Meta-analysis of gene-level tests for rare variant association.
The majority of reported complex disease associations for common genetic variants have been identified through meta-analysis, a powerful approach that enables the use of large sample sizes while protecting against common artifacts due to population structure and repeated small-sample analyses sharin...
প্রধান লেখক: | Liu, D, Peloso, G, Zhan, X, Holmen, O, Zawistowski, M, Feng, S, Nikpay, M, Auer, P, Goel, A, Zhang, H, Peters, U, Farrall, M, Orho-Melander, M, Kooperberg, C, McPherson, R, Watkins, H, Willer, C, Hveem, K, Melander, O, Kathiresan, S, Abecasis, G |
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বিন্যাস: | Journal article |
ভাষা: | English |
প্রকাশিত: |
2014
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অনুরূপ উপাদানগুলি
অনুরূপ উপাদানগুলি
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Meta-analysis of gene-level tests for rare variant association
অনুযায়ী: Liu, D, অন্যান্য
প্রকাশিত: (2014) -
Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemia.
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Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia
অনুযায়ী: Stitziel, N, অন্যান্য
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New insights into impaired muscle glycogen synthesis.
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Variants in the calpain-10 gene predispose to insulin resistance and elevated free fatty acid levels.
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