Author

O. Bernard

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Cell Biology· 1 Ecology· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:ecology & biodiversity· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

A. Forman· 1 shared A. Fritsche· 1 shared A. Hansen· 1 shared A. Sciandra· 1 shared A.-C. Baudoux· 1 shared A.M. Nielsen· 1 shared Adem Y. DawediD· 1 shared Agnete Troen LundgaardiD· 1 shared

Activity by Year

2018-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetics

A. Forman

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

A thermal trade-off between viral production and degradation drives phytoplankton-virus population dynamics

D. Demory, J. Weitz, A.-C. Baudoux, S. Touzeau, N. Simon, S. Ranbouille, A. Sciandra, O. Bernard

The paper models how temperature affects viral production and degradation in phytoplankton-virus interactions, showing climate change could alter host-virus dynamics.

bioRxiv · Aug 18, 2020Ecology

Variation in the plasma membrane monoamine transporter (PMAT, encoded in SLC29A4) and organic cation transporter 1 (OCT1, encoded in SLC22A1) and gastrointestinal intolerance to metformin in type 2 diabetes: an IMI DIRECT study

Adem Y. Dawed, Kaixin Zhou, Nienke van Leeuwen, Anubha Mahajan, Neil Robertson, Robert Wilhelm Koivula, Petra J. M. Elders, Simone P. Rauh, Angus G. Jones, Reinhard Walter Holl, Julia Stingl, Paul W. Franks, Mark I. McCarthy, Leen M. ‘t Hart, Ewan R. Pearson, , A. Forman

This study investigates the association between genetic variants in PMAT and OCT1 transporters and metformin gastrointestinal intolerance in type 2 diabetes patients.

Diabetes Care · Mar 18, 2019Peer-reviewedGenetics

Inhibition of platelet function by targeting the platelet cytoskeleton via the LIMK-signaling pathway.

J. Antonipillai, S. Rigby, N. Bassler, K. Peter, O. Bernard

This study investigates how inhibiting LIMK activity affects platelet function by modulating actin dynamics, suggesting it could inhibit platelet aggregation and thrombus formation.

bioRxiv · Oct 8, 2018 · PreprintCell Biology