J. J. Pointon

发表

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Simon C. Potter, P. Donnelly, C. Spencer, 2007, Nature.

Novel Mutations in ACVR1 Result in Atypical Features in Two Fibrodysplasia Ossificans Progressiva Patients

J. J. Pointon, M. Brown, B. P. Wordsworth, 2009, PloS one.

Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results

J. J. Pointon, J. Crowe, P. Gasparini, 1999, Nature Genetics.

Multicentric origin of hemochromatosis gene (HFE) mutations.

J. J. Pointon, D. Weatherall, C. Fisher, 1999, American journal of human genetics.

Major histocompatibility complex associations of ankylosing spondylitis are complex and involve further epistasis with ERAP1

John D Reveille, Michael H Weisman, Linda A Bradbury, 2015, Nature Communications.

Major histocompatibility complex associations of ankylosing spondylitis are complex and involve further epistasis with ERAP 1

David M. Evans, L. Bradbury, J. J. Pointon, 2015 .

Effect of vitamin D deficiency on sarcoplasmic reticulum function and troponin C concentration of rabbit skeletal muscle.

J. J. Pointon, M. Francis, R. Smith, 1979, Clinical science.

Occurrence of ornithine decarboxylase and polyamines in cartilage.

P. D. Conroy, J. J. Pointon, D. M. Simms, 1977, The Biochemical journal.

A targeted approach significantly increases the identification rate of patients with undiagnosed haemochromatosis

J. J. Pointon, J. Emery, Jennifer J. Pointon, 2003, Journal of internal medicine.