell network profiling (SCNP) is stable in longtitudinal samples of peripheral blood mononuclear cells (PBMC) from healthy donors (HD) across multiple immune cell subsets (TECH1P.839) (2014) (0)
The Genotype and Phenotype (GaP) registry: a living biobank for the analysis of quantitative traits (2015) (0)
New Genetic Risk Loci for the Radiographic Severity of Rheumatoid Arthritis (2012) (0)
IDENTIFICATION OF NOVEL OSTEOARTHRITIS GENES USING ZEBRAFISH (2012) (0)
Genotyping of Risk Loci in Black South Africans with Rheumatoid Arthritis using the Immunochip: An Association study (2013) (0)
28 COLLECTION OF DE-IDENTIFIED HUMAN BIOLOGICAL SPECIMENS FOR RESEARCH. (2004) (0)
Fine-mapping and functional studies highlight potential causal variants for rheumatoid arthritis and type 1 diabetes (2018) (0)
THU0469 Genetic Variants in IL-6, IL-10, C5-TRAF1 and FCRL3 and Progression of Joint Damage in Rheumatoid Arthritis; A Study on Six Cohorts (2014) (0)
1622: Macrophage Migration Inhibitory Factor (MIF) Gene Polymorphisms are Associated with Susceptibility and Severity of Prostate Cancer (2007) (0)
Detective work reveals new secrets about rheumatoid arthritis (2013) (0)
Gene Set Enrichment Analysis of Ki-67 high CLL Clones Suggests Complex Interactions of B-Cell Receptor Signaling and Normal Cell Interactions in the Disease (2011) (0)
Effect of Polymorphisms in p53 Pathway Proteins and B-Chronic Lymphocytic Leukemia Disease Progression, (2011) (0)
OR.28. Macrophages Remember Neural Signals that Teach Attenuation of Responses to Bacterial Endotoxin (2008) (0)
Relationship of DR3 T cell recognition determinants to protein sequence (1988) (0)
Abstract A32: Single-cell RNA-seq analysis of primary tumor and corresponding metastatic lesion in high-grade serous ovarian cancer (2018) (0)
1291 DIFFERENTIAL EXPRESSION OF MICRORNA IN RADICAL PROSTATECTOMY SPECIMENS: COMPARING FOCI OF PROSTATE CANCER TO AREAS OF BENIGN GLANDULAR ARCHITECTURE (2011) (0)
University of Groningen Identification of Novel Genetic Markers Associated with Clinical Phenotypes of Systemic Sclerosis through a Genome-Wide Association Strategy Gorlova, (2011) (0)

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