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

Should TSPYL1 mutation screening be included in routine diagnostics of male idiopathic infertility?

Fertility and sterility - 1 Feb 2012

Javaher Poupak, Stuhrmann Manfred, Wilke Christina, Frenzel Eileen, Manukjan Georgi, Grosshenig Anika, Dechend Frank, Schwaab Eva, Schmidtke Jörg, Schubert Stephanie

Abstract excerpt

OBJECTIVE: To investigate a putative role of TSPYL1 in male idiopathic infertility. DESIGN: Clinical article. SETTING: University hospital. PATIENT(S): A total of 104 infertile men were selected with idiopathic nonobstructive azoospermia, cryptozoospermia, oligozoospermia, oligonecrozoospermia, and oligoasthenoteratozoospermia (OAT) syndrome, along with a control group of 106 men with proven paternity....

Read the complete abstract on PubMed

Topics

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

Share to Chi-Square Distribution
Share to Fertility

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Germany

Share to Infertility, Male

Share to Nuclear Proteins

Share to Predictive Value of Tests

Share to Risk Assessment

Source

Identifiers

PMID: 22137496
DOI: 10.1016/j.fertnstert.2011.11.002

Genes

TSPYL1
OAT

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Should TSPYL1 mutation screening be included in routine diagnostics of male idiopathic infertility?PMID 22137496Read ↗

Sequence recombination in exon 1 of the TSPY gene in men with impaired fertility.Semantic proximity Read ↗

Novel Mutations of TSPY1 Gene Associate Spermatogenic Failure Among Men.Semantic proximity Read ↗

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

Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility.Semantic proximity Read ↗

DMRT1 mutations are rarely associated with male infertility.Semantic proximity Read ↗

Role of testis‑specific serine kinase 1B in undiagnosed male infertility.Semantic proximity Read ↗

Analysis of 29 Targeted Genes for Non-obstructive Azoospermia: the Relationship Between Genetic Testing and Testicular HistologySemantic proximity Read ↗

An M1AP homozygous splice-site mutation associated with severe oligozoospermia in a consanguineous family.Semantic proximity Read ↗

Novel RHOXF1 mutation causes male infertility by inducing severe oligoasthenozoospermia.Semantic proximity Read ↗

Analysis of the correlation of CATSPER single nucleotide polymorphisms (SNPs) with idiopathic asthenospermia.Semantic proximity Read ↗

Identification of the PRM1 gene mutations in oligoasthenoteratozoospermic men.Semantic proximity Read ↗

TSPY gene copy number as a potential new risk factor for male infertilitySemantic proximity Read ↗

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