1. Biallelic mutations in PSMC3IP are associated with secondary amenorrhea: expanding the spectrum of premature ovarian insufficiency
   Fabio Sirchia et al, 2022, J Assist Reprod Genet CrossRef
2. Selected Genetic Factors Associated with Primary Ovarian Insufficiency
   Mengchi Chen et al, 2023, IJMS CrossRef
3. DNA double-strand break genetic variants in patients with premature ovarian insufficiency
   Xuechun Ding et al, 2023, J Ovarian Res CrossRef
4. The landscape of genetic variations in non-syndromic primary ovarian insufficiency in the MENA region: a systematic review
   Asma Allouch et al, 2024, Front. Endocrinol. CrossRef
5. TP63 truncating mutation causes increased cell apoptosis and premature ovarian insufficiency by enhanced transcriptional activation of CLCA2
   Yali Fan et al, 2024, J Ovarian Res CrossRef
6. Identification of novel variants and candidate genes in women with 46,XX complete gonadal dysgenesis
   Leilei Ding et al, 2024, Reprod Biol Endocrinol CrossRef