Elodie Persyn

An atlas of genetic scores to predict multi-omic traits

J. Danesh, M. Inouye, C. Foguet, 2022, bioRxiv.

The genetic case for cardiorespiratory fitness as a clinical vital sign and the routine prescription of physical activity in healthcare

M. Hamer, J. Coleman, K. Hanscombe, 2020, Genome Medicine.

DoEstRare: A statistical test to identify local enrichments in rare genomic variants associated with disease

R. Redon, C. Dina, D. Campion, 2017, PloS one.

Genome-wide association study of MRI markers of cerebral small vessel disease in 42,310 participants

C. Lewis, J. Howson, H. Markus, 2020, Nature Communications.

The impact of a fine-scale population stratification on rare variant association test results

R. Redon, C. Dina, E. Persyn, 2018, PloS one.

Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome.

R. Redon, C. Dina, R. Teusan, 2015, Human molecular genetics.

Systematic Mendelian randomization using the human plasma proteome to discover potential therapeutic targets for stroke

J. Danesh, W. Ouwehand, N. Watkins, 2022, Nature Communications.

Genetically predicted levels of the human plasma proteome and risk of stroke: a Mendelian Randomization study

J. Danesh, W. Ouwehand, N. Watkins, 2021, medRxiv.

Graft Fibrosis Over 10 to 15 Years in Pediatric Liver Transplant Recipients: Multicenter Study of Paired, Longitudinal Surveillance Biopsies

A. Demetris, S. Feng, Mercedes Martinez, 2022, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.

Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies

V. Salomaa, C. Lewis, P. Rothwell, 2021, The Lancet Neurology.

Genetically personalised organ-specific metabolic models in health and disease

J. Danesh, M. Inouye, C. Foguet, 2022, Nature Communications.

Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19

J. Danesh, C. Gieger, T. Assimes, 2021, medRxiv.

An atlas of genetic scores to predict multi-omic traits

J. Danesh, M. Inouye, C. Foguet, 2023, Nature.