Author

Sandra Whalen

Hôpital Armand-TrousseauORCID 0000-0001-9156-5047Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 1 Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:differential expression· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Organism:mouse· 1

Frequent Co-Authors

Abdelamdjid Benmansour· 1 shared Alain VerloèsiD· 1 shared Albert David· 1 shared Alexandra AfenjariD· 1 shared Alexandre MathieuiD· 1 shared Amelie Brugger· 1 shared Angèle Tingaud‐Sequeira· 1 shared Anne Dieux‐CoëslieriD· 1 shared

Activity by Year

2017-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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1 shared paperGenetics

Abdelamdjid Benmansour

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Developmental BiologybioRxivPreprintOct 13, 2024

MMP21 behaves as a fluid flow transported morphogen to impart laterality during development

Tim Ott, Amelie Brugger, Emmanuelle Szenker‐Ravi…·Axel Schweickert

The paper identifies MMP21 as a morphogen transported by leftward fluid flow to specify left-sided development in Xenopus embryos, revealing its role in heterotaxy.

1 citation

mousehuman

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Genetic & Genomic MedicinePigment Cell & Melanoma ResearchPeer-reviewedAug 31, 2023

Unsuspected consequences of synonymous and missense variants in can be detected in blood cell RNA samples of patients with albinism

Vincent Michaud, Angèle Tingaud‐Sequeira, Elina Mercier…·Sophie Javerzat

The paper shows that blood cell RNA analysis can detect the effects of OCA2 variants on exon skipping and mRNA levels, helping to reclassify variants of unknown significance as pathogenic.

10 citations

humanbulk RNA-seq

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GeneticsbioRxivPreprintMar 18, 2017

A framework to identify modifier genes in patients with Phelan-McDermid syndrome

Anne‐Claude Tabet, Thomas Rolland, Marie Ducloy…·Thomas Bourgeron

This study identifies modifier genes in Phelan-McDermid syndrome patients by analyzing 22q13 rearrangements and their association with clinical features.

1 citation

humanstatistical model

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