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

Whole-genome sequencing identifies new candidate genes for nonobstructive azoospermia.

Andrology - 1 Nov 2022

Malcher Agnieszka, Stokowy Tomasz, Berman Andrea, Olszewska Marta, Jedrzejczak Piotr, Sielski Dawid, Nowakowski Adam, Rozwadowska Natalia, Yatsenko Alexander N, Kurpisz Maciej K

Abstract excerpt

BACKGROUND: Genetic causes that lead to spermatogenetic failure in patients with nonobstructive azoospermia (NOA) have not been yet completely established. OBJECTIVE: To identify low-frequency NOA-associated single nucleotide variants (SNVs) using whole-genome sequencing (WGS). MATERIALS AND METHODS: Men with various types of NOA (n = 39), including samples that had been previously tested with whole-exome...

Read the complete abstract on PubMed

Topics

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

Share to Argonaute Proteins
Share to Azoospermia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Calcium-Binding Proteins

Share to DNA Helicases

Share to Exome Sequencing

Share to Immunoglobulins

Share to N-Acetylglucosaminyltransferases

Share to Nucleotides

Source

Open in PubMed Open full text

Identifiers

PMID: 36017582
DOI: 10.1111/andr.13269
PMCID: PMC9826517

Genes

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Whole-genome sequencing identifies new candidate genes for nonobstructive azoospermia.PMID 36017582Read ↗

Whole-exome sequencing of a large Chinese azoospermia and severe oligospermia cohort identifies novel infertility causative variants and genes.Semantic proximity Read ↗

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

Next-generation sequencing: toward an increase in the diagnostic yield in patients with apparently idiopathic spermatogenic failure.Semantic proximity Read ↗

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

Genetic profiling of azoospermic men to identify the etiology and predict reproductive potential.Semantic proximity Read ↗

Identification of risk genes in Chinese nonobstructive azoospermia patients based on whole-exome sequencing.Semantic proximity Read ↗

How exome sequencing improves the diagnostics and management of men with non‐syndromic infertilitySemantic proximity Read ↗

Whole exome sequencing analysis of 167 men with primary infertilitySemantic proximity Read ↗

Genetics of Azoospermia.Semantic proximity Read ↗

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

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

Copy number variations in spermatogenic failure patients with chromosomal abnormalities and unexplained azoospermia.Semantic proximity Read ↗

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