Associated Papers
Case Report and Literature Review: A 46,XX Infant with Atypical Genitalia Diagnosed with Primary Ovarian Insufficiency Caused by HFM1 Gene Variants.
Yuan Z et al.
Hormone Research in Paediatrics, 2025
DNA double-strand break genetic variants in patients with premature ovarian insufficiency.
Ding X et al.
Journal of Ovarian Research, 2023
Novel deleterious splicing variant in HFM1 causes gametogenesis defect and recurrent implantation failure: concerning the risk of chromosomal abnormalities in embryos.
Tang F et al.
Journal of Assisted Reproduction and Genetics, 2023
Novel pathogenic splicing variants in helicase for meiosis 1 (HFM1) are associated with diminished ovarian reserve and poor pregnancy outcomes.
Yu L et al.
Journal of Assisted Reproduction and Genetics, 2022
Meiotic Recombination Defects and Premature Ovarian Insufficiency.
Huang C et al.
Frontiers in Cell and Developmental Biology, 2021
The ChinaMAP analytics of deep whole genome sequences in 10,588 individuals.
Cao Y et al.
Cell Research, 2020
32355288 (PubMed )
Supplement: 41422_2020_322_MOESM14_ESM.xlsx › S7
Association analysis between HFM1 variation and primary ovarian insufficiency in Chinese women.
Pu D et al.
Clinical Genetics, 2016
Variation analysis of EXO1 gene in Chinese patients with premature ovarian failure.
Su S et al.
Reproductive Biomedicine Online, 2016
Mutations in HFM1 in recessive primary ovarian insufficiency.
Wang J et al.
The New England Journal of Medicine, 2014
Genetics of primary ovarian insufficiency: new developments and opportunities.
Qin Y et al.
Human Reproduction Update, 0
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