Author

Camille Level

CHU Dijon BourgogneORCID 0000-0002-0185-8207Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:benchmarking· 2 Organism:human· 2 Approach:benchmark study· 1 Assay:electronic health records· 1 Approach:machine learning (classical)· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Aaron J. GoldenbergiD· 1 shared Aditi SatijaiD· 1 shared Alberte Lundquist· 1 shared Aldona Zygmunt· 1 shared Alessandra FerliniiD· 1 shared Alexandra BenachiiD· 1 shared Alexandra Wiedemann· 1 shared Alice Tuff-Lacey· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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Focal author (center)Selected co-authorORCID co-authorUnlinked name

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1 shared paperGenetic & Genomic Medicine

Aaron J. GoldenbergORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

How parents judge newborn screening expansion in the genomic era: a theory-informed survey in France from the SeDeN-p3 study

Camille Level, Laurence Olivier Faivre, Margot LEMAITRE, Dominique Salvi, Isabelle MARCHETTI-WATERNAUX, Élisabeth Cudry, Emmanuel G. Simon, Nicolas Bourgon, Alexandra Benachi, Nhut-Thanh VAN, Camille Coppola, Christine Binquet, Christel Thauvin‐Robinet, Frédéric Huet, Christine Peyron

This study surveys French parents' views on expanding newborn screening to include genomic testing, finding high support but nuanced concerns about uncertainty and equity.

medRxiv · Feb 24, 2026 · PreprintGenetic & Genomic Medicine

Data-driven consideration of genetic disorders for global genomic newborn screening programs

Thomas Minten, Sarah Bick, Sophia M. Adelson, Nils Gehlenborg, Laura M. Amendola, François Boemer, Alison J. Coffey, Nicolas Encina, Alessandra Ferlini, Janbernd Kirschner, Bianca E. Russell, Laurent Servais, Kristen Lipscomb Sund, Ryan J. Taft, Petros Tsipouras, , Dominique C. Pichard

The paper develops a machine learning model to prioritize genes for newborn sequencing programs based on factors like evidence of disease natural history and treatment efficacy.

Genetics in Medicine · May 9, 2025Peer-reviewedGenetic & Genomic Medicine