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For: Gao F, Chang D, Biddanda A, Ma L, Guo Y, Zhou Z, Keinan A. XWAS: A Software Toolset for Genetic Data Analysis and Association Studies of the X Chromosome. J Hered 2015;106:666-71. [PMID: 26268243 DOI: 10.1093/jhered/esv059] [Cited by in Crossref: 59] [Cited by in F6Publishing: 52] [Article Influence: 8.4] [Reference Citation Analysis]
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4 Andlauer TFM, Mühleisen TW, Hoffstaedter F, Teumer A, Wittfeld K, Teuber A, Reinbold CS, Grotegerd D, Bülow R, Caspers S, Dannlowski U, Herms S, Hoffmann P, Kircher T, Minnerup H, Moebus S, Nenadić I, Teismann H, Völker U, Etkin A, Berger K, Grabe HJ, Nöthen MM, Amunts K, Eickhoff SB, Sämann PG, Müller-Myhsok B, Cichon S. Genetic factors influencing a neurobiological substrate for psychiatric disorders. Transl Psychiatry 2021;11:192. [PMID: 33782385 DOI: 10.1038/s41398-021-01317-7] [Reference Citation Analysis]
5 Liu W, Wang B, Liu-fu G, Fung WK, Zhou J. X-chromosome genetic association test incorporating X-chromosome inactivation and imprinting effects. J Genet 2019;98. [DOI: 10.1007/s12041-019-1146-6] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
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7 Schurz H, Salie M, Tromp G, Hoal EG, Kinnear CJ, Möller M. The X chromosome and sex-specific effects in infectious disease susceptibility. Hum Genomics 2019;13:2. [PMID: 30621780 DOI: 10.1186/s40246-018-0185-z] [Cited by in Crossref: 114] [Cited by in F6Publishing: 105] [Article Influence: 38.0] [Reference Citation Analysis]
8 Song Y, Biernacka JM, Winham SJ. Testing and estimation of X-chromosome SNP effects: Impact of model assumptions. Genet Epidemiol 2021;45:577-92. [PMID: 34082482 DOI: 10.1002/gepi.22393] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Bruiners N, Schurz H, Daya M, Salie M, van Helden PD, Kinnear CJ, Hoal EG, Möller M, Gey van Pittius NC. A regulatory variant in the C1Q gene cluster is associated with tuberculosis susceptibility and C1qA plasma levels in a South African population. Immunogenetics 2020;72:305-14. [PMID: 32556499 DOI: 10.1007/s00251-020-01167-5] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Fontaine A, Filipovic I, Fansiri T, Hoffmann AA, Cheng C, Kirkpatrick M, Rašic G, Lambrechts L. Extensive Genetic Differentiation between Homomorphic Sex Chromosomes in the Mosquito Vector, Aedes aegypti. Genome Biol Evol 2017;9:2322-35. [PMID: 28945882 DOI: 10.1093/gbe/evx171] [Cited by in Crossref: 22] [Cited by in F6Publishing: 16] [Article Influence: 5.5] [Reference Citation Analysis]
11 Swietlik EM, Gräf S, Morrell NW. The role of genomics and genetics in pulmonary arterial hypertension. Glob Cardiol Sci Pract 2020;2020:e202013. [PMID: 33150157 DOI: 10.21542/gcsp.2020.13] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
12 Wawrusiewicz-Kurylonek N, Chorąży M, Posmyk R, Zajkowska O, Zajkowska A, Krętowski AJ, Tarasiuk J, Kochanowicz J, Kułakowska A. The FOXP3 rs3761547 Gene Polymorphism in Multiple Sclerosis as a Male-Specific Risk Factor. Neuromolecular Med 2018;20:537-43. [PMID: 30229436 DOI: 10.1007/s12017-018-8512-z] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 2.5] [Reference Citation Analysis]
13 Li M, Yuan Y, Zhu B, Wang K, Fung WK, Zhou J. Gene-Based Methods for Estimating the Degree of the Skewness of X Chromosome Inactivation. Genes 2022;13:827. [DOI: 10.3390/genes13050827] [Reference Citation Analysis]
14 Hu B, Shen N, Li JJ, Kang H, Hong J, Fletcher J, Greenberg J, Mailick MR, Lu Q. Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness. PLoS Genet 2019;15:e1007973. [PMID: 30946739 DOI: 10.1371/journal.pgen.1007973] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
15 Rodrigues PM, Perugorria MJ, Santos-laso A, Bujanda L, Beuers U, Banales JM. Primary biliary cholangitis: A tale of epigenetically-induced secretory failure? Journal of Hepatology 2018;69:1371-83. [DOI: 10.1016/j.jhep.2018.08.020] [Cited by in Crossref: 20] [Cited by in F6Publishing: 16] [Article Influence: 5.0] [Reference Citation Analysis]
