Similar articles for PMID: 25676666

Year	Number of Results
1948	1
1985	1
1987	2
1995	2
1996	2
1997	2
1999	2
2000	5
2001	3
2002	1
2003	1
2004	4
2005	1
2006	10
2007	7
2008	8
2009	5
2010	15
2011	14
2012	4
2013	8
2014	5
2015	3
2016	1
2017	3
2019	1
2020	5
2021	2
2024	0

1

Premature ovarian failure caused by a heterozygous missense mutation in POF1B and a reciprocal translocation 46,X,t(X;3)(q21.1;q21.3).

Ledig S, Preisler-Adams S, Morlot S, Liehr T, Wieacker P. Ledig S, et al. Sex Dev. 2015;9(2):86-90. doi: 10.1159/000373906. Epub 2015 Feb 11. Sex Dev. 2015. PMID: 25676666

2

A teenager with a t(X;17)(q22;q25) and ovarian failure.

Martínez-Valenzuela M, Rivera H, Mundo-Ayala JN, González-Mercado MG, Davalos-Rodríguez IP. Martínez-Valenzuela M, et al. Genet Couns. 2010;21(3):269-75. Genet Couns. 2010. PMID: 20964116

3

Translocation t(X;11)(q22;q25) in a woman with premature ovarian failure.

Saranya B, Kavitha Devi D, Chandra RS, Jayashankar M, Santhiya ST. Saranya B, et al. Sex Dev. 2013;7(4):216-21. doi: 10.1159/000346958. Epub 2013 Feb 16. Sex Dev. 2013. PMID: 23429171

4

Disruption of HDX gene in premature ovarian failure.

Okten G, Gunes S, Onat OE, Tukun A, Ozcelik T, Kocak I. Okten G, et al. Syst Biol Reprod Med. 2013 Aug;59(4):218-22. doi: 10.3109/19396368.2013.769028. Epub 2013 Feb 26. Syst Biol Reprod Med. 2013. PMID: 23441923

5

Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B.

Bione S, Rizzolio F, Sala C, Ricotti R, Goegan M, Manzini MC, Battaglia R, Marozzi A, Vegetti W, Dalprà L, Crosignani PG, Ginelli E, Nappi R, Bernabini S, Bruni V, Torricelli F, Zuffardi O, Toniolo D. Bione S, et al. Hum Reprod. 2004 Dec;19(12):2759-66. doi: 10.1093/humrep/deh502. Epub 2004 Sep 30. Hum Reprod. 2004. PMID: 15459172

6

Disruption of POF1B binding to nonmuscle actin filaments is associated with premature ovarian failure.

Lacombe A, Lee H, Zahed L, Choucair M, Muller JM, Nelson SF, Salameh W, Vilain E. Lacombe A, et al. Am J Hum Genet. 2006 Jul;79(1):113-9. doi: 10.1086/505406. Epub 2006 May 26. Am J Hum Genet. 2006. PMID: 16773570 Free PMC article.

7

Premature ovarian failure with 46,XX,t(1;4)(p34.1;q34): first case report and literature review.

Vichinsartvichai P, Manolertthewan C, Promrungrueng P. Vichinsartvichai P, et al. Climacteric. 2015;18(4):656-8. doi: 10.3109/13697137.2014.992013. Epub 2015 Feb 4. Climacteric. 2015. PMID: 25427618 Review.

8

The first case described: monozygotic twin sisters with the fragile X premutation but with a different phenotype for premature ovarian failure.

Johnston-MacAnanny EB, Koty P, Pettenati M, Brady M, Yalcinkaya TM, Schmidt DW. Johnston-MacAnanny EB, et al. Fertil Steril. 2011 Jun;95(7):2431.e13-5. doi: 10.1016/j.fertnstert.2011.01.039. Epub 2011 Feb 5. Fertil Steril. 2011. PMID: 21300345 Free article.

9

[Xq;Yq translocation in a patient with premature ovarian insufficiency].

Yang S, Zhang Y, Hu J, Hu R, Jia Z, Xi H, Wang H. Yang S, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Sep 10;37(9):942-945. doi: 10.3760/cma.j.cn511374-20191001-00505. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32820504 Chinese.

10

Skewed X chromosome inactivation and breast and ovarian cancer status: evidence for X-linked modifiers of BRCA1.

Lose F, Duffy DL, Kay GF, Kedda MA, Spurdle AB; Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer; Australian Ovarian Cancer Study Management Group. Lose F, et al. J Natl Cancer Inst. 2008 Nov 5;100(21):1519-29. doi: 10.1093/jnci/djn345. Epub 2008 Oct 28. J Natl Cancer Inst. 2008. PMID: 18957670

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