Kliesch S - Search Results

1

Large-scale analyses of the X chromosome in 2,354 infertile men discover recurrently affected genes associated with spermatogenic failure.

Riera-Escamilla A, Vockel M, Nagirnaja L, Xavier MJ, Carbonell A, Moreno-Mendoza D, Pybus M, Farnetani G, Rosta V, Cioppi F, Friedrich C, Oud MS, van der Heijden GW, Soave A, Diemer T, Ars E, Sánchez-Curbelo J, Kliesch S, O'Bryan MK, Ruiz-Castañe E; GEMINI Consortium; Azorín F, Veltman JA, Aston KI, Conrad DF, Tüttelmann F, Krausz C. Riera-Escamilla A, et al. Among authors: kliesch s. Am J Hum Genet. 2022 Aug 4;109(8):1458-1471. doi: 10.1016/j.ajhg.2022.06.007. Epub 2022 Jul 8. Am J Hum Genet. 2022. PMID: 35809576 Free PMC article.

2

Both protamine-1 to protamine-2 mRNA ratio and Bcl2 mRNA content in testicular spermatids and ejaculated spermatozoa discriminate between fertile and infertile men.

Steger K, Wilhelm J, Konrad L, Stalf T, Greb R, Diemer T, Kliesch S, Bergmann M, Weidner W. Steger K, et al. Among authors: kliesch s. Hum Reprod. 2008 Jan;23(1):11-6. doi: 10.1093/humrep/dem363. Epub 2007 Nov 13. Hum Reprod. 2008. PMID: 18003625

3

[Genetics of male infertility].

Tüttelmann F, Gromoll J, Kliesch S. Tüttelmann F, et al. Among authors: kliesch s. Urologe A. 2008 Dec;47(12):1561-2, 1564-7. doi: 10.1007/s00120-008-1804-4. Urologe A. 2008. PMID: 18953522 Review. German.

4

Aquaporins in the human testis and spermatozoa - identification, involvement in sperm volume regulation and clinical relevance.

Yeung CH, Callies C, Tüttelmann F, Kliesch S, Cooper TG. Yeung CH, et al. Among authors: kliesch s. Int J Androl. 2010 Aug 1;33(4):629-41. doi: 10.1111/j.1365-2605.2009.00998.x. Epub 2009 Oct 12. Int J Androl. 2010. PMID: 19840149

5

Clinical experience with azoospermia: aetiology and chances for spermatozoa detection upon biopsy.

Tüttelmann F, Werny F, Cooper TG, Kliesch S, Simoni M, Nieschlag E. Tüttelmann F, et al. Among authors: kliesch s. Int J Androl. 2011 Aug;34(4):291-8. doi: 10.1111/j.1365-2605.2010.01087.x. Epub 2010 Jun 28. Int J Androl. 2011. PMID: 20609027

6

Copy number variants in patients with severe oligozoospermia and Sertoli-cell-only syndrome.

Tüttelmann F, Simoni M, Kliesch S, Ledig S, Dworniczak B, Wieacker P, Röpke A. Tüttelmann F, et al. Among authors: kliesch s. PLoS One. 2011 Apr 29;6(4):e19426. doi: 10.1371/journal.pone.0019426. PLoS One. 2011. PMID: 21559371 Free PMC article.

7

Bilateral histological evaluation of exocrine testicular function in men with obstructive azoospermia: condition of spermatogenesis and andrological implications?

Pühse G, Hense J, Bergmann M, Kliesch S. Pühse G, et al. Among authors: kliesch s. Hum Reprod. 2011 Oct;26(10):2606-12. doi: 10.1093/humrep/der257. Epub 2011 Aug 12. Hum Reprod. 2011. PMID: 21840906

8

Comprehensive sequence analysis of the NR5A1 gene encoding steroidogenic factor 1 in a large group of infertile males.

Röpke A, Tewes AC, Gromoll J, Kliesch S, Wieacker P, Tüttelmann F. Röpke A, et al. Among authors: kliesch s. Eur J Hum Genet. 2013 Sep;21(9):1012-5. doi: 10.1038/ejhg.2012.290. Epub 2013 Jan 9. Eur J Hum Genet. 2013. PMID: 23299922 Free PMC article.

9

DNA methylation in spermatozoa as a prospective marker in andrology.

Kläver R, Tüttelmann F, Bleiziffer A, Haaf T, Kliesch S, Gromoll J. Kläver R, et al. Among authors: kliesch s. Andrology. 2013 Sep;1(5):731-40. doi: 10.1111/j.2047-2927.2013.00118.x. Andrology. 2013. PMID: 23970452 Free article.

10

Y-chromosome microdeletions are not associated with SHOX haploinsufficiency.

Chianese C, Lo Giacco D, Tüttelmann F, Ferlin A, Ntostis P, Vinci S, Balercia G, Ars E, Ruiz-Castañé E, Giglio S, Forti G, Kliesch S, Krausz C. Chianese C, et al. Among authors: kliesch s. Hum Reprod. 2013 Nov;28(11):3155-60. doi: 10.1093/humrep/det322. Epub 2013 Sep 5. Hum Reprod. 2013. PMID: 24008148

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