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Family-based genetic risk prediction of multifactorial disease
Genome-wide association studies have detected dozens of variants underlying complex diseases, although it is uncertain how often these discoveries will translate into clinically useful predictors. Here, to improve genetic risk prediction, we consider including phenotypic and genotypic information fr...
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| 主要な著者: | , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2010
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2829927/ https://ncbi.nlm.nih.gov/pubmed/20193047 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gm123 |
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