Professor of Medicine, University Alabama
Rheumatology
Dr. Robert P. Kimberly, MD
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Robert P. Kimberly works in the field of Rheumatology. He graduated from Harvard Medical School. Harvard Medical School is one of the top medical schools in the US. Harvard Medical School has a rank of 1 in research and a 12 in primary care He over the years received 3 awards: "America's Top Doctors", "Elected Member" and "Whos Who in Medicine and Healthcare". Dr. Robert P. Kimberly is a published doctor and has 87 publications published. The lastest was: 'Estimation of Cell-Type Composition Including T and B Cell Subtypes for Whole Blood Methylation Microarray Data.' He accepts Medicare payments and is listed with Medicare.gov.
Publications
- Characterization of Genetic Loci That Affect Susceptibility to Inflammatory Bowel Diseases in African Americans.
- Genetic association of CD247 (CD3ζ) with SLE in a large-scale multiethnic study.
- Preferential association of a functional variant in complement receptor 2 with antibodies to double-stranded DNA.
- The IRF5-TNPO3 association with systemic Lupus erythematosus (SLE) has two components that other autoimmune disorders variably share.
- Lack of Association of the APOL1 G3 Haplotype in African Americans with ESRD.
- Brief Report: A Polymorphism in TLR2 Is Associated With Arterial Thrombosis in a Multiethnic Population of Patients With Systemic Lupus Erythematosus.
- Lupus Nephritis Susceptibility Loci in Women with Systemic Lupus Erythematosus.
- GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region.
- Fcγ Receptor IIIa Single-Nucleotide Polymorphisms and Haplotypes Affect Human IgG Binding and Are Associated With Lupus Nephritis in African Americans.
- Two Functional Lupus-Associated BLK Promoter Variants Control Cell-Type- and Developmental-Stage-Specific Transcription.
- Targeting the Fc receptor in autoimmune Disease.
- End-Stage Renal Disease in African Americans With Lupus Nephritis Is Associated With APOL1.
- Allelic-dependent expression of an activating fc receptor on B cells enhances humoral immune responses.
- FcγRIIIa SNPs and haplotypes affect human IgG binding and association with Lupus nephritis in African Americans.
- Preferential binding to Elk-1 by SLE-associated IL10 risk allele upregulates IL10 expression.
- End-stage kidney disease in African Americans with Lupus nephritis associates with APOL1.
- Genome-Wide DNA Methylation Analysis of Systemic Lupus Erythematosus Reveals Persistent Hypomethylation of Interferon Genes and Compositional Changes to CD4+ T-cell Po...
- Variable Association of Reactive Intermediate Genes with Systemic Lupus Erythematosus in Populations with Different African Ancestry.
- Genome-Wide Association Study and Gene Expression Analysis Identifies CD84 as a Predictor of Response to Etanercept Therapy in Rheumatoid Arthritis.
- Fine mapping of Xq28: both MECP2 and IRAK1 contribute to risk for systemic Lupus erythematosus in multiple ancestral groups.
- MicroRNA-3148 Modulates Allelic Expression of Toll-Like Receptor 7 Variant Associated with Systemic Lupus Erythematosus.
- Admixture Mapping in Lupus Identifies Multiple Functional Variants within IFIH1 Associated with Apoptosis, Inflammation, and Autoantibody Production.
- Brief Report: Single-nucleotide polymorphisms in VKORC1 are risk factors for systemic Lupus erythematosus in Asians.
- Impact of genetic ancestry and socio-demographic status on the clinical expression of systemic Lupus erythematosus in Amerindian-European populations.
- Two independent functional risk haplotypes in TNIP1 are associated with systemic Lupus erythematosus.
- The Unique Cytoplasmic Domain of Human FcγRIIIA Regulates Receptor-Mediated Function.
- Variation in the ICAM1-ICAM4-ICAM5 locus is associated with systemic Lupus erythematosus susceptibility in multiple ancestries.
- Association of single-nucleotide polymorphisms in CCR6, TAGAP, and TNFAIP3 with rheumatoid Arthritis in African Americans.
