Genetic Causes of Male Infertility

1. Ferlin A, Arredi B, Foresta C. Genetic causes of male infertility. Reprod Toxicol. 2006; 22(2): 133-141.10.1016/j.reprotox.2006.04.016Search in Google Scholar

2. Gekas J, Thepot F, Turleau C, et al. Chromosomal factors of infertility in candidate couples for ICSI: an equal risk of constitutional aberrations in women and men. Hum Reprod. 2001; 16(1): 82-90.10.1093/humrep/16.1.82Search in Google Scholar

3. Foresta C, Ferlin A, Moro E, Scandellari C. Y chromosome. Lancet. 2000; 355(9199): 234-235.10.1016/S0140-6736(05)72111-5Search in Google Scholar

4. Krausz C, Forti G, McElreavey K. The Y chromosome and male fertility and infertility. Int J Androl. 2003; 26(2): 70-75.10.1046/j.1365-2605.2003.00402.x12641824Search in Google Scholar

5. Simoni M, Kamischke A, Nieschlag E. Current status of the molecular diagnosis of Y-chromosomal microdeletions in the work-up of male infertility. Initiative for international quality control. Hum Reprod. 1998; 13(7): 1764-1768.10.1093/humrep/13.7.17649740417Search in Google Scholar

6. Plaseski T, Dimitrovski C, Kocevska B, Efremov GD, Plaseska-Karanfilska D. The prevalence of Y chromosome microdeletions among infertile males from the Republic of Macedonia. Balkan J Med Genet. 2003; 6(1&2): 39-44.Search in Google Scholar

7. Plaseski T, Novevski P, Kocevska B, Dimitrovski C, Efremov GD, Plaseska-Karanfilska D. AZF deletions in infertile men from the Republic of Macedonia. Prilozi. 2006; 27(1): 5-16.Search in Google Scholar

8. Plaseski T, Noveski P, Trivodalieva S, Efremov GD, Plaseska-Karanfilska D. Quantitative fluorescent- PCR detection of sex chromosome aneuploidies and AZF deletions/duplications. Genet Test. 2008; 12(4): 595-605.10.1089/gte.2008.006819072570Search in Google Scholar

9. Vogt PH. AZF deletions and Y chromosomal haplogroups: history and update based on sequence. Hum Reprod Update. 2005; 11(4): 319-336.10.1093/humupd/dmi01715890785Search in Google Scholar

10. Repping S, Skaletsky H, Brown L, et al. Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection. Nat Genet. 2003; 35(3): 247-251.10.1038/ng125014528305Search in Google Scholar

11. Repping S, van Daalen SK, Korver CM, et al. A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region. Genomics. 2004; 83(6): 1046-1052.10.1016/j.ygeno.2003.12.01815177557Search in Google Scholar

12. Lin YW, Hsu LC, Kuo PL, et al. Partial duplication at AZFc on the Y chromosome is a risk factor for impaired spermatogenesis in Han Chinese in Taiwan. Hum Mutat. 2007; 28(5): 486-494.10.1002/humu.2047317285591Search in Google Scholar

13. Plaseska-Karanfilska D, Noveski P, Plaseski T. PNaTP, detection of the most common genetic causes of male infertility by quantitative fluorescent (QF)-PCR analysis. In: Plaseska-Karanfilska, Ed. Genetics of Human Diseases. Rijeka: Croatia. 2011: 203-222.10.5772/33229Search in Google Scholar

14. Yang Y, Ma M, Li L, et al. Y chromosome haplogroups may confer susceptibility to partial AZFc deletions and deletion effect on spermatogenesis impairment. Hum Reprod. 2008; 23(9): 2167-2172.10.1093/humrep/den22918579508Search in Google Scholar

15. Noveski P, Trivodalieva S, Efremov GD, Plaseska- Karanfilska D. Y-chromosome single nucleotide polymorphisms typing by SNaPshot minisequencing. Balkan J Med Genet. 2010; 13(1): 9-16.10.2478/v10034-010-0013-9Search in Google Scholar

16. Krausz C, Giachini C. Genetic risk factors in male infertility. Arch Androl. 2007; 53(3): 125-133.10.1080/0148501070127178617612870Search in Google Scholar

17. Plaseski T, Noveski P, Kocevska B, Dimitrovski C, Efremov GD, Plaseska-Karanfilska D. CAG repeat polymorphism of the mitrochondrial DNA polymerase gamma gene in Macedonian infertile and fertile men. Balkan J Med Genet. 2007; 10(2): 37-41.10.2478/v10034-008-0005-1Search in Google Scholar

18. Plaseski T, Noveski P, Kocevska B, Dimitrovski C, Efremov GD, Plaseska-Karanfilska D. CAG repeat number in androgen receptor gene and male infertility. Balkan J Med Genet. 2007; 10(1): 19-24.10.2478/v10034-007-0003-8Search in Google Scholar

19. Plaseski T, Noveski P, Popeska Z, Efremov GD, Plaseska-Karanfilska D. Association study of single nucleotide polymorphisms in FASLG, JMJDIA,LOC203413, TEX15, BRDT, OR2W3, INSR and TAS2R38 genes with male infertility. J Androl. 2011; 33(4): 675-683.10.2164/jandrol.111.01399522016351Search in Google Scholar

20. Tuttelmann F, Simoni M, Kliesch S, et al. Copy number variants in patients with severe oligozoospermia and Sertoli-cell-only syndrome. PLoS One. 2011; 6(4): e19426. 10.1371/journal.pone.0019426308485321559371Search in Google Scholar