Pharmacogenetics of FSH action

por Laan, Maris, Grigorova, Marina, Huhtaniemi, Ilpo T.
Publicado em 2012

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

por Grigorova, Marina, Punab, Margus, Ausmees, Kristo, Laan, Maris
Publicado em 2008

Genomics and genetics of gonadotropin beta-subunit genes: Unique FSHB and duplicated LHB/CGB loci

por Nagirnaja, Liina, Rull, Kristiina, Uusküla, Liis, Hallast, Pille, Grigorova, Marina, Laan, Maris
Publicado em 2010

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

por Grigorova, Marina, Punab, Margus, Poolamets, Olev, Adler, Mart, Vihljajev, Vladimir, Laan, Maris
Publicado no J Endocr Soc (2017)

Increased Prevalance of the −211 T Allele of Follicle Stimulating Hormone (FSH) β Subunit Promoter Polymorphism and Lower Serum FSH in Infertile Men

por Grigorova, Marina, Punab, Margus, Poolamets, Olev, Kelgo, Piret, Ausmees, Kristo, Korrovits, Paul, Vihljajev, Vladimir, Laan, Maris
Publicado em 2010

Genetically Determined Dosage of Follicle-Stimulating Hormone (FSH) Affects Male Reproductive Parameters

por Grigorova, Marina, Punab, Margus, Ẑilaitienė, Birutė, Erenpreiss, Juris, Ausmees, Kristo, Matuleviĉius, Valentinas, Tsarev, Igor, Jørgensen, Niels, Laan, Maris
Publicado em 2011

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

por Grigorova, Marina, Punab, Margus, Punab, Anna Maria, Poolamets, Olev, Vihljajev, Vladimir, Žilaitienė, Birutė, Erenpreiss, Juris, Matulevičius, Valentinas, Laan, Maris
Publicado em 2014

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

por Kasak, Laura, Punab, Margus, Nagirnaja, Liina, Grigorova, Marina, Minajeva, Ave, Lopes, Alexandra M., Punab, Anna Maria, Aston, Kenneth I., Carvalho, Filipa, Laasik, Eve, Smith, Lee B., Conrad, Donald F., Laan, Maris
Publicado no Am J Hum Genet (2018)

A common 1.6 mb Y-chromosomal inversion predisposes to subsequent deletions and severe spermatogenic failure in humans

por Hallast, Pille, Kibena, Laura, Punab, Margus, Arciero, Elena, Rootsi, Siiri, Grigorova, Marina, Flores, Rodrigo, Jobling, Mark A, Poolamets, Olev, Pomm, Kristjan, Korrovits, Paul, Rull, Kristiina, Xue, Yali, Tyler-Smith, Chris, Laan, Maris
Publicado no eLife (2021)

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

por Shi, Wentao, Louzada, Sandra, Grigorova, Marina, Massaia, Andrea, Arciero, Elena, Kibena, Laura, Ge, Xiangyu Jack, Chen, Yuan, Ayub, Qasim, Poolamets, Olev, Tyler-Smith, Chris, Punab, Margus, Laan, Maris, Yang, Fengtang, Hallast, Pille, Xue, Yali
Publicado no Hum Mol Genet (2019)