Christine Bellanné-Chantelot

18PUBLICATIONS
69CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Haematological tumoursEpigenetics (incl. genome methylation and epigenomics)Models of care and place of birthImmunogenetics (incl. genetic immunology)
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Publications (18)

|Apr 17, 2026
Co-occurrence of Loss-of-Function GCK and ABCC8 Variants in a Pedigree With a Spectrum of Dysglycemia.

|Oct 07, 2025
Germ line LCP1 mutations cause immunodeficiency with neutropenia, monocytopenia, lymphopenia, and defective cytokinesis.

Thijs van Bergen, Dennis A Bosch, Christine Bellanné-Chantelot

|Jun 13, 2025
Expanding the phenotypic and genetic landscape of congenital neutropenia through whole-exome and genome sequencing.

Séverine Marti, Philippe Pellet, Blandine Beaupain

|Jun 05, 2025
RNA-based diagnostic studies in genetics: Review and guidance from a multidisciplinary French network.

Marie-Pierre Buisine, Christine Bellanne-Chantelot, Nadège Calmels

|Apr 14, 2025
Evaluation in Monogenic Diabetes of the Impact of GCK, HNF1A, and HNF4A Variants on Splicing through the Combined Use of In Silico Tools and Minigene Assays.

Delphine Bouvet, Amélie Blondel, Jean-Madeleine de Sainte Agathe

|Feb 19, 2025
Pregnancy and neonatal outcomes in women with GCK-MODY: an observational study based on standardised insulin modalities.

Cécile Ciangura, Aurélien Seco, Cécile Saint-Martin

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Frequent Collaborators

4 joint publications

Jean Donadieu

4 joint publications

Isabelle Plo

3 joint publications

Cécile Saint-Martin

3 joint publications

Alan J Warren