188 related articles for article (PubMed ID: 22009789)
1. Incorporating model uncertainty in detecting rare variants: the Bayesian risk index.
Quintana MA; Berstein JL; Thomas DC; Conti DV
Genet Epidemiol; 2011 Nov; 35(7):638-49. PubMed ID: 22009789
[TBL] [Abstract][Full Text] [Related]
2. Incorporating prior biologic information for high-dimensional rare variant association studies.
Quintana MA; Schumacher FR; Casey G; Bernstein JL; Li L; Conti DV
Hum Hered; 2012; 74(3-4):184-95. PubMed ID: 23594496
[TBL] [Abstract][Full Text] [Related]
3. Comparing the frequency of common genetic variants and haplotypes between carriers and non-carriers of BRCA1 and BRCA2 deleterious mutations in Australian women diagnosed with breast cancer before 40 years of age.
Turkovic L; Gurrin LC; Bahlo M; Dite GS; Southey MC; Hopper JL
BMC Cancer; 2010 Sep; 10():466. PubMed ID: 20807450
[TBL] [Abstract][Full Text] [Related]
4. Hierarchical Bayesian model for rare variant association analysis integrating genotype uncertainty in human sequence data.
He L; Pitkäniemi J; Sarin AP; Salomaa V; Sillanpää MJ; Ripatti S
Genet Epidemiol; 2015 Feb; 39(2):89-100. PubMed ID: 25395270
[TBL] [Abstract][Full Text] [Related]
5. Assessment of rare BRCA1 and BRCA2 variants of unknown significance using hierarchical modeling.
Capanu M; Concannon P; Haile RW; Bernstein L; Malone KE; Lynch CF; Liang X; Teraoka SN; Diep AT; Thomas DC; Bernstein JL; ; Begg CB
Genet Epidemiol; 2011 Jul; 35(5):389-97. PubMed ID: 21520273
[TBL] [Abstract][Full Text] [Related]
6. False discovery rates for rare variants from sequenced data.
Capanu M; Seshan VE
Genet Epidemiol; 2015 Feb; 39(2):65-76. PubMed ID: 25556339
[TBL] [Abstract][Full Text] [Related]
7. Reconsidering association testing methods using single-variant test statistics as alternatives to pooling tests for sequence data with rare variants.
Kinnamon DD; Hershberger RE; Martin ER
PLoS One; 2012; 7(2):e30238. PubMed ID: 22363423
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Dynamic Bayesian testing of sets of variants in complex diseases.
Zhang Y; Ghosh S; Hakonarson H
Genetics; 2014 Nov; 198(3):867-78. PubMed ID: 25217050
[TBL] [Abstract][Full Text] [Related]
10. Characterization of BRCA1 and BRCA2 variants in multi-ethnic Asian cohort from a Malaysian case-control study.
Lai KN; Ho WK; Kang IN; Kang PC; Phuah SY; Mariapun S; Yip CH; Mohd Taib NA; Teo SH
BMC Cancer; 2017 Feb; 17(1):149. PubMed ID: 28222693
[TBL] [Abstract][Full Text] [Related]
11. Radiation Treatment, ATM, BRCA1/2, and CHEK2*1100delC Pathogenic Variants and Risk of Contralateral Breast Cancer.
Reiner AS; Robson ME; Mellemkjær L; Tischkowitz M; John EM; Lynch CF; Brooks JD; Boice JD; Knight JA; Teraoka SN; Liang X; Woods M; Shen R; Shore RE; Stram DO; Thomas DC; Malone KE; Bernstein L; Riaz N; Woodward W; Powell S; Goldgar D; Concannon P; ; Bernstein JL
J Natl Cancer Inst; 2020 Dec; 112(12):1275-1279. PubMed ID: 32119081
[TBL] [Abstract][Full Text] [Related]
12. Robust and Powerful Affected Sibpair Test for Rare Variant Association.
Lin KH; Zöllner S
Genet Epidemiol; 2015 Jul; 39(5):325-33. PubMed ID: 25966809
[TBL] [Abstract][Full Text] [Related]
13. Evaluating the breast cancer predisposition role of rare variants in genes associated with low-penetrance breast cancer risk SNPs.
Li N; Rowley SM; Thompson ER; McInerny S; Devereux L; Amarasinghe KC; Zethoven M; Lupat R; Goode D; Li J; Trainer AH; Gorringe KL; James PA; Campbell IG
Breast Cancer Res; 2018 Jan; 20(1):3. PubMed ID: 29316957
[TBL] [Abstract][Full Text] [Related]
14. Breast cancer risk associated with BRCA1/2 variants in the Pakistani population.
Abbas S; Siddique A; Shahid N; Khan RT; Fatima W
Breast Cancer; 2019 May; 26(3):365-372. PubMed ID: 30430339
[TBL] [Abstract][Full Text] [Related]
15. A powerful association test of multiple genetic variants using a random-effects model.
Cheng KF; Lee JY; Zheng W; Li C
Stat Med; 2014 May; 33(11):1816-27. PubMed ID: 24338936
[TBL] [Abstract][Full Text] [Related]
16. A variational Bayes discrete mixture test for rare variant association.
Logsdon BA; Dai JY; Auer PL; Johnsen JM; Ganesh SK; Smith NL; Wilson JG; Tracy RP; Lange LA; Jiao S; Rich SS; Lettre G; Carlson CS; Jackson RD; O'Donnell CJ; Wurfel MM; Nickerson DA; Tang H; Reiner AP; Kooperberg C;
Genet Epidemiol; 2014 Jan; 38(1):21-30. PubMed ID: 24482836
[TBL] [Abstract][Full Text] [Related]
17. Reclassification of
Lee JS; Oh S; Park SK; Lee MH; Lee JW; Kim SW; Son BH; Noh DY; Lee JE; Park HL; Kim MJ; Cho SI; Lee YK; Park SS; Seong MW
J Med Genet; 2018 Dec; 55(12):794-802. PubMed ID: 30415210
[TBL] [Abstract][Full Text] [Related]
18. Evaluation of the contribution of germline variants in BRCA1 and BRCA2 to uveal and cutaneous melanoma.
Johansson PA; Nathan V; Bourke LM; Palmer JM; Zhang T; Symmons J; Howlie M; Patch AM; Read J; Holland EA; Schmid H; Warrier S; Glasson W; Höiom V; Wadt K; Jönsson G; Olsson H; Ingvar C; Mann G; Brown KM; Hayward NK; Pritchard AL
Melanoma Res; 2019 Oct; 29(5):483-490. PubMed ID: 31464824
[TBL] [Abstract][Full Text] [Related]
19. Comprehensive profiling of BRCA1 and BRCA2 variants in breast and ovarian cancer in Chinese patients.
Gao X; Nan X; Liu Y; Liu R; Zang W; Shan G; Gai F; Zhang J; Li L; Cheng G; Song L
Hum Mutat; 2020 Mar; 41(3):696-708. PubMed ID: 31825140
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]