Recent Advances in the Genetics of Autoimmune Disease

PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses

2007 • 29,581 citations

Repertoires of Autophagy in the Pathogenesis of Ocular Diseases

2015 • 15,801 citations

Principal components analysis corrects for stratification in genome-wide association studies

2006 • 9,771 citations

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

2007 • 9,332 citations

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

2001 • 5,526 citations

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

2001 • 4,997 citations

A second generation human haplotype map of over 3.1 million SNPs

2007 • 4,436 citations

STATs: transcriptional control and biological impact

2002 • 3,050 citations

A Genome-Wide Association Study Identifies IL23R as an Inflammatory Bowel Disease Gene

2006 • 2,903 citations

Strong Association of De Novo Copy Number Mutations with Autism

2007 • 2,782 citations

The Wellcome Trust Case Control Consortium, U.K.

2008 • 2,762 citations

A new multipoint method for genome-wide association studies by imputation of genotypes

2007 • 2,593 citations

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

2008 • 2,577 citations

Large-Scale Copy Number Polymorphism in the Human Genome

2004 • 2,542 citations

Projection of an Immunological Self Shadow Within the Thymus by the Aire Protein

2002 • 2,371 citations

B-Cell Depletion with Rituximab in Relapsing–Remitting Multiple Sclerosis

2008 • 2,239 citations

In Vivo Analysis of Autophagy in Response to Nutrient Starvation Using Transgenic Mice Expressing a Fluorescent Autophagosome Marker

2003 • 2,218 citations

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

2003 • 2,181 citations

Interferon-inducible gene expression signature in peripheral blood cells of patients with severe lupus

2003 • 2,133 citations

Replication validity of genetic association studies

2001 • 1,845 citations

A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1

2006 • 1,843 citations

Efficacy and safety of ustekinumab, a human interleukin-12/23 monoclonal antibody, in patients with psoriasis: 76-week results from a randomised, double-blind, placebo-controlled trial (PHOENIX 1)

2008 • 1,788 citations

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

2007 • 1,750 citations

Risk Alleles for Multiple Sclerosis Identified by a Genomewide Study

2007 • 1,681 citations

IRFs: master regulators of signalling by Toll-like receptors and cytosolic pattern-recognition receptors

2006 • 1,564 citations

A Missense Single-Nucleotide Polymorphism in a Gene Encoding a Protein Tyrosine Phosphatase (PTPN22) Is Associated with Rheumatoid Arthritis

2004 • 1,489 citations

A new model for an etiology of rheumatoid arthritis: Smoking may trigger HLA–DR (shared epitope)–restricted immune reactions to autoantigens modified by citrullination

2005 • 1,444 citations

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

2007 • 1,426 citations

A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes

2004 • 1,392 citations

Failure to Regulate TNF-Induced NF-κB and Cell Death Responses in A20-Deficient Mice

2000 • 1,374 citations

Germline Mutations in the Extracellular Domains of the 55 kDa TNF Receptor, TNFR1, Define a Family of Dominantly Inherited Autoinflammatory Syndromes

1999 • 1,363 citations

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

2007 • 1,358 citations

Impaired IL-12 responses and enhanced development of Th2 cells in Stat4-deficient mice

1996 • 1,277 citations

Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci

2008 • 1,273 citations

Efficacy and safety of ustekinumab, a human interleukin-12/23 monoclonal antibody, in patients with psoriasis: 52-week results from a randomised, double-blind, placebo-controlled trial (PHOENIX 2)

2008 • 1,268 citations

Inflammatory Bowel Disease

1991 • 1,264 citations

Induction of Dendritic Cell Differentiation by IFN-α in Systemic Lupus Erythematosus

2001 • 1,245 citations

Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility

2007 • 1,145 citations

Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis

2003 • 1,143 citations

Mapping and sequencing of structural variation from eight human genomes

2008 • 1,132 citations

A Large-Scale Genetic Association Study Confirms IL12B and Leads to the Identification of IL23R as Psoriasis-Risk Genes

2007 • 1,070 citations

Horror Autoinflammaticus: The Molecular Pathophysiology of Autoinflammatory Disease

2009 • 1,024 citations

STAT4and the Risk of Rheumatoid Arthritis and Systemic Lupus Erythematosus

2007 • 1,008 citations

Integral role of IRF-5 in the gene induction programme activated by Toll-like receptors

2005 • 973 citations

Mapping of a susceptibility locus for Crohn's disease on chromosome 16

1996 • 961 citations

CARD15 mutations in Blau syndrome

2001 • 945 citations

The insulin gene is transcribed in the human thymus and transcription levels correlate with allelic variation at the INS VNTR-IDDM2 susceptibility locus for type 1 diabetes

