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For: Chang D, Gao F, Slavney A, Ma L, Waldman YY, Sams AJ, Billing-Ross P, Madar A, Spritz R, Keinan A. Accounting for eXentricities: analysis of the X chromosome in GWAS reveals X-linked genes implicated in autoimmune diseases. PLoS One 2014;9:e113684. [PMID: 25479423 DOI: 10.1371/journal.pone.0113684] [Cited by in Crossref: 71] [Cited by in F6Publishing: 62] [Article Influence: 8.9] [Reference Citation Analysis]
Number Citing Articles
1 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]
2 Ding N, Li R, Shi W, He C. CENPI is overexpressed in colorectal cancer and regulates cell migration and invasion. Gene 2018;674:80-6. [PMID: 29936263 DOI: 10.1016/j.gene.2018.06.067] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.8] [Reference Citation Analysis]
3 Prins BP, Leitsalu L, Pärna K, Fischer K, Metspalu A, Haller T, Snieder H. Advances in Genomic Discovery and Implications for Personalized Prevention and Medicine: Estonia as Example. J Pers Med 2021;11:358. [PMID: 33946982 DOI: 10.3390/jpm11050358] [Reference Citation Analysis]
4 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]
5 Powers MS, Smith PH, McKee SA, Ehringer MA. From sexless to sexy: Why it is time for human genetics to consider and report analyses of sex. Biol Sex Differ 2017;8:15. [PMID: 28473910 DOI: 10.1186/s13293-017-0136-8] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 1.4] [Reference Citation Analysis]
6 Capaldo CT, Powell DN, Kalman D. Layered defense: how mucus and tight junctions seal the intestinal barrier. J Mol Med (Berl). 2017;95:927-934. [PMID: 28707083 DOI: 10.1007/s00109-017-1557-x] [Cited by in Crossref: 81] [Cited by in F6Publishing: 74] [Article Influence: 16.2] [Reference Citation Analysis]
7 Syed ZA, Zhang L, Ten Hagen KG. In vivo models of mucin biosynthesis and function. Adv Drug Deliv Rev 2022;184:114182. [PMID: 35278522 DOI: 10.1016/j.addr.2022.114182] [Reference Citation Analysis]
8 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]
9 Schöneberg T, Meister J, Knierim AB, Schulz A. The G protein-coupled receptor GPR34 - The past 20 years of a grownup. Pharmacol Ther 2018;189:71-88. [PMID: 29684466 DOI: 10.1016/j.pharmthera.2018.04.008] [Cited by in Crossref: 13] [Cited by in F6Publishing: 11] [Article Influence: 3.3] [Reference Citation Analysis]
10 Zhou J, Liu C, Sun Y, Huang W, Ye K. Cognitive disorders associated with hospitalization of COVID-19: Results from an observational cohort study. Brain Behav Immun 2021;91:383-92. [PMID: 33148439 DOI: 10.1016/j.bbi.2020.10.019] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 5.0] [Reference Citation Analysis]
11 D'Amico F, Skarmoutsou E, Lo LJ, Granata M, Trovato C, Rossi GA, Bellocchi C, Marchini M, Scorza R, Mazzarino MC, Keinan A. Association between rs2294020 in X-linked CCDC22 and susceptibility to autoimmune diseases with focus on systemic lupus erythematosus. Immunol Lett 2017;181:58-62. [PMID: 27888057 DOI: 10.1016/j.imlet.2016.11.011] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
12 Credendino SC, Neumayer C, Cantone I. Genetics and Epigenetics of Sex Bias: Insights from Human Cancer and Autoimmunity. Trends Genet 2020;36:650-63. [PMID: 32736810 DOI: 10.1016/j.tig.2020.06.016] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
13 Luciano M, Davies G, Summers KM, Hill WD, Hayward C, Liewald DC, Porteous DJ, Gale CR, McIntosh AM, Deary IJ. The influence of X chromosome variants on trait neuroticism. Mol Psychiatry 2021;26:483-91. [PMID: 30842574 DOI: 10.1038/s41380-019-0388-2] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
