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For: Sauteraud R, Stahl JM, James J, Englebright M, Chen F, Zhan X, Carrel L, Liu DJ. Inferring genes that escape X-Chromosome inactivation reveals important contribution of variable escape genes to sex-biased diseases. Genome Res 2021;31:1629-37. [PMID: 34426515 DOI: 10.1101/gr.275677.121] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Ahern DT, Bansal P, Armillei MK, Faustino IV, Kondaveeti Y, Glatt-Deeley HR, Banda EC, Pinter SF. Monosomy X in isogenic human iPSC-derived trophoblast model impacts expression modules preserved in human placenta. Proc Natl Acad Sci U S A 2022;119:e2211073119. [PMID: 36161909 DOI: 10.1073/pnas.2211073119] [Reference Citation Analysis]
2 Keur N, Ricaño-Ponce I, Kumar V, Matzaraki V. A systematic review of analytical methods used in genetic association analysis of the X-chromosome. Brief Bioinform 2022:bbac287. [PMID: 35901513 DOI: 10.1093/bib/bbac287] [Reference Citation Analysis]
3 Gupta M, Srikrishna G, Klein SL, Bishai WR. Genetic and hormonal mechanisms underlying sex-specific immune responses in tuberculosis. Trends in Immunology 2022. [DOI: 10.1016/j.it.2022.06.004] [Reference Citation Analysis]
4 Wren G, Davies W. Sex-linked genetic mechanisms and atrial fibrillation risk. European Journal of Medical Genetics 2022. [DOI: 10.1016/j.ejmg.2022.104459] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
5 San Roman AK, Godfrey AK, Skaletsky H, Bellott DW, Groff AF, Harris HL, Blanton LV, Hughes JF, Brown L, Phou S, Buscetta A, Kruszka P, Banks N, Dutra A, Pak E, Lasutschinkow PC, Keen C, Davis SM, Tartaglia NR, Samango-sprouse C, Muenke M, Page DC. Quantitative analysis of gene expression on the inactive human X chromosome.. [DOI: 10.1101/2021.08.09.455676] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]