1997 • 931 citations

PAD, a growing family of citrullinating enzymes: genes, features and involvement in disease

2003 • 924 citations

The genetics and immunopathogenesis of inflammatory bowel disease

2008 • 920 citations

Association of Systemic Lupus Erythematosus withC8orf13–BLKandITGAM–ITGAX

2008 • 887 citations

Unveiling the roles of autophagy in innate and adaptive immunity

2007 • 861 citations

Genotype, haplotype and copy-number variation in worldwide human populations

2008 • 858 citations

Strong association of de novo copy number mutations with sporadic schizophrenia

2008 • 822 citations

TRAF1–C5as a Risk Locus for Rheumatoid Arthritis — A Genomewide Study

2007 • 816 citations

Interleukin-23 drives innate and T cell–mediated intestinal inflammation

2006 • 814 citations

Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locus

1997 • 806 citations

A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans

2002 • 756 citations

Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant

2005 • 707 citations

A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region

2006 • 677 citations

Interleukin 12 signaling in T helper type 1 (Th1) cells involves tyrosine phosphorylation of signal transducer and activator of transcription (Stat)3 and Stat4.

1995 • 675 citations

Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 are associated with systemic lupus erythematosus

2007 • 674 citations

Genetic Association of the R620W Polymorphism of Protein Tyrosine Phosphatase PTPN22 with Human SLE

2004 • 665 citations

IL-23 stimulates epidermal hyperplasia via TNF and IL-20R2–dependent mechanisms with implications for psoriasis pathogenesis

2006 • 662 citations

A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21

2007 • 662 citations

A common haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus

2006 • 661 citations

Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease

2008 • 653 citations

A Genome-Wide Association Study of Psoriasis and Psoriatic Arthritis Identifies New Disease Loci

2008 • 649 citations

Interleukin 7 receptor α chain ( IL7R ) shows allelic and functional association with multiple sclerosis

2007 • 628 citations

Autophagy promotes MHC class II presentation of peptides from intracellular source proteins

2005 • 619 citations

Analysis of Families in the Multiple Autoimmune Disease Genetics Consortium (MADGC) Collection: the PTPN22 620W Allele Associates with Multiple Autoimmune Phenotypes

2005 • 597 citations

Polymorphisms in the Tyrosine Kinase 2 and Interferon Regulatory Factor 5 Genes Are Associated with Systemic Lupus Erythematosus

2005 • 591 citations

Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles

2008 • 589 citations

Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus

2008 • 574 citations

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 • 559 citations

The Many Faces of IL-7: From Lymphopoiesis to Peripheral T Cell Maintenance

2005 • 551 citations

Two independent alleles at 6q23 associated with risk of rheumatoid arthritis

2007 • 549 citations

Signaling by IL‐12 and IL‐23 and the immunoregulatory roles of STAT4

2004 • 547 citations

Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A

2007 • 544 citations

A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene

2007 • 532 citations

Common variants at CD40 and other loci confer risk of rheumatoid arthritis

2008 • 524 citations

Replication of an Association Between the Lymphoid Tyrosine Phosphatase Locus (LYP/PTPN22) With Type 1 Diabetes, and Evidence for Its Role as a General Autoimmunity Locus

2004 • 496 citations

Fc gamma RIIA alleles are heritable risk factors for lupus nephritis in African Americans.

1996 • 476 citations

Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus

2008 • 467 citations

The Codon 620 Tryptophan Allele of the Lymphoid Tyrosine Phosphatase (LYP) Gene Is a Major Determinant of Graves’ Disease

2004 • 464 citations

FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity

2007 • 460 citations

Immunity to Citrullinated Proteins in Rheumatoid Arthritis

2008 • 451 citations

Multiple polymorphisms in the TNFAIP3 region are independently associated with systemic lupus erythematosus

2008 • 448 citations

A biosynthetic pathway for anandamide

2006 • 446 citations

Three functional variants of IFN regulatory factor 5 ( IRF5 ) define risk and protective haplotypes for human lupus

2007 • 441 citations

Detecting Disease Associations due to Linkage Disequilibrium Using Haplotype Tags: A Class of Tests and the Determinants of Statistical Power

2003 • 424 citations

Expanded T cells from pancreatic lymph nodes of type 1 diabetic subjects recognize an insulin epitope

2005 • 417 citations

Large-scale genetic fine mapping and genotype-phenotype associations implicate polymorphism in the IL2RA region in type 1 diabetes

2007 • 413 citations

High serum IFN-α activity is a heritable risk factor for systemic lupus erythematosus