- Evidence for gene-gene epistatic interactions among susceptibility loci for systemic Lupus erythematosus.
- Lupus-associated causal mutation in neutrophil cytosolic factor 2 (NCF2) brings unique insights to the structure and function of NADPH oxidase.
- Association of discoid Lupus with clinical manifestations and damage accrual in profile: A multiethnic Lupus cohort.
- IgA and IgG antineutrophil cytoplasmic antibody engagement of Fc receptor genetic variants influences Granulomatosis with polyangiitis.
- IRF5 haplotypes demonstrate diverse serological associations which predict serum interferon alpha activity and explain the majority of the genetic association with sys...
- Identification of novel genetic susceptibility loci in African American Lupus patients in a candidate gene association study.
- Treatment of Arthritis by macrophage depletion and immunomodulation: Testing an apoptosis-mediated therapy in a humanized death receptor mouse model.
- Serine phosphorylation of Fc{gamma}RI cytoplasmic domain directs lipid raft localization and interaction with protein 4.1G.
- FAS mRNA editing in human systemic Lupus erythematosus.
- Genetic analyses of interferon pathway-related genes reveals multiple new loci associated with systemic Lupus erythematosus (SLE).
- Human FasL Gene Is a Target of ?-Catenin/T-Cell Factor Pathway and Complex FasL Haplotypes Alter Promoter Functions.
- Most common single-nucleotide polymorphisms associated with rheumatoid Arthritis in persons of European ancestry confer risk of rheumatoid Arthritis in African Americans.
- Most common SNPs associated with rheumatoid Arthritis in subjects of European ancestry confer risk of rheumatoid Arthritis in African-Americans.
- Genetic factors predisposing to systemic Lupus erythematosus and Lupus nephritis.
- Wegener's Granulomatosis: a model of auto-antibodies in mucosal autoimmunity.
- The role of genetic variation near interferon-kappa in systemic Lupus erythematosus.
- Retraction: an African ancestry-specific allele of CTLA4 confers protection against rheumatoid Arthritis in African Americans.
- A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic Lupus erythematosus.
- The FCRL3-169CT promoter single-nucleotide polymorphism, which is associated with systemic Lupus erythematosus in a Japanese population, predicts expression of recepto...
- A polymorphism within IL21R confers risk for systemic Lupus erythematosus.
- Variants within MECP2, a key transcription regulator, are associated with increased susceptibility to Lupus and differential gene expression in patients with systemic ...
- An African ancestry-specific allele of CTLA4 confers protection against rheumatoid Arthritis in African Americans.
- Functional expression of IgA receptor FcalphaRI on human platelets.
- Klinefelter's Syndrome (47,XXY) in male systemic lupus erythematosus patients: support for the notion of a gene-dose effect from the X chromosome.
- Immune opsonins modulate BLyS/BAFF release in a receptor-specific fashion.
- IgA1-secreting cell lines from patients with IgA nephropathy produce aberrantly glycosylated IgA1.
- A nonsynonymous functional variant in integrin-alpha(M) (encoded by ITGAM) is associated with systemic Lupus erythematosus.
- Common variants within MECP2 confer risk of systemic Lupus erythematosus.
- Variation in the relative copy number of the TLR7 gene in patients with systemic Lupus erythematosus and healthy control subjects.
- FcalphaRI (CD89) alleles determine the proinflammatory potential of serum IgA.
- Expression profile of FcgammaRIIb on leukocytes and its dysregulation in systemic Lupus erythematosus.
- Dectin-2 is a pattern recognition receptor for fungi that couples with the Fc receptor gamma chain to induce innate immune responses.
- Association of a transmembrane polymorphism of Fcgamma receptor IIb (FCGR2B) with systemic Lupus erythematosus in Taiwanese patients.
- JAB1 determines the response of rheumatoid Arthritis synovial fibroblasts to tumor necrosis factor-alpha.
- Regional admixture mapping and structured association testing: conceptual unification and an extensible general linear model.
