Author

Smaranda Leu‐Semenescu

Sorbonne UniversitéORCID 0000-0001-9556-4527Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Isabelle ArnulfiD· 3 shared Delphine OudietteiD· 2 shared Pauline DodetiD· 2 shared Pierre ChampetieriD· 2 shared A.C.N. Chen· 1 shared Aditya AmbatiiD· 1 shared Alix RomieriD· 1 shared Amélie Barbier· 1 shared

Activity by Year

2021-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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3 shared papersNeuroscience

Isabelle ArnulfORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

NeurosciencebioRxivPreprintAug 27, 2025

Live access to the emotional dynamics of REM sleep dreams in lucid dreamers with narcolepsy

Jean‐Baptiste Maranci, Pierre Champetier, Delphine Oudiette…·Isabelle Arnulf

This study investigates the emotional dynamics of REM sleep dreams in lucid dreamers with narcolepsy by collecting real-time emotional valence reports during naps.

DOI 10.1101/2025.08.27.672557

humanimaging

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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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