A Review on CYP11A1, CYP17A1, and CYP19A1 Polymorphism Studies: Candidate Susceptibility Genes for Polycystic Ovary Syndrome (PCOS) and Infertility

R Heidarzadehpilehrood, M Pirhoushiaran… - Genes, 2022 - mdpi.com
Polycystic ovary syndrome is a multifactorial condition associated with reproductive and
endocrine organs and might cause infertility and metabolic abnormalities in childbearing …

Genetic predictors of controlled ovarian hyperstimulation: where do we stand today?

S Altmäe, O Hovatta, A Stavreus-Evers… - Human reproduction …, 2011 - academic.oup.com
BACKGROUND Nowadays, the use of IVF has improved the prospects of infertility treatment.
The expected outcome of IVF depends greatly on the effectiveness of controlled ovarian …

[HTML][HTML] Impact of various parameters as predictors of the success rate of in vitro fertilization

RD Rezaeiye, A Mehrara, AMA Pour… - … Journal of Fertility & …, 2022 - ncbi.nlm.nih.gov
Infertility is one of the major problems faced in medicine. There are numerous factors that
play a role in infertility. For example, numerous studies mention the impact of the quantity …

Polymorphisms in ESR1, ESR2 and HSD17B1 genes are associated with fertility status in endometriosis

M Lamp, M Peters, E Reinmaa… - Gynecological …, 2011 - Taylor & Francis
Objective. To investigate whether polymorphisms in genes involved in biosynthesis and
signalling of sex steroids influence susceptibility to endometriosis and to infertility associated …

[HTML][HTML] Transcriptional, hormonal and histological alterations in the ovaries of BALB/c mice exposed to TCDD in connection with multigenerational female infertility

N Aldeli, C Soukkarie, A Hanano - Ecotoxicology and Environmental Safety, 2023 - Elsevier
Abstract 2, 3, 7, 8-tetrachlorodibenzo-p-dioxin (TCDD), the most toxic congener of dioxins,
has a proven reproductive toxicity. Due to the lack of evidence on the multigenerational …

No evidence for mutations in NLRP7, NLRP2 or KHDC3L in women with unexplained recurrent pregnancy loss or infertility

L Aghajanova, S Mahadevan, S Altmäe… - Human …, 2015 - academic.oup.com
STUDY QUESTION Are mutations in NLRP2/7 (NACHT, LRR and PYD domains-containing
protein 2/7) or KHDC3L (KH Domain Containing 3 Like) associated with recurrent …

[HTML][HTML] Genetic variation in the sex hormone metabolic pathway and endometriosis risk: an evaluation of candidate genes

B Trabert, SM Schwartz, U Peters, AJ De Roos… - Fertility and sterility, 2011 - Elsevier
OBJECTIVE: To evaluate the relationship between common genetic variation in genes
involved in the biosynthesis and signaling of estrogen and progesterone and endometriosis …

Genetics of ovarian hyperstimulation syndrome

B Rizk - Reproductive biomedicine online, 2009 - Elsevier
Ovarian hyperstimulation syndrome (OHSS) is typically iatrogenic following the
administration of gonadotrophins. Sporadic and familial cases of spontaneous OHSS have …

Association between the luteinizing hormone/chorionic gonadotropin receptor (LHCGR) rs4073366 polymorphism and ovarian hyperstimulation syndrome during …

TJ O'Brien, MM Kalmin, AF Harralson, AM Clark… - Reproductive biology …, 2013 - Springer
Background The aim of this study was to determine the relationship between a purported
luteinizing hormone/chorionic gonadotropin (LHCGR) high function polymorphism …

[HTML][HTML] Sequence variants in FSHR and CYP19A1 genes and the ovarian response to controlled ovarian stimulation

D Song, X Huang, L Hong, J Yu, Z Zhang, H Zhang… - Fertility and …, 2019 - Elsevier
Objective To examine whether sequence variants within the FSHR and CYP19A1 genes are
related to the ovarian response to controlled ovarian stimulation (COS). Design Genetic …