Author

S. Boughorbel

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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Immunology· 4

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 4 Organism:human· 4 Assay:bulk RNA-seq· 3 Research Focus:differential expression· 3 Approach:experimental assay· 3 Research Focus:database / resource· 2 Approach:statistical model· 2 Research Focus:cell-cell communication· 1

Frequent Co-Authors

D. Chaussabel· 4 shared N. Marr· 3 shared M. Garand· 2 shared M. Toufiq· 2 shared S. Bougarn· 2 shared A. Guerin· 1 shared B. Bigio· 1 shared B. S. A. Kabeer· 1 shared

Activity by Year

2017-2019 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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4 shared papersImmunology

D. Chaussabel

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Author profile →

4 papers

Recent·Most cited

A curated transcriptome dataset collection to investigate inborn errors of immunity.

S. Bougarn, S. Boughorbel, D. Chaussabel, N. Marr

The paper compiles a curated transcriptome dataset collection from PID patients and controls to enable meta-analysis and improve understanding of inborn errors of immunity.

bioRxiv · Feb 1, 2019Immunology

A curated collection of transcriptome datasets to investigate the molecular mechanisms of immunoglobulin E-mediated atopic diseases

S. Huang, F. Al Ali, S. Boughorbel, M. Toufiq, D. Chaussabel, M. Garand

The paper curates 30 transcriptomic datasets from GEO to study IgE-mediated atopic diseases and provides an online tool for data visualization and metadata annotation.

bioRxiv · Jan 20, 2019Immunology

The abundance of Nudix hydrolase 16 transcripts is elevated in human sepsis: perspectives gained during a hands-on reductionist investigation workshop.

M. Garand, D. Rinchai, B. S. A. Kabeer, M. Toufiq, M. Alfaki, J. Roelands, W. Hendrickx, S. Boughorbel, N. Marr, D. Bedognetti, D. Chaussabel

The paper investigates NUDT16 transcript abundance in sepsis using omics data and public datasets, finding elevated levels in septic patients compared to controls.

bioRxiv · Dec 9, 2018 · PreprintImmunology

IRF4 haploinsufficiency in a family with Whipples disease

A. Guerin, G. Kerner, N. Marr, J. G. Markle, F. Fenollar, N. Wong, S. Boughorbel, D. T. Avery, C. Ma, S. Bougarn, M. Bouaziz, V. Beziat, E. Della Mina, T. Lazarovt, L. Worley, , J.-L. Casanova

This study identifies IRF4 haploinsufficiency as the genetic cause of Whipples disease in a family, showing age-dependent incomplete penetrance and chronic Tw carriage preceding disease onset.

bioRxiv · Oct 3, 2017Immunology