14 Zhu J, Zhou Q, Xia Y, Lin L, Li J, Peng M, Zhang R, Zhang M. GIT/PIX Condensates Are Modular and Ideal for Distinct Compartmentalized Cell Signaling. Molecular Cell 2020;79:782-796.e6. [DOI: 10.1016/j.molcel.2020.07.004] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 4.5] [Reference Citation Analysis]
15 Yap CX, Sidorenko J, Wu Y, Kemper KE, Yang J, Wray NR, Robinson MR, Visscher PM. Dissection of genetic variation and evidence for pleiotropy in male pattern baldness. Nat Commun 2018;9:5407. [PMID: 30573740 DOI: 10.1038/s41467-018-07862-y] [Cited by in Crossref: 24] [Cited by in F6Publishing: 21] [Article Influence: 6.0] [Reference Citation Analysis]
16 [DOI: 10.1101/346940] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
17 Kukurba KR, Parsana P, Balliu B, Smith KS, Zappala Z, Knowles DA, Favé MJ, Davis JR, Li X, Zhu X, Potash JB, Weissman MM, Shi J, Kundaje A, Levinson DF, Awadalla P, Mostafavi S, Battle A, Montgomery SB. Impact of the X Chromosome and sex on regulatory variation. Genome Res 2016;26:768-77. [PMID: 27197214 DOI: 10.1101/gr.197897.115] [Cited by in Crossref: 57] [Cited by in F6Publishing: 48] [Article Influence: 9.5] [Reference Citation Analysis]
18 Xu W, Hao M. A unified partial likelihood approach for X-chromosome association on time-to-event outcomes. Genet Epidemiol 2018;42:80-94. [DOI: 10.1002/gepi.22097] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 1.8] [Reference Citation Analysis]
19 Gordon D, Londono D, Patel P, Kim W, Finch SJ, Heiman GA. An Analytic Solution to the Computation of Power and Sample Size for Genetic Association Studies under a Pleiotropic Mode of Inheritance. Hum Hered 2016;81:194-209. [PMID: 28315880 DOI: 10.1159/000457135] [Cited by in Crossref: 2] [Article Influence: 0.4] [Reference Citation Analysis]
20 Cummings RD. "Stuck on sugars - how carbohydrates regulate cell adhesion, recognition, and signaling". Glycoconj J 2019;36:241-57. [PMID: 31267247 DOI: 10.1007/s10719-019-09876-0] [Cited by in Crossref: 41] [Cited by in F6Publishing: 32] [Article Influence: 13.7] [Reference Citation Analysis]
21 . Accounting for sex in the genome. Nat Med 2017;23:1243-1243. [DOI: 10.1038/nm.4445] [Cited by in Crossref: 30] [Cited by in F6Publishing: 25] [Article Influence: 6.0] [Reference Citation Analysis]
22 Ma L, Hoffman G, Keinan A. X-inactivation informs variance-based testing for X-linked association of a quantitative trait. BMC Genomics 2015;16:241. [PMID: 25880738 DOI: 10.1186/s12864-015-1463-y] [Cited by in Crossref: 15] [Cited by in F6Publishing: 13] [Article Influence: 2.1] [Reference Citation Analysis]
23 Chiaroni-clarke RC, Munro JE, Ellis JA. Sex bias in paediatric autoimmune disease – Not just about sex hormones? Journal of Autoimmunity 2016;69:12-23. [DOI: 10.1016/j.jaut.2016.02.011] [Cited by in Crossref: 17] [Cited by in F6Publishing: 14] [Article Influence: 2.8] [Reference Citation Analysis]
24 Basit S, Al-Edressi HM, Sairafi MH, Hashmi JA, Alharby E, Safar R, Ramzan K. Centromere protein I (CENPI) is a candidate gene for X-linked steroid sensitive nephrotic syndrome. J Nephrol 2020;33:763-9. [PMID: 31912435 DOI: 10.1007/s40620-019-00692-1] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
25 Mirkov MU, Verstockt B, Cleynen I. Genetics of inflammatory bowel disease: beyond NOD2. Lancet Gastroenterol Hepatol. 2017;2:224-234. [PMID: 28404137 DOI: 10.1016/s2468-1253(16)30111-x] [Cited by in Crossref: 58] [Cited by in F6Publishing: 32] [Article Influence: 11.6] [Reference Citation Analysis]
26 Gerussi A, Carbone M, Corpechot C, Schramm C, Asselta R, Invernizzi P. The genetic architecture of primary biliary cholangitis. Eur J Med Genet 2021;64:104292. [PMID: 34303876 DOI: 10.1016/j.ejmg.2021.104292] [Reference Citation Analysis]
