Author

Zakaria Mougin

Centre National de la Recherche ScientifiqueORCID 0000-0001-9429-2865Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Approach:benchmark study· 1 Research Focus:cell-cell communication· 1 Research Focus:clustering· 1 Research Focus:database / resource· 1 Research Focus:gene regulatory network inference· 1 Assay:imaging· 1

Frequent Co-Authors

AIMS-2-Trials A-Reps group· 1 shared Alexandre GuilhemiD· 1 shared Alexandre MathieuiD· 1 shared Aline LefebvreiD· 1 shared Aline VitraciD· 1 shared Anaël AyrollesiD· 1 shared Angélique Bibimbou· 1 shared Anita BeggiatoiD· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

AIMS-2-Trials A-Reps group

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintNov 24, 2025

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

Mathis Fleury, Zakaria Mougin, Claire S. Leblond…·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.

2 citations

humanwhole-genome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintMay 2, 2025

Loss of function variants in ADAMTS6: Connective tissue, Heart defect, thoracic Aortic aneurysm and Neuro developmental Syndrome (CHANS)

Júlia Huguet Herrero, Pauline Arnaud, Angélique Bibimbou…·Carine Le Goff

The paper identifies loss-of-function variants in ADAMTS6 in patients with vascular and neurodevelopmental disorders, linking them to connective tissue defects and proposing a new syndrome called CHANS.

2 citations

humanwhole-exome sequencing

𝕏 PostBluesky