Author

Stanie Gaëte

Centre Hospitalier Universitaire Pointe-à-PitreORCID 0000-0002-2248-8989Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Andrea K. Thoma‐KressiD· 1 shared Anika Marie-Delcasse· 1 shared Annie LannuzeliD· 1 shared Antoine DuquetteiD· 1 shared Ariane Veilleux CarpentieriD· 1 shared Arnaud Lecante· 1 shared B. TressièresiD· 1 shared Benoı̂t BarbeauiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperMolecular Biology

Andrea K. Thoma‐KressORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Antagonistic regulation of HBZ splicing by hnRNPA1 and hnRNPH1 drives HTLV-1 leukemogenesis.

Julie Tram, Célima Mourouvin, Laetitia Marty, Anika Marie-Delcasse, Arnaud Lecante, Raymond Césaire, Philippe Hélias, Stanie Gaëte, Véronique Baccini, Benoı̂t Barbeau, Norbert Donhauser, Andrea K. Thoma‐Kress, Jean-Michel Mesnard, Jean‐Marie Péloponèse

This paper identifies HBZ splicing regulation by hnRNPA1 and hnRNPH1 as a key driver of HTLV-1 leukemogenesis, showing that HBZ_SP1 promotes transformation and chemoresistance in ATL.

bioRxiv · Jul 21, 2026 · PreprintMolecular Biology

Ancestry-specific immune signatures in Parkinson's disease: a rare variant burden analysis in Montreal and Guadeloupe cohorts

Lovatiana Andriamboavonjy, Marjorie Labrecque, Lalla Yasmine Al Idrissi, B. Tressières, Ariane Veilleux Carpentier, Juliette Chaumont, Hugo Chaumont, Stanie Gaëte, Sylvie Ravion, Antoine Duquette, Sylvain Chouinard, Michel Panisset, Annie Lannuzel, Martine Tétreault

This study identifies ancestry-specific immune signatures in Parkinson's disease through rare variant analysis in Montreal and Guadeloupe cohorts, revealing divergent molecular pathways associated with disease.

medRxiv · May 4, 2026 · PreprintGenetic & Genomic Medicine