Author

Houda Hamdi‐Rozé

Centre National de la Recherche ScientifiqueORCID 0000-0003-2175-9190Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Approach:benchmark study· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 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

2018-2018 · 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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1 paper

Recent·Most cited

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