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Items: 1 to 20 of 99

1.

Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits.

Rafnar T, Gunnarsson B, Stefansson OA, Sulem P, Ingason A, Frigge ML, Stefansdottir L, Sigurdsson JK, Tragante V, Steinthorsdottir V, Styrkarsdottir U, Stacey SN, Gudmundsson J, Arnadottir GA, Oddsson A, Zink F, Halldorsson G, Sveinbjornsson G, Kristjansson RP, Davidsson OB, Salvarsdottir A, Thoroddsen A, Helgadottir EA, Kristjansdottir K, Ingthorsson O, Gudmundsson V, Geirsson RT, Arnadottir R, Gudbjartsson DF, Masson G, Asselbergs FW, Jonasson JG, Olafsson K, Thorsteinsdottir U, Halldorsson BV, Thorleifsson G, Stefansson K.

Nat Commun. 2018 Sep 7;9(1):3636. doi: 10.1038/s41467-018-05428-6.

2.

Genetic predisposition to uterine leiomyoma is determined by loci for genitourinary development and genome stability.

Välimäki N, Kuisma H, Pasanen A, Heikinheimo O, Sjöberg J, Bützow R, Sarvilinna N, Heinonen HR, Tolvanen J, Bramante S, Tanskanen T, Auvinen J, Uimari O, Alkodsi A, Lehtonen R, Kaasinen E, Palin K, Aaltonen LA.

Elife. 2018 Sep 18;7. pii: e37110. doi: 10.7554/eLife.37110.

3.

Characterization of uterine leiomyomas by whole-genome sequencing.

Mehine M, Kaasinen E, Mäkinen N, Katainen R, Kämpjärvi K, Pitkänen E, Heinonen HR, Bützow R, Kilpivaara O, Kuosmanen A, Ristolainen H, Gentile M, Sjöberg J, Vahteristo P, Aaltonen LA.

N Engl J Med. 2013 Jul 4;369(1):43-53. doi: 10.1056/NEJMoa1302736. Epub 2013 Jun 5.

4.

Polymorphic (CAG)n repeats in the androgen receptor gene: a risk marker for endometriosis and uterine leiomyomas.

Shaik NA, Govindan S, Kodati V, Rao KP, Hasan Q.

Hematol Oncol Stem Cell Ther. 2009;2(1):289-93.

5.

Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets.

Rahmioglu N, Nyholt DR, Morris AP, Missmer SA, Montgomery GW, Zondervan KT.

Hum Reprod Update. 2014 Sep-Oct;20(5):702-16. doi: 10.1093/humupd/dmu015. Epub 2014 Mar 27.

6.

Genetic Association Studies in Uterine Fibroids: Risk Alleles Presage the Path to Personalized Therapies.

Gallagher CS, Morton CC.

Semin Reprod Med. 2016 Jul;34(4):235-41. doi: 10.1055/s-0036-1585401. Epub 2016 Aug 11. Review.

PMID:
27513025
7.

Genotype distribution of estrogen receptor-alpha, catechol-O-methyltransferase, and cytochrome P450 17 gene polymorphisms in Caucasian women with uterine leiomyomas.

Denschlag D, Bentz EK, Hefler L, Pietrowski D, Zeillinger R, Tempfer C, Tong D.

Fertil Steril. 2006 Feb;85(2):462-7.

PMID:
16595228
8.

Epidemiological and genetic clues for molecular mechanisms involved in uterine leiomyoma development and growth.

Commandeur AE, Styer AK, Teixeira JM.

Hum Reprod Update. 2015 Sep-Oct;21(5):593-615. doi: 10.1093/humupd/dmv030. Epub 2015 Jul 3. Review.

9.

Aberrant DNA methylation status in human uterine leiomyoma.

Yamagata Y, Maekawa R, Asada H, Taketani T, Tamura I, Tamura H, Ogane J, Hattori N, Shiota K, Sugino N.

Mol Hum Reprod. 2009 Apr;15(4):259-67. doi: 10.1093/molehr/gap010. Epub 2009 Feb 14.

PMID:
19218588
10.

Analysis of potential protein-modifying variants in 9000 endometriosis patients and 150000 controls of European ancestry.

Sapkota Y, Vivo I, Steinthorsdottir V, Fassbender A, Bowdler L, Buring JE, Edwards TL, Jones S, O D, Peterse D, Rexrode KM, Ridker PM, Schork AJ, Thorleifsson G, Wallace LM; iPSYCH-SSI-Broad Group, Kraft P, Morris AP, Nyholt DR, Edwards DRV, Nyegaard M, D'Hooghe T, Chasman DI, Stefansson K, Missmer SA, Montgomery GW.

