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

Genetic Architecture of Azoospermia—Time to Advance the Standard of Care

8 Jun 2022

Abstract excerpt

No abstract is available from the source.

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 Reproductive biology and impacts on aquatic species
Share to Sperm and Testicular Function

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 35690514
DOI: 10.1016/j.eururo.2022.05.011

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic Architecture of Azoospermia—Time to Advance the Standard of CarePMID 35690514Read ↗

Evaluating genetic causes of azoospermia: What can we learn from a complex cellular structure and single-cell transcriptomics of the human testis?Semantic proximity Read ↗

Role of Genetics in AzoospermiaSemantic proximity Read ↗

Genetic defects in human azoospermiaSemantic proximity Read ↗

Summarizing the human genes and their variants causative of non-obstructive azoospermia uncovered using whole genome/exome sequencingSemantic proximity Read ↗

Genetics of Azoospermia.Semantic proximity Read ↗

Genetic Landscape of Nonobstructive Azoospermia and New Perspectives for the ClinicSemantic proximity Read ↗

Review of AzoospermiaSemantic proximity Read ↗

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

Genetics: Mutations underlying azoospermia identified on the X chromosome.Semantic proximity Read ↗

Unraveling epigenomic abnormality in azoospermic human males by WGBS, RNA-Seq, and transcriptome profiling analysesSemantic proximity Read ↗

Diverse Monogenic Subforms of Human Spermatogenic FailureSemantic proximity Read ↗

Diverse monogenic subforms of human spermatogenic failureSemantic proximity Read ↗

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