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Genome-wide association study identifies candidate genes for male fertility traits in humans

Genome-wide association study identifies candidate genes for male fertility traits in humans

http://www.wikidata.org/entity/Q36017107

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The Biodemography of Fertility: A Review and Future Research Frontiers Variations in Antioxidant Genes and Male Infertility What should it take to describe a substance or product as 'sperm-safe'Expression Quantitative Trait Locus Mapping Studies in Mid-secretory Phase Endometrial Cells Identifies HLA-F and TAP2 as Fecundability-Associated Genes A model-based approach for identifying signatures of ancient balancing selection in genetic data Anogenital distance as a marker of androgen exposure in humans.Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.A single nucleotide polymorphism in COQ9 affects mitochondrial and ovarian function and fertility in Holstein cows†.Genomic patterns of introgression in rainbow and westslope cutthroat trout illuminated by overlapping paired-end RAD sequencing The "omics" of human male infertility: integrating big data in a systems biology approach.Glutathione S-transferase P1 Ile105Val Polymorphism and Male Infertility Risk: An Updated Meta-analysis.Genetic loci associated with coronary artery disease harbor evidence of selection and antagonistic pleiotropy A genome-wide analysis of open chromatin in human epididymis epithelial cells reveals candidate regulatory elements for genes coordinating epididymal function.Strong association of SLC1A1 and DPF3 gene variants with idiopathic male infertility in Han Chinese.Genetic susceptibility to male infertility: news from genome-wide association studies.Genome-wide association study identifies phospholipase C zeta 1 (PLCz1) as a stallion fertility locus in Hanoverian warmblood horses Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family.Male Reproductive Disorders and Fertility Trends: Influences of Environment and Genetic Susceptibility.Environmentally induced epigenetic transgenerational inheritance of male infertility.Large genomic region free of GWAS-based common variants contains fertility-related genes Targeted Germline Modifications in Rats Using CRISPR/Cas9 and Spermatogonial Stem Cells Clinically relevant known and candidate genes for obesity and their overlap with human infertility and reproduction.Acetylproteomic analysis reveals functional implications of lysine acetylation in human spermatozoa (sperm)Genome-wide association studies in Africans and African Americans: expanding the framework of the genomics of human traits and disease.Molecular Effects of Polymorphism in the 3'UTR of Unc-5 homolog C Associated with Conception Rate in Holsteins.Severe impairment of male reproductive organ development in a low SMN expressing mouse model of spinal muscular atrophy Genetics of the polycystic ovary syndrome.Improved detection of disease-associated variation by sex-specific characterization and prediction of genes required for fertility New genetic markers for male fertility.Genetic variants determining survival and fertility in an adverse African environment: a population-based large-scale candidate gene association study.Association of progesterone receptor gene polymorphism with male infertility and clinical outcome of ICSI.Detection of mutations in the CYP21A2 gene: genotype-phenotype correlation in Slovenian couples with conceiving problems.Genetic links between post-reproductive lifespan and family size in Framingham.Variants in DPF3 and DSCAML1 are associated with sperm morphology.Seminal plasma as a diagnostic fluid for male reproductive system disorders.Global human tissue profiling and protein network analysis reveals distinct levels of transcriptional germline-specificity and identifies target genes for male infertility.A familial study of azoospermic men identifies three novel causative mutations in three new human azoospermia genes.Correlation between SHBG gene polymorphism and male infertility in Han population of Henan province of China: A STROBE-compliant article.Genome-wide Loci linked to non-obstructive azoospermia susceptibility may be independent of reduced sperm production in males with normozoospermia.Implication of FKBP6 for male fertility in horses.

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Genome-wide association study identifies candidate genes for male fertility traits in humans

http://www.wikidata.org/entity/Q36017107

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J.AJHG.2012.04.016

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American Journal of Human Genetics

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Genome-wide association study ...... ale fertility traits in humans

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Gail S Prins

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Gülüm Kosova

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P2860

Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function

The ubiquitin-like protein FAT10 mediates NF-kappaB activation

Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) gene.

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

Inbreeding effects on fertility in humans: evidence for reproductive compensation.

Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13

Regulatory mechanisms involved in the control of ubiquitin homeostasis

Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6q

Statistical tests for detection of misspecified relationships by use of genome-screen data.

Isolation and expression profiling of genes upregulated in the peripheral blood cells of systemic lupus erythematosus patients.

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genome-wide association study

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