scholarly article | Q13442814 |
review article | Q7318358 |
P356 | DOI | 10.1016/S0140-6736(05)67601-5 |
P698 | PubMed publication ID | 16243094 |
P50 | author | George Davey Smith | Q21003878 |
Shah Ebrahim | Q90615321 | ||
Anna Hansell | Q61087747 | ||
Lyle J. Palmer | Q30512610 | ||
Sarah J Lewis | Q37613585 | ||
P2093 | author name string | Paul R Burton | |
P2860 | cites work | Commentary: Mendelian randomization--an update on its use to evaluate allogeneic stem cell transplantation in leukaemia | Q79904916 |
Commentary: development of Mendelian randomization: from hypothesis test to 'Mendelian deconfounding' | Q79904933 | ||
Lipid-related genes and myocardial infarction in 4685 cases and 3460 controls: discrepancies between genotype, blood lipid concentrations, and coronary disease risk | Q80346156 | ||
Prenatal screening for cystic fibrosis: an early report card | Q80539134 | ||
The family history--more important than ever | Q81059123 | ||
‘Mendelian randomization’: can genetic epidemiology contribute to understanding environmental determinants of disease?* | Q22066036 | ||
Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease | Q22337234 | ||
How many diseases does it take to map a gene with SNPs? | Q22337263 | ||
Searching for genetic determinants in the new millennium | Q22337300 | ||
Scientific and ethical aspects of genetic screening of workers for cancer risk: The case of the n-acetyltransferase phenotype | Q24169682 | ||
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis | Q24310146 | ||
Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies | Q24531993 | ||
Effect of supplemental vitamin E for the prevention and treatment of cardiovascular disease | Q24550510 | ||
The role of genetic polymorphisms in environmental health | Q24815139 | ||
The International HapMap Project | Q27860695 | ||
Apolipoprotein E epsilon4 count affects age at onset of Alzheimer disease, but not lifetime susceptibility: The Cache County Study | Q47658804 | ||
Shattuck lecture--medical and societal consequences of the Human Genome Project. | Q48582472 | ||
Long-term cognitive and emotional impact of genetic testing for carriers of cystic fibrosis: the effects of test result and gender. | Q50974548 | ||
Incorrect recall of residual risk three years after carrier screening for cystic fibrosis: a comparison of two-step and couple screening. | Q51983120 | ||
Epidemiology faces its limits. | Q52877590 | ||
Genetically reduced antioxidative protection and increased ischemic heart disease risk: The Copenhagen City Heart Study. | Q55037941 | ||
Apolipoprotein E isoforms, serum cholesterol, and cancer. | Q55060187 | ||
Amount of DNA in plasma and cancer risk: A prospective study | Q57037855 | ||
Association of C-Reactive Protein With Blood Pressure and Hypertension | Q57110219 | ||
Commentary: The rough world of nutritional epidemiology: Does dietary fibre prevent large bowel cancer? | Q57128163 | ||
Parameters for reliable results in genetic association studies in common disease | Q57240978 | ||
Genome scans and candidate gene approaches in the study of common diseases and variable drug responses | Q57840862 | ||
Pharmacogenetics of Inflammatory Bowel Disease | Q58037975 | ||
The case for a US prospective cohort study of genes and environment | Q59051741 | ||
CANALIZATION OF DEVELOPMENT AND THE INHERITANCE OF ACQUIRED CHARACTERS | Q59064935 | ||
Can family history be used as a tool for public health and preventive medicine? | Q64127919 | ||
Mendelian randomisation: a new spin or real progress? | Q64134143 | ||
Lactase deficiency: prevalence in osteoporosis | Q67364196 | ||
Does lactose intolerance predispose to low bone density? A population-based study of perimenopausal Finnish women | Q71589430 | ||
Osteoporosis, Intestinal Lactase Deficiency and Low Dietary Calcium Intake | Q72344117 | ||
Translating biomedical research to the bedside: a national crisis and a call to action | Q73116855 | ||
Cystic fibrosis gene testing a challenge: experts say widespread use is creating unnecessary risks | Q73508822 | ||
Population screening for cystic fibrosis: knowledge and emotional consequences 18 months later | Q73589507 | ||
Population screening for cystic fibrosis in Western Australia: community response | Q74108588 | ||
Pharmacogenetics | Q74843888 | ||
Dissecting a population genome for targeted screening of disease mutations | Q77373277 | ||
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease | Q27860821 | ||
Relation between plasma ascorbic acid and mortality in men and women in EPIC-Norfolk prospective study: a prospective population study. European Prospective Investigation into Cancer and Nutrition | Q28204672 | ||
ELAC2/HPC2 polymorphisms, prostate-specific antigen levels, and prostate cancer | Q28208394 | ||
A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis | Q28267921 | ||
Homocysteine and coronary heart disease in the Caerphilly cohort: a 10 year follow up | Q28345971 | ||
The future of genetic studies of complex human diseases | Q29547215 | ||
Replication validity of genetic association studies | Q29615456 | ||
The effect of vitamin E and beta carotene on the incidence of lung cancer and other cancers in male smokers | Q29616096 | ||
Hypothesis: is low prenatal vitamin D a risk-modifying factor for schizophrenia? | Q33819585 | ||
Genetic polymorphism of thiopurine methyltransferase and its clinical relevance for childhood acute lymphoblastic leukemia | Q33891379 | ||
