PubMed for id: 9968

Year	Number of Results
1993	1
1996	4
1997	2
1998	1
1999	4
2000	1
2001	2
2002	9
2003	8
2004	3
2005	4
2006	8
2007	6
2008	8
2009	3
2010	5
2011	6
2012	12
2013	19
2014	14
2015	30
2016	18
2017	19
2018	20
2019	9
2020	16
2021	21
2022	23
2023	10
2024	7

1

Racial disparity in uterine leiomyoma: new insights of genetic and environmental burden in myometrial cells.

Khan NH, McNally R, Kim JJ, Wei JJ. Khan NH, et al. Mol Hum Reprod. 2024 Feb 29;30(3):gaae004. doi: 10.1093/molehr/gaae004. Mol Hum Reprod. 2024. PMID: 38290796 Review.

2

The Effect of Race/Ethnicity and MED12 Mutation on the Expression of Long Non-Coding RNAs in Uterine Leiomyoma and Myometrium.

Chuang TD, Ton N, Rysling S, Boos D, Khorram O. Chuang TD, et al. Int J Mol Sci. 2024 Jan 21;25(2):1307. doi: 10.3390/ijms25021307. Int J Mol Sci. 2024. PMID: 38279317 Free PMC article.

3

Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathy.

Ghasemi S, Mahdavi M, Maleki M, Salahshourifar I, Kalayinia S. Ghasemi S, et al. BMC Med Genomics. 2023 Dec 21;16(1):334. doi: 10.1186/s12920-023-01780-9. BMC Med Genomics. 2023. PMID: 38129817 Free PMC article.

4

RISING STARS: Role of MED12 mutation in the pathogenesis of uterine fibroids.

Ishikawa H, Kobayashi T, Kaneko M, Saito Y, Shozu M, Koga K. Ishikawa H, et al. J Mol Endocrinol. 2023 Sep 29;71(4):e230039. doi: 10.1530/JME-23-0039. Print 2023 Nov 1. J Mol Endocrinol. 2023. PMID: 37668348

5

The Mediator Complex Subunit 12 (MED-12) Gene and Uterine Fibroids: a Systematic Review.

Amendola ILS, Spann M, Segars J, Singh B. Amendola ILS, et al. Reprod Sci. 2024 Feb;31(2):291-308. doi: 10.1007/s43032-023-01297-7. Epub 2023 Jul 29. Reprod Sci. 2024. PMID: 37516697 Review.

6

MED12 variants associated with X-linked recessive partial epilepsy without intellectual disability.

Yang JH, Liu ZG, Liu CL, Zhang MR, Jia YL, Zhai QX, He MF, He N, Qiao JD. Yang JH, et al. Seizure. 2024 Mar;116:30-36. doi: 10.1016/j.seizure.2023.02.018. Epub 2023 Feb 27. Seizure. 2024. PMID: 36894399

7

Differential Expression of MED12-Associated Coding RNA Transcripts in Uterine Leiomyomas.

Chuang TD, Gao J, Quintanilla D, McSwiggin H, Boos D, Yan W, Khorram O. Chuang TD, et al. Int J Mol Sci. 2023 Feb 13;24(4):3742. doi: 10.3390/ijms24043742. Int J Mol Sci. 2023. PMID: 36835153 Free PMC article.

8

XLID syndrome gene Med12 promotes Ig isotype switching through chromatin modification and enhancer RNA regulation.

Haque F, Honjo T, Begum NA. Haque F, et al. Sci Adv. 2022 Nov 25;8(47):eadd1466. doi: 10.1126/sciadv.add1466. Epub 2022 Nov 25. Sci Adv. 2022. PMID: 36427307 Free PMC article.

9

MED12 mutation as a potential predictive biomarker for immune checkpoint inhibitors in pan-cancer.

Zhou Y, Tan Y, Zhang Q, Duan Q, Chen J. Zhou Y, et al. Eur J Med Res. 2022 Oct 29;27(1):225. doi: 10.1186/s40001-022-00856-z. Eur J Med Res. 2022. PMID: 36309740 Free PMC article.

10

Missense MED12 variants in 22 males with intellectual disability: From nonspecific symptoms to complete syndromes.

Maia N, Ibarluzea N, Misra-Isrie M, Koboldt DC, Marques I, Soares G, Santos R, Marcelis CLM, Keski-Filppula R, Guitart M, Gabau Vila E, Lehman A, Hickey S, Mori M, Terhal P, Valenzuela I, Lasa-Aranzasti A, Cueto-González AM, Chhouk BH, Yeh RC, Neil JE, Abu-Libde B, Kleefstra T, Elting MW, Császár A, Kárteszi J, Bessenyei B, van Bokhoven H, Jorge P, van Hagen JM, de Brouwer APM. Maia N, et al. Am J Med Genet A. 2023 Jan;191(1):135-143. doi: 10.1002/ajmg.a.63004. Epub 2022 Oct 22. Am J Med Genet A. 2023. PMID: 36271811 Free PMC article.

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