2007 • 400 citations

Rheumatoid arthritis association at 6q23

2007 • 385 citations

Heterozygous Mutations in TREX1 Cause Familial Chilblain Lupus and Dominant Aicardi-Goutières Syndrome

2007 • 379 citations

PEST Domain-Enriched Tyrosine Phosphatase (PEP) Regulation of Effector/Memory T Cells

2004 • 376 citations

Interleukin-2 gene variation impairs regulatory T cell function and causes autoimmunity

2007 • 367 citations

Regulatory regions and critical residues of NOD2 involved in muramyl dipeptide recognition

2004 • 358 citations

Localization of a Type 1 Diabetes Locus in the IL2RA/CD25 Region by Use of Tag Single-Nucleotide Polymorphisms

2005 • 350 citations

Genetic Variation in PTPN22 Corresponds to Altered Function of T and B Lymphocytes

2007 • 339 citations

The type I interferon system in systemic lupus erythematosus

2006 • 335 citations

Safety and efficacy of additional courses of rituximab in patients with active rheumatoid arthritis: An open‐label extension analysis

2007 • 326 citations

The T Cell Protein Tyrosine Phosphatase Is a Negative Regulator of Janus Family Kinases 1 and 3

2002 • 325 citations

Both IL-12p70 and IL-23 are synthesized during active Crohnʼs disease and are down-regulated by treatment with anti-IL-12 p40 monoclonal antibody

2005 • 319 citations

Both integrated and differential regulation of components of the IL-2/IL-2 receptor system

2006 • 310 citations

Discerning the Ancestry of European Americans in Genetic Association Studies

2008 • 309 citations

A nonsynonymous functional variant in integrin-αM (encoded by ITGAM) is associated with systemic lupus erythematosus

2008 • 304 citations

Association between the PTPN22 gene and rheumatoid arthritis and juvenile idiopathic arthritis in a UK population: Further support that PTPN22 is an autoimmunity gene

2005 • 296 citations

CTLA4 gene polymorphism and autoimmunity

2005 • 282 citations

A Candidate Gene Approach Identifies the TRAF1/C5 Region as a Risk Factor for Rheumatoid Arthritis

2007 • 274 citations

Both donor and recipient NOD2/CARD15 mutations associate with transplant-related mortality and GvHD following allogeneic stem cell transplantation

2004 • 273 citations

Polymorphisms of the IL12B and IL23R Genes Are Associated with Psoriasis

2008 • 266 citations

Regulation of IL-8 and IL-1 expression in Crohn's disease associated NOD2/CARD15 mutations

2004 • 264 citations

Association of the IRF5 risk haplotype with high serum interferon‐α activity in systemic lupus erythematosus patients

2008 • 259 citations

A20 inhibits NF-κB activation by dual ubiquitin-editing functions

2004 • 254 citations

Ethnic differences in allele frequency of autoimmune-disease-associated SNPs

2005 • 233 citations

PTPN22 Genetic Variation: Evidence for Multiple Variants Associated with Rheumatoid Arthritis

2005 • 230 citations

Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci

2007 • 219 citations

Specificity of the STAT4 Genetic Association for Severe Disease Manifestations of Systemic Lupus Erythematosus

2008 • 217 citations

A C/T Single-Nucleotide Polymorphism in the Region of the CD40 Gene is Associated with Graves' Disease

2002 • 212 citations

Novel Association in Chromosome 4q27 Region with Rheumatoid Arthritis and Confirmation of Type 1 Diabetes Point to a General Risk Locus for Autoimmune Diseases

2007 • 211 citations

The emerging role of interferon in human systemic lupus erythematosus

2004 • 207 citations

A risk haplotype of STAT4 for systemic lupus erythematosus is over-expressed, correlates with anti-dsDNA and shows additive effects with two risk alleles of IRF5

2008 • 202 citations

A decade of AIRE

2007 • 188 citations

Inducible Expression of Stat4 in Dendritic Cells and Macrophages and Its Critical Role in Innate and Adaptive Immune Responses

2001 • 187 citations

Nonreceptor Protein-Tyrosine Phosphatases in Immune Cell Signaling

2007 • 185 citations

An insertion deletion polymorphism in the Interferon Regulatory Factor 5 (IRF5) gene confers risk of inflammatory bowel diseases

2007 • 182 citations

BANK regulates BCR-induced calcium mobilization by promoting tyrosine phosphorylation of IP3 receptor

2002 • 180 citations

Association of the TSHR gene with Graves' disease: the first disease specific locus

