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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1973 1
1976 2
1977 1
1998 1
2000 3
2002 80
2003 173
2004 179
2005 223
2006 193
2007 216
2008 196
2009 197
2010 242
2011 219
2012 192
2013 152
2014 159
2015 128
2016 113
2017 131
2018 119
2019 133
2020 132
2021 88
2022 29
2023 27
2024 40

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3,003 results

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Page 1
The human Y and inactive X chromosomes similarly modulate autosomal gene expression.
San Roman AK, Skaletsky H, Godfrey AK, Bokil NV, Teitz L, Singh I, Blanton LV, Bellott DW, Pyntikova T, Lange J, Koutseva N, Hughes JF, Brown L, Phou S, Buscetta A, Kruszka P, Banks N, Dutra A, Pak E, Lasutschinkow PC, Keen C, Davis SM, Lin AE, Tartaglia NR, Samango-Sprouse C, Muenke M, Page DC. San Roman AK, et al. Cell Genom. 2024 Jan 10;4(1):100462. doi: 10.1016/j.xgen.2023.100462. Epub 2023 Dec 13. Cell Genom. 2024. PMID: 38190107 Free PMC article.
X-chromosome genetics and human cancer.
Spatz A, Borg C, Feunteun J. Spatz A, et al. Nat Rev Cancer. 2004 Aug;4(8):617-29. doi: 10.1038/nrc1413. Nat Rev Cancer. 2004. PMID: 15286741 Review. No abstract available.
The impact of sex on gene expression across human tissues.
Oliva M, Muñoz-Aguirre M, Kim-Hellmuth S, Wucher V, Gewirtz ADH, Cotter DJ, Parsana P, Kasela S, Balliu B, Viñuela A, Castel SE, Mohammadi P, Aguet F, Zou Y, Khramtsova EA, Skol AD, Garrido-Martín D, Reverter F, Brown A, Evans P, Gamazon ER, Payne A, Bonazzola R, Barbeira AN, Hamel AR, Martinez-Perez A, Soria JM; GTEx Consortium; Pierce BL, Stephens M, Eskin E, Dermitzakis ET, Segrè AV, Im HK, Engelhardt BE, Ardlie KG, Montgomery SB, Battle AJ, Lappalainen T, Guigó R, Stranger BE. Oliva M, et al. Science. 2020 Sep 11;369(6509):eaba3066. doi: 10.1126/science.aba3066. Science. 2020. PMID: 32913072 Free PMC article.
Triple X syndrome: a review of the literature.
Otter M, Schrander-Stumpel CT, Curfs LM. Otter M, et al. Eur J Hum Genet. 2010 Mar;18(3):265-71. doi: 10.1038/ejhg.2009.109. Epub 2009 Jul 1. Eur J Hum Genet. 2010. PMID: 19568271 Free PMC article. Review.
GCTA: a tool for genome-wide complex trait analysis.
Yang J, Lee SH, Goddard ME, Visscher PM. Yang J, et al. Am J Hum Genet. 2011 Jan 7;88(1):76-82. doi: 10.1016/j.ajhg.2010.11.011. Epub 2010 Dec 17. Am J Hum Genet. 2011. PMID: 21167468 Free PMC article.
The contribution of X-linked coding variation to severe developmental disorders.
Martin HC, Gardner EJ, Samocha KE, Kaplanis J, Akawi N, Sifrim A, Eberhardt RY, Tavares ALT, Neville MDC, Niemi MEK, Gallone G, McRae J; Deciphering Developmental Disorders Study; Wright CF, FitzPatrick DR, Firth HV, Hurles ME. Martin HC, et al. Nat Commun. 2021 Jan 27;12(1):627. doi: 10.1038/s41467-020-20852-3. Nat Commun. 2021. PMID: 33504798 Free PMC article.
Targeting Xist with compounds that disrupt RNA structure and X inactivation.
Aguilar R, Spencer KB, Kesner B, Rizvi NF, Badmalia MD, Mrozowich T, Mortison JD, Rivera C, Smith GF, Burchard J, Dandliker PJ, Patel TR, Nickbarg EB, Lee JT. Aguilar R, et al. Nature. 2022 Apr;604(7904):160-166. doi: 10.1038/s41586-022-04537-z. Epub 2022 Mar 30. Nature. 2022. PMID: 35355011
The X chromosome and male infertility.
Vockel M, Riera-Escamilla A, Tüttelmann F, Krausz C. Vockel M, et al. Hum Genet. 2021 Jan;140(1):203-215. doi: 10.1007/s00439-019-02101-w. Epub 2019 Dec 24. Hum Genet. 2021. PMID: 31875237 Free PMC article. Review.
3,003 results