K. Lievers

发表

The 2756A>G variant in the gene encoding methionine synthase: its relation with plasma homocysteine levels and risk of coronary heart disease in a Dutch case-control study.

H. Blom, L. Kluijtmans, M. den Heijer, 2003, Thrombosis research.

Bioavailability of polyglutamyl folic acid relative to that of monoglutamyl folic acid in subjects with different genotypes of the glutamate carboxypeptidase II gene.

H. Blom, A. Melse-Boonstra, P. Verhoef, 2004, The American journal of clinical nutrition.

The -323Ins10 polymorphism for factor VII is not associated with coronary atherosclerosis in symptomatic men. The REGRESS study group.

A. Zwinderman, J. Jukema, E. Schouten, 2000, Thrombosis research.

MAJOR HISTOCOMPATIBILITY COMPLEX VARIATION IN THE ARABIAN ORYX

P. Hedrick, A. Rattink, G. Gutiérrez-Espeleta, 2000, Evolution; international journal of organic evolution.

A second common variant in the methylenetetrahydrofolate reductase (MTHFR) gene and its relationship to MTHFR enzyme activity, homocysteine, and cardiovascular disease risk

H. Blom, G. Boers, M. Heijer, 2001, Journal of Molecular Medicine.

Influence of a glutamate carboxypeptidase II (GCPII) polymorphism (1561C-->T) on plasma homocysteine, folate and vitamin B(12) levels and its relationship to cardiovascular disease risk.

H. Blom, G. Boers, L. Kluijtmans, 2002, Atherosclerosis.

Betaine-homocysteine methyltransferase (BHMT): genomic sequencing and relevance to hyperhomocysteinemia and vascular disease in humans.

H. Blom, G. Boers, M. Heijer, 2000, Molecular Genetics and Metabolism.

Genetics of hyperhomocysteinaemia in cardiovascular disease

H. Blom, L. Kluijtmans, K. Lievers, 2003, Annals of clinical biochemistry.

Single nucleotide polymorphisms in the transcobalamin gene: relationship with transcobalamin concentrations and risk for neural tube defects

H. Blom, F. Trijbels, L. Afman, 2002, European Journal of Human Genetics.

Polymorphisms in the transcobalamin gene: association with plasma homocysteine in healthy individuals and vascular disease patients.

H. Blom, G. Boers, L. Kluijtmans, 2002, Clinical chemistry.

Association of a 31 bp VNTR in the CBS gene with postload homocysteine concentrations in the Framingham Offspring Study

P. Wilson, J. Ordovás, H. Blom, 2006, European Journal of Human Genetics.

Cystathionine β-synthase polymorphisms and hyperhomocysteinaemia: an association study

H. Blom, G. Boers, M. Heijer, 2003, European Journal of Human Genetics.

A 31 bp VNTR in the cystathionine β-synthase (CBS) gene is associated with reduced CBS activity and elevated post-load homocysteine levels

H. Blom, G. Boers, M. Heijer, 2001, European Journal of Human Genetics.

Gene-gene interaction between the cystathionine beta-synthase 31 base pair variable number of tandem repeats and the methylenetetrahydrofolate reductase 677C > T polymorphism on homocysteine levels and risk for neural tube defects.

H. Blom, L. Kluijtmans, F. Trijbels, 2003, Molecular genetics and metabolism.