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17 Schurz H, Kinnear CJ, Gignoux C, Wojcik G, van Helden PD, Tromp G, Henn B, Hoal EG, Möller M. A Sex-Stratified Genome-Wide Association Study of Tuberculosis Using a Multi-Ethnic Genotyping Array. Front Genet 2018;9:678. [PMID: 30713548 DOI: 10.3389/fgene.2018.00678] [Cited by in Crossref: 9] [Cited by in F6Publishing: 13] [Article Influence: 3.0] [Reference Citation Analysis]
18 Agopian AJ, Hoang TT, Goldmuntz E, Hakonarson H, Musfee FI, Mitchell LE; Pediatric Cardiac Genomics Consortium. X-chromosome association studies of congenital heart defects. Am J Med Genet A 2020;182:250-4. [PMID: 31729158 DOI: 10.1002/ajmg.a.61411] [Reference Citation Analysis]
19 Chen B, Craiu RV, Strug LJ, Sun L. The X factor: A robust and powerful approach to X-chromosome-inclusive whole-genome association studies. Genet Epidemiol 2021. [PMID: 34224641 DOI: 10.1002/gepi.22422] [Reference Citation Analysis]
20 Zhao B, Luo T, Li T, Li Y, Zhang J, Shan Y, Wang X, Yang L, Zhou F, Zhu Z, Zhu H; Alzheimer’s Disease Neuroimaging Initiative., Pediatric Imaging, Neurocognition and Genetics. Genome-wide association analysis of 19,629 individuals identifies variants influencing regional brain volumes and refines their genetic co-architecture with cognitive and mental health traits. Nat Genet 2019;51:1637-44. [PMID: 31676860 DOI: 10.1038/s41588-019-0516-6] [Cited by in Crossref: 70] [Cited by in F6Publishing: 48] [Article Influence: 23.3] [Reference Citation Analysis]
21 Gerussi A, Paraboschi EM, Cappadona C, Caime C, Binatti E, Cristoferi L, Asselta R, Invernizzi P. The Role of Epigenetics in Primary Biliary Cholangitis. Int J Mol Sci 2022;23:4873. [PMID: 35563266 DOI: 10.3390/ijms23094873] [Reference Citation Analysis]
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24 Deschepper CF. Viewing the male-specific chromosome Y in a new light. Eur J Hum Genet 2017;25:1177-8. [PMID: 28853719 DOI: 10.1038/ejhg.2017.135] [Reference Citation Analysis]
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26 Vaura F, Palmu J, Aittokallio J, Kauko A, Niiranen T. Genetic, Molecular, and Cellular Determinants of Sex-Specific Cardiovascular Traits. Circ Res 2022;130:611-31. [PMID: 35175841 DOI: 10.1161/CIRCRESAHA.121.319891] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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29 Webster TH, Couse M, Grande BM, Karlins E, Phung TN, Richmond PA, Whitford W, Wilson MA. Identifying, understanding, and correcting technical artifacts on the sex chromosomes in next-generation sequencing data. Gigascience 2019;8:giz074. [PMID: 31289836 DOI: 10.1093/gigascience/giz074] [Cited by in Crossref: 22] [Cited by in F6Publishing: 15] [Article Influence: 11.0] [Reference Citation Analysis]
30 Traglia M, Bseiso D, Gusev A, Adviento B, Park DS, Mefford JA, Zaitlen N, Weiss LA. Genetic Mechanisms Leading to Sex Differences Across Common Diseases and Anthropometric Traits. Genetics 2017;205:979-92. [PMID: 27974502 DOI: 10.1534/genetics.116.193623] [Cited by in Crossref: 33] [Cited by in F6Publishing: 27] [Article Influence: 5.5] [Reference Citation Analysis]
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32 Povysil G, Petrovski S, Hostyk J, Aggarwal V, Allen AS, Goldstein DB. Rare-variant collapsing analyses for complex traits: guidelines and applications. Nat Rev Genet 2019;20:747-59. [PMID: 31605095 DOI: 10.1038/s41576-019-0177-4] [Cited by in Crossref: 50] [Cited by in F6Publishing: 36] [Article Influence: 16.7] [Reference Citation Analysis]
33 Lee HS, Oh H, Yang SK, Baek J, Jung S, Hong M, Kim KM, Shin HD, Kim KJ, Park SH, Ye BD, Han B, Song K. X Chromosome-wide Association Study Identifies a Susceptibility Locus for Inflammatory Bowel Disease in Koreans. J Crohns Colitis 2017;11:820-30. [PMID: 28333213 DOI: 10.1093/ecco-jcc/jjx023] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
34 Yu WY, Zhang Y, Li MK, Yang ZY, Fung WK, Zhao PZ, Zhou JY. BEXCIS: Bayesian methods for estimating the degree of the skewness of X chromosome inactivation. BMC Bioinformatics 2022;23:193. [PMID: 35610583 DOI: 10.1186/s12859-022-04721-y] [Reference Citation Analysis]
