P. Gallagher

Functional modeling of vitamin responsiveness in yeast: a common pyridoxine-responsive cystathionine beta-synthase mutation in homocystinuria.

P. Ueland, A. Guttormsen, H. Refsum, 1997, Human molecular genetics.

The role of hereditary hemochromatosis in aseptic loosening following primary total hip arthroplasty

J. Crowe, M. Kaliszer, P. Murray, 2005, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

Characterization of mutations in the cystathionine beta-synthase gene in Irish patients with homocystinuria.

M. Tsai, N. Hanson, K. Schwichtenberg, 1998, Molecular genetics and metabolism.

Are common mutations of cystathionine β‐synthase involved in the aetiology of neural tube defects?

D. Weir, A. Molloy, J. Scott, 1997, Clinical genetics.

A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects.

D C Shields, A M Molloy, D. Shields, 1995, QJM : monthly journal of the Association of Physicians.

Homocysteine and risk of premature coronary heart disease. Evidence for a common gene mutation.

A. Evans, R. Rozen, D. Shields, 1996, Circulation.