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

Copy number variations in female infertility in China

1 Jun 2019

Abstract excerpt

Abstract Copy number variation (CNV) is a main cause of male infertility, yet its influence still remains elusive in that of females. To investigate the correlation between CNV and female infertility, we applied whole-genome CNV analyses by next generation Sequencing (NGS), and analyzed 324 female infertility samples in Xinjiang Province, People's Republic of China. We identified 29 CNVs in total, of which 10...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomal and Genetic Variations
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 31523614
DOI: 10.2478/bjmg-2019-0005

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Copy number variations in female infertility in ChinaPMID 31523614Read ↗

[Genome-wide copy number scan in Chinese patients with premature ovarian failure].Semantic proximity Read ↗

The search for SNPs, CNVs, and epigenetic variants associated with the complex disease of male infertility.Semantic proximity Read ↗

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

Characterization of Copy-Number Variations and Possible Candidate Genes in Recurrent Pregnancy Losses.Semantic proximity Read ↗

Systematic mapping and in silico reevaluation of genomic copy number variations in primary ovarian insufficiency.Semantic proximity Read ↗

Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases.Semantic proximity Read ↗

IDDB: a comprehensive resource featuring genes, variants and characteristics associated with infertility.Semantic proximity Read ↗

A genomics approach to females with infertility and recurrent pregnancy loss.Semantic proximity Read ↗

Copy Number Variants in Premature Ovarian Failure and Ovarian DysgenesisSemantic proximity Read ↗

A Comprehensive Genetic Study of Microtubule-Associated Gene Clusters for Male Infertility in a Taiwanese Cohort.Semantic proximity Read ↗

Compilation of copy number variants identified in phenotypically normal and parous Japanese women.Semantic proximity Read ↗

Improved detection of disease-associated variation by sex-specific characterization and prediction of genes required for fertility.Semantic proximity Read ↗

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