Associated Papers
Identification of novel variants underlying non-syndromic primary ovarian insufficiency using a targeted NGS gene panel.
Veneziano C et al.
Frontiers in Endocrinology, 2025
41458559 (PubMed )
Supplement: Table4.xlsx › sheet1
Searching for the 'X' factor: investigating the genetics of primary ovarian insufficiency.
Knight A et al.
Journal of Ovarian Research, 2024
Screening of premature ovarian insufficiency associated genes in Hungarian patients with next generation sequencing.
Illés A et al.
Bmc Medical Genomics, 2024
Bi-allelic mutation in SEC16B alters collagen trafficking and increases ER stress.
El-Gazzar A et al.
Embo Molecular Medicine, 2023
36916446 (PubMed )
Supplement: EMMM-15-e16834-s012.xlsx › WES_SEC16B_mutant
Exome sequencing of early-onset patients supports genetic heterogeneity in colorectal cancer.
Fernández-Rozadilla C et al.
Scientific Reports, 2021
34045552 (PubMed )
Supplement: 41598_2021_90590_MOESM1_ESM.docx
Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B.
Bione S et al.
Human Reproduction (oxford, England), 2004
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