Paco Derouault
Limoges, France
Last Updated: 09/26/2026
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Found 24 publications
A Wet Lab Procedure for Gene Fusion Analysis by Targeted RNA Next-Generation Sequencing in Lung Cancer.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: July 23, 2025
CLL-like stereotyped BCRs are equally produced in young and old healthy adults, share features of public clonotypes and may be stuck at a pre-germinal centre stage.
Journal: British journal of haematology
Published: April 04, 2025
Revisiting proliferative glomerulonephritis with monoclonal immunoglobulin deposits through immunoglobulin repertoire sequencing.
Journal: Kidney international
Published: January 06, 2025
The First Large Deletion of ATL3 Identified in a Patient Presenting with a Sensory Polyneuropathy.
Journal: Biomedicines
Published: April 13, 2023
From Negative to Positive Diagnosis: Structural Variation Could Be the Second Mutation You Are Looking for in a Recessive Autosomal Gene.
Journal: Journal of personalized medicine
Published: January 09, 2022
UnAIDed Class Switching in Activated B-Cells Reveals Intrinsic Features of a Self-Cleaving IgH Locus.
Journal: Frontiers in immunology
Published: July 06, 2021
New structural variations responsible for Charcot-Marie-Tooth disease: The first two large KIF5A deletions detected by CovCopCan software.
Journal: Computational and structural biotechnology journal
Published: May 03, 2021
RNA-based immunoglobulin repertoire sequencing is a new tool for the management of monoclonal gammopathy of renal (kidney) significance.
Journal: Kidney international
Published: January 12, 2021
One Multilocus Genomic Variation Is Responsible for a Severe Charcot-Marie-Tooth Axonal Form.
Journal: Brain sciences
Published: November 17, 2020
Pharmacoresistant Epilepsy in Childhood: Think of the Cerebral Folate Deficiency, a Treatable Disease.
Journal: Brain sciences
Published: September 25, 2020
Flow cytometry detection of CD138 expression continuum between monotypic B and plasma cells is associated with both high IgM peak levels and MYD88 mutation and contributes to diagnosis of Waldenström macroglobulinemia.
Journal: Cytometry. Part B, Clinical cytometry
Published: July 24, 2020
Last Updated: 09/26/2026