Similar articles for PMID: 25677961

Year	Number of Results
1998	1
2004	2
2005	1
2008	1
2009	1
2010	7
2011	6
2012	7
2013	16
2014	12
2015	12
2016	3
2017	3
2018	3
2019	3
2020	2
2021	2
2022	2
2024	0

1

Xq25 duplication: the crucial role of the STAG2 gene in this novel human cohesinopathy.

Leroy C, Jacquemont ML, Doray B, Lamblin D, Cormier-Daire V, Philippe A, Nusbaum S, Patrat C, Steffann J, Colleaux L, Vekemans M, Romana S, Turleau C, Malan V. Leroy C, et al. Clin Genet. 2016 Jan;89(1):68-73. doi: 10.1111/cge.12567. Epub 2015 Mar 5. Clin Genet. 2016. PMID: 25677961

2

Definition of minimal duplicated region encompassing the XIAP and STAG2 genes in the Xq25 microduplication syndrome.

Di Benedetto D, Musumeci SA, Avola E, Alberti A, Buono S, Scuderi C, Grillo L, Galesi O, Spalletta A, Giudice ML, Luciano D, Vinci M, Bianca S, Romano C, Fichera M. Di Benedetto D, et al. Am J Med Genet A. 2014 Aug;164A(8):1923-30. doi: 10.1002/ajmg.a.36570. Epub 2014 Apr 14. Am J Med Genet A. 2014. PMID: 24733578

3

Microduplication of chromosome Xq25 encompassing STAG2 gene in a boy with intellectual disability.

Yingjun X, Wen T, Yujian L, Lingling X, Huimin H, Qun F, Junhong C. Yingjun X, et al. Eur J Med Genet. 2015 Feb;58(2):116-21. doi: 10.1016/j.ejmg.2014.10.002. Epub 2014 Oct 24. Eur J Med Genet. 2015. PMID: 25450604

4

Xq25 duplications encompassing GRIA3 and STAG2 genes in two families convey recognizable X-linked intellectual disability with distinctive facial appearance.

Philippe A, Malan V, Jacquemont ML, Boddaert N, Bonnefont JP, Odent S, Munnich A, Colleaux L, Cormier-Daire V. Philippe A, et al. Am J Med Genet A. 2013 Jun;161A(6):1370-5. doi: 10.1002/ajmg.a.35307. Epub 2013 May 1. Am J Med Genet A. 2013. PMID: 23637084

5

Increased STAG2 dosage defines a novel cohesinopathy with intellectual disability and behavioral problems.

Kumar R, Corbett MA, Van Bon BW, Gardner A, Woenig JA, Jolly LA, Douglas E, Friend K, Tan C, Van Esch H, Holvoet M, Raynaud M, Field M, Leffler M, Budny B, Wisniewska M, Badura-Stronka M, Latos-Bieleńska A, Batanian J, Rosenfeld JA, Basel-Vanagaite L, Jensen C, Bienek M, Froyen G, Ullmann R, Hu H, Love MI, Haas SA, Stankiewicz P, Cheung SW, Baxendale A, Nicholl J, Thompson EM, Haan E, Kalscheuer VM, Gecz J. Kumar R, et al. Hum Mol Genet. 2015 Dec 20;24(25):7171-81. doi: 10.1093/hmg/ddv414. Epub 2015 Oct 6. Hum Mol Genet. 2015. PMID: 26443594

6

Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions.

El-Hattab AW, Fang P, Jin W, Hughes JR, Gibson JB, Patel GS, Grange DK, Manwaring LP, Patel A, Stankiewicz P, Cheung SW. El-Hattab AW, et al. J Med Genet. 2011 Dec;48(12):840-50. doi: 10.1136/jmedgenet-2011-100125. Epub 2011 Oct 8. J Med Genet. 2011. PMID: 21984752 Free article.

7

Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?

Li F, Shen Y, Köhler U, Sharkey FH, Menon D, Coulleaux L, Malan V, Rio M, McMullan DJ, Cox H, Fagan KA, Gaunt L, Metcalfe K, Heinrich U, Hislop G, Maye U, Sutcliffe M, Wu BL, Thiel BD, Mulchandani S, Conlin LK, Spinner NB, Murphy KM, Batista DA. Li F, et al. Eur J Med Genet. 2010 Mar-Apr;53(2):93-9. doi: 10.1016/j.ejmg.2010.01.004. Epub 2010 Feb 2. Eur J Med Genet. 2010. PMID: 20132918

8

Xq12q13.1 microduplication encompassing the EFNB1 gene in a boy with congenital diaphragmatic hernia.

Petit F, Andrieux J, Holder-Espinasse M, Bouquillon S, Pennaforte T, Storme L, Manouvrier-Hanu S. Petit F, et al. Eur J Med Genet. 2011 Sep-Oct;54(5):e525-7. doi: 10.1016/j.ejmg.2011.06.011. Epub 2011 Jul 14. Eur J Med Genet. 2011. PMID: 21782985

9

STAG2 microduplication in a patient with eyelid myoclonia and absences and a review of EMA-related reported genes.

Gokce-Samar Z, de Bellescize J, Arzimanoglou A, Putoux A, Chatron N, Lesca G, Portes VD. Gokce-Samar Z, et al. Eur J Med Genet. 2022 Dec;65(12):104636. doi: 10.1016/j.ejmg.2022.104636. Epub 2022 Oct 7. Eur J Med Genet. 2022. PMID: 36216271 Review.

10

Clinical characterization of int22h1/int22h2-mediated Xq28 duplication/deletion: new cases and literature review.

El-Hattab AW, Schaaf CP, Fang P, Roeder E, Kimonis VE, Church JA, Patel A, Cheung SW. El-Hattab AW, et al. BMC Med Genet. 2015 Mar 14;16:12. doi: 10.1186/s12881-015-0157-2. BMC Med Genet. 2015. PMID: 25927380 Free PMC article.

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