J. J. Pointon

Global prevalence of putative haemochromatosis mutations.

Alison T. Merryweather‐Clarke, J. J. Pointon, Jeremy D. Shearman et al. · Journal of Medical Genetics · 1997 · 791 citations · Full text

Biology, Amino Acid 282, Haplotype Determination +14

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation

Samantha J.L. Knight, A Flannery, Mark C. Hirst et al. · Cell · 1993 · 520 citations

Cpg Island, Genetic Disorder, Genetics +6

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

David M. Evans, Chris C. A. Spencer, J. J. Pointon et al. · UWA Profiles and Research Repository (University of Western Australia) · 2011 · 253 citations

Multicentric Origin of Hemochromatosis Gene (HFE) Mutations

Jacques Rochette, J. J. Pointon, Christopher A. Fisher et al. · The American Journal of Human Genetics · 1999 · 150 citations · Full text

Genetic Disorder, Genetics, Molecular Genetics +3

Elucidating the chromosome 9 association with AS; CARD9 is a candidate gene

J. J. Pointon, David Harvey, Tugce Karaderi et al. · Genes and Immunity · 2010 · 71 citations · Full text

Cytogenetics, Genetics, Human Polymorphism +8