Ryanodine receptor mutations in malignant hyperthermia and central core disease | Q33903152 | ||
Case-control association studies for the genetics of complex respiratory diseases | Q33933058 | ||
MRC/BHF Heart Protection Study of antioxidant vitamin supplementation in 20,536 high-risk individuals: a randomised placebo-controlled trial | Q33960122 | ||
Large upward bias in estimation of locus-specific effects from genomewide scans | Q34044873 | ||
Association between presence of HLA-B*5701, HLA-DR7, and HLA-DQ3 and hypersensitivity to HIV-1 reverse-transcriptase inhibitor abacavir | Q34117815 | ||
Principles for the buffering of genetic variation | Q34171380 | ||
Problems of reporting genetic associations with complex outcomes | Q34184173 | ||
Association study designs for complex diseases | Q34186026 | ||
Reflections on the limitations to epidemiology | Q34215778 | ||
Pharmacogenetics: potential for individualized drug therapy through genetics | Q34273202 | ||
Mendelian randomization: prospects, potentials, and limitations | Q34312296 | ||
Vitamin E consumption and the risk of coronary heart disease in men. | Q34363912 | ||
1998 ASHG presidential address. Making genomic medicine a reality | Q34388472 | ||
Experiences in molecular-based prenatal screening for Ashkenazi Jewish genetic diseases | Q34399100 | ||
Epidemiological methods for studying genes and environmental factors in complex diseases | Q34421625 | ||
Genetic hemochromatosis, a Celtic disease: is it now time for population screening? | Q34517626 | ||
Finnish Disease Heritage I: characteristics, causes, background | Q34531986 | ||
Gene-environment interaction and aetiology of cancer: what does it mean and how can we measure it? | Q34564801 | ||
Strategies for early diagnosis of haemochromatosis | Q34601551 | ||
Estrogen replacement therapy and coronary heart disease: a quantitative assessment of the epidemiologic evidence | Q34748119 | ||
MTHFR 677C-->T polymorphism and risk of coronary heart disease: a meta-analysis. | Q34974721 | ||
Population screening in the age of genomic medicine | Q35037759 | ||
An epidemiologic assessment of genomic profiling for measuring susceptibility to common diseases and targeting interventions | Q40537645 | ||
Familial risk and genetic susceptibility for breast cancer | Q40654778 | ||
Clustering of risk factors and social class in childhood and adulthood in British women's heart and health study: cross sectional analysis | Q40762277 | ||
Psychological and social impact of carrier screening for cystic fibrosis among pregnant woman--a pilot study | Q40943638 | ||
Practice guideline development task force of the College of American Pathologists. Hereditary hemochromatosis | Q41161614 | ||
Canalization: a molecular genetic perspective | Q41396336 | ||
The new genetics in clinical practice | Q41728150 | ||
Comparison of the genomic structure and variation in the two human sodium-dependent vitamin C transporters, SLC23A1 and SLC23A2. | Q42633800 | ||
The effect of the C677T and A1298C polymorphisms in the methylenetetrahydrofolate reductase gene on homocysteine levels in elderly men and women from the British regional heart study | Q43546770 | ||
Candidate-gene approaches for studying complex genetic traits: practical considerations | Q44636099 | ||
Validity of self-report in alcoholism research: results of a Veterans Administration Cooperative Study | Q44774125 | ||
Commentary: Katan's remarkable foresight: genes and causality 18 years on. | Q44838036 | ||
Commentary: Mendelian randomization and gene-environment interaction | Q44838041 | ||
Pharmacogenetic study of statin therapy and cholesterol reduction | Q44938097 | ||
Using pharmacogenetics to improve drug safety and efficacy | Q44938100 | ||
Use of regularly scheduled albuterol treatment in asthma: genotype-stratified, randomised, placebo-controlled cross-over trial | Q45121026 | ||
Commentary: the concept of 'Mendelian Randomization'. | Q46041775 | ||
Commentary: hormone replacement therapy and coronary heart disease: four lessons | Q46054104 | ||
Laboratory standards and guidelines for population-based cystic fibrosis carrier screening | Q46673370 | ||
Molecular genetic risk screening | Q35044209 | ||
Genetic associations in large versus small studies: an empirical assessment | Q35070873 | ||
Pharmacogenetics and personalised medicine | Q35071836 | ||
Locating gene–environment interaction: at the intersections of genetics and public health | Q35116439 | ||
Pharmacogenetics of Drug Metabolising Enzymes: Importance for Personalised Medicine | Q35127786 | ||
N-Acetyltransferase phenotype and risk in urinary bladder cancer: approaches in molecular epidemiology. Preliminary results in Sweden and Denmark | Q35133059 | ||
The opportunities and challenges of personalized genome-based molecular therapies for cancer: targets, technologies, and molecular chaperones | Q35159851 | ||
Genetic evaluation for coronary artery disease | Q35179025 | ||
Genomic profiling to promote a healthy lifestyle: not ready for prime time | Q35201468 | ||
Genomics as a probe for disease biology | Q35211343 | ||
Risk and protective effects of the APOE gene towards Alzheimer's disease in the Kungsholmen project: variation by age and sex. | Q35481029 | ||
Design, objectives, and lessons from a pilot 25 year follow up re-survey of survivors in the Whitehall study of London Civil Servants | Q35558356 | ||
