[1. de Kretser DM, Loveland KL, Meinhardt A, Simorangkir D, Wreford N. Spermatogenesis. Hum Reprod. 1998; 13(Suppl 1): 1-8.10.1093/humrep/13.suppl_1.1]Search in Google Scholar
[2. Ferlin A, Arredi B, Foresta C. Genetic causes of male infertility. Reprod Toxicol. 2006; 22(2): 133-141.10.1016/j.reprotox.2006.04.016]Search in Google Scholar
[3. Plaseska-Karanfilska D, Noveski P, Plaseski T, Maleva I, Madjunkova S, Moneva Z. Genetic causes of male infertility. Balkan J Med Genet. 2012; 15(Suppl): 31-34.10.2478/v10034-012-0015-x]Search in Google Scholar
[4. Dohle GR, Colpi GM, Hargreave TB, Papp GK, Jungwirth A, Weidner W; EAU Working Group on Male Infertility. EAU guidelines on male infertility. Eur Urol. 2005; 48(5): 703-711.10.1016/j.eururo.2005.06.002]Search in Google Scholar
[5. Sivakumaran S, Agakov F, Theodoratou E, Prendergast JG, Zgaga L, Manolio T, et al. Abundant pleiotropy in human complex diseases and traits. Am J Hum Genet. 2011; 89(5): 607-618.10.1016/j.ajhg.2011.10.004]Search in Google Scholar
[6. Aston KI, Krausz C, Laface I, Ruiz-Castane E, Carrell DT. Evaluation of 172 candidate polymorphisms for association with oligozoospermia or azoospermia in a large cohort of men of European descent. Hum Reprod. 2010; 25(6): 1383-1397.10.1093/humrep/deq081]Search in Google Scholar
[7. 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. 2012; 33(4): 675-683.10.2164/jandrol.111.013995]Search in Google Scholar
[8. Sloan JL, Mager S. Cloning and functional expression of a human Na+ and Cl--dependent neutral and cationic amino acid transporter B0+. J Biol Chem. 1999; 274(34): 23740-23745.10.1074/jbc.274.34.23740]Search in Google Scholar
[9. Suviolahti E, Oksanen LJ, Ohman M, Cantor RM, Ridderstrale M, Tuomi T, et al. The SLC6A14 gene shows evidence of association with obesity. J Clin Invest. 2003; 112(11): 1762-1772.10.1172/JCI200317491]Search in Google Scholar
[10. Durand E, Boutin P, Meyre D, Charles MA, Clement K, Dina C, et al. Polymorphisms in the amino acid transporter solute carrier family 6 (neurotransmitter transporter) member 14 gene contribute to polygenic obesity in French Caucasians. Diabetes. 2004; 53(9): 2483-2486.10.2337/diabetes.53.9.2483]Search in Google Scholar
[11. Corpeleijn E, Petersen L, Holst C, Saris WH, Astrup A, Langin D, et al. Obesity-related polymorphisms and their associations with the ability to regulate fat oxidation in obese Europeans: the NUGENOB study. Obesity (Silver Spring). 2010; 18(7): 1369-1377.10.1038/oby.2009.377]Search in Google Scholar
[12. Sun L, Rommens JM, Corvol H, Li W, Li X, Chiang TA, et al. Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis. Nat Genet. 2012; 44(5): 562-569.10.1038/ng.2221]Search in Google Scholar
[13. Li W, Soave D, Miller MR, Keenan K, Lin F, Gong J, et al. Unraveling the complex genetic model for cystic fibrosis: Pleiotropic effects of modifier genes on early cystic fibrosis-related morbidities. Hum Genet. 2014; 133(2): 151-161.10.1007/s00439-013-1363-7]Search in Google Scholar
[14. Aragon MA, Ayala ME, Marin M, Aviles A, Damian-Matsumura P, Dominguez R. Serotoninergic system blockage in the prepubertal rat inhibits spermatogenesis development. Reproduction. 2005; 129(6): 717-727.10.1530/rep.1.00598]Search in Google Scholar
[15. Tinajero JC, Fabbri A, Ciocca DR, Dufau ML. Serotonin secretion from rat Leydig cells. Endocrinology. 1993; 133(6): 3026-3029.10.1210/endo.133.6.8243331]Search in Google Scholar
[16. Collin O, Damber JE, Bergh A. 5-Hydroxytryptamine - A local regulator of testicular blood flow and vasomotion in rats. J Reprod Fertil. 1996; 106(1): 17-22.10.1530/jrf.0.1060017]Search in Google Scholar
[17. Barrett JC, Fry B, Maller J, Daly MJ. Haploview: Analysis and visualization of LD and haplotype maps. Bioinformatics. 2005; 21(2): 263-265.10.1093/bioinformatics/bth457]Search in Google Scholar
[18. Sabarinathan R, Tafer H, Seemann SE, Hofacker IL, Stadler PF, Gorodkin J. The RNAsnp web server: Predicting SNP effects on local RNA secondary structure. Nucleic Acids Res. 2013; 41(Web Server issue): W475-W479.10.1093/nar/gkt291]Search in Google Scholar
[19. Barrett LW, Fletcher S, Wilton SD. Regulation of eukaryotic gene expression by the untranslated gene regions and other non-coding elements. Cell Mol Life Sci. 2012; 69(21): 3613-3634.10.1007/s00018-012-0990-9]Search in Google Scholar
[20. Chatterjee S, Pal JK. Role of 5’- and 3’-untranslated regions of mRNAs in human diseases. Biol Cell. 2009; 101(5): 251-262.10.1042/BC20080104]Search in Google Scholar
[21. Haas U, Sczakiel G, Laufer SD. MicroRNAmediated regulation of gene expression is affected by disease-associated SNPs within the 3’-UTR via altered RNA structure. RNA Biol. 2012; 9(6): 924-937.10.4161/rna.20497]Search in Google Scholar
[22. Ritz J, Martin JS, Laederach A. Evaluating our ability to predict the structural disruption of RNA by SNPs. BMC Genomics. 2012; 13(Suppl 4): S6.10.1186/1471-2164-13-S4-S6]Search in Google Scholar