Family history aggregation unit-based tests to detect rare genetic variant associations with application to the Framingham Heart Study-Reference-Cited by-同舟云学术

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Family history aggregation unit-based tests to detect rare genetic variant associations with application to the Framingham Heart Study

Published:2022-04 Issue:4 Volume:109 Page:738-749
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Wang Yanbing^ORCID,Chen Han,Peloso Gina M.,Meigs James B.,Beiser Alexa S.,Seshadri Sudha,DeStefano Anita L.,Dupuis Josée

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference26 articles.

1. Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data;Li;Am. J. Hum. Genet.,2008

2. Rare-variant association testing for sequencing data with the sequence kernel association test;Wu;Am. J. Hum. Genet.,2011

3. Optimal tests for rare variant effects in sequencing association studies;Lee;Biostatistics,2012

4. Testing for an unusual distribution of rare variants;Neale;PLoS Genet.,2011

5. Sequence kernel association test for quantitative traits in family samples;Chen;Genet. Epidemiol.,2013

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Leveraging family history in genetic association analyses of binary traits;BMC Genomics;2022-10-01

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