P. A. Dyer

STRONG ASSOCIATION BETWEEN IDIOPATHIC MEMBRANOUS NEPHROPATHY AND HLA-DRW3.

P. T. Klouda, Elise Acheson, F Goldby et al. · The Lancet · 1979 · 177 citations

Glomerular Disease, Glomerulonephritis, Autoimmune Disease +14

Pulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21-hydroxylase and complement C4 gene repeats in 21-hydroxylase deficiency haplotypes.

Simon Collier, P. J. Sinnott, P. A. Dyer et al. · The EMBO Journal · 1989 · 115 citations · Full text

Allelic Variant, Genetic Disorder, Genetics +7

Mannose binding lectin (MBL) genotype distributions with relation to serum levels in UK Caucasoids

D. Crosdale, William Ollier, Wendy Thomson et al. · European Journal of Immunogenetics · 2000 · 97 citations

“Homozygosity” for the HLA–DR shared epitope contributes the highest risk for rheumatoid arthritis concordance in identical twins

Damini Jawaheer, Wendy Thomson, Alex J. MacGregor et al. · Arthritis & Rheumatism · 1994 · 96 citations

Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiency.

P. J. Sinnott, Simon Collier, Colm Costigan et al. · Proceedings of the National Academy of Sciences · 1990 · 68 citations · Full text

Disease Haplotype, Genetics, Genomic Mechanism +18