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Clinical Endocrinology|December 9, 2020
NR5A1 c.991-1G > C splice-site variant causes familial 46,XY partial gonadal dysgenesis with incomplete penetranceMaris Laan, Laura Kasak, Kęstutis Timinskas, et al.Human Reproduction (Oxford, England)|April 7, 2017
Semen quality of young men from the general population in Baltic countriesJuris Erenpreiss, Margus Punab, Birute Zilaitiene, et al.The Journal of Clinical Endocrinology and Metabolism|July 8, 2011
Genetically determined dosage of follicle-stimulating hormone (FSH) affects male reproductive parametersMarina Grigorova, Margus Punab, Birutė Zilaitienė, et al.Journal of Andrology|November 21, 2009
Analysis of polymorphisms in the SRD5A2 gene and semen parameters in Estonian menMaire Peters, Merli Saare, Tanel Kaart, et al.Human Reproduction (Oxford, England)|December 3, 2025
Microdeletion and microduplication syndromes, including recurrent rearrangements at 16p11.2 and 22q11.21, are enriched in unexplained male infertilityTriin Kikas, Avirup Dutta, Rain Inno, et al.Plos One|April 11, 2014
Reproductive physiology in young men is cumulatively affected by FSH-action modulating genetic variants: FSHR -29G/A and c.2039 A/G, FSHB -211G/TMarina Grigorova, Margus Punab, Anna Maria Punab, et al.Journal of Assisted Reproduction and Genetics|November 10, 2018
Chromosomal scan of single sperm cells by combining fluorescence-activated cell sorting and next-generation sequencingQuoc Ty Tran, Tatjana Jatsenko, Olev Poolamets, et al.Asian Journal of Andrology|June 23, 2026
The long (GGN)n repeat tract in the androgen receptor gene exerts a negative effect on quantitative sperm parametersKristel Ehala-Aleksejev, Triin Kikas, Marina Grigorova, et al.Human Reproduction Open|March 10, 2025
Significantly increased load of hereditary cancer-linked germline variants in infertile menAnu Valkna, Anna-Grete Juchnewitsch, Lisanna Põlluaas, et al.Andrology|October 26, 2021
Prevalence of congenital cryptorchidism in EstoniaViljo Kübarsepp, Karin Varik, Heili Varendi, et al.Pageof 14