Xavier Vanhoye

5PUBLICATIONS
17CO-AUTHORS
Haematological tumoursMedical molecular engineering of nucleic acids and proteinsGene mappingGene expression (incl. microarray and other genome-wide approaches)Medical biochemistry - lipids
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Publications (5)

|Oct 04, 2025
Prenatal Recurrence of Ductal Plate Malformations Leads to PKHD1 Variant Reclassification.

Mario Abaji, Laurent Nasca, Marie-Pierre Audrezet

|Dec 09, 2024
Authors' Reply: Using VNtyper from Whole Exome Sequencing Data to Detect Pathogenic Variants in the MUC1 Gene.

Ilias Bensouna, Thomas Robert, Xavier Vanhoye

|Sep 26, 2024
Systematic Screening of Autosomal Dominant Tubulointerstitial Kidney Disease- MUC1 27dupC Pathogenic Variant through Exome Sequencing.

Ilias Bensouna, Thomas Robert, Xavier Vanhoye

|Sep 22, 2022
Exome sequencing as a first-tier test for copy number variant detection: retrospective evaluation and prospective screening in 2418 cases.

Quentin Testard, Xavier Vanhoye, Kevin Yauy

|Apr 23, 2022
APOB CRISPR-Cas9 Engineering in Hypobetalipoproteinemia: A Promising Tool for Functional Studies of Novel Variants.

Xavier Vanhoye, Alexandre Janin, Amandine Caillaud

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Frequent Collaborators

2 joint publications

Laurent Mesnard

2 joint publications

Thomas Robert

2 joint publications

Ilias Bensouna

1 joint publications

Antoine Rimbert