221 related articles for article (PubMed ID: 21047260)
21. Utilising family-based designs for detecting rare variant disease associations.
Preston MD; Dudbridge F
Ann Hum Genet; 2014 Mar; 78(2):129-40. PubMed ID: 24571231
[TBL] [Abstract][Full Text] [Related]
22. Using population isolates in genetic association studies.
Hatzikotoulas K; Gilly A; Zeggini E
Brief Funct Genomics; 2014 Sep; 13(5):371-7. PubMed ID: 25009120
[TBL] [Abstract][Full Text] [Related]
23. Enhancing GTEx by bridging the gaps between genotype, gene expression, and disease.
eGTEx Project
Nat Genet; 2017 Dec; 49(12):1664-1670. PubMed ID: 29019975
[TBL] [Abstract][Full Text] [Related]
24. The effect of phenotypic outliers and non-normality on rare-variant association testing.
Auer PL; Reiner AP; Leal SM
Eur J Hum Genet; 2016 Aug; 24(8):1188-94. PubMed ID: 26733287
[TBL] [Abstract][Full Text] [Related]
25. [Family-based association tests for rare variants].
Chen X; Wang SY; Xue EC; Wang XH; Peng HX; Fan M; Wang MY; Wu YQ; Qin XY; Li J; Wu T; Zhu J; Li ZP; Zhou DF; Chen YH; Hu Y
Zhonghua Liu Xing Bing Xue Za Zhi; 2022 Sep; 43(9):1497-1502. PubMed ID: 36117360
[TBL] [Abstract][Full Text] [Related]
26. Gene-based partial least-squares approaches for detecting rare variant associations with complex traits.
Turkmen AS; Lin S
BMC Proc; 2011 Nov; 5 Suppl 9(Suppl 9):S19. PubMed ID: 22373126
[TBL] [Abstract][Full Text] [Related]
27. Genomewide association studies and human disease.
Hardy J; Singleton A
N Engl J Med; 2009 Apr; 360(17):1759-68. PubMed ID: 19369657
[No Abstract] [Full Text] [Related]
28. Detecting genes in complex disease: does phenotype accuracy limit the horizon?
Lee K; Sawcer S
Trends Genet; 2010 Jun; 26(6):241-2; author reply 242-3. PubMed ID: 20417577
[No Abstract] [Full Text] [Related]
29. Overcoming the challenges of imputation of rare variants in a Taiwanese cohort.
Chattopadhyay A; Lu TP
Transl Cancer Res; 2020 Jul; 9(7):4065-4069. PubMed ID: 35117776
[No Abstract] [Full Text] [Related]
30. Rare-variant association analysis: study designs and statistical tests.
Lee S; Abecasis GR; Boehnke M; Lin X
Am J Hum Genet; 2014 Jul; 95(1):5-23. PubMed ID: 24995866
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Rare-variant association testing for sequencing data with the sequence kernel association test.
Wu MC; Lee S; Cai T; Li Y; Boehnke M; Lin X
Am J Hum Genet; 2011 Jul; 89(1):82-93. PubMed ID: 21737059
[TBL] [Abstract][Full Text] [Related]
33. Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies.
Lee S; Emond MJ; Bamshad MJ; Barnes KC; Rieder MJ; Nickerson DA; ; Christiani DC; Wurfel MM; Lin X
Am J Hum Genet; 2012 Aug; 91(2):224-37. PubMed ID: 22863193
[TBL] [Abstract][Full Text] [Related]
34. The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease.
Moutsianas L; Agarwala V; Fuchsberger C; Flannick J; Rivas MA; Gaulton KJ; Albers PK; ; McVean G; Boehnke M; Altshuler D; McCarthy MI
PLoS Genet; 2015 Apr; 11(4):e1005165. PubMed ID: 25906071
[TBL] [Abstract][Full Text] [Related]
35. Power analysis and sample size estimation for sequence-based association studies.
Wang GT; Li B; Santos-Cortez RP; Peng B; Leal SM
Bioinformatics; 2014 Aug; 30(16):2377-8. PubMed ID: 24778108
[TBL] [Abstract][Full Text] [Related]
36. Sequence kernel association tests for the combined effect of rare and common variants.
Ionita-Laza I; Lee S; Makarov V; Buxbaum JD; Lin X
Am J Hum Genet; 2013 Jun; 92(6):841-53. PubMed ID: 23684009
[TBL] [Abstract][Full Text] [Related]
37. Meta-analysis of gene-level tests for rare variant association.
Liu DJ; Peloso GM; Zhan X; Holmen OL; Zawistowski M; Feng S; Nikpay M; Auer PL; Goel A; Zhang H; Peters U; Farrall M; Orho-Melander M; Kooperberg C; McPherson R; Watkins H; Willer CJ; Hveem K; Melander O; Kathiresan S; Abecasis GR
Nat Genet; 2014 Feb; 46(2):200-4. PubMed ID: 24336170
[TBL] [Abstract][Full Text] [Related]
38. Optimal tests for rare variant effects in sequencing association studies.
Lee S; Wu MC; Lin X
Biostatistics; 2012 Sep; 13(4):762-75. PubMed ID: 22699862
[TBL] [Abstract][Full Text] [Related]
39. Comparison of statistical tests for disease association with rare variants.
Basu S; Pan W
Genet Epidemiol; 2011 Nov; 35(7):606-19. PubMed ID: 21769936
[TBL] [Abstract][Full Text] [Related]
40.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
