Author

Bertrand Fin

Commissariat à l'Énergie Atomique et aux Énergies Alternatives

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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Genetic & Genomic Medicine· 2 Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 4 Organism:human· 3 Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Approach:benchmark study· 1 Research Focus:cell-cell communication· 1 Research Focus:clustering· 1 Research Focus:database / resource· 1

Frequent Co-Authors

Jean‐François DeleuzeiD· 3 shared Anne BolandiD· 2 shared Robert OlasoiD· 2 shared Thomas BourgeroniD· 2 shared A.L. Fitzpatrick· 1 shared AB Kuzma· 1 shared Adam Christian NajiD· 1 shared Adelina OrellanaiD· 1 shared

Activity by Year

2018-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 23 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Jean‐François DeleuzeORCID

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Neoantigenic properties of TP53 variants modify cancer risk in individuals with Li-Fraumeni syndrome

Emilie Montellier, Olivier Manches, Jonathan Gaucher, Claire Freyçon, D B Collantes Hoyos, Sandrine Blanchet, Murielle Verboom, Christina M. Dutzmann, Sophie Coutant, Jacqueline Bou, Bertrand Fin, Robert Olaso, Jean‐François Deleuze, Thierry Frébourg, Benjamin D. Greenbaum, , Pierre L. Hainaut

The paper analyzes how neoantigenic properties of TP53 variants correlate with cancer risk and presentation in Li-Fraumeni syndrome carriers.

EBioMedicine · Dec 9, 2025Peer-reviewedGenetic & Genomic Medicine

LEAP-InovAND a multiscale resource to explore genetics, brain imaging and clinical data in autism

Mathis Fleury, Zakaria Mougin, Claire S. Leblond, Freddy Cliquet, Alexandre Mathieu, Bethany F. M. Oakley, Anna Maruani, Jean‐Madeleine de Sainte Agathe, Selin Korkmaz, Rosemary Holt, Aline Vitrac, Frédérique Amsellem, Aria Batut, Gaelle Botton-Amiot, Thomas Rolland, , Thomas Bourgeron

The paper introduces a multiscale resource integrating genetics, brain imaging, and clinical data from autistic individuals and their relatives to explore genetic and neurobiological patterns in autism.

medRxiv · Nov 24, 2025 · PreprintGenetic & Genomic Medicine

Excessive self-grooming, gene dysregulation and imbalance between the striosome and matrix compartments in the striatum of Shank3 mutant mice

Allain-Thibeault Le Sourd Ferhat, Elisabeth Verpy, Anne Biton, Benoît Forget, Fabrice de Chaumont, Florian Mueller, Le Sourd Anne-Marie, Sabrina Coqueran, Julien Schmitt, Christelle Rochefort, Laure Rondi‐Reig, Aziliz Leboucher, Anne Boland, Bertrand Fin, Jean‐François Deleuze, , Thomas Bourgeron

This study identifies gene dysregulation and striosome-matrix imbalance in Shank3 mutant mice, linking these changes to behavioral abnormalities associated with autism.

bioRxiv · Jan 19, 2022 · PreprintNeuroscience

Meta-analysis of genetic association with diagnosed Alzheimer’s disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing

B K Kunkle, Benjamin Grenier‐Boley, Rebecca Sims, Joshua C. Bis, Adam Christian Naj, Anne Boland, Maria Vronskaya, Sven J. van der Lee, Alexandre Amlie‐Wolf, Céline Bellenguez, Aura Frizzati, Vincent Antoine Chouraki, Eden R. Martin, Kristel Sleegers, Nandini Badarinarayan, , Clive Holmes

This study performs a large GWAS of Alzheimer's disease, identifies four new risk loci, and highlights pathways involving immunity, lipid metabolism, and APP/Aβ processing.

bioRxiv · Apr 5, 2018 · PreprintGenetics