Author

F. Fenollar

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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Microbiology· 2 Immunology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:host-pathogen & immune response· 2 Assay:proteomics· 2 Research Focus:cell type annotation· 1 Organism:human· 1 Organism:mouse· 1 Organism:non-human primate· 1 Organism:rat· 1

Frequent Co-Authors

B. Davoust· 2 shared D. Raoult· 2 shared N. Orain· 2 shared O. Mediannikov· 2 shared S. Edouard· 2 shared A. Guerin· 1 shared B. Bigio· 1 shared C. Deswarte· 1 shared

Activity by Year

2017-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 28 mutual co-author links

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2 shared papersMicrobiology

B. Davoust

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Evidence of antibodies against SARS-CoV-2 in wild mustelids from Brittany (France)

B. Davoust, P. Guerin, N. Orain, C. Fligny, F. Flirden, F. Fenollar, O. Mediannikov, S. Edouard

The paper reports seropositivity for SARS-CoV-2 in wild mustelids in Brittany, France, detected via western blot and ELISA, despite negative PCR results.

bioRxiv · Jan 20, 2022Microbiology

Stool serology: development of a non-invasive immunological method for the detection of Enterovirus-specific antibodies in Congo gorilla faeces

Y. Sereme, S. M. Zarza, H. Medkour, I. Amona, F. Fenollar, J. Akiana, S. Mezouar, N. Orain, J. Vitte, B. Davoust, D. Raoult, O. Mediannikov

The paper develops a non-invasive method to detect Enterovirus-specific antibodies in gorilla faeces, finding specific antibodies in 4/16 gorilla samples and 2/3 human samples.

bioRxiv · Nov 28, 2020Microbiology

IRF4 haploinsufficiency in a family with Whipples disease

A. Guerin, G. Kerner, N. Marr, J. G. Markle, F. Fenollar, N. Wong, S. Boughorbel, D. T. Avery, C. Ma, S. Bougarn, M. Bouaziz, V. Beziat, E. Della Mina, T. Lazarovt, L. Worley, , J.-L. Casanova

This study identifies IRF4 haploinsufficiency as the genetic cause of Whipples disease in a family, showing age-dependent incomplete penetrance and chronic Tw carriage preceding disease onset.

bioRxiv · Oct 3, 2017Immunology