Genetics of human male infertility.
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Summary
The current estimate is that about 30 percent of men seeking help at the infertility clinic are found to have oligozoospermia or azoospermia of unknown aetiology, and there is a need to find the cause of infertility.
- Type
- article
- Published
- 2009-04-01
- Cited by
- 368
- References
- 49
- OpenAlex
- https://openalex.org/W2262973066
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:29192350
Keywords
Azoospermia, Male infertility, Infertility, Azoospermia factor, Y chromosome
References
- Degeneracy in human multicopy RBM (YRRM), a candidate spermatogenesis gene
- Main presentations of sexually transmitted infections in men
- Practical Laboratory Andrology
- Sperm mitochondrial mutations as a cause of low sperm motility.
- Mitochondrial DNA damage is more extensive and persists longer than nuclear DNA damage in human cells following oxidative stress.
- Genetic disorders and spermatogenesis.
- Case-control study of whether subfertility in men is familial
- Semen quality and reproductive health of young Czech men exposed to seasonal air pollution.
- Safety issues in assisted reproduction technology: should ICSI patients have genetic testing before treatment? A practical proposition to help patient information.
- Cystic fibrosis mutation screening before assisted reproduction.
- The human Y chromosome: a 43-interval map based on naturally occurring deletions.
- Genetic dissection of mammalian fertility pathways.
- Cloning and characterization of the human mitochondrial DNA polymerase, DNA polymerase gamma.
- Mitochondrial DNA Content of Human Spermatozoa1
- Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human y chromosome long arm
- High incidence of single nucleotide substitutions in the mitochondrial genome is associated with poor semen parameters in men.
- The influence of varicocele on parameters of fertility in a large group of men presenting to infertility clinics
- Role of the AZFd locus in spermatogenesis.
- The choice and outcome of the fertility treatment of 38 couples in whom the male partner has a Yq microdeletion.
- Identification of two novel proteins that interact with germ-cell-specific RNA-binding proteins DAZ and DAZL1.
Cited by
- A review of genome-wide approaches to study the genetic basis for spermatogenic defects.
- Mild androgen insensitivity syndrome (MAIS): the identification of c.1783C>T mutation in two unrelated infertile men
- The significance of Y chromosome microdeletion analysis in subfertile men with clinical variocele
- The prevalence of Y chromosome microdeletions in Pakistani infertile men
- Sperm selection: effect on sperm DNA quality.
- Comprehensive Genomic Study in Patients with Idiopathic Azoospermia and Oligoasthenoteratozoospermia
- The clinical utility of the Halosperm assay and the development of a simplified method of human semen storage for the testing of sperm DNA fragmentation
- Roles of regulatory T cells in endometriosis-associated infertility
- Étude de gènes impliqués dans la fertilité humaine à partir d'un modèle de souris interspécifiques recombinantes congéniques (IRCS)
- Pilot study for early prognosis of Azoospermia in relation to Y-STR Profiling
- The association of LEP gene Arg105Trp polymorphism and female infertility in the population of Guilan
- The frequency of Yq microdeletion in azoospermic and oligospermic Iranian infertile men
- Chromosome aberrations and spermatogenic disorders in mice with Robertsonian translocation (11; 13).
- Androgen receptor‐CAG repeats in infertile Egyptian men
- Comparison of Sperm Parameters in Patients with Infertility Induced by Genital Infection versus Varicocele.
- Experimental tests of sex allocation theory in a simultaneous hermaphrodite using phenotypic engineering
- Genetic screening for AZF Y chromosome microdeletions in Jordanian azoospermic infertile men.
- Êxpression of inducible nitric oxide synthase (iNOS) in the azoospermic human testis
- Analysis of the AZF Region in Slovak Men with Azoospermia
- Metabolomics fingerprinting of the human seminal plasma of asthenozoospermic patients
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