Fellow of The Academy of Medical Sciences, United Kingdom
His primary scientific interests are in Immunology, Genetics, Haplotype, Lupus erythematosus and Single-nucleotide polymorphism. His research in Immunology intersects with topics in Systemic lupus erythematosus, Disease, Genome-wide association study and Genetic association. His research integrates issues of Autoantibody and Pathogenesis in his study of Systemic lupus erythematosus.
Allele, Autoimmunity, Linkage disequilibrium, Major histocompatibility complex and Locus are the primary areas of interest in his Genetics study. His research in Lupus erythematosus focuses on subjects like Minor allele frequency, which are connected to Cohort, Malaria, FCGR2B and Virology. His Single-nucleotide polymorphism research is multidisciplinary, relying on both Regulation of gene expression and Candidate gene.
His primary areas of investigation include Immunology, Genetics, Single-nucleotide polymorphism, Genome-wide association study and Haplotype. His research on Immunology often connects related topics like Systemic lupus erythematosus. His Genetics study focuses mostly on Locus, Allele, Gene, Genetic association and Linkage disequilibrium.
His Single-nucleotide polymorphism research includes themes of Odds ratio, Case-control study and Genetic variation. His Genome-wide association study study integrates concerns from other disciplines, such as Expression quantitative trait loci and Disease. His Haplotype study which covers Human leukocyte antigen that intersects with Major histocompatibility complex.
His scientific interests lie mostly in Genome-wide association study, Disease, Genetics, Internal medicine and Single-nucleotide polymorphism. His Genome-wide association study research includes elements of Computational biology, Epigenetics and Genetic association. His work in Locus, Expression quantitative trait loci, Human leukocyte antigen, Haplotype and Autoimmune disease is related to Genetics.
His Human leukocyte antigen research incorporates themes from Allele and Major histocompatibility complex. His study explores the link between Gene and topics such as Lupus erythematosus that cross with problems in Candidate Disease Gene and Phenotype. His study in Immunology focuses on Autoantibody in particular.
Disease, Immunology, Lupus erythematosus, Genetics and Single-nucleotide polymorphism are his primary areas of study. The Disease study combines topics in areas such as Genome-wide association study, Antiphospholipid syndrome, Quartile, Medical genetics and Survival analysis. His Immunology research focuses on subjects like Cell, which are linked to Cohort.
As part of one scientific family, he deals mainly with the area of Lupus erythematosus, narrowing it down to issues related to the Gene, and often TLR7, Autoimmune disease and Interferon. His biological study spans a wide range of topics, including Family aggregation and Rheumatology. His Single-nucleotide polymorphism research incorporates elements of Human leukocyte antigen, Allele, Haplotype and Arthritis.
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Human polymorphism at microRNAs and microRNA target sites.
Liuqing Yang;Chunru Lin;Chunyu Jin;Joy C. Yang.
Frontiers in Genetics (2013)
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.
John B. Harley;John B. Harley;John B. Harley;Marta E. Alarcón-Riquelme;Lindsey A. Criswell;Chaim O. Jacob.
Nature Genetics (2008)
Genetic Analysis of Autoimmune Disease
Timothy J Vyse;John A Todd.
A high resolution HLA and SNP haplotype map for disease association studies in the extended human MHC
Paul I W de Bakker;Gil McVean;Pardis C Sabeti;Marcos M Miretti.
Nature Genetics (2006)
Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans
Timothy J. Aitman;Rong Dong;Timothy J. Vyse;Penny J. Norsworthy.
Defining the Role of the MHC in Autoimmunity: A Review and Pooled Analysis
Michelle M. A. Fernando;Christine R. Stevens;Emily C. Walsh;Philip Lawrence De Jager;Philip Lawrence De Jager;Philip Lawrence De Jager.
PLOS Genetics (2008)
Expansion of circulating T cells resembling follicular helper T cells is a fixed phenotype that identifies a subset of severe systemic lupus erythematosus.
Nicholas Simpson;Paul A. Gatenby;Anastasia Wilson;Shreya Malik.
Arthritis & Rheumatism (2010)
Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosus.
Min Ae Lee-Kirsch;Maolian Gong;Dipanjan Chowdhury;Lydia Senenko.
Nature Genetics (2007)
Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.
Robert R Graham;Chris Cotsapas;Chris Cotsapas;Leela Davies;Rachel Hackett.
Nature Genetics (2008)
FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity
Manuela Fanciulli;Penny J Norsworthy;Enrico Petretto;Rong Dong.
Nature Genetics (2007)
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