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GLP-1s for ME/CFS and long COVID: hype, hope and hidden dangers

The promise of GLP-1s is real but so is the risk of getting it wrong, particularly in patient populations such as ME/CFS and long COVID

Publication

POSTER: ME & Long COVID - Genetics, Tests, GLP-1s and other Drugs

Novel reproducible genetic associations, disease overlaps, clinical studies, protective biology, and repurposing opportunities

Publication

PRESENTATION: Genetic Risk Factors for Endometriosis Identified and Validated

Combinatorial analysis reveals and reproduces the genetic drivers of endometriosis, unlocking new understanding of the disease biology

Publication

PRESENTATION: Uncovering the Genetic Drivers of Female Infertility in Endometriosis

New insights from combinatorial analysis reveal distinct biological mechanisms underpinning infertility risk

Blog

Predicting GLP-1 response: building the foundation for precision prescribing

PrecisionLife and Ovation aim to make it possible to predict which patients are most likely to benefit from specific GLP-1 therapies before treatment begins.

Publication

POSTER: Genetic Risk Factors and Shared Biology in ME/CFS and Long COVID

Shared genetic risk factors between ME/CFS and Long COVID strengthens biological understanding and creates opportunities for earlier diagnosis, mechanism-guided therapy, and preventive interventions

Disease Study

Unraveling the biology of ME/CFS and long COVID

See the progress that we've made in understanding ME/CFS and long COVID to find new diagnostic and therapeutic options for patients

Publication

POSTER: Characterizing the Genetic and Biological Differences Between Endometriosis and Adenomyosis

Furthering our understanding of the overlapping and unique disease mechanisms driving each condition, with direct implications for personalized diagnosis and treatment

Publication

PAPER: Reproducibility of Genetic Risk Factors Identified for Long COVID Using Combinatorial Analysis

First ever confirmation of long COVID genetic associations identified in reproduction of results across US and UK patient cohorts with diverse ancestries

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