2005 • 176 citations

Protein Tyrosine Phosphatases in Autoimmunity

2008 • 175 citations

Association of STAT4 with Rheumatoid Arthritis in the Korean Population

2007 • 173 citations

Variant form of STAT4 is associated with primary Sjögren's syndrome

2008 • 168 citations

Association of the interleukin‐2 receptor alpha (IL‐2Rα)/CD25 gene region with Graves’ disease using a multilocus test and tag SNPs

2007 • 160 citations

<scp>TRAF</scp>‐Mediated <scp>TNFR</scp>‐Family Signaling

2002 • 160 citations

Association analysis of the 1858C&gt;T polymorphism in the PTPN22 gene in juvenile idiopathic arthritis and other autoimmune diseases

2005 • 154 citations

CD4+CD25+FoxP3+ regulatory T cells in autoimmune diseases

2007 • 154 citations

Association of STAT4 with susceptibility to rheumatoid arthritis and systemic lupus erythematosus in the Japanese population

2008 • 151 citations

The multifaceted roles of TRAFs in the regulation of B-cell function

2004 • 151 citations

What Can Genome-Wide Association Studies Tell Us about the Genetics of Common Disease?

2008 • 146 citations

Human receptors for immunoglobulin G: Key elements in the pathogenesis of rheumatic disease

2001 • 139 citations

Spondyloarthritis: update on pathogenesis and management

2005 • 137 citations

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

2008 • 134 citations

High-density SNP analysis of 642 Caucasian families with rheumatoid arthritis identifies two new linkage regions on 11p12 and 2q33

2006 • 132 citations

Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians

2008 • 128 citations

Expression of Jak3, STAT1, STAT4, and STAT6 in inflammatory arthritis: unique Jak3 and STAT4 expression in dendritic cells in seropositive rheumatoid arthritis

2005 • 128 citations

Multiple SNPs in Intron 7 of Thyrotropin Receptor Are Associated with Graves’ Disease

2005 • 127 citations

Lymphoid tyrosine phosphatase (PTPN22/LYP) variant and Graves’ disease in a Polish population: association and gene dose‐dependent correlation with age of onset

2005 • 126 citations

IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations

2008 • 124 citations

Association of the PTPN22*R620W polymorphism with autoimmune myasthenia gravis

2006 • 121 citations

Expression of CD40 identifies a unique pathogenic T cell population in type 1 diabetes

2002 • 117 citations

Genetic risk factors for rheumatoid arthritis differ in caucasian and Korean populations

2009 • 116 citations

Haplotype analysis revealed no association between the PTPN22 gene and RA in a Japanese population

2006 • 115 citations

Genomic Polymorphism at the Interferon-Induced Helicase (IFIH1) Locus Contributes to Graves’ Disease Susceptibility

2007 • 112 citations

Cooperation between TNF Receptor-Associated Factors 1 and 2 in CD40 Signaling

2006 • 109 citations

The PTPN22 620W allele confers susceptibility to systemic sclerosis: Findings of a large case–control study of European Caucasians and a meta‐analysis

2008 • 108 citations

A Costimulatory Function for T Cell CD40

2007 • 107 citations

Tumor Necrosis Factor Receptor-associated Factor (TRAF) 1 Regulates CD40-induced TRAF2-mediated NF-κB Activation

2003 • 101 citations

Inflammatory Bowel Disease Genetics: Nod2

2006 • 101 citations

A CD40 Kozak sequence polymorphism and susceptibility to antibody-mediated autoimmune conditions: the role of CD40 tissue-specific expression

2007 • 100 citations

Several Regions in the Major Histocompatibility Complex Confer Risk for Anti-CCP-Antibody Positive Rheumatoid Arthritis, Independent of the DRB1 Locus

2008 • 99 citations

Pleiotropic effects of the 8.1 HLA haplotype in patients with autoimmune myasthenia gravis and thymus hyperplasia

2004 • 95 citations

BANK Negatively Regulates Akt Activation and Subsequent B Cell Responses

2006 • 94 citations

Finnish case–control and family studies support PTPN22 R620W polymorphism as a risk factor in rheumatoid arthritis, but suggest only minimal or no effect in juvenile idiopathic arthritis

2005 • 94 citations

Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease

2008 • 92 citations

HLA class I alleles tag HLA-DRB1 * 1501 haplotypes for differential risk in multiple sclerosis susceptibility

2008 • 89 citations

A Large-Scale Rheumatoid Arthritis Genetic Study Identifies Association at Chromosome 9q33.2

2008 • 86 citations

Surface expression of gp165/95, the complement receptor CR3, as a marker of disease activity in systemic lupus erythematosus

