Genetics and female infertility

Genetic causes of female infertility

Molecular mechanisms behind women's biological clock

Pre-selected for an award: Chromosome errors in human eggs shape natural fertility

Genes involved in menopause and POI

Genetics and male infertility

Genetic causes of male infertility

Current clinical application of DNA fragmentation analysis based on evidences and potential effects on the offspring

The microbiome as a marker of male fertility potential

SNP, CGH and NGS in the characterization of male infertility

Chromosomal aberrations in male reproductive disorders: evolving diagnosis tools and related genetic counselling

Infertility and heritable diseases

Gene editing

PGT-M

Carrier Screening

Mitochondrial dna copy number

Preventing mitochondrial disease

Development of new technologies to reduce the risk of transmitting mitochondrial DNA mutations

Expanded carrier screening

Development, Diagnostic sensitivity and clinical utility of expanded carrier screening

ESHRE ethics committees recommendations on expanded carrier screening in MAR

Cost-effectiveness consideration for ECS over disease management

PGT

Recommendations for good practice in PGT

The ESHRE PGD Consortium, a Brief History and Summary of Activities

Non-invasive PGT

PGT-A

PGT-A for everyone. Pro / con debate

New evidence on mosaic developmental potential: multicentric study of 822 mosaic embryos diagnosed by preimplantation genetic testing with trophectoderm biopsy

PGT-M

Cell-based non-invasive prenatal testing (cbNIPT): an alternative to chorionic villus sampling to confirm diagnosis of unaffected fetuses following preimplantation genetic testing for monogenic disorders (PGT-M)

A novel long-range DNA sequencing approach improves the design of new protocols for preimplantation genetic testing of monogenic disease (PGT-M).

PGT-M current approaches