Author

Pauline Dodet

Sorbonne UniversitéORCID 0000-0002-7078-8345Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Assay:electronic health records· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Approach:machine learning (classical)· 1

Frequent Co-Authors

Isabelle ArnulfiD· 3 shared Birgit HögliD· 2 shared Smaranda Leu‐SemenescuiD· 2 shared Yves A DauvilliersiD· 2 shared Abubaker IbrahimiD· 1 shared Aditya AmbatiiD· 1 shared Alex DésautelsiD· 1 shared Álex IranzoiD· 1 shared

Activity by Year

2021-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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

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3 shared papersGenetic & Genomic Medicine

Isabelle ArnulfORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintSep 5, 2025

Post-traumatic stress disorder and REM-sleep behavior disorder: exploring genetic associations and causal links

Morvarid Ghamgosar Shahkhali, Lang Liu, Mohammad H. Ghamgosar Shahkhali…·Ziv Gan‐Or

The paper investigates genetic and causal links between post-traumatic stress disorder and rapid-eye-movement sleep behavior disorder using polygenic risk scores, genetic correlation, and Mendelian randomization analyses.

DOI 10.1101/2025.09.05.25335205

humanstatistical model

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NeurosciencebioRxivPreprintMay 26, 2025

EEG Signature of Idiopathic Hypersomnia: Insights from Sleep Microarchitecture and Hypnodensity Metrics

Arthur Le Coz, Raphael Vollhardt, Pierre Champetier…·Thomas Andrillon

The paper identifies EEG features distinguishing idiopathic hypersomnia from controls using sleep microarchitecture and hypnodensity metrics.

1 citation

humanelectronic health records

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Genetic & Genomic MedicineProceedings of the National Academy of SciencesPeer-reviewedMar 18, 2021

Kleine Levin syndrome is associated with birth difficulties and genetic variants in the TRANK1 gene loci.

Aditya Ambati, Ryan P. Hillary, Smaranda Leu‐Semenescu…·Emmanuel Jean-Marie Mignot

This study identifies a genetic association between Kleine-Levin Syndrome and variants in the TRANK1 gene, with increased risk linked to birth difficulties.

55 citationstop 3%

humanstatistical model

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