27 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]
28 You XP, Zou QL, Li JL, Zhou JY. Likelihood Ratio Test for Excess Homozygosity at Marker Loci on X Chromosome. PLoS One 2015;10:e0145032. [PMID: 26671781 DOI: 10.1371/journal.pone.0145032] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.7] [Reference Citation Analysis]
29 Zeng J, Aryal RP, Stavenhagen K, Luo C, Liu R, Wang X, Chen J, Li H, Matsumoto Y, Wang Y, Wang J, Ju T, Cummings RD. Cosmc deficiency causes spontaneous autoimmunity by breaking B cell tolerance. Sci Adv 2021;7:eabg9118. [PMID: 34613773 DOI: 10.1126/sciadv.abg9118] [Reference Citation Analysis]
30 Snell DM, Turner JMA. Sex Chromosome Effects on Male-Female Differences in Mammals. Curr Biol 2018;28:R1313-24. [PMID: 30458153 DOI: 10.1016/j.cub.2018.09.018] [Cited by in Crossref: 35] [Cited by in F6Publishing: 27] [Article Influence: 8.8] [Reference Citation Analysis]
31 Stein MM, Conery M, Magnaye KM, Clay SM, Billstrand C, Nicolae R, Naughton K, Ober C, Thompson EE. Sex-specific differences in peripheral blood leukocyte transcriptional response to LPS are enriched for HLA region and X chromosome genes. Sci Rep 2021;11:1107. [PMID: 33441806 DOI: 10.1038/s41598-020-80145-z] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
32 Kang Y, Park H, Choe B, Kang B. The Role and Function of Mucins and Its Relationship to Inflammatory Bowel Disease. Front Med 2022;9:848344. [DOI: 10.3389/fmed.2022.848344] [Reference Citation Analysis]
33 Haltrich I, Pikó H, Pamjav H, Somogyi A, Völgyi A, David D, Beke A, Garamvölgyi Z, Kiss E, Karcagi V, Fekete G. Complex X chromosome rearrangement associated with multiorgan autoimmunity. Mol Cytogenet 2015;8:51. [PMID: 26191082 DOI: 10.1186/s13039-015-0152-5] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
34 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]
35 Winham SJ, Jenkins GD, Biernacka JM. Modeling X Chromosome Data Using Random Forests: Conquering Sex Bias. Genet Epidemiol 2016;40:123-32. [PMID: 26639183 DOI: 10.1002/gepi.21946] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.6] [Reference Citation Analysis]
36 Loley C, Alver M, Assimes TL, Bjonnes A, Goel A, Gustafsson S, Hernesniemi J, Hopewell JC, Kanoni S, Kleber ME, Lau KW, Lu Y, Lyytikäinen LP, Nelson CP, Nikpay M, Qu L, Salfati E, Scholz M, Tukiainen T, Willenborg C, Won HH, Zeng L, Zhang W, Anand SS, Beutner F, Bottinger EP, Clarke R, Dedoussis G, Do R, Esko T, Eskola M, Farrall M, Gauguier D, Giedraitis V, Granger CB, Hall AS, Hamsten A, Hazen SL, Huang J, Kähönen M, Kyriakou T, Laaksonen R, Lind L, Lindgren C, Magnusson PK, Marouli E, Mihailov E, Morris AP, Nikus K, Pedersen N, Rallidis L, Salomaa V, Shah SH, Stewart AF, Thompson JR, Zalloua PA, Chambers JC, Collins R, Ingelsson E, Iribarren C, Karhunen PJ, Kooner JS, Lehtimäki T, Loos RJ, März W, McPherson R, Metspalu A, Reilly MP, Ripatti S, Sanghera DK, Thiery J, Watkins H, Deloukas P, Kathiresan S, Samani NJ, Schunkert H, Erdmann J, König IR. No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis. Sci Rep 2016;6:35278. [PMID: 27731410 DOI: 10.1038/srep35278] [Cited by in Crossref: 19] [Cited by in F6Publishing: 18] [Article Influence: 3.2] [Reference Citation Analysis]
37 de Lange KM, Barrett JC. Understanding inflammatory bowel disease via immunogenetics. J Autoimmun 2015;64:91-100. [PMID: 26257098 DOI: 10.1016/j.jaut.2015.07.013] [Cited by in Crossref: 87] [Cited by in F6Publishing: 81] [Article Influence: 12.4] [Reference Citation Analysis]
