Author

Charlotte Mouden

Centre National de la Recherche Scientifique

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioinformatics· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:variant calling· 2 Approach:benchmark study· 1 Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Research Focus:phylogenetics / evolution· 1

Frequent Co-Authors

Abdel AbdellaouiiD· 1 shared Albert Hofman DiD· 1 shared Alexandros KanterakisiD· 1 shared Anne BolandiD· 1 shared Anton J.M. de CraeniD· 1 shared Artem KimiD· 1 shared Arthur KoiD· 1 shared Barbera D. C. van SchaikiD· 1 shared

Activity by Year

2018-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Abdel AbdellaouiORCID

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2 papers

Recent·Most cited

DiscoSnp-RAD: de novo detection of small variants for population genomics

Jérémy Gauthier, Charlotte Mouden, Tomasz Suchan, Nadir Álvarez, Nils Arrigo, Chloé Riou, Claire Lemaitre, Pierre Peterlongo

DiscoSnp-RAD efficiently detects small variants in RAD-Seq data, revealing population structure and outperforming existing tools in speed.

PeerJ · Jun 10, 2020Peer-reviewedBioinformatics

Integrated Clinical and Omics Approach to Rare Diseases: Novel Genes and Oligogenic Inheritance in Holoprosencephaly

Artem Kim, Clara Savary, Christèle Dubourg, Wilfrid Carré, Charlotte Mouden, Houda Hamdi‐Rozé, Hélène Guyodo, Jérôme Le Douce, Emmanuelle Génin, Dominique Campion, Jean‐François Dartigues, Jean‐François Deleuze, Jean‐Charles Lambert, Richard Redon, Thomas E Ludwig, , Tania Attié‐Bitach

This study identifies novel HPE genes and oligogenic inheritance patterns in holoprosencephaly by integrating clinical data with exome sequencing and gene prioritization.

Brain · Oct 29, 2018Peer-reviewedGenetics