Author

Francis Fidelle

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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Genomics· 2

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Research Focus:fine-mapping· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Carole Moreno‐RomieuxiD· 2 shared Céline André· 2 shared Florence Plisson‐Petit· 2 shared Florent Woloszyn· 2 shared I. Granado-TajadaiD· 2 shared Julien Sarry· 2 shared Maxime Ben BraiekiD· 2 shared Philippe BardouiD· 2 shared

Activity by Year

2023-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Carole Moreno‐RomieuxORCID

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2 papers

Recent·Most cited

A single base pair duplication in SLC33A1 gene causes fetal losses and neonatal lethality in Manech Tete Rousse dairy sheep

Maxime Ben Braiek, Soline Szymczak, Céline André, Philippe Bardou, Francis Fidelle, I. Granado-Tajada, Florence Plisson‐Petit, Julien Sarry, Florent Woloszyn, Carole Moreno‐Romieux, Stéphane Fabre

The paper identifies a single base pair duplication in SLC33A1 causing fetal losses and neonatal lethality in MTR sheep through whole genome sequencing and breeding studies.

bioRxiv · Mar 13, 2023 · PreprintGenomics

Homozygous haplotype deficiency in Manech Tete Rousse dairy sheep revealed a nonsense variant in MMUT gene affecting newborn lamb viability

Maxime Ben Braiek, Carole Moreno‐Romieux, Céline André, Jean‐Michel Astruc, Philippe Bardou, Arnaud Bordes, Frédéric Debat, Francis Fidelle, I. Granado-Tajada, Chris Hozé, Florence Plisson‐Petit, François Rivemale, Julien Sarry, Némuel Tadi, Florent Woloszyn, Stéphane Fabre

The paper identifies recessive deleterious variants in Manech Tete Rousse dairy sheep using genome scans, finds a nonsense mutation in MMUT causing lamb mortality, and links other haplotypes to morphological traits.

bioRxiv · Mar 10, 2023 · PreprintGenomics