Author

Camille Humbert

Inserm

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Biology Disciplines

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Genetics· 2 Evolutionary Biology· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 3 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Organism:mouse· 1 Research Focus:variant calling· 1

Frequent Co-Authors

André MégarbanéiD· 2 shared Christel Castro· 2 shared Karine BertauxiD· 2 shared Nathalie Bernard‐MarissaliD· 2 shared Nathalie Roëckel· 2 shared Nicolas LenfantiD· 2 shared Rosette A. JabbouriD· 2 shared Valérie DelagueiD· 2 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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2 shared papersGenetics

André MégarbanéORCID

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3 papers

Recent·Most cited

Rethinking human AMY1 copy number evolution in light of demographic history

Andrea Soler i Nunez, Cécile Jolly, Camille Humbert, Afifa Chowdhury, Susanne T. Green, Pakou Haréna, Lebarama Bakrobena, Forka Leypey Mathew Fomine, Peter Ebbesen, Zelalem G. Tolesa, Wendawek Abebe Mengesha, Minique H. de Castro, Vinet Coetzee, Himla Soodyall, Leon Mundeke, , Carina M. Schlebusch

This study re-evaluates AMY1 copy number evolution using ancestry-aware models and finds demographic history, not diet, drives global variation.

bioRxiv · Feb 18, 2026 · PreprintEvolutionary Biology

Bi-allelic mutations in KCTD11 cause a new form of autosomal recessive intermediate Charcot-Marie-Tooth disease

Jihane Gadacha, Zahraa Haidar, Nathalie Roëckel, Amandine Pauset, Christel Castro, Coralie Provost, Zeinab Hamzé, Camille Humbert, Karine Bertaux, Nicolas Lenfant, Marion Masingue, Alix de Becdelièvre, Marina Konyukh, Nathalie Bonello‐Palot, Anne‐Sophie Lia, , Valérie Delague

This paper identifies bi-allelic mutations in KCTD11 as a cause of autosomal recessive intermediate Charcot-Marie-Tooth disease and elucidates its role in myelin homeostasis through molecular mechanisms.

bioRxiv · Jun 30, 2025 · PreprintGenetics

Altered NRG1/ErbB4 signaling and cholesterol metabolism dysregulation are key pathomechanisms in VRK1-related motor neuropathies and motor neuron diseases

Zeinab Hamzé, Camille Humbert, Khalil Rihan, Nathalie Roëckel, Christel Castro, Nicolas Lenfant, Catherine Aubert, Karine Bertaux, Rosette A. Jabbour, Nathalie Bernard‐Marissal, André Mégarbané, Valérie Delague

The paper investigates VRK1-related motor neuropathies using hiPSC-MNs and bulk mRNA-Seq, identifying altered NRG1/ErbB4 signaling and cholesterol metabolism dysregulation as key pathomechanisms.

bioRxiv · Feb 19, 2024 · PreprintGenetics