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

Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia.

Journal of andrology - 1 Jan 2000

Aston Kenneth I, Carrell Douglas T

Abstract excerpt

Male infertility affects a large proportion of the population. In spite of the magnitude of the problem and the considerable research effort that has been made to understand its causes, a large proportion of male infertility cases remain idiopathic in nature. This pilot genome-wide association study employed genotyping microarray technology to interrogate over 370,000 single-nucleotide polymorphisms (SNPs) in men...

Read the complete abstract on PubMed

Topics

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

Share to Azoospermia
Share to Gene Frequency
Share to Genome-Wide Association Study

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infertility, Male

Share to Oligonucleotide Array Sequence Analysis

Share to Oligospermia

Share to Polymorphism, Single Nucleotide

Share to White People

Source

Identifiers

PMID: 19478329
DOI: 10.2164/jandrol.109.007971

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

Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia.PMID 19478329Read ↗

Evaluation of 172 candidate polymorphisms for association with oligozoospermia or azoospermia in a large cohort of men of European descent.Semantic proximity Read ↗

Mate-pair genome sequencing reveals structural variants for idiopathic male infertilitySemantic proximity Read ↗

Evaluation of five candidate genes from GWAS for association with oligozoospermia in a Han Chinese population.Semantic proximity Read ↗

Genome-wide expression of azoospermia testes demonstrates a specific profile and implicates ART3 in genetic susceptibility.Semantic proximity Read ↗

Genetic susceptibility to male infertility: news from genome-wide association studies.Semantic proximity Read ↗

Progress in the genetic studies of spermatogenesis abnormalities.Semantic proximity Read ↗

Single gene defects leading to sperm quantitative anomaliesSemantic proximity Read ↗

Pathogenic variants screening in five non-obstructive azoospermia-associated genes.Semantic proximity Read ↗

Associations of single nucleotide polymorphisms in the Pygo2 coding sequence with idiopathic oligospermia and azoospermia.Semantic proximity Read ↗

Multicenter study of genetic abnormalities associated with severe oligospermia and non-obstructive azoospermiaSemantic proximity Read ↗

Genetic Testing for Monogenic Forms of Male Infertility Contributes to the Clinical Diagnosis of Men with Severe Idiopathic Male InfertilitySemantic proximity Read ↗

Genetic aspects of idiopathic asthenozoospermia as a cause of male infertilitySemantic proximity Read ↗

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