Next generation sequencing in women affected by nonsyndromic premature ovarian failure displays new potential causative genes and mutations.
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Summary
Next generation sequencing (NGS) is recommended as a powerful tool for identifying new molecular actors in POF and for future diagnostic/prognostic purposes.
- Type
- article
- Published
- 2015-07-01
- Cited by
- 66
- References
- 68
- Access
- Open access
- OpenAlex
- https://openalex.org/W25989972
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:22510042
Keywords
Art
References
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Cited by
- Genetics of primary ovarian insufficiency: new developments and opportunities
- Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencing.
- A novel follicle-stimulating hormone receptor mutation causing primary ovarian failure: a fertility application of whole exome sequencing.
- Primary ovarian insufficiency associated with autosomal abnormalities: from chromosome to genome-wide and beyond
- Ovarian Physiology and GWAS: Biobanks, Biology, and Beyond
- Primary Ovarian Insufficiency
- Array-CGH diagnosis in ovarian failure: identification of new molecular actors for ovarian physiology
- Genetics of primary ovarian insufficiency
- Molecular approaches for HPV genotyping and HPV-DNA physical status
- A potential functional association between mutant BMPR2 and primary ovarian insufficiency
- New mutations in non-syndromic primary ovarian insufficiency patients identified via whole-exome sequencing
- The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing.
- Novel genes and mutations in patients affected by recurrent pregnancy loss
- Ovarian Follicular Theca Cell Recruitment, Differentiation, and Impact on Fertility: 2017 Update.
- Premature Ovarian Insufficiency - an update on recent advances in understanding and management
- GENOME WIDE ANALYSIS IN A COHORT OF 46,XX PATIENTS AFFECTED BY AN EXTREME PHENOTYPE OF PRIMARY OVARIAN INSUFFICIENCY: AN EFFICIENT TOOL TO IDENTIFY NEW GENES INVOLVED IN OOCYTE MATURATION AND DIFFERENTIATION
- Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian Insufficiency.
- Molecular Genetics of Premature Ovarian Insufficiency.
- Connecting links between genetic factors defining ovarian reserve and recurrent miscarriages
- A survey of undetected, clinically relevant chromosome abnormalities when replacing postnatal karyotyping by Whole Genome Sequencing.
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