Laan M - Search Results

1

Genetics of Sex Hormone-Binding Globulin and Testosterone Levels in Fertile and Infertile Men of Reproductive Age.

Grigorova M, Punab M, Poolamets O, Adler M, Vihljajev V, Laan M. Grigorova M, et al. Among authors: laan m. J Endocr Soc. 2017 Apr 11;1(6):560-576. doi: 10.1210/js.2017-00050. eCollection 2017 Jun 1. J Endocr Soc. 2017. PMID: 29264510 Free PMC article.

2

Putative predictors of antibodies against follicle-stimulating hormone in female infertility: a study based on in vitro fertilization patients.

Haller K, Salumets A, Grigorova M, Talja I, Salur L, Béné MC, Laan M, Uibo R. Haller K, et al. Among authors: laan m. Am J Reprod Immunol. 2007 Mar;57(3):193-200. doi: 10.1111/j.1600-0897.2006.00462.x. Am J Reprod Immunol. 2007. PMID: 17295898

3

FSHB promoter polymorphism within evolutionary conserved element is associated with serum FSH level in men.

Grigorova M, Punab M, Ausmees K, Laan M. Grigorova M, et al. Among authors: laan m. Hum Reprod. 2008 Sep;23(9):2160-6. doi: 10.1093/humrep/den216. Epub 2008 Jun 21. Hum Reprod. 2008. PMID: 18567894 Free PMC article.

4

Combined effects of the variants FSHB -211G>T and FSHR 2039A>G on male reproductive parameters.

Tüttelmann F, Laan M, Grigorova M, Punab M, Sõber S, Gromoll J. Tüttelmann F, et al. Among authors: laan m. J Clin Endocrinol Metab. 2012 Oct;97(10):3639-47. doi: 10.1210/jc.2012-1761. Epub 2012 Jul 12. J Clin Endocrinol Metab. 2012. PMID: 22791757

5

Reproductive physiology in young men is cumulatively affected by FSH-action modulating genetic variants: FSHR -29G/A and c.2039 A/G, FSHB -211G/T.

Grigorova M, Punab M, Punab AM, Poolamets O, Vihljajev V, Zilaitienė B, Erenpreiss J, Matulevičius V, Laan M. Grigorova M, et al. Among authors: laan m. PLoS One. 2014 Apr 9;9(4):e94244. doi: 10.1371/journal.pone.0094244. eCollection 2014. PLoS One. 2014. PMID: 24718625 Free PMC article.

6

FSHB -211 G>T is a major genetic modulator of reproductive physiology and health in childbearing age women.

Rull K, Grigorova M, Ehrenberg A, Vaas P, Sekavin A, Nõmmemees D, Adler M, Hanson E, Juhanson P, Laan M. Rull K, et al. Among authors: laan m. Hum Reprod. 2018 May 1;33(5):954-966. doi: 10.1093/humrep/dey057. Hum Reprod. 2018. PMID: 29617818

7

Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia.

Kasak L, Punab M, Nagirnaja L, Grigorova M, Minajeva A, Lopes AM, Punab AM, Aston KI, Carvalho F, Laasik E, Smith LB; GEMINI Consortium; Conrad DF, Laan M. Kasak L, et al. Among authors: laan m. Am J Hum Genet. 2018 Aug 2;103(2):200-212. doi: 10.1016/j.ajhg.2018.07.005. Am J Hum Genet. 2018. PMID: 30075111 Free PMC article.

8

Evolutionary and functional analysis of RBMY1 gene copy number variation on the human Y chromosome.

Shi W, Louzada S, Grigorova M, Massaia A, Arciero E, Kibena L, Ge XJ, Chen Y, Ayub Q, Poolamets O, Tyler-Smith C, Punab M, Laan M, Yang F, Hallast P, Xue Y. Shi W, et al. Among authors: laan m. Hum Mol Genet. 2019 Aug 15;28(16):2785-2798. doi: 10.1093/hmg/ddz101. Hum Mol Genet. 2019. PMID: 31108506 Free PMC article.

9

Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia.

Salas-Huetos A, Tüttelmann F, Wyrwoll MJ, Kliesch S, Lopes AM, Goncalves J, Boyden SE, Wöste M, Hotaling JM; GEMINI Consortium; Nagirnaja L, Conrad DF, Carrell DT, Aston KI. Salas-Huetos A, et al. Hum Genet. 2021 Jan;140(1):217-227. doi: 10.1007/s00439-020-02236-1. Epub 2020 Nov 19. Hum Genet. 2021. PMID: 33211200 Free PMC article.

10

NR5A1 c.991-1G > C splice-site variant causes familial 46,XY partial gonadal dysgenesis with incomplete penetrance.

Laan M, Kasak L, Timinskas K, Grigorova M, Venclovas Č, Renaux A, Lenaerts T, Punab M. Laan M, et al. Clin Endocrinol (Oxf). 2021 Apr;94(4):656-666. doi: 10.1111/cen.14381. Epub 2020 Dec 9. Clin Endocrinol (Oxf). 2021. PMID: 33296094

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