168 related articles for article (PubMed ID: 29281626)
1. Integrated rare variant-based risk gene prioritization in disease case-control sequencing studies.
Lin JR; Zhang Q; Cai Y; Morrow BE; Zhang ZD
PLoS Genet; 2017 Dec; 13(12):e1007142. PubMed ID: 29281626
[TBL] [Abstract][Full Text] [Related]
2. Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation.
Susak H; Serra-Saurina L; Demidov G; Rabionet R; Domènech L; Bosio M; Muyas F; Estivill X; Escaramís G; Ossowski S
PLoS Comput Biol; 2021 Feb; 17(2):e1007784. PubMed ID: 33606672
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 22865616
[TBL] [Abstract][Full Text] [Related]
4. A permutation method for detecting trend correlations in rare variant association studies.
Liu L; Wang P; Meng J; Chen L; Zhu W; Ma W
Genet Res (Camb); 2019 Dec; 101():e13. PubMed ID: 31831092
[TBL] [Abstract][Full Text] [Related]
5. Discovery of rare variants via sequencing: implications for the design of complex trait association studies.
Li B; Leal SM
PLoS Genet; 2009 May; 5(5):e1000481. PubMed ID: 19436704
[TBL] [Abstract][Full Text] [Related]
6. No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients.
Guipponi M; Santoni F; Schneider M; Gehrig C; Bustillo XB; Kates WR; Morrow B; Armando M; Vicari S; Sloan-Béna F; Gagnebin M; Shashi V; Hooper SR; Eliez S; Antonarakis SE
Transl Psychiatry; 2017 Feb; 7(2):e1039. PubMed ID: 28221368
[TBL] [Abstract][Full Text] [Related]
7. A phenome-wide association study of 26 mendelian genes reveals phenotypic expressivity of common and rare variants within the general population.
Tcheandjieu C; Aguirre M; Gustafsson S; Saha P; Potiny P; Haendel M; Ingelsson E; Rivas MA; Priest JR
PLoS Genet; 2020 Nov; 16(11):e1008802. PubMed ID: 33226994
[TBL] [Abstract][Full Text] [Related]
8. A new testing strategy to identify rare variants with either risk or protective effect on disease.
Ionita-Laza I; Buxbaum JD; Laird NM; Lange C
PLoS Genet; 2011 Feb; 7(2):e1001289. PubMed ID: 21304886
[TBL] [Abstract][Full Text] [Related]
9. An evaluation of statistical approaches to rare variant analysis in genetic association studies.
Morris AP; Zeggini E
Genet Epidemiol; 2010 Feb; 34(2):188-93. PubMed ID: 19810025
[TBL] [Abstract][Full Text] [Related]
10. Statistical power and significance testing in large-scale genetic studies.
Sham PC; Purcell SM
Nat Rev Genet; 2014 May; 15(5):335-46. PubMed ID: 24739678
[TBL] [Abstract][Full Text] [Related]
11. Enabling genome-wide association testing with multiple diseases and no healthy controls.
Tom J; Chang D; Wuster A; Mukhyala K; Cuenco K; Cowgill A; Vogel J; Reeder J; Yaspan B; Hunkapiller J; Brauer M; Behrens T; Forrest W; Bhangale T
Gene; 2019 Feb; 684():118-123. PubMed ID: 30366082
[TBL] [Abstract][Full Text] [Related]
12. Improved detection of rare genetic variants for diseases.
Zhang L; Pei YF; Li J; Papasian CJ; Deng HW
PLoS One; 2010 Nov; 5(11):e13857. PubMed ID: 21079782
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Methodology for the analysis of rare genetic variation in genome-wide association and re-sequencing studies of complex human traits.
Moutsianas L; Morris AP
Brief Funct Genomics; 2014 Sep; 13(5):362-70. PubMed ID: 24916163
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. Variant discovery and breakpoint region prediction for studying the human 22q11.2 deletion using BAC clone and whole genome sequencing analysis.
Guo X; Delio M; Haque N; Castellanos R; Hestand MS; Vermeesch JR; Morrow BE; Zheng D
Hum Mol Genet; 2016 Sep; 25(17):3754-3767. PubMed ID: 27436579
[TBL] [Abstract][Full Text] [Related]
19. A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variants.
Bacchelli E; Cainazzo MM; Cameli C; Guerzoni S; Martinelli A; Zoli M; Maestrini E; Pini LA
J Headache Pain; 2016 Dec; 17(1):114. PubMed ID: 27957625
[TBL] [Abstract][Full Text] [Related]
20. Association Tests for Rare Variants.
Nicolae DL
Annu Rev Genomics Hum Genet; 2016 Aug; 17():117-30. PubMed ID: 27147090
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