1988 • 81 citations

Genetic association of IRF5 with SLE in Mexicans: higher frequency of the risk haplotype and its homozygozity than Europeans

2007 • 77 citations

Replication of reported genetic associations of PADI4, FCRL3, SLC22A4 and RUNX1 genes with rheumatoid arthritis: results of an independent Japanese population and evidence from meta-analysis of East Asian studies

2007 • 76 citations

Reduced Expression of STAT4 and IFN-γ in Macrophages from BALB/c Mice

2002 • 72 citations

PTPN22 Is Genetically Associated with Risk of Generalized Vitiligo, but CTLA4 Is Not

2008 • 71 citations

Changes in synovial tissue Jak-STAT expression in rheumatoid arthritis in response to successful DMARD treatment

2006 • 67 citations

Association of CD40 Gene Polymorphism (C-1T) with Susceptibility and Phenotype of Graves' Disease

2005 • 64 citations

Targeting of the Transcription Factor STAT4 by Antisense Phosphorothioate Oligonucleotides Suppresses Collagen-Induced Arthritis

2007 • 64 citations

Gene copy number variation in schizophrenia

2007 • 63 citations

Association of a C/T Single-Nucleotide Polymorphism in the 5' Untranslated Region of the CD40 Gene with Graves' Disease in Japanese

2006 • 62 citations

Replication of the genetic effects of IFN regulatory factor 5 (IRF5) on systemic lupus erythematosus in a Korean population

2007 • 59 citations

Thymic expression of peripheral tissue antigens in humans: a remarkable variability among individuals

2005 • 58 citations

A unique T cell subset described as CD4loCD40+ T cells (TCD40) in human type 1 diabetes

2007 • 58 citations

Selective Availability of IL-2 Is a Major Determinant Controlling the Production of CD4+CD25+Foxp3+ T Regulatory Cells

2006 • 56 citations

The R620W polymorphism in PTPN22 confers general susceptibility for the development of alopecia areata

2007 • 53 citations

A single nucleotide polymorphism in the IRF5 promoter region is associated with susceptibility to rheumatoid arthritis in the Japanese population

2008 • 51 citations

Nuclear Localization in the Biology of the CD40 Receptor in Normal and Neoplastic Human B Lymphocytes

2006 • 51 citations

STAT4 is a target of the hematopoietic zinc‐finger transcription factor Ikaros in T cells

2005 • 46 citations

Nuclear CD40 interacts with c-Rel and enhances proliferation in aggressive B-cell lymphoma

2007 • 44 citations

Architectural Defects in the Spleens of Nkx2-3-Deficient Mice Are Intrinsic and Associated with Defects in Both B Cell Maturation and T Cell-Dependent Immune Responses

2003 • 44 citations

Disruption of the homeostatic balance between autoaggressive (CD4+CD40+) and regulatory (CD4+CD25+FoxP3+) T cells promotes diabetes

2008 • 43 citations

Negative regulation of constitutive NF‐κB and JNK signaling by PKN1‐mediated phosphorylation of TRAF1

2008 • 40 citations

Evaluating the role of the 620W allele of protein tyrosine phosphatase PTPN22 in Crohn's disease and multiple sclerosis

2005 • 39 citations

Increased expression of CD40 on thymocytes and peripheral T cells in autoimmunity: a mechanism for acquiring changes in the peripheral T cell receptor repertoire.

1999 • 37 citations

NF-κB is required for STAT-4 expression during dendritic cell maturation

2006 • 37 citations

Amplification of the synovial inflammatory response through activation of mitogen‐activated protein kinases and nuclear factor κB using ligation of CD40 on CD14+ synovial cells from patients with rheumatoid arthritis

2004 • 35 citations

High Distribution of CD40 and TRAF2 in Th40 T Cell Rafts Leads to Preferential Survival of this Auto-Aggressive Population in Autoimmunity

2008 • 35 citations

Fine-Mapping Chromosome 20 in 230 Systemic Lupus Erythematosus Sib Pair and Multiplex Families: Evidence for Genetic Epistasis with Chromosome 16q12

2006 • 28 citations

A novel polymorphism of the human CD40 receptor with enhanced function

2008 • 23 citations

Identification and characterization of two CD40-inducible enhancers in the mouse TRAF1 gene locus

2000 • 20 citations

Gene copy number variation in schizophrenia

2007 • 11 citations

Analysis of variation in NF-κB genes and expression levels of NF-κB-regulated molecules

2007 • 11 citations

Complex organizational defects of fibroblast architecture in the mouse spleen with Nkx2.3 homeodomain deficiency

2007 • 8 citations