Associated Papers
Genetics Investigation of Idiopathic Premature Ovarian Insufficiency: Contribution of Array-CGH and Next-Generation Sequencing.
Cozette C et al.
Genes, 2025
Identification and characterization of two functional variants in the human longevity gene FOXO3.
Flachsbart F et al.
Nature Communications, 2017
29234056 (PubMed )
Supplement: 41467_2017_2183_MOESM1_ESM.pdf
Genetics of primary ovarian insufficiency.
Rossetti R et al.
Clinical Genetics, 2017
Ethnic specificity of variants of the ESR1, HK3, BRSK1 genes and the 8q22.3 locus: no association with premature ovarian failure (POF) in Serbian women.
Qin Y et al.
Maturitas, 2014
Genetic aspects of premature ovarian failure: a literature review.
Cordts EB et al.
Archives of Gynecology and Obstetrics, 2011
Analysis of FOXO3 mutation in 114 Chinese women with premature ovarian failure.
Wang B et al.
Reproductive Biomedicine Online, 2010
Mutational screening of FOXO3A and FOXO1A in women with premature ovarian failure.
Watkins WJ et al.
Fertility and Sterility, 2006
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