159 related articles for article (PubMed ID: 32864779)
1. Detecting X-linked common and rare variant effects in family-based sequencing studies.
Turkmen AS; Lin S
Genet Epidemiol; 2021 Feb; 45(1):36-45. PubMed ID: 32864779
[TBL] [Abstract][Full Text] [Related]
2. Identifying rare variants associated with complex traits via sequencing.
Li B; Liu DJ; Leal SM
Curr Protoc Hum Genet; 2013 Jul; Chapter 1():Unit 1.26. PubMed ID: 23853079
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Contribution of rare whole-genome sequencing variants to plasma protein levels and the missing heritability.
Kierczak M; Rafati N; Höglund J; Gourlé H; Lo Faro V; Schmitz D; Ek WE; Gyllensten U; Enroth S; Ekman D; Nystedt B; Karlsson T; Johansson Å
Nat Commun; 2022 May; 13(1):2532. PubMed ID: 35534486
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Advances in the Genetics of Hypertension: The Effect of Rare Variants.
Russo A; Di Gaetano C; Cugliari G; Matullo G
Int J Mol Sci; 2018 Feb; 19(3):. PubMed ID: 29495593
[TBL] [Abstract][Full Text] [Related]
8. [Less common variants association study and statistical analysis].
Liao X; Deng J; Xun JY; Yan JX
Zhonghua Liu Xing Bing Xue Za Zhi; 2017 Jul; 38(7):977-982. PubMed ID: 28738478
[TBL] [Abstract][Full Text] [Related]
9. GxGrare: gene-gene interaction analysis method for rare variants from high-throughput sequencing data.
Kwon M; Leem S; Yoon J; Park T
BMC Syst Biol; 2018 Mar; 12(Suppl 2):19. PubMed ID: 29560826
[TBL] [Abstract][Full Text] [Related]
10. Effective discovery of rare variants by pooled target capture sequencing: A comparative analysis with individually indexed target capture sequencing.
Ryu S; Han J; Norden-Krichmar TM; Schork NJ; Suh Y
Mutat Res; 2018 May; 809():24-31. PubMed ID: 29677560
[TBL] [Abstract][Full Text] [Related]
11. GWASeq: targeted re-sequencing follow up to GWAS.
Salomon MP; Li WL; Edlund CK; Morrison J; Fortini BK; Win AK; Conti DV; Thomas DC; Duggan D; Buchanan DD; Jenkins MA; Hopper JL; Gallinger S; Le Marchand L; Newcomb PA; Casey G; Marjoram P
BMC Genomics; 2016 Mar; 17():176. PubMed ID: 26940994
[TBL] [Abstract][Full Text] [Related]
12. Polygenic architecture of rare coding variation across 394,783 exomes.
Weiner DJ; Nadig A; Jagadeesh KA; Dey KK; Neale BM; Robinson EB; Karczewski KJ; O'Connor LJ
Nature; 2023 Feb; 614(7948):492-499. PubMed ID: 36755099
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. A modified association test for rare and common variants based on affected sib-pair design.
Guo Y; Zhou Y
J Theor Biol; 2019 Apr; 467():1-6. PubMed ID: 30707975
[TBL] [Abstract][Full Text] [Related]
15. A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next-generation sequencing.
Chiu CY; Jung J; Wang Y; Weeks DE; Wilson AF; Bailey-Wilson JE; Amos CI; Mills JL; Boehnke M; Xiong M; Fan R
Genet Epidemiol; 2017 Jan; 41(1):18-34. PubMed ID: 27917525
[TBL] [Abstract][Full Text] [Related]
16. Detecting Multiethnic Rare Variants.
Ouyang W; Zhu X; Qin H
Methods Mol Biol; 2017; 1666():527-538. PubMed ID: 28980263
[TBL] [Abstract][Full Text] [Related]
17. FARVATX: Family-Based Rare Variant Association Test for X-Linked Genes.
Choi S; Lee S; Qiao D; Hardin M; Cho MH; Silverman EK; Park T; Won S
Genet Epidemiol; 2016 Sep; 40(6):475-85. PubMed ID: 27325607
[TBL] [Abstract][Full Text] [Related]
18. Rare-variant genome-wide association studies: a new frontier in genetic analysis of complex traits.
Wagner MJ
Pharmacogenomics; 2013 Mar; 14(4):413-24. PubMed ID: 23438888
[TBL] [Abstract][Full Text] [Related]
19. Association studies for next-generation sequencing.
Luo L; Boerwinkle E; Xiong M
Genome Res; 2011 Jul; 21(7):1099-108. PubMed ID: 21521787
[TBL] [Abstract][Full Text] [Related]
20. The Nature of Genetic Variation for Complex Traits Revealed by GWAS and Regional Heritability Mapping Analyses.
Caballero A; Tenesa A; Keightley PD
Genetics; 2015 Dec; 201(4):1601-13. PubMed ID: 26482794
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]