Genomic Priorities and Public Health | Q35566970 | ||
Pharmacogenetics goes genomic | Q35590351 | ||
Prenatal screening for cystic fibrosis: past, present and future | Q35623356 | ||
Genetic testing for cardiovascular disease susceptibility: a useful clinical management tool or possible misinformation? | Q35625535 | ||
Population genetic screening programmes: principles, techniques, practices, and policies | Q35626856 | ||
The complex interplay among factors that influence allelic association. | Q35634519 | ||
Fibrinogen, C-reactive protein and coronary heart disease: does Mendelian randomization suggest the associations are non-causal? | Q35672053 | ||
Moving towards individualized medicine with pharmacogenomics | Q35784527 | ||
The emergence of epidemiology in the genomics age. | Q35866648 | ||
Hereditary cancer: guidelines in clinical practice. Breast and ovarian cancer genetics. | Q35914662 | ||
Pharmacogenetics of HMG-CoA reductase inhibitors: exploring the potential for genotype-based individualization of coronary heart disease management | Q35941950 | ||
Neurodevelopment, neuroplasticity, and new genes for schizophrenia | Q35974517 | ||
Mechanisms of BCR-ABL in the pathogenesis of chronic myelogenous leukaemia | Q36047171 | ||
What can mendelian randomisation tell us about modifiable behavioural and environmental exposures? | Q36119363 | ||
Cancer prevention and diet: help from single nucleotide polymorphisms | Q36181606 | ||
Alcohol, ALDH2, and esophageal cancer: a meta-analysis which illustrates the potentials and limitations of a Mendelian randomization approach | Q36231579 | ||
Key concepts in genetic epidemiology | Q36254149 | ||
Shaking the tree: mapping complex disease genes with linkage disequilibrium | Q36274243 | ||
Estimating the survival benefits gained from providing national cancer genetic services to women with a family history of breast cancer. | Q36694081 | ||
The APC variants I1307K and E1317Q are associated with colorectal tumors, but not always with a family history. | Q37484741 | ||
P433 | issue | 9495 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | public health | Q189603 |
P304 | page(s) | 1484-1498 | |
P577 | publication date | 2005-10-01 | |
P1433 | published in | The Lancet | Q939416 |
P1476 | title | Genetic epidemiology and public health: hope, hype, and future prospects | |
P478 | volume | 366 |
Q38905976 | "The Google of Healthcare": enabling the privatization of genetic bio/databanking. |
Q48555506 | 2006 Council Lecture: Lancelot to the rescue: realizing the promise of genomic medicine. |
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Q30365147 | A gentle introduction to SNP analysis: resources and tools. |
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Q43922635 | Adjusting for bias and unmeasured confounding in Mendelian randomization studies with binary responses |
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Q91444729 | Assessing pleiotropy and mediation in genetic loci associated with chronic obstructive pulmonary disease |
Q35801330 | Assessing the impact of nicotine dependence genes on the risk of facial clefts: An example of the use of national registry and biobank data. |
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Q37083131 | Basis for korean genome study |
Q33725581 | Being more realistic about the public health impact of genomic medicine |
Q36916960 | Beta2-adrenoceptor polymorphisms and obstructive airway diseases: important issues of study design |
Q58047301 | Beyond odds ratios — communicating disease risk based on genetic profiles |
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Q26767428 | Biobanks in the era of personalized medicine: objectives, challenges, and innovation: Overview |
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Q46833945 | C-reactive protein and its role in metabolic syndrome: mendelian randomisation study |
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Q33314841 | Correction of population stratification in large multi-ethnic association studies |
Q36006147 | Credible Mendelian randomization studies: approaches for evaluating the instrumental variable assumptions |
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Q36072265 | Demographic differences in willingness to provide broad and narrow consent for biobank research |
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Q83880570 | Designs combining instrumental variables with case-control: estimating principal strata causal effects |
Q33263590 | Dietetic guidelines on food and nutrition in the secondary prevention of cardiovascular disease - evidence from systematic reviews of randomized controlled trials (second update, January 2006). |
Q36470922 | Differences in preferences for models of consent for biobanks between Black and White women. |
Q92729186 | Dispositional negativity, cognition, and anxiety disorders: An integrative translational neuroscience framework |
Q37598897 | Drug-induced liver injury: insights from genetic studies. |
Q36497096 | EUDRAGENE: European collaboration to establish a case-control DNA collection for studying the genetic basis of adverse drug reactions |
Q45746397 | EpiHealth: a large population-based cohort study for investigation of gene-lifestyle interactions in the pathogenesis of common diseases |
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