| 1 |
Kong Y, Li S, Wang K, Zhu B, Yuan Y, Li M, Zhou J. An Efficient Bayesian Method for Estimating the Degree of the Skewness of X Chromosome Inactivation Based on the Mixture of General Pedigrees and Unrelated Females. Biomolecules 2023;13:543. [DOI: 10.3390/biom13030543] [Reference Citation Analysis]
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| 2 |
Chappell K, Colle R, Bouligand J, Trabado S, Fève B, Becquemont L, Corruble E, Verstuyft C. The MAOA rs979605 Genetic Polymorphism Is Differentially Associated with Clinical Improvement Following Antidepressant Treatment between Male and Female Depressed Patients. Int J Mol Sci 2022;24. [PMID: 36613935 DOI: 10.3390/ijms24010497] [Reference Citation Analysis]
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| 3 |
Zhang L, Sun L. Unifying genetic association tests via regression: Prospective and retrospective, parametric and nonparametric, and genotype‐ and allele‐based tests. Can J Statistics. [DOI: 10.1002/cjs.11729] [Reference Citation Analysis]
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| 4 |
Yang ZY, Liu W, Yuan YX, Kong YF, Zhao PZ, Fung WK, Zhou JY. Robust association tests for quantitative traits on the X chromosome. Heredity (Edinb) 2022. [PMID: 36085362 DOI: 10.1038/s41437-022-00560-y] [Reference Citation Analysis]
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| 5 |
Sugolov A, Emmenegger E, Paterson AD, Sun L. Statistical learning of large-scale genetic data: How to run a genome-wide association study of gene-expression data using the 1000 Genomes Project data.. [DOI: 10.1101/2022.09.03.506492] [Reference Citation Analysis]
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| 6 |
Lin B, Sun L. An empirical study of sex-stratified vs. sex-combined analysis in the presence of genetic effect heterogeneity.. [DOI: 10.1101/2022.06.08.495202] [Reference Citation Analysis]
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| 7 |
Yoo S, Garg E, Elliott L, Hung R, Halevy A, Brooks J, Bull S, Gagnon F, Greenwood C, Lawless J, Paterson A, Sun L, Zawati M, Lerner-ellis J, Abraham R, Birol I, Bourque G, Garant J, Gosselin C, Li J, Whitney J, Thiruvahindrapuram B, Herbrick J, Lorenti M, Reuter M, Liu S, Allen U, Bernier F, Biggs C, Cheung A, Cowan J, Herridge M, Maslove D, Modi B, Mooser V, Morris S, Ostrowski M, Parekh R, Pfeffer G, Suchowersky O, Taher J, Turvey S, Upton J, Warren R, Yeung R, Aziz N, Knoppers B, Lathrop M, Jones S, Scherer S, Strug L. HostSeq: A Canadian Whole Genome Sequencing and Clinical Data Resource.. [DOI: 10.1101/2022.05.06.22274627] [Reference Citation Analysis]
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| 8 |
Wang Z, Sun L, Paterson AD. Major sex differences in allele frequencies for X chromosomal variants in both the 1000 Genomes Project and gnomAD. PLoS Genet 2022;18:e1010231. [PMID: 35639794 DOI: 10.1371/journal.pgen.1010231] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
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| 9 |
Deng WQ, Sun L. gJLS2: an R package for generalized joint location and scale analysis in X-inclusive genome-wide association studies. G3 Genes|Genomes|Genetics 2022;12. [DOI: 10.1093/g3journal/jkac049] [Reference Citation Analysis]
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| 10 |
Zhang L, Sun L. Unifying genetic association tests via regression: Prospective and retrospective, parametric and non-parametric, and genotype- and allele-based tests.. [DOI: 10.1101/2022.03.31.486648] [Reference Citation Analysis]
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| 11 |
Zhang C, Ye Y, Zhao H. Comparison of Methods Utilizing Sex-Specific PRSs Derived From GWAS Summary Statistics. Front Genet 2022;13:892950. [PMID: 35873490 DOI: 10.3389/fgene.2022.892950] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
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| 12 |
Wang Z, Sun L, Paterson AD. Major sex differences in allele frequencies for X chromosome variants in the 1000 Genomes Project data.. [DOI: 10.1101/2021.10.27.466015] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
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| 13 |
Deng WQ, Sun L. gJLS2: An R package for generalized joint location and scale analysis in X-inclusive genome-wide association studies.. [DOI: 10.1101/2021.10.11.463951] [Reference Citation Analysis]
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