A. Whitehead

发表

Whole-blood folate values in subjects with different methylenetetrahydrofolate reductase genotypes: differences between the radioassay and microbiological assays.

J. Mills, A. Whitehead, D. Weir, 1998, Clinical chemistry.

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.

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.

C5 DEFICIENCY IN A/J MICE IS NOT ASSOCIATED WITH RESISTANCE TO THE DEVELOPMENT OF SECONDARY AMYLOIDOSIS

A. Davis, K. Zahedi, A. Whitehead, 1992, European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics.

Resistance to Secondary Amyloidosis in A/J Mice is Not Significantly Associated with Allelic Variants Linked to the Serum Amyloid A Gene Cluster

A. Butler, A. Whitehead, A. Whitehead, 1994, Scandinavian journal of immunology.

Association between historically high frequencies of neural tube defects and the human T homologue of mouse T (Brachyury).

D. Shields, J. Mills, D. Weir, 2000, American journal of medical genetics.

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

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

The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother.

D. Shields, J. Mills, A. Whitehead, 1999, American journal of human genetics.

Low blood folates in NTD pregnancies are only partly explained by thermolabile 5,10-methylenetetrahydrofolate reductase: low folate status alone may be the critical factor.

J. Mills, D. Weir, J. Scott, 1998, American journal of medical 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.

Increased prevalence of methylenetetrahydrofolate reductase C677T variant in patients with inflammatory bowel disease, and its clinical implications

R. Corbally, A. Whitehead, D. Weir, 1999, Gut.

Wallaby Serum Amyloid A Protein: cDNA Cloning, Sequence and Evolutionary Analysis

D. Shields, G. Schreiber, C. Uhlar, 1996, Scandinavian journal of immunology.

The transcobalamin (TCN2) 776C>G polymorphism affects homocysteine concentrations among subjects with low vitamin B12 status

J. Yarnell, J. Woodside, I. Young, 2010, European Journal of Clinical Nutrition.

Warfarin Response and Vitamin K Epoxide Reductase Complex 1 in African Americans and Caucasians

C. Thorn, F. Samaha, J. Christie, 2007, Clinical pharmacology and therapeutics.

Changes in MTHFR genotype frequencies over time

AS Whitehead, A. Whitehead, 1998, The Lancet.