35 Scelsi MA, Khan RR, Lorenzi M, Christopher L, Greicius MD, Schott JM, Ourselin S, Altmann A. Genetic study of multimodal imaging Alzheimer's disease progression score implicates novel loci. Brain 2018;141:2167-80. [PMID: 29860282 DOI: 10.1093/brain/awy141] [Cited by in Crossref: 31] [Cited by in F6Publishing: 20] [Article Influence: 10.3] [Reference Citation Analysis]
36 Khramtsova EA, Heldman R, Derks EM, Yu D, Davis LK, Stranger BE; Tourette Syndrome/Obsessive-Compulsive Disorder Working Group of the Psychiatric Genomics Consortium. Sex differences in the genetic architecture of obsessive-compulsive disorder. Am J Med Genet B Neuropsychiatr Genet 2019;180:351-64. [PMID: 30456828 DOI: 10.1002/ajmg.b.32687] [Cited by in Crossref: 18] [Cited by in F6Publishing: 19] [Article Influence: 4.5] [Reference Citation Analysis]
37 Su Y, Hu J, Yin P, Jiang H, Chen S, Dai M, Chen Z, Wang P. XCMAX4: A Robust X Chromosomal Genetic Association Test Accounting for Covariates. Genes 2022;13:847. [DOI: 10.3390/genes13050847] [Reference Citation Analysis]
38 Shen JJ, Wang YF, Yang W. Sex-Interacting mRNA- and miRNA-eQTLs and Their Implications in Gene Expression Regulation and Disease. Front Genet 2019;10:313. [PMID: 31024623 DOI: 10.3389/fgene.2019.00313] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
39 Simcoe MJ, Khawaja AP, Mahroo OA, Hammond CJ, Hysi PG; UK Biobank Eye and Vision Consortium. The Role of Chromosome X in Intraocular Pressure Variation and Sex-Specific Effects. Invest Ophthalmol Vis Sci 2020;61:20. [PMID: 32926103 DOI: 10.1167/iovs.61.11.20] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
40 Wang P, Xu SQ, Wang BQ, Fung WK, Zhou JY. A robust and powerful test for case-control genetic association study on X chromosome. Stat Methods Med Res 2019;28:3260-72. [PMID: 30232923 DOI: 10.1177/0962280218799532] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
41 Anguita-Ruiz A, Plaza-Diaz J, Ruiz-Ojeda FJ, Rupérez AI, Leis R, Bueno G, Gil-Campos M, Vázquez-Cobela R, Cañete R, Moreno LA, Gil Á, Aguilera CM. X chromosome genetic data in a Spanish children cohort, dataset description and analysis pipeline. Sci Data 2019;6:130. [PMID: 31332195 DOI: 10.1038/s41597-019-0109-3] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
42 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: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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44 Mielke MM, Miller VM. Improving clinical outcomes through attention to sex and hormones in research. Nat Rev Endocrinol 2021. [PMID: 34316045 DOI: 10.1038/s41574-021-00531-z] [Reference Citation Analysis]
45 Lopez-Lee C, Kodama L, Gan L. Sex Differences in Neurodegeneration: The Role of the Immune System in Humans. Biol Psychiatry 2021:S0006-3223(21)00039-1. [PMID: 33715827 DOI: 10.1016/j.biopsych.2021.01.002] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 9.0] [Reference Citation Analysis]
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48 Zhang Y, Xu SQ, Liu W, Fung WK, Zhou JY. A robust test for X-chromosome genetic association accounting for X-chromosome inactivation and imprinting. Genet Res (Camb) 2020;102:e2. [PMID: 32234109 DOI: 10.1017/S0016672320000026] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
49 Ruiz-Ojeda FJ, Anguita-Ruiz A, Rupérez AI, Gomez-Llorente C, Olza J, Vázquez-Cobela R, Gil-Campos M, Bueno G, Leis R, Cañete R, Moreno LA, Gil A, Aguilera CM. Effects of X-chromosome Tenomodulin Genetic Variants on Obesity in a Children's Cohort and Implications of the Gene in Adipocyte Metabolism. Sci Rep 2019;9:3979. [PMID: 30850679 DOI: 10.1038/s41598-019-40482-0] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
50 Asselta R, Paraboschi EM, Gerussi A, Cordell HJ, Mells GF, Sandford RN, Jones DE, Nakamura M, Ueno K, Hitomi Y, Kawashima M, Nishida N, Tokunaga K, Nagasaki M, Tanaka A, Tang R, Li Z, Shi Y, Liu X, Xiong M, Hirschfield G, Siminovitch KA, Carbone M, Cardamone G, Duga S, Gershwin ME, Seldin MF, Invernizzi P; Canadian-US PBC Consortium., Italian PBC Genetics Study Group., UK-PBC Consortium., Japan PBC-GWAS Consortium. X Chromosome Contribution to the Genetic Architecture of Primary Biliary Cholangitis. Gastroenterology 2021;160:2483-2495.e26. [PMID: 33675743 DOI: 10.1053/j.gastro.2021.02.061] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
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