Author

Mathilde Boissel

Centre National de la Recherche ScientifiqueORCID 0000-0001-5719-8749Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:differential expression· 2 Assay:DNA methylation· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Approach:deep learning· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1

Frequent Co-Authors

Amélie BonnefondiD· 3 shared Lijiao NingiD· 3 shared Philippe FrogueliD· 3 shared Amna KhamisiD· 2 shared Bénédicte Toussaint· 2 shared François N. PattouiD· 2 shared Inga ProkopenkoiD· 2 shared Mehdi DerhourhiiD· 2 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Amélie BonnefondORCID

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3 papers

Recent·Most cited

Molecular BiologybioRxivPreprintOct 10, 2025

Deep learning models reading clinical data and liver omics strongly distinguish NASH from steatosis and suggest new genes involved in liver disease severity

Nicolas Gambardella Le Novère, Smaïn Fettem, Mathilde Boissel…·Amélie Bonnefond

The paper develops a deep learning model combining clinical data, gene expression, and DNA methylation to distinguish NASH from steatosis and identifies new genes involved in liver disease severity.

1 citation

humanbulk RNA-seq

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Genetic & Genomic MedicineNature CommunicationsPeer-reviewedNov 20, 2024

A framework for conducting time-varying genome-wide association studies: An application to body mass index across childhood in six multiethnic cohorts

Kimberley Burrows, Anni Heiskala, Jonathan P. Bradfield…·Nicole M. Warrington

The paper introduces a framework for time-varying GWAS to identify age-varying genetic effects on BMI across childhood, finding 28 genome-wide significant variants, including a novel one in DAOA.

16 citationstop 4%

humanGWAS summary statistics

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Genetic & Genomic MedicinemedRxivPreprintDec 30, 2022

Epigenetics of PNLIPRP1 in human pancreas reveals a molecular path between type 2 diabetes and pancreatic cancer

Lucas Maurin, Lorella Marselli, Lijiao Ning…·Amna Khamis

The paper identifies hypermethylation of PNLIPRP1 in T2D patients and shows its association with acinar-to-ductal metaplasia and PDAC risk.

1 citation

humanDNA methylation

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