Associated Papers
Revisiting GDF9 variants in primary ovarian insufficiency: A shift from dominant to recessive pathogenicity?
Jordan P et al.
Gene, 2024
Dendritic Spine in Autism Genetics: Whole-Exome Sequencing Identifying De Novo Variant of CTTNBP2 in a Quad Family Affected by Autism Spectrum Disorder.
Xie Y et al.
Children (basel, Switzerland), 2022
36670631 (PubMed )
Supplement: children-10-00080-s001.zip › children-2044403-supplementary › children-2044403-Supplementary › Supplementary_Tables-R1.xlsx › STS5
Ovarian insufficiency and secondary amenorrhea in a patient with a novel variant within GDF9 gene.
Marinakis NM et al.
Menopause (new York, N.y.), 2022
Next Generation Sequencing Should Be Proposed to Every Woman With "Idiopathic" Primary Ovarian Insufficiency.
Eskenazi S et al.
Journal of the Endocrine Society, 2021
Aberrant GDF9 expression and activation are associated with common human ovarian disorders.
Simpson CM et al.
The Journal of Clinical Endocrinology and Metabolism, 2014
Identification of novel missense mutations of GDF9 in Chinese women with polycystic ovary syndrome.
Wang B et al.
Reproductive Biomedicine Online, 2010
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