- A membrane form of TNF-alpha presented by exosomes delays T cell activation-induced cell death.
- Murine mammary carcinoma exosomes promote tumor growth by suppression of NK cell function.
- Genetics of susceptibility and severity in systemic Lupus erythematosus.
- Cleavage of p53-vimentin complex enhances tumor necrosis factor-related apoptosis-inducing ligand-mediated apoptosis of rheumatoid Arthritis synovial fibroblasts.
- Differential gene expression modulated by the cytoplasmic domain of Fc gamma RIa (CD64) alpha-chain.
- The influence of genetic variation in the HLA-DRB1 and LTA-TNF regions on the response to treatment of early rheumatoid Arthritis with methotrexate or etanercept.
- Associations, populations, and the truth: recommendations for genetic association studies in Arthritis & Rheumatism.
- A promoter haplotype of the immunoreceptor tyrosine-based inhibitory motif-bearing FcgammaRIIb alters receptor expression and associates with autoimmunity. I. Regulato...
- A promoter haplotype of the immunoreceptor tyrosine-based inhibitory motif-bearing FcgammaRIIb alters receptor expression and associates with autoimmunity. II. Differe...
- Control of spontaneous B lymphocyte autoimmunity with adenovirus-encoded soluble TACI.
- Fc gamma RIIIb allele-sensitive release of alpha-defensins: anti-neutrophil cytoplasmic antibody-induced release of chemotaxins.
- A novel polymorphism in the Fcgamma receptor IIB (CD32B) transmembrane region alters receptor signaling.
- Fc gamma Rs modulate cytotoxicity of anti-Fas antibodies: implications for agonistic antibody-based therapeutics.
- A novel polymorphic CAAT/enhancer-binding protein beta element in the FasL gene promoter alters Fas ligand expression: a candidate Background gene in African American ...
- The CY domain of the Fcgamma RIa alpha-chain (CD64) alters gamma-chain tyrosine-based signaling and phagocytosis.
- Genetic linkage and association of Fcgamma receptor IIIA (CD16A) on chromosome 1q23 with human systemic Lupus erythematosus.
- Immunobiology of tumor necrosis factor receptor superfamily.
- Diversity and duplicity: human FCgamma receptors in host defense and autoimmunity.
- Differential Regulation of Fcgamma Receptor Isoforms: Implications for Therapeutic Intervention.
- Estimation of Cell-Type Composition Including T and B Cell Subtypes for Whole Blood Methylation Microarray Data.
- Genetic analysis of the pathogenic molecular sub-phenotype interferon-alpha identifies multiple novel loci involved in systemic Lupus erythematosus.
- Lupus risk variants in the PXK locus alter B-cell receptor internalization.
- PTPN22 Association in Systemic Lupus Erythematosus (SLE) with Respect to Individual Ancestry and Clinical Sub-Phenotypes.
Schools
Harvard Medical School
Johns Hopkins University School of Medicine
Procedures Preformed
- Joint Drainage
Conditions Treated
- Ankylosing Spondylitis
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- Bursitis
- Carpal Tunnel Background: yellow;'>Syndrome
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Doctors Specialties
- Rheumatology
Accepted Insurances
Awards
- America's Top Doctors
- Elected Member
- Whos Who in Medicine and Healthcare
Education
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Hospital for Special Surgery -
University of Pennsylvania Health System -
Harvard Medical School
Hospital
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University of Alabama Hospital -
Birmingham Veterans Affairs Medical Center
Drug Facts
| NPI NUMBER | 1750318267 | |
| NPPES Provider LastName | KIMBERLY | |
| NPPES Provider FirstName | ROBERT | |
| NPPES Provider ZIPCode | 35233 | |
| NPPES Provider State | AL | |
| Specialty Description | Rheumatology | |
| Total Claim Count | 572.0 | |
| Distinct Opioid Count | 1.0 | |
| Opioid Claim Count | 33.0 | |
| Percent Opioid Claims | 5.77 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1750318267 |
| Last Name Of The Provider | KIMBERLY |
| First Name Of The Provider | ROBERT |
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