Personal information

Applied statistics; genetics; genetic association studies
United Kingdom

Activities

Employment (3)

University of Cambridge: Cambridge, GB

2021-02 to present | Research Associate (Department of Public Health and Primary Care)
Employment
Source: Self-asserted source
Elodie Persyn

King's College London: London, London, GB

2018-02 to 2021-02 | Research Associate in Statistical Genetics (Medical and Molecular Genetics)
Employment
Source: Self-asserted source
Elodie Persyn

INSERM UMR1087: Nantes, FR

2017-10 to 2018-01 | Research Engineer
Employment
Source: Self-asserted source
Elodie Persyn

Education and qualifications (3)

Université de Nantes: Nantes, Pays de la Loire, FR

2014-10 to 2017-10 | PhD (l'institut du thorax, INSERM UMR1087)
Education
Source: Self-asserted source
Elodie Persyn

AGROCAMPUS OUEST: Rennes, Bretagne, FR

2013-09 to 2014-09 | Master Applied Statistics in Agronomic and Food Sciences
Education
Source: Self-asserted source
Elodie Persyn

AGROCAMPUS OUEST: Rennes, Bretagne, FR

2010-09 to 2013-09 | Master Celular and Molecular Sciences
Education
Source: Self-asserted source
Elodie Persyn

Works (10)

The common VTE-protective G haplotype of F5 increases factor V-short, TFPI function, and risk of bleeding

Blood Advances
2025-01-14 | Journal article
Contributors: Matthew C. Sims; Magdalena Gierula; Jonathan C. Stephens; Alex Tokolyi; Luca Stefanucci; Elodie Persyn; Luanluan Sun; Janine H. Collins; Emma E. Davenport; Emanuele Di Angelantonio et al.
Source: check_circle
Crossref

Metabolic reaction fluxes as amplifiers and buffers of risk alleles for coronary artery disease

2024-08-20 | Preprint
Contributors: Carles Foguet; Xilin Jiang; Scott C. Ritchie; Elodie Persyn; Yu Xu; Chief Ben-Eghan; Emanuele Di Angelantonio; John Danesh; Adam S. Butterworth; Samuel A. Lambert et al.
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Crossref

Genetic determinants of blood gene expression and splicing and their contribution to molecular phenotypes and health outcomes

2023-11-27 | Preprint
Contributors: Alex Tokolyi; Elodie Persyn; Artika P. Nath; Katie L. Burnham; Jonathan Marten; Thomas Vanderstichele; Manuel Tardaguila; David Stacey; Ben Farr; Vivek Iyer et al.
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Crossref

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

Nature Communications
2022-10-17 | Journal article
Contributors: Lingyan Chen; James E. Peters; Bram Prins; Elodie Persyn; Matthew Traylor; Praveen Surendran; Savita Karthikeyan; Ekaterina Yonova-Doing; Emanuele Di Angelantonio; David J. Roberts et al.
Source: check_circle
Crossref

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

2021-11-15 | Preprint
Contributors: Lingyan Chen; James Peters; Bram Prins; Elodie Persyn; Matthew Traylor; Praveen Surendran; Savita Karthikeyan; Ekaterina Yonova-Doing; Emanuele Di Angelantonio; David Roberts et al.
Source: check_circle
Crossref

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

2020-12-09 | Other
Contributors: Ken B. Hanscombe; Elodie Persyn; Matthew Traylor; Kylie P. Glanville; Mark Hamer; Jonathan R. I. Coleman; Cathryn M. Lewis
Source: check_circle
Crossref

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

Nature Communications
2020-05-01 | Journal article
Contributors: Elodie Persyn; Ken B. Hanscombe; Joanna M. M. Howson; Cathryn M. Lewis; Matthew Traylor; Hugh S. Markus
Source: check_circle
Crossref

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

PLOS ONE
2018-12-06 | Journal article
Contributors: Elodie Persyn; David Meyre; Richard Redon; Lise Bellanger; Christian Dina
Source: check_circle
Crossref

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

PLOS ONE
2017-07-24 | Journal article
Contributors: Elodie Persyn; Kai Wang; Matilde Karakachoff; Solena Le Scouarnec; Camille Le Clézio; Dominique Campion; French Exome Consortium; Jean-Jacques Schott; Richard Redon; Lise Bellanger et al.
Source: check_circle
Crossref

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

Human Molecular Genetics
2015 | Journal article
ARXIV:

/oup/backfile/content_public/journal/hmg/24/10/10.1093_hmg_ddv036/1/ddv036.pdf

Source: Self-asserted source
Elodie Persyn
grade
Preferred source (of 2)‎

Peer review (2 reviews for 1 publication/grant)

Review activity for Cell genomics. (2)