Female Infertility Genetic Testing for Better Fertility Outcomes

Advanced genetic evaluation helps identify hidden DNA-level factors behind unexplained infertility and supports more personalised fertility care for improved pregnancy planning.
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Understanding Female Infertility Through Genetic Testing

For many women, infertility, recurrent pregnancy loss, or poor response to fertility treatment may be influenced by genetic factors. As part of our reproductive genetics services, female infertility genetic testing helps identify chromosomal variations, gene polymorphisms, and inherited conditions that may affect reproductive outcomes.

At our advanced genetic testing center, specialised female infertility gene panel testing using next-generation sequencing (NGS) provides deeper insights into ovarian function, hormonal response, and implantation potential – enabling clinicians to personalise fertility care.

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Who Should Consider Female Infertility Genetic Testing?

Female infertility genetic testing may be recommended for women who meet the following clinical criteria:
Premature Ovarian Ageing
Women experiencing low egg counts or early menopause.
Recurrent Pregnancy Loss
Patients who have experienced two or more consecutive miscarriages.
History of IVF Failure
Women who have had multiple failed embryo transfers or poor ovarian response to follicle-stimulating hormones.
Advanced Maternal Age
Women over 35 seeking evaluation of chromosomal and reproductive genetic risks.

Genetic Causes of Female Infertility

Understanding the genetic factors that may influence fertility can help identify underlying causes of infertility and guide more personalised reproductive care.

Chromosomal Abnormalities

Structural or numerical chromosome variations, such as balanced translocations or mosaicism, may affect egg quality, implantation, and pregnancy outcomes.

Ovarian Reserve Genes

Variations in genes related to ovarian function can influence egg quantity, hormonal regulation, and the risk of premature ovarian insufficiency.

Hormonal Receptor Polymorphisms

Genetic differences in hormone receptor genes, such as FSHR and LHCGR, may alter ovarian response to fertility treatments and ovulation induction.

Implantation Genetics

Genetic and molecular factors affecting endometrial receptivity can influence embryo implantation success and early pregnancy maintenance.

Female Infertility Genetic Evaluation

The process of a comprehensive genetic evaluation involves high-precision testing tailored to a woman’s unique reproductive history:

Constitutional Karyotyping

Chromosomal analysis helps detect structural or numerical abnormalities such as balanced translocations or mosaicism that may affect fertility, implantation, or pregnancy outcomes.
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We screen for FMR1 gene premutation or full mutation ‑ a leading cause of Primary Ovarian Insufficiency (POI) and early menopause.

Fragile X FMR1 Test

FSHR Gene Test for Female Infertility

This test evaluates the follicle-stimulating hormone receptor to predict how your ovaries will respond to IVF stimulation, preventing “poor responder” cycles.

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By analysing the luteinising hormone receptor, we can fine-tune the "trigger" timing during ovulation induction to maximise egg maturity.

LHCGR Polymorphism Test

GeneSight EVA Female Panel

A genetic evaluation of factors influencing ovarian function and reproductive hormonal pathways to evaluate genetic factors influencing endometrial receptivity and implantation potential.

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Based on genetic evaluation findings, assisted reproductive options such as IVF with preimplantation genetic testing (PGT-A or PGT-M) may be recommended in selected cases.
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Looking for Answers to Your Fertility Challenges?

Turn Genetic Insights into New Beginnings.
Female infertility genetic testing can help identify underlying genetic factors and support more informed decisions on your path to pregnancy.
Consult Our Genetics Team

Clinical Benefits of Female Infertility Genetic Testing

Integrating a female infertility gene panel into your care supports better reproductive planning and may improve the chances of achieving a healthy live birth.
Using results from the FSHR gene test for female infertility, specialists can customise hormone dosages, which may help optimise ovarian response and improve egg yield.
Detecting chromosomal abnormalities or inherited risk factors helps guide personalised fertility care and pregnancy planning to minimise the chances of pregnancy loss.
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Insights from the GeneSight EVA female panel and LHCGR polymorphism testing may help optimise embryo transfer timing and support improved IVF outcomes.