Rethinking Endometriosis and Fertility Through Genomics at EEC 2026 – PrecisionLife
PrecisionLife shared a post on LinkedIn:
“We’re continuing our series of talks at the European Endometriosis Congress 2026 with a second presentation focused on validation of novel genetic insights.
‘Identification and validation of novel genetic risk factors for endometriosis across multiple UK and US patient cohorts’
25 April | 11:30–13:00
Presenter: Krystyna Taylor, VP Product Strategy, PrecisionLife
This work demonstrates how multi-SNP disease signatures identified using combinatorial analytics can be robustly reproduced across independent, multi-ancestry cohorts – addressing one of the biggest limitations of traditional genetic studies.
Key highlights include:
- 1,700+ endometriosis genetic signatures identified in UK Biobank
- Strong validation in US All of Us data, with reproducibility up to 88%
- Identification of 75 novel genes not captured by prior GWAS studies
Together, these findings reinforce the value of moving beyond single-variant analysis to uncover causal biology and clinically relevant patient stratification in complex women’s health conditions.
If you’re attending EEC, come and speak with us.
Connect with Krystyna Taylor and our Chief Medical Officer, Veronique Bouchet, to explore how PrecisionLife is translating these insights into scalable Precision Medicine approaches.
Work in Womens Health? Comment ‘Endometriosis ‘ below to receive a summary of the talk, key findings, and a pre-print of the full study.”
Krystyna Taylor, VP Product Strategy at PrecisionLife, shared PrecisionLife’s post, adding:
“We’ve identified novel genomic signatures linked to infertility that have reproduced across multiple endometriosis cohorts – looking forward to presenting this research at EEC2026 this week in Bologna.”
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