| scholarly article | Q13442814 |
| P50 | author | John Ioannidis | Q6251482 |
| Muin J. Khoury | Q64746271 | ||
| Ramal Moonesinghe | Q64751074 | ||
| W Dana Flanders | Q92676300 | ||
| Quanhe Yang | Q114425216 | ||
| P2093 | author name string | Benedict I Truman | |
| P2860 | cites work | Consistency of genome-wide associations across major ancestral groups | Q44515366 |
| 'Racial' differences in genetic effects for complex diseases | Q44586727 | ||
| Differences in diabetes prevalence, incidence, and mortality among the elderly of four racial/ethnic groups: whites, blacks, hispanics, and asians | Q45183051 | ||
| Founder mutations | Q46729491 | ||
| Detection of genotype-environment interaction in case-control studies of birth defects: how big a sample size? | Q47355457 | ||
| Disparities in infant mortality: what's genetics got to do with it? | Q80406095 | ||
| Prevalence in the United States of selected candidate gene variants. Third National Health and Nutrition Examination Survey, 1991- 1994 | Q23917519 | ||
| A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity | Q24650037 | ||
| Genetic research and health disparities | Q24650579 | ||
| Assessing genetic contributions to phenotypic differences among 'racial' and 'ethnic' groups | Q28290021 | ||
| Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits | Q29614593 | ||
| ''R"--project for statistical computing | Q29618640 | ||
| Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP. | Q33323357 | ||
| Worldwide population differentiation at disease-associated SNPs | Q33340690 | ||
| Admixture mapping of 15,280 African Americans identifies obesity susceptibility loci on chromosomes 5 and X. | Q33450573 | ||
| Genetic variants associated with complex human diseases show wide variation across multiple populations | Q33714507 | ||
| Prediction of individual genetic risk to disease from genome-wide association studies | Q34676890 | ||
| Validating, augmenting and refining genome-wide association signals | Q34976245 | ||
| Implication of genetic variants near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in type 2 diabetes and obesity in 6,719 Asians | Q36807593 | ||
| Population-wide generalizability of genome-wide discovered associations | Q43725415 | ||
| P433 | issue | 8 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 831-6 | |
| P577 | publication date | 2012-08-01 | |
| P1433 | published in | European Journal of Human Genetics | Q2155433 |
| P1476 | title | Estimating the contribution of genetic variants to difference in incidence of disease between population groups | |
| P478 | volume | 20 |
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| Q55027605 | Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population. |
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| Q26829341 | The contribution of genomic research to explaining racial disparities in cardiovascular disease: a systematic review |
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