38 Brazil JC, Parkos CA. Finding the sweet spot: glycosylation mediated regulation of intestinal inflammation. Mucosal Immunol 2021. [PMID: 34782709 DOI: 10.1038/s41385-021-00466-8] [Reference Citation Analysis]
39 Slavney A, Arbiza L, Clark AG, Keinan A. Strong Constraint on Human Genes Escaping X-Inactivation Is Modulated by their Expression Level and Breadth in Both Sexes. Mol Biol Evol 2016;33:384-93. [PMID: 26494842 DOI: 10.1093/molbev/msv225] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 1.6] [Reference Citation Analysis]
40 Bove R, Gilmore W. Hormones and MS: Risk factors, biomarkers, and therapeutic targets. Mult Scler 2018;24:17-21. [DOI: 10.1177/1352458517737396] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 1.8] [Reference Citation Analysis]
41 Chen Y, Qi X, Bian C, Ling C, Yi T, Mu X, Zhao X. The association of FOXP3 gene polymorphisms with cancer susceptibility: a comprehensive systemic review and meta-analysis. Biosci Rep 2019;39:BSR20181809. [PMID: 30782783 DOI: 10.1042/BSR20181809] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
42 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]
43 Watson HJ, Yilmaz Z, Thornton LM, Hübel C, Coleman JRI, Gaspar HA, Bryois J, Hinney A, Leppä VM, Mattheisen M, Medland SE, Ripke S, Yao S, Giusti-Rodríguez P, Hanscombe KB, Purves KL, Adan RAH, Alfredsson L, Ando T, Andreassen OA, Baker JH, Berrettini WH, Boehm I, Boni C, Perica VB, Buehren K, Burghardt R, Cassina M, Cichon S, Clementi M, Cone RD, Courtet P, Crow S, Crowley JJ, Danner UN, Davis OSP, de Zwaan M, Dedoussis G, Degortes D, DeSocio JE, Dick DM, Dikeos D, Dina C, Dmitrzak-Weglarz M, Docampo E, Duncan LE, Egberts K, Ehrlich S, Escaramís G, Esko T, Estivill X, Farmer A, Favaro A, Fernández-Aranda F, Fichter MM, Fischer K, Föcker M, Foretova L, Forstner AJ, Forzan M, Franklin CS, Gallinger S, Giegling I, Giuranna J, Gonidakis F, Gorwood P, Mayora MG, Guillaume S, Guo Y, Hakonarson H, Hatzikotoulas K, Hauser J, Hebebrand J, Helder SG, Herms S, Herpertz-Dahlmann B, Herzog W, Huckins LM, Hudson JI, Imgart H, Inoko H, Janout V, Jiménez-Murcia S, Julià A, Kalsi G, Kaminská D, Kaprio J, Karhunen L, Karwautz A, Kas MJH, Kennedy JL, Keski-Rahkonen A, Kiezebrink K, Kim YR, Klareskog L, Klump KL, Knudsen GPS, La Via MC, Le Hellard S, Levitan RD, Li D, Lilenfeld L, Lin BD, Lissowska J, Luykx J, Magistretti PJ, Maj M, Mannik K, Marsal S, Marshall CR, Mattingsdal M, McDevitt S, McGuffin P, Metspalu A, Meulenbelt I, Micali N, Mitchell K, Monteleone AM, Monteleone P, Munn-Chernoff MA, Nacmias B, Navratilova M, Ntalla I, O'Toole JK, Ophoff RA, Padyukov L, Palotie A, Pantel J, Papezova H, Pinto D, Rabionet R, Raevuori A, Ramoz N, Reichborn-Kjennerud T, Ricca V, Ripatti S, Ritschel F, Roberts M, Rotondo A, Rujescu D, Rybakowski F, Santonastaso P, Scherag A, Scherer SW, Schmidt U, Schork NJ, Schosser A, Seitz J, Slachtova L, Slagboom PE, Slof-Op 't Landt MCT, Slopien A, Sorbi S, Świątkowska B, Szatkiewicz JP, Tachmazidou I, Tenconi E, Tortorella A, Tozzi F, Treasure J, Tsitsika A, Tyszkiewicz-Nwafor M, Tziouvas K, van Elburg AA, van Furth EF, Wagner G, Walton E, Widen E, Zeggini E, Zerwas S, Zipfel S, Bergen AW, Boden JM, Brandt H, Crawford S, Halmi KA, Horwood LJ, Johnson C, Kaplan AS, Kaye WH, Mitchell JE, Olsen CM, Pearson JF, Pedersen NL, Strober M, Werge T, Whiteman DC, Woodside DB, Stuber GD, Gordon S, Grove J, Henders AK, Juréus A, Kirk KM, Larsen JT, Parker R, Petersen L, Jordan J, Kennedy M, Montgomery GW, Wade TD, Birgegård A, Lichtenstein P, Norring C, Landén M, Martin NG, Mortensen PB, Sullivan PF, Breen G, Bulik CM; Anorexia Nervosa Genetics Initiative., Eating Disorders Working Group of the Psychiatric Genomics Consortium. Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa. Nat Genet 2019;51:1207-14. [PMID: 31308545 DOI: 10.1038/s41588-019-0439-2] [Cited by in Crossref: 236] [Cited by in F6Publishing: 194] [Article Influence: 78.7] [Reference Citation Analysis]
