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Items: 1 to 20 of 309

1.

Two adaptive weighting methods to test for rare variant associations in family-based designs.

Fang S, Sha Q, Zhang S.

Genet Epidemiol. 2012 Jul;36(5):499-507. doi: 10.1002/gepi.21646.

PMID:
22674630
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Detecting association of rare and common variants by testing an optimally weighted combination of variants.

Sha Q, Wang X, Wang X, Zhang S.

Genet Epidemiol. 2012 Sep;36(6):561-71. doi: 10.1002/gepi.21649.

PMID:
22714994
4.

A fast and noise-resilient approach to detect rare-variant associations with deep sequencing data for complex disorders.

Cheung YH, Wang G, Leal SM, Wang S.

Genet Epidemiol. 2012 Nov;36(7):675-85. doi: 10.1002/gepi.21662.

PMID:
22865616
5.

Weighted selective collapsing strategy for detecting rare and common variants in genetic association study.

Dai Y, Jiang R, Dong J.

BMC Genet. 2012 Feb 6;13:7. doi: 10.1186/1471-2156-13-7.

6.

Test of rare variant association based on affected sib-pairs.

Sha Q, Zhang S.

Eur J Hum Genet. 2015 Feb;23(2):229-37. doi: 10.1038/ejhg.2014.43.

7.

A robust model-free approach for rare variants association studies incorporating gene-gene and gene-environmental interactions.

Fan R, Lo SH.

PLoS One. 2013 Dec 17;8(12):e83057. doi: 10.1371/journal.pone.0083057. Erratum in: PLoS One. 2014;9(5):e98083.

8.

Joint Analysis of Multiple Traits in Rare Variant Association Studies.

Wang Z, Wang X, Sha Q, Zhang S.

Ann Hum Genet. 2016 May;80(3):162-71. doi: 10.1111/ahg.12149.

PMID:
26990300
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10.

Robust and Powerful Affected Sibpair Test for Rare Variant Association.

Lin KH, Zöllner S.

Genet Epidemiol. 2015 Jul;39(5):325-33. doi: 10.1002/gepi.21903.

11.

Comparison of six statistics of genetic association regarding their ability to discriminate between causal variants and genetically linked markers.

Lorenzo Bermejo J, Garcia Perez A, Brandt A, Hemminki K, Matthews AG.

Hum Hered. 2011;72(2):142-52. doi: 10.1159/000332006.

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Detecting rare variants for quantitative traits using nuclear families.

Guo W, Shugart YY.

Hum Hered. 2012;73(3):148-58. doi: 10.1159/000338439.

PMID:
22699804
14.

A new association test using haplotype similarity.

Sha Q, Chen HS, Zhang S.

Genet Epidemiol. 2007 Sep;31(6):577-93.

PMID:
17443704
15.

On optimal gene-based analysis of genome scans.

Bacanu SA.

Genet Epidemiol. 2012 May;36(4):333-9. doi: 10.1002/gepi.21625.

PMID:
22508187
16.

KNOWLEDGE DRIVEN BINNING AND PHEWAS ANALYSIS IN MARSHFIELD PERSONALIZED MEDICINE RESEARCH PROJECT USING BIOBIN.

Basile AO, Wallace JR, Peissig P, McCarty CA, Brilliant M, Ritchie MD.

Pac Symp Biocomput. 2016;21:249-60.

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Optimal tests for rare variant effects in sequencing association studies.

Lee S, Wu MC, Lin X.

Biostatistics. 2012 Sep;13(4):762-75. doi: 10.1093/biostatistics/kxs014.

20.

TATES: efficient multivariate genotype-phenotype analysis for genome-wide association studies.

van der Sluis S, Posthuma D, Dolan CV.

PLoS Genet. 2013;9(1):e1003235. doi: 10.1371/journal.pgen.1003235.

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