Katrien Stouffs Team

Genetic aspects of male infertility

Papers in international peer-reviewed journals

Tanyalcin I, Al Assaf C, Gheldof A, Stouffs K, Lissens W, Jansen AC. I-PV: a CIRCOS module for interactive protein sequence visualization. Bioinformatics. 2015 Oct 10. pii: btv579

Santos-Ribeiro S, Polyzos NP, Stouffs K, De Vos M, Seneca S, Tournaye H, Blockeel C. Ovarian hyperstimulation syndrome after gonadotropin-releasing hormone agonist triggering and "freeze-all": in-depth analysis of genetic predisposition. (2015) J Assist Reprod Genet.32:1063-1068.

Vancampenhout K, Caljon B, Spits C, Stouffs K, Jonckheere A, De Meirleir L, Lissens W, Vanlander A, Smet J, De Paepe B, Van Coster R, Seneca S.A bumpy ride on the diagnostic bench of massive parallel sequencing, the case of the mitochondrial genome (2014) PLoS One. 9(11):e112950.

Stouffs K, Seneca S, Lissens W. Genetic causes of male infertility. Ann Endocrinol (Paris). 2014 Apr 23. doi: 10.1016/j.ando.2014.03.004.

Seneca S, Vancampenhout K, Van Coster R, Smet J, Lissens W, Vanlander A, De Paepe B, Jonckheere A, Stouffs K, De Meirleir L. (2015) Analysis of the whole mitochondrial genome: translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench? Eur J Hum Genet. 23:41-48.

Stouffs, K., Lissens, W. (November 2013) X Chromosome and Spermatogenesis Defects. In: eLS. John Wiley & Sons, Ltd: Chichester. DOI: 10.1002/9780470015902.a0025311

Stouffs, K., Lissens, W. X chromosomal mutations and spermatogenic failure (2012). BBA - Molecular basis of disease. 1822:1864-1872.

Stouffs, K., Vandermaelen, D., Massart, A., Menten, B., Liebaers, I., Tournaye, H., Lissens, W. (2012) Array comparative genomic hybridisation in male infertility. Hum. Reprod. 27, 921-929.

Massart, A., Lissens, W., Stouffs, K. (2012) Genetics of spermatogenesis defects, Asian J Androl, 14, 40-48.

Stouffs, K., Vandermaelen, D., Tournaye, H., Liebaers, I. and Lissens, W. (2011) Mutation analysis of three genes in patients with maturation arrest of spermatogenesis and couples with recurrent miscarriages. RBMonline, 22, 65-71.

Stouffs, K., Lissens, W., Tournaye, H., Haentjens, P. (2011) What about gr/gr deletions and male infertility? Systematic review and meta-analysis. Hum Reprod Update, 17, 197-209.

Stouffs, K., Tournaye, H., Liebaers, I. and Lissens, W (2009) Male infertility and the involvement of the X chromosome. Hum Reprod Update, 15, 623-637.

Stouffs, K., Tournaye, H., Van der Elst, J., Haentjens, P., Liebaers, I. and Lissens, W. (2008) Do we need to search for gr/gr deletions in infertile men in a clinical setting? Hum. Reprod., 23, 1193-1199.

Stouffs, K., Tournaye, H., Van der Elst, J., Liebaers, I. and Lissens, W. (2008) Is there a role for NXF2 in male infertility? Fertil. Steril., 90, 1787-1791.

Stouffs, K., Lissens, W., Tournaye, H., Van Steirteghem, A. and Liebaers (2006) Alterations of the USP26 gene in Caucasian men. Int. J. Androl., 29, 614-617.

Stouffs, K., Willems, A., Lissens, W., Tournaye, H., Van Steirteghem, A. and Liebaers, I. (2006) The role of the testis-specific gene TAF7L in the etiology of male infertility. Mol. Hum. Reprod., 12, 263-267.

Stouffs, K., Lissens, W., Tournaye, H., Van Steirteghem, A. and Liebaers, I. (2005) SYCP3 mutations are uncommon in patients with azoospermia. Fertil. Steril., 84, 1019-1020.

Stouffs, K., Lissens, W., Tournaye, H., Van Steirteghem, A. and Liebaers, I. (2005) The choice and outcome of the fertility treatment of 38 couples in whom the male partner has a Yq microdeletion. Hum. Reprod., 20,1887-1896.

Stouffs, K., Lissens, W., Tournaye, H., Van Steirteghem, A. and Liebaers, I. (2005) Possible role of USP26 in patients with severely impaired spermatogenesis. Eur. J. Hum. Genet., 13, 336-340.

Stouffs, K., Lissens, W., Verheyen, G., Van Landuyt, L., Goossens, A., Tournaye, H., Van Steirteghem, A. and Liebaers, I. (2004) Expression pattern of the Y-linked PRY gene suggests a function in apoptosis but not in spermatogenesis. Mol. Hum. Reprod., 10, 15-21.

Van Landuyt, L., Lissens, W., Stouffs, K., Tournaye, H., Liebaers, I. and Van Steirteghem, A. (2001) The role of USP9Y and DBY in infertile patients with severely impaired spermatogenesis. Mol. Hum. Reprod., 7, 691-693.

Stouffs, K., Lissens, W., Van Landuyt, L., Tournaye, H., Van Steirteghem, A. and Liebaers, I. (2001) Characterization of the genomic organization, localization and expression of four PRY genes (PRY1, PRY2, PRY3 and PRY4). Mol. Hum. Reprod., 7, 603-610.

Van Landuyt, L., Lissens, W., Stouffs, K., Tournaye, H., Liebaers, I. and Van Steirteghem, A. (2000) Validation of a simple Yq deletion screening programme in an ICSI candidate population. Mol. Hum. Reprod., 6, 291-297.

Book Chapters

Lissens, W., Stouffs, K. Severe male factor: Genetic consequences and recommendations for genetic testing. Textbook of assisted reproductive techniques. Volume One: Laboratory Perspectives, Fourth Edition David K. Gardner, Ariel Weissman, Colin M. Howles, Zeev Shoham. DOI: 10.3109/9781841849713.025

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