44 Hanes MS, Moremen KW, Cummings RD. Biochemical characterization of functional domains of the chaperone Cosmc. PLoS One 2017;12:e0180242. [PMID: 28665962 DOI: 10.1371/journal.pone.0180242] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 1.8] [Reference Citation Analysis]
45 Chenoweth MJ, Cox LS, Nollen NL, Ahluwalia JS, Benowitz NL, Lerman C, Knight J, Tyndale RF. Analyses of nicotine metabolism biomarker genetics stratified by sex in African and European Americans. Sci Rep 2021;11:19572. [PMID: 34599228 DOI: 10.1038/s41598-021-98883-z] [Reference Citation Analysis]
46 Jin Y, Andersen G, Yorgov D, Ferrara TM, Ben S, Brownson KM, Holland PJ, Birlea SA, Siebert J, Hartmann A, Lienert A, van Geel N, Lambert J, Luiten RM, Wolkerstorfer A, Wietze van der Veen JP, Bennett DC, Taïeb A, Ezzedine K, Kemp EH, Gawkrodger DJ, Weetman AP, Kõks S, Prans E, Kingo K, Karelson M, Wallace MR, McCormack WT, Overbeck A, Moretti S, Colucci R, Picardo M, Silverberg NB, Olsson M, Valle Y, Korobko I, Böhm M, Lim HW, Hamzavi I, Zhou L, Mi QS, Fain PR, Santorico SA, Spritz RA. Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants. Nat Genet 2016;48:1418-24. [PMID: 27723757 DOI: 10.1038/ng.3680] [Cited by in Crossref: 132] [Cited by in F6Publishing: 102] [Article Influence: 22.0] [Reference Citation Analysis]
47 Trincot CE, Caron KM. Lymphatic Function and Dysfunction in the Context of Sex Differences. ACS Pharmacol Transl Sci 2019;2:311-24. [PMID: 32259065 DOI: 10.1021/acsptsci.9b00051] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.7] [Reference Citation Analysis]
48 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]
49 Backenroth D, Carmi S. A test for deviations from expected genotype frequencies on the X chromosome for sex-biased admixed populations. Heredity (Edinb) 2019;123:470-8. [PMID: 31101879 DOI: 10.1038/s41437-019-0233-z] [Cited by in Crossref: 2] [Article Influence: 0.7] [Reference Citation Analysis]
50 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]
51 Li YR, Li J, Zhao SD, Bradfield JP, Mentch FD, Maggadottir SM, Hou C, Abrams DJ, Chang D, Gao F, Guo Y, Wei Z, Connolly JJ, Cardinale CJ, Bakay M, Glessner JT, Li D, Kao C, Thomas KA, Qiu H, Chiavacci RM, Kim CE, Wang F, Snyder J, Richie MD, Flatø B, Førre Ø, Denson LA, Thompson SD, Becker ML, Guthery SL, Latiano A, Perez E, Resnick E, Russell RK, Wilson DC, Silverberg MS, Annese V, Lie BA, Punaro M, Dubinsky MC, Monos DS, Strisciuglio C, Staiano A, Miele E, Kugathasan S, Ellis JA, Munro JE, Sullivan KE, Wise CA, Chapel H, Cunningham-Rundles C, Grant SF, Orange JS, Sleiman PM, Behrens EM, Griffiths AM, Satsangi J, Finkel TH, Keinan A, Prak ET, Polychronakos C, Baldassano RN, Li H, Keating BJ, Hakonarson H. Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. Nat Med 2015;21:1018-27. [PMID: 26301688 DOI: 10.1038/nm.3933] [Cited by in Crossref: 128] [Cited by in F6Publishing: 114] [Article Influence: 18.3] [Reference Citation Analysis]
52 Haller-Kikkatalo K, Alnek K, Metspalu A, Mihailov E, Metsküla K, Kisand K, Pisarev H, Salumets A, Uibo R. Demographic associations for autoantibodies in disease-free individuals of a European population. Sci Rep 2017;7:44846. [PMID: 28349935 DOI: 10.1038/srep44846] [Cited by in Crossref: 14] [Cited by in F6Publishing: 13] [Article Influence: 2.8] [Reference Citation Analysis]
53 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]
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