Sci Rep. 2017 Sep 12;7(1):11380. doi: 10.1038/s41598-017-10440-9.

11.

Association between HSD17B1 rs605059 polymorphisms and the risk of uterine diseases: a systemic review and meta-analysis.

Mu X, Du X, Yao K, Zhao J, Bian C, Wang Q, Ma H, Yi T, Wu Y, Zhao X.

Int J Clin Exp Pathol. 2015 Jun 1;8(6):6012-8. eCollection 2015. Review.

12.

Variants in BET1L and TNRC6B associate with increasing fibroid volume and fibroid type among European Americans.

Edwards TL, Hartmann KE, Velez Edwards DR.

Hum Genet. 2013 Dec;132(12):1361-9. doi: 10.1007/s00439-013-1340-1. Epub 2013 Jul 28.

13.

Analysis of MED12 Mutation in Multiple Uterine Leiomyomas in South Korean patients.

Lee M, Cheon K, Chae B, Hwang H, Kim HK, Chung YJ, Song JY, Cho HH, Kim JH, Kim MR.

Int J Med Sci. 2018 Jan 1;15(2):124-128. doi: 10.7150/ijms.21856. eCollection 2018.

14.

Genome-wide association meta-analysis identifies new endometriosis risk loci.

Nyholt DR, Low SK, Anderson CA, Painter JN, Uno S, Morris AP, MacGregor S, Gordon SD, Henders AK, Martin NG, Attia J, Holliday EG, McEvoy M, Scott RJ, Kennedy SH, Treloar SA, Missmer SA, Adachi S, Tanaka K, Nakamura Y, Zondervan KT, Zembutsu H, Montgomery GW.

Nat Genet. 2012 Dec;44(12):1355-9. doi: 10.1038/ng.2445. Epub 2012 Oct 28.

15.

African ancestry and genetic risk for uterine leiomyomata.

Wise LA, Ruiz-Narvaez EA, Palmer JR, Cozier YC, Tandon A, Patterson N, Radin RG, Rosenberg L, Reich D.

Am J Epidemiol. 2012 Dec 15;176(12):1159-68. doi: 10.1093/aje/kws276. Epub 2012 Nov 15.

16.

Estrogen receptor alpha polymorphism and susceptibility to uterine leiomyoma.

Villanova FE, Andrade PM, Otsuka AY, Gomes MT, Leal ES, Castro RA, Girão MJ, Nishimura E, Baracat EC, Silva ID.

Steroids. 2006 Nov;71(11-12):960-5. Epub 2006 Aug 28.

PMID:
16935316
17.

A possible role of the cytochrome P450c17alpha gene (CYP17) polymorphism in the pathobiology of uterine leiomyomas from black South African women: a pilot study.

Amant F, Dorfling CM, de Brabanter J, Vandewalle J, Vergote I, Lindeque BG, van Rensburg EJ.

Acta Obstet Gynecol Scand. 2004 Mar;83(3):234-9.

PMID:
14995917
18.

Highly heterogeneous genomic landscape of uterine leiomyomas by whole exome sequencing and genome-wide arrays.

Yatsenko SA, Mittal P, Wood-Trageser MA, Jones MW, Surti U, Edwards RP, Sood AK, Rajkovic A.

Fertil Steril. 2017 Feb;107(2):457-466.e9. doi: 10.1016/j.fertnstert.2016.10.035. Epub 2016 Nov 23.

PMID:
27889101
19.

Genome-wide DNA methylation analysis reveals a potential mechanism for the pathogenesis and development of uterine leiomyomas.

Maekawa R, Sato S, Yamagata Y, Asada H, Tamura I, Lee L, Okada M, Tamura H, Takaki E, Nakai A, Sugino N.

PLoS One. 2013 Jun 20;8(6):e66632. doi: 10.1371/journal.pone.0066632. Print 2013.

20.

A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids.

Edwards TL, Giri A, Hellwege JN, Hartmann KE, Stewart EA, Jeff JM, Bray MJ, Pendergrass SA, Torstenson ES, Keaton JM, Jones SH, Gogoi RP, Kuivaniemi H, Jackson KL, Kho AN, Kullo IJ, McCarty CA, Im HK, Pacheco JA, Pathak J, Williams MS, Tromp G, Kenny EE, Peissig PL, Denny JC, Roden DM, Velez Edwards DR.

Front Genet. 2019 Jun 12;10:511. doi: 10.3389/fgene.2019.00511. eCollection 2019.

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