| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | John Scott | |
| P2860 | cites work | 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. | Q24540193 |
| Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls | Q24550675 | ||
| A Polymorphism, R653Q, in the Trifunctional Enzyme Methylenetetrahydrofolate Dehydrogenase/Methenyltetrahydrofolate Cyclohydrolase/Formyltetrahydrofolate Synthetase Is a Maternal Genetic Risk Factor for Neural Tube Defects | Q24632141 | ||
| Genomewide association analysis of coronary artery disease | Q24658344 | ||
| A haplotype map of the human genome | Q24679827 | ||
| Regulation of iron metabolism by hepcidin | Q28252744 | ||
| A HapMap harvest of insights into the genetics of common disease | Q29614875 | ||
| Genome-wide association studies for common diseases and complex traits | Q29615822 | ||
| Hereditary hemochromatosis--a new look at an old disease | Q34324340 | ||
| Gene-environment interactions in human diseases | Q34407923 | ||
| Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium | Q34724404 | ||
| Impact of the MTHFR C677T polymorphism on risk of neural tube defects: case-control study. | Q35211162 | ||
| Iron, ferritin, and nutrition | Q35799890 | ||
| Genetic epidemiology and public health: hope, hype, and future prospects | Q36293973 | ||
| A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes | Q36492194 | ||
| Genome-wide association studies provide new insights into type 2 diabetes aetiology | Q36912145 | ||
| Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population | Q57677550 | ||
| Folate levels and neural tube defects. Implications for prevention | Q57677635 | ||
| Folate levels and neural tube defects. Implications for prevention | Q71516278 | ||
| Population variation of common cystic fibrosis mutations. The Cystic Fibrosis Genetic Analysis Consortium | Q71670536 | ||
| Hereditary hemochromatosis | Q79927316 | ||
| Adult cystic fibrosis | Q81448681 | ||
| P433 | issue | 2 | |
| P921 | main subject | public health | Q189603 |
| genetic variation | Q349856 | ||
| P304 | page(s) | 113-121 | |
| P577 | publication date | 2009-02-11 | |
| P1433 | published in | Proceedings of the Nutrition Society | Q15817594 |
| P1476 | title | Symposium on 'The challenge of translating nutrition research into public health nutrition'. Session 2: Personalised nutrition. Genetic variation and disease risk: new advances | |
| P478 | volume | 68 |
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