James A. Traherne

Genetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history.

Splice variation in the cytoplasmic domains of myelin oligodendrocyte glycoprotein affects its cellular localisation and transport.

Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project.

Human MHC architecture and evolution: implications for disease association studies.

Cellular expression, trafficking, and function of two isoforms of human ULBP5/RAET1G.

Mechanisms of copy number variation and hybrid gene formation in the KIR immune gene complex.

Genetic variation, Fcγ receptors, KIRs and infection: the evolution of autoimmunity.

Electrostatic modifications of the human leukocyte antigen-DR P9 peptide-binding pocket and susceptibility to primary sclerosing cholangitis.

Copy number variation leads to considerable diversity for B but not A haplotypes of the human KIR genes encoding NK cell receptors.

Killer cell immunoglobulin-like receptor (KIR) genes and their HLA-C ligands in a Ugandan population.

Copy number and nucleotide variation of the LILR family of myelomonocytic cell activating and inhibitory receptors.

TAPBPR isoforms exhibit altered association with MHC class I.

Killer-cell Immunoglobulin-like Receptor gene linkage and copy number variation analysis by droplet digital PCR.

A hybrid qPCR/SNP array approach allows cost efficient assessment of KIR gene copy numbers in large samples.

KIR diversity in Māori and Polynesians: populations in which HLA-B is not a significant KIR ligand.

Refinement of the MHC risk map in a scandinavian primary sclerosing cholangitis population.

High-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis.

A KIR B centromeric region present in Africans but not Europeans protects pregnant women from pre-eclampsia.

Surveillance of cell and tissue perturbation by receptors in the LRC.

Imputation of KIR Types from SNP Variation Data.

LILRA6 copy number variation correlates with susceptibility to atopic dermatitis.

Defining KIR and HLA Class I Genotypes at Highest Resolution via High-Throughput Sequencing.

qKAT: a high-throughput qPCR method for KIR gene copy number and haplotype determination.

Deciphering the killer-cell immunoglobulin-like receptor system at super-resolution for natural killer and T-cell biology.

Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's disease.

Novel KIR genotypes and gene copy number variations in northeastern Thais.

High-Resolution Genetic and Phenotypic Analysis of KIR2DL1 Alleles and Their Association with Pre-Eclampsia.

Report from the Killer-cell Immunoglobulin-like Receptors (KIR) component of the 17th International HLA and Immunogenetics Workshop.

A novel antibody combination to identify KIR2DS2 natural killer cells in KIR2DL3/L2/S2 heterozygous donors.

Inhibitory killer cell immunoglobulin-like receptors strengthen CD8 T cell-mediated control of HIV-1, HCV, and HTLV-1.