| Thermolabile methylenetetrahydrofolate reductase in coronary artery disease LAJ Kluijtmans, JJP Kastelein, J Lindemans, GHJ Boers, SG Heil, ... Circulation 96 (8), 2573-2577, 1997 | 307 | 1997 |
| Sequence analysis of the coding region of human methionine synthase: relevance to hyperhomocysteinaemia in neural-tube defects and vascular disease. NM Van der Put, EF Van der Molen, LA Kluijtmans, SG Heil, JM Trijbels, ... QJM: monthly journal of the Association of Physicians 90 (8), 511-517, 1997 | 254 | 1997 |
| Effect of the methylenetetrahydrofolate reductase 677C→ T mutation on the relations among folate intake and plasma folate and homocysteine concentrations in a general … A de Bree, WMM Verschuren, AL Bjørke-Monsen, NMJ Van der Put, ... The American journal of clinical nutrition 77 (3), 687-693, 2003 | 228 | 2003 |
| Thermolabile methylenetetrahydrofolate reductase and factor V Leiden in the risk of deep-vein thrombosis LAJ Kluijtmans, M Den Heijer, PH Reitsma, SG Heil, HJ Blom, ... Thrombosis and haemostasis 79 (02), 254-258, 1998 | 209 | 1998 |
| Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD (methylenetetrahydrofolate‐dehydrogenase, methenyltetrahydrofolate‐cyclohydrolase … FA Hol, NMJ van der Put, MPA Geurds, SG Heil, FJM Trijbels, BCJ Hamel, ... Clinical genetics 53 (2), 119-125, 1998 | 199 | 1998 |
| Challenging homeostasis to define biomarkers for nutrition related health B van Ommen, J Keijer, SG Heil, J Kaput Molecular nutrition & food research 53 (7), 795-804, 2009 | 194 | 2009 |
| Is mutated serine hydroxymethyltransferase (SHMT) involved in the etiology of neural tube defects? SG Heil, NMJ Van der Put, ET Waas, M Den Heijer, FJM Trijbels, HJ Blom Molecular genetics and metabolism 73 (2), 164-172, 2001 | 193 | 2001 |
| Homocysteine and DNA methylation: a review of animal and human literature PR Mandaviya, L Stolk, SG Heil Molecular genetics and metabolism 113 (4), 243-252, 2014 | 186 | 2014 |
| Genetic variation in genes of folate metabolism and neural-tube defect risk IJM van der Linden, LA Afman, SG Heil, HJ Blom Proceedings of the Nutrition Society 65 (2), 204-215, 2006 | 171 | 2006 |
| Vitamin B12 intake from animal foods, biomarkers, and health aspects R Obeid, SG Heil, MMA Verhoeven, EGHM Van den Heuvel, LC De Groot, ... Frontiers in nutrition 6, 93, 2019 | 169 | 2019 |
| The effects of long-term daily folic acid and vitamin B12 supplementation on genome-wide DNA methylation in elderly subjects DEG Kok, RAM Dhonukshe-Rutten, C Lute, SG Heil, AG Uitterlinden, ... Clinical epigenetics 7, 1-14, 2015 | 141 | 2015 |
| Interaction between hyperhomocysteinemia, mutated methylenetetrahydrofolatereductase (MTHFR) and inherited thrombophilic factors in recurrent venous thrombosis MBAJ KeiJzer, M Den Heijer, HJ Blom, GMJ Bos, HPJ Willems, ... Thrombosis and haemostasis 88 (11), 723-728, 2002 | 132 | 2002 |
| A common mutation in the 5, 10-methylenetetrahydrofolate reductase gene as a new risk factor for placental vasculopathy EF van der Molen, GE Arends, WLDM Nelen, NJM van der Put, SG Heil, ... American journal of obstetrics and gynecology 182 (5), 1258-1263, 2000 | 128 | 2000 |
| Gene-environment and gene-gene interaction in the determination of plasma homocysteine levels in healthy middle-aged men V Dekou, V Gudnason, E Hawe, GJ Miller, D Stansbie, SE Humphries Thrombosis and haemostasis 85 (01), 67-74, 2001 | 127 | 2001 |
| Genetic determinants of plasma total homocysteine H Gellekink, M Den Heijer, SG Heil, HJ Blom Seminars in vascular medicine 5 (02), 98-109, 2005 | 104 | 2005 |
| Screening for metabolic vitamin B12 deficiency by holotranscobalamin in patients suspected of vitamin B12 deficiency: a multicentre study SG Heil, R de Jonge, MCFJ de Rotte, M van Wijnen, ... Annals of Clinical Biochemistry 49 (2), 184-189, 2012 | 98 | 2012 |
| Betaine-homocysteine methyltransferase (BHMT): genomic sequencing and relevance to hyperhomocysteinemia and vascular disease in humans SG Heil, KJA Lievers, GH Boers, P Verhoef, M Den Heijer, FJM Trijbels, ... Molecular genetics and metabolism 71 (3), 511-519, 2000 | 96 | 2000 |
| ABCB1 and ABCC3 gene polymorphisms are associated with first-year response to methotrexate in juvenile idiopathic arthritis MCFJ de ROTTE, M Bulatovic, MW Heijstek, G Jansen, SG Heil, ... The Journal of rheumatology 39 (10), 2032-2040, 2012 | 95 | 2012 |
| Intermediate and severe hyperhomocysteinemia with thrombosis: a study of genetic determinants M Gaustadnes, N Rüdiger, K Rasmussen, J Ingerslev Thrombosis and haemostasis 83 (04), 554-558, 2000 | 87 | 2000 |
| Measuring methotrexate polyglutamates in red blood cells: a new LC-MS/MS-based method E den Boer, RJW Meesters, BD Van Zelst, TM Luider, JMW Hazes, ... Analytical and bioanalytical chemistry 405, 1673-1681, 2013 | 84 | 2013 |
