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

Analysis of copy number variation in men with non‐obstructive azoospermia

30 Aug 2022

Abstract excerpt

BACKGROUND: Recent findings demonstrate that single nucleotide variants can cause non-obstructive azoospermia (NOA). In contrast, copy number variants (CNVs) were only analysed in few studies in infertile men. Some have reported a higher prevalence of CNVs in infertile versus fertile men. OBJECTIVES: This study aimed to elucidate if CNVs are associated with NOA. MATERIALS AND METHODS: We performed array-based...

Read the complete abstract on PubMed

Topics

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

Share to Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 36041235
DOI: 10.1111/andr.13267

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analysis of copy number variation in men with non‐obstructive azoospermiaPMID 36041235Read ↗

Genetic and epigenetic insights into non-obstructive azoospermia: mechanisms, biomarkers, and clinical perspectivesSemantic proximity Read ↗

Novel copy number variations within SYCE1 caused meiotic arrest and non-obstructive azoospermia.Semantic proximity Read ↗

Systematic molecular analyses for 115 karyotypically normal men with isolated non-obstructive azoospermia.Semantic proximity Read ↗

Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermiaSemantic proximity Read ↗

Whole-genome sequencing identifies new candidate genes for nonobstructive azoospermia.Semantic proximity Read ↗

Genetic insights into non-obstructive azoospermia: Implications for diagnosis and TESE outcomesSemantic proximity Read ↗

Actionable secondary findings following exome sequencing of 836 non-obstructive azoospermia cases and their value in patient managementSemantic proximity Read ↗

Genetic and functional analysis reveals novel mutations in meiotic genes underlying non-obstructive azoospermia.Semantic proximity Read ↗

Point-of-care whole-exome sequencing of idiopathic male infertility.Semantic proximity Read ↗

Genetic Factors of Non-Obstructive Azoospermia: Consequences on Patients’ and Offspring HealthSemantic proximity Read ↗

DDX3Y is likely the key spermatogenic factor in the AZFa region that contributes to human non-obstructive azoospermiaSemantic proximity Read ↗

Genetic determinants of testicular sperm extraction outcomes: insights from a large multicentre study of men with non-obstructive azoospermiaSemantic proximity Read ↗

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