Associated Papers
Understanding the Mechanisms of Diminished Ovarian Reserve: Insights from Genetic Variants and Regulatory Factors.
Zhu Q et al.
Reproductive Sciences (thousand Oaks, Calif.), 2024
The landscape of genetic variations in non-syndromic primary ovarian insufficiency in the MENA region: a systematic review.
Allouch A et al.
Frontiers in Endocrinology, 2023
Association of BMP15 and GDF9 variants to premature ovarian insufficiency.
Santos M et al.
Journal of Assisted Reproduction and Genetics, 2019
NOBOX is a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency.
Bouali N et al.
Clinical Genetics, 2016
Single nucleotide polymorphisms in premature ovarian failure-associated genes in a Chinese Hui population.
Ma L et al.
Molecular Medicine Reports, 2015
Gene variation and premature ovarian failure: a meta-analysis.
Pu D et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology, 2014
Variants of the BMP15 gene in a cohort of patients with premature ovarian failure.
Tiotiu D et al.
Human Reproduction (oxford, England), 2010
Genes governing premature ovarian failure.
Dixit H et al.
Reproductive Biomedicine Online, 2010
Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning.
Zhao ZZ et al.
Human Reproduction (oxford, England), 2008
Missense mutations in the BMP15 gene are associated with ovarian failure.
Dixit H et al.
Human Genetics, 2006
Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure.
Laissue P et al.
European Journal of Endocrinology, 2006
Genetics of primary ovarian insufficiency: new developments and opportunities.
Qin Y et al.
Human Reproduction Update, 0
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