177 related articles for article (PubMed ID: 21368279)
1. An optimal weighted aggregated association test for identification of rare variants involved in common diseases.
Sul JH; Han B; He D; Eskin E
Genetics; 2011 May; 188(1):181-8. PubMed ID: 21368279
[TBL] [Abstract][Full Text] [Related]
2. Increasing power of groupwise association test with likelihood ratio test.
Sul JH; Han B; Eskin E
J Comput Biol; 2011 Nov; 18(11):1611-24. PubMed ID: 21919745
[TBL] [Abstract][Full Text] [Related]
3. How important are rare variants in common disease?
Saint Pierre A; Génin E
Brief Funct Genomics; 2014 Sep; 13(5):353-61. PubMed ID: 25005607
[TBL] [Abstract][Full Text] [Related]
4. A novel genome-information content-based statistic for genome-wide association analysis designed for next-generation sequencing data.
Luo L; Zhu Y; Xiong M
J Comput Biol; 2012 Jun; 19(6):731-44. PubMed ID: 22651812
[TBL] [Abstract][Full Text] [Related]
5. Efficient unified rare variant association test by modeling the population genetic distribution in case-control studies.
Li H; Chen J
Genet Epidemiol; 2016 Nov; 40(7):579-590. PubMed ID: 27550412
[TBL] [Abstract][Full Text] [Related]
6. Detecting rare and common variants for complex traits: sibpair and odds ratio weighted sum statistics (SPWSS, ORWSS).
Feng T; Elston RC; Zhu X
Genet Epidemiol; 2011 Jul; 35(5):398-409. PubMed ID: 21594893
[TBL] [Abstract][Full Text] [Related]
7. Identifying rare and common disease associated variants in genomic data using Parkinson's disease as a model.
Lin YC; Hsieh AR; Hsiao CL; Wu SJ; Wang HM; Lian IeB; Fann CS
J Biomed Sci; 2014 Aug; 21(1):88. PubMed ID: 25175702
[TBL] [Abstract][Full Text] [Related]
8. A general statistic to test an optimally weighted combination of common and/or rare variants.
Zhang J; Wu B; Sha Q; Zhang S; Wang X
Genet Epidemiol; 2019 Dec; 43(8):966-979. PubMed ID: 31498476
[TBL] [Abstract][Full Text] [Related]
9. GENOME-WIDE ASSOCIATION MAPPING AND RARE ALLELES: FROM POPULATION GENOMICS TO PERSONALIZED MEDICINE - Session Introduction.
DE LA Vega FM; Bustamante CD; Leal SM
Pac Symp Biocomput; 2011; ():74-5. PubMed ID: 21121034
[TBL] [Abstract][Full Text] [Related]
10. DoEstRare: A statistical test to identify local enrichments in rare genomic variants associated with disease.
Persyn E; Karakachoff M; Le Scouarnec S; Le Clézio C; Campion D; Consortium FE; Schott JJ; Redon R; Bellanger L; Dina C
PLoS One; 2017; 12(7):e0179364. PubMed ID: 28742119
[TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 22674630
[TBL] [Abstract][Full Text] [Related]
12. Power Analysis for Genetic Association Test (PAGEANT) provides insights to challenges for rare variant association studies.
Derkach A; Zhang H; Chatterjee N
Bioinformatics; 2018 May; 34(9):1506-1513. PubMed ID: 29194474
[TBL] [Abstract][Full Text] [Related]
13. A groupwise association test for rare mutations using a weighted sum statistic.
Madsen BE; Browning SR
PLoS Genet; 2009 Feb; 5(2):e1000384. PubMed ID: 19214210
[TBL] [Abstract][Full Text] [Related]
14. Two-stage design of sequencing studies for testing association with rare variants.
Yang F; Thomas DC
Hum Hered; 2011; 71(4):209-20. PubMed ID: 21734405
[TBL] [Abstract][Full Text] [Related]
15. Estimating genetic effects and quantifying missing heritability explained by identified rare-variant associations.
Liu DJ; Leal SM
Am J Hum Genet; 2012 Oct; 91(4):585-96. PubMed ID: 23022102
[TBL] [Abstract][Full Text] [Related]
16. Rare variant association test with multiple phenotypes.
Lee S; Won S; Kim YJ; Kim Y; ; Kim BJ; Park T
Genet Epidemiol; 2017 Apr; 41(3):198-209. PubMed ID: 28039885
[TBL] [Abstract][Full Text] [Related]
17. Weighted selective collapsing strategy for detecting rare and common variants in genetic association study.
Dai Y; Jiang R; Dong J
BMC Genet; 2012 Feb; 13():7. PubMed ID: 22309429
[TBL] [Abstract][Full Text] [Related]
18. Association screening of common and rare genetic variants by penalized regression.
Zhou H; Sehl ME; Sinsheimer JS; Lange K
Bioinformatics; 2010 Oct; 26(19):2375-82. PubMed ID: 20693321
[TBL] [Abstract][Full Text] [Related]
19. Uncovering the roles of rare variants in common disease through whole-genome sequencing.
Cirulli ET; Goldstein DB
Nat Rev Genet; 2010 Jun; 11(6):415-25. PubMed ID: 20479773
[TBL] [Abstract][Full Text] [Related]
20. An efficient and flexible test for rare variant effects.
Sugasawa S; Noma H; Otani T; Nishino J; Matsui S
Eur J Hum Genet; 2017 Jun; 25(6):752-757. PubMed ID: 28401900
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
