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 association study of RNF8 and BRDT variants with non-obstructive azoospermia in the Chinese Han population.

Systems biology in reproductive medicine - 1 Jan 2015

Zhang Yan, Song Bing, Du Wei-Dong, He Xiao-Jin, Ruan Jian, Zhou Fu-Sheng, Zuo Xian-Bo, Ye Lei, Xie Xu-Shi, Cao Yun-Xia

Abstract excerpt

Increasing evidence indicates that polymorphisms in genes relevant to spermatogenesis might modulate the efficiency of reproduction in men. Ring finger protein 8 (RNF8) and bromodomain testis-specific (BRDT) are two candidate genes associated with spermatogenesis. Here, we considered potential associations of 14 single nucleotide polymorphisms (SNPs) in RNF8 and BRDT genes in Chinese patients with non-obstructive...

Read the complete abstract on PubMed

Topics

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

Share to Azoospermia
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA-Binding Proteins

Share to Ethnicity

Share to Genome-Wide Association Study

Share to Nuclear Proteins

Share to Ubiquitin-Protein Ligases

Source

Identifiers

PMID: 25374327
DOI: 10.3109/19396368.2014.979513

Genes

RNF8
BRDT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic association study of RNF8 and BRDT variants with non-obstructive azoospermia in the Chinese Han population.PMID 25374327Read ↗

Genetic study of Hormad1 and Hormad2 with non-obstructive azoospermia patients in the male Chinese population.Semantic proximity Read ↗

Excess of rare variants in genes that are key epigenetic regulators of spermatogenesis in the patients with non-obstructive azoospermia.Semantic proximity Read ↗

Association of genetic variants in SOHLH1 and SOHLH2 with non-obstructive azoospermia risk in the Chinese population.Semantic proximity Read ↗

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

A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia.Semantic proximity Read ↗

Genome-wide Loci linked to non-obstructive azoospermia susceptibility may be independent of reduced sperm production in males with normozoospermia.Semantic proximity Read ↗

Association of single nucleotide polymorphisms in the USF1, GTF2A1L and OR2W3 genes with non-obstructive azoospermia in the Chinese population.Semantic proximity Read ↗

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

Association study between polymorphisms of PRMT6, PEX10, SOX5, and nonobstructive azoospermia in the Han Chinese population.Semantic proximity Read ↗

Genetic variants in TEX15 gene conferred susceptibility to spermatogenic failure in the Chinese Han population.Semantic proximity Read ↗

PRDM9 gene polymorphism may not be associated with defective spermatogenesis in the Chinese Han population.Semantic proximity Read ↗

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

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