Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Screening of premature ovarian insufficiency associated genes in Hungarian patients with next generation sequencing.

BMC medical genomics - 22 Apr 2024

Illés Anett, Pikó Henriett, Árvai Kristóf, Donka Veronika, Szepesi Olívia, Kósa János, Lakatos Péter, Beke Artúr

Abstract excerpt

BACKGROUND: Premature ovarian insuffiency (POI) is one of the main cause behind infertility. The genetic analysis of POI should be part of the clinical diagnostics, as several genes have been implicated in the genetic background of it. The aim of our study was to analyse the genetic background of POI in a Hungarian cohort. METHODS: The age of onset was between 15 and 39 years. All patients had the 46,XX karyotype...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to High-Throughput Nucleotide Sequencing

Share to Hungary

Share to Mutation

Share to Primary Ovarian Insufficiency

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 38649916
DOI: 10.1186/s12920-024-01873-z
PMCID: PMC11036647

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Screening of premature ovarian insufficiency associated genes in Hungarian patients with next generation sequencing.PMID 38649916Read ↗

Next Generation Sequencing Should Be Proposed to Every Woman With “Idiopathic” Primary Ovarian InsufficiencySemantic proximity Read ↗

Whole-exome sequencing in patients with premature ovarian insufficiency: early detection and early interventionSemantic proximity Read ↗

Genetics of ovarian insufficiency and defects of folliculogenesis.Semantic proximity Read ↗

Screening of targeted panel genes in Brazilian patients with primary ovarian insufficiencySemantic proximity Read ↗

Landscape of pathogenic mutations in premature ovarian insufficiency.Semantic proximity Read ↗

Targeted Next-Generation Sequencing Indicates a Frequent Oligogenic Involvement in Primary Ovarian Insufficiency Onset.Semantic proximity Read ↗

Next-generation sequencing of 500 POI patients identified novel responsible monogenic and oligogenic variants.Semantic proximity Read ↗

Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of DiseaseSemantic proximity Read ↗

Genetic landscape of a large cohort of Primary Ovarian Insufficiency: New genes and pathways and implications for personalized medicineSemantic proximity Read ↗

Monogenic causes of Premature Ovarian Insufficiency are rare and mostly recessiveSemantic proximity Read ↗

A Tiered Approach to Exome Sequencing Analysis in Early-Onset Primary Ovarian Insufficiency.Semantic proximity Read ↗

Investigation of the molecular genetic causes of non-syndromic primary ovarian ınsufficiency by next generation sequencing analysis.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.