230 related articles for article (PubMed ID: 26268243)
1. XWAS: A Software Toolset for Genetic Data Analysis and Association Studies of the X Chromosome.
Gao F; Chang D; Biddanda A; Ma L; Guo Y; Zhou Z; Keinan A
J Hered; 2015; 106(5):666-71. PubMed ID: 26268243
[TBL] [Abstract][Full Text] [Related]
2. Accounting for eXentricities: analysis of the X chromosome in GWAS reveals X-linked genes implicated in autoimmune diseases.
Chang D; Gao F; Slavney A; Ma L; Waldman YY; Sams AJ; Billing-Ross P; Madar A; Spritz R; Keinan A
PLoS One; 2014; 9(12):e113684. PubMed ID: 25479423
[TBL] [Abstract][Full Text] [Related]
3. X-inactivation informs variance-based testing for X-linked association of a quantitative trait.
Ma L; Hoffman G; Keinan A
BMC Genomics; 2015 Mar; 16(1):241. PubMed ID: 25880738
[TBL] [Abstract][Full Text] [Related]
4. A systematic review of analytical methods used in genetic association analysis of the X-chromosome.
Keur N; Ricaño-Ponce I; Kumar V; Matzaraki V
Brief Bioinform; 2022 Sep; 23(5):. PubMed ID: 35901513
[TBL] [Abstract][Full Text] [Related]
5. Detecting associated single-nucleotide polymorphisms on the X chromosome in case control genome-wide association studies.
Chen Z; Ng HK; Li J; Liu Q; Huang H
Stat Methods Med Res; 2017 Apr; 26(2):567-582. PubMed ID: 25253574
[TBL] [Abstract][Full Text] [Related]
6. Statistics for X-chromosome associations.
Özbek U; Lin HM; Lin Y; Weeks DE; Chen W; Shaffer JR; Purcell SM; Feingold E
Genet Epidemiol; 2018 Sep; 42(6):539-550. PubMed ID: 29900581
[TBL] [Abstract][Full Text] [Related]
7. GCTA: a tool for genome-wide complex trait analysis.
Yang J; Lee SH; Goddard ME; Visscher PM
Am J Hum Genet; 2011 Jan; 88(1):76-82. PubMed ID: 21167468
[TBL] [Abstract][Full Text] [Related]
8. Chromosome X-wide association study identifies Loci for fasting insulin and height and evidence for incomplete dosage compensation.
Tukiainen T; Pirinen M; Sarin AP; Ladenvall C; Kettunen J; Lehtimäki T; Lokki ML; Perola M; Sinisalo J; Vlachopoulou E; Eriksson JG; Groop L; Jula A; Järvelin MR; Raitakari OT; Salomaa V; Ripatti S
PLoS Genet; 2014 Feb; 10(2):e1004127. PubMed ID: 24516404
[TBL] [Abstract][Full Text] [Related]
9. Analytical strategies to include the X-chromosome in variance heterogeneity analyses: Evidence for trait-specific polygenic variance structure.
Deng WQ; Mao S; Kalnapenkis A; Esko T; Mägi R; Paré G; Sun L
Genet Epidemiol; 2019 Oct; 43(7):815-830. PubMed ID: 31332826
[TBL] [Abstract][Full Text] [Related]
10. How to include chromosome X in your genome-wide association study.
König IR; Loley C; Erdmann J; Ziegler A
Genet Epidemiol; 2014 Feb; 38(2):97-103. PubMed ID: 24408308
[TBL] [Abstract][Full Text] [Related]
11. Sex bias in celiac disease: XWAS and monocyte eQTLs in women identify TMEM187 as a functional candidate gene.
Hernangomez-Laderas A; Cilleros-Portet A; Martínez Velasco S; Marí S; Legarda M; González-García BP; Tutau C; García-Santisteban I; Irastorza I; Fernandez-Jimenez N; Bilbao JR
Biol Sex Differ; 2023 Dec; 14(1):86. PubMed ID: 38072919
[TBL] [Abstract][Full Text] [Related]
12. Robust association tests for quantitative traits on the X chromosome.
Yang ZY; Liu W; Yuan YX; Kong YF; Zhao PZ; Fung WK; Zhou JY
Heredity (Edinb); 2022 Oct; 129(4):244-256. PubMed ID: 36085362
[TBL] [Abstract][Full Text] [Related]
13. X chromosome association testing in genome wide association studies.
Hickey PF; Bahlo M
Genet Epidemiol; 2011 Nov; 35(7):664-70. PubMed ID: 21818774
[TBL] [Abstract][Full Text] [Related]
14. Testing for association on the X chromosome.
Clayton D
Biostatistics; 2008 Oct; 9(4):593-600. PubMed ID: 18441336
[TBL] [Abstract][Full Text] [Related]
15. VEGAS2: Software for More Flexible Gene-Based Testing.
Mishra A; Macgregor S
Twin Res Hum Genet; 2015 Feb; 18(1):86-91. PubMed ID: 25518859
[TBL] [Abstract][Full Text] [Related]
16. Evaluating the Calibration and Power of Three Gene-Based Association Tests of Rare Variants for the X Chromosome.
Ma C; Boehnke M; Lee S;
Genet Epidemiol; 2015 Nov; 39(7):499-508. PubMed ID: 26454253
[TBL] [Abstract][Full Text] [Related]
17. Influence of sex and genetic variability on expression of X-linked genes in human monocytes.
Castagné R; Zeller T; Rotival M; Szymczak S; Truong V; Schillert A; Trégouët DA; Münzel T; Ziegler A; Cambien F; Blankenberg S; Tiret L
Genomics; 2011 Nov; 98(5):320-6. PubMed ID: 21763416
[TBL] [Abstract][Full Text] [Related]
18. EPIQ-efficient detection of SNP-SNP epistatic interactions for quantitative traits.
Arkin Y; Rahmani E; Kleber ME; Laaksonen R; März W; Halperin E
Bioinformatics; 2014 Jun; 30(12):i19-25. PubMed ID: 24931983
[TBL] [Abstract][Full Text] [Related]
19. Endometrial vezatin and its association with endometriosis risk.
Holdsworth-Carson SJ; Fung JN; Luong HT; Sapkota Y; Bowdler LM; Wallace L; Teh WT; Powell JE; Girling JE; Healey M; Montgomery GW; Rogers PA
Hum Reprod; 2016 May; 31(5):999-1013. PubMed ID: 27005890
[TBL] [Abstract][Full Text] [Related]
20. Common X-Chromosome Variants Are Associated with Parkinson Disease Risk.
Le Guen Y; Napolioni V; Belloy ME; Yu E; Krohn L; Ruskey JA; Gan-Or Z; Kennedy G; Eger SJ; Greicius MD
Ann Neurol; 2021 Jul; 90(1):22-34. PubMed ID: 33583074
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]