Citations for
1BCORL1
Human X chromosome exome sequencing identifies BCORL1 as contributor to spermatogenesis
Lu C, Zhang Y, Qin Y, Xu Q, Zhou R, Cui Y, Zhu Y, Zhang X, Zhang J, Wei X, Wang M, Hang B, Mao JH, Snijders AM, Liu M, Hu Z, Shen H, Zhou Z, Guo X, Wu X, Wang X, Xia Y.
J Med Genet. Jan;58(1):56-65. doi: 10.1136/jmedgenet-2019-106598.Epub 2020 May 6. 2021
2BCOR, BCORL1
Age-Related Co-Expression of BCOR and BCORL1 mRNA in Acute Myeloid Leukemia
Coskun FR, Percin-Pacal F, Emrence Z, Ar MC, Abaci N, Unuvar A, Eskazan AE, Elverdi T, Salihoglu A, Seflekci Y, Karakas Z, Soysal T, Sirma-Ekmekci S.
Clin Lab. Aug 1;66(8). doi: 10.7754/Clin.Lab.2020.191119. 2020
3BCORL1, IDBDD
Variants in the transcriptional corepressor BCORL1 are associated with an X-linked disorder of intellectual disability, dysmorphic features, and behavioral abnormalities
Shukla A, Girisha KM, Somashekar PH, Nampoothiri S, McClellan R, Vernon HJ.
Am J Med Genet A. May;179(5):870-874. doi: 10.1002/ajmg.a.61118. Epub 2019 Apr 2 2019
4BCOR, BCORL1
Usefulness of BCOR gene mutation as a prognostic factor in acute myeloid leukemia with intermediate cytogenetic prognosis
Terada K, Yamaguchi H, Ueki T, Usuki K, Kobayashi Y, Tajika K, Gomi S, Kurosawa S, Saito R, Furuta Y, Miyadera K, Tokura T, Marumo A, Omori I, Sakaguchi M, Fujiwara Y, Yui S, Ryotokuji T, Arai K, Kitano T, Wakita S, Fukuda T, Inokuchi K
Genes Chromosomes Cancer. Aug;57(8):401-408. doi: 10.1002/gcc.22542. 2018
5BCOR, BCORL1
Whole-exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemia
Shiba N, Yoshida K, Shiraishi Y, Okuno Y, Yamato G, Hara Y, Nagata Y, Chiba K, Tanaka H, Terui K, Kato M, Park MJ, Ohki K, Shimada A, Takita J, Tomizawa D, Kudo K, Arakawa H, Adachi S, Taga T, Tawa A, Ito E, Horibe K, Sanada M, Miyano S, Ogawa S, Hayashi Y.
Br J Haematol. Nov;175(3):476-489. doi: 10.1111/bjh.14247. Epub 2016 Jul 29. 2016
6BCORL1
Age-related mutations associated with clonal hematopoietic expansion and malignancies
Xie M, Lu C, Wang J, McLellan MD, Johnson KJ, Wendl MC, McMichael JF, Schmidt HK, Yellapantula V, Miller CA, Ozenberger BA, Welch JS, Link DC, Walter MJ, Mardis ER, Dipersio JF, Chen F, Wilson RK, Ley TJ, Ding L
Nat Med. Dec;20(12):1472-8. doi: 10.1038/nm.3733. Epub 2014 Oct 19 2014
7BCORL1, CRTRD, DDHD2, IDBDD, MCM3AP, PNRIID, PTPRT, SLC6A8, SPG54, SYNE1, ZNF528
Identification of pathogenic gene variants in small families with intellectually disabled siblings by exome sequencing.
Schuurs-Hoeijmakers JH, Vulto-van Silfhout AT, Vissers LE, van de Vondervoort II, van Bon BW, de Ligt J, Gilissen C, Hehir-Kwa JY, Neveling K, del Rosario M, Hira G, Reitano S, Vitello A, Failla P, Greco D, Fichera M, Galesi O, Kleefstra T, Greally MT, Ockeloen CW, Willemsen MH, Bongers EM, Janssen IM, Pfundt R, Veltman JA, Romano C, Willemsen MA, van Bokhoven H, Brunner HG, de Vries BB, de Brouwer AP.
J Med Genet. Dec;50(12):802-11. doi: 10.1136/jmedgenet-2013-101644. Epub 2013 Oct 11. 2013
8BCORL1
A novel corepressor, BCoR-L1, represses transcription through an interaction with CtBP.
Pagan JK, Arnold J, Hanchard KJ, Kumar R, Bruno T, Jones MJ, Richard DJ, Forrest A, Spurdle A, Verdin E, Crossley M, Fanciulli M, Chenevix-Trench G, Young DB, Khanna KK.
J Biol Chem 282(20):15248-57. Epub 2007 Mar 22. 2007
9BCORL1
BCoR-L1 variation and breast cancer.
Lose F, Arnold J, Young DB, Brown CJ, Mann GJ, Pupo GM; Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer, Khanna KK, Chenevix-Trench G, Spurdle AB.
Breast Cancer Res 9(4):R54. 2007
10BCORL1, ELF4, POF1, SASH3, ZDHHC9
X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genes.
Mumm S, Herrera L, Waeltz PW, Scardovi A, Nagaraja R, Esposito T, Schlessinger D, Rocchi M, Forabosco A.
Genomics 76(1-3):30-6. 2001