Jean-baptiste C. Gaillard
Montpellier, France
Last Updated: 09/26/2026
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Found 18 publications
Optical genome mapping improves detection and characterisation of cytogenetic abnormalities in non-Hodgkin lymphomas.
Journal: British journal of haematology
Published: March 02, 2026
Somatic STAT5BN642H mutations shape variable immune landscapes resulting in heterogenous immune diseases.
Journal: The Journal of allergy and clinical immunology
Published: September 09, 2025
Effective requesting method to detect fusion transcripts in chronic myelomonocytic leukemia RNA-seq.
Effective requesting method to detect fusion transcripts in chronic myelomonocytic leukemia RNA-seq.
Journal: NAR genomics and bioinformatics
Published: January 29, 2024
Molecular landscape of mature B-cell lymphoproliferative disorders with BCL3-translocation: A Groupe Francophone de Cytogénétique Hématologique (GFCH)/French Innovative Leukemia Organization (FILO) study.
Journal: American journal of hematology
Published: November 28, 2023
Cytogenetics in the management of hematological malignancies: An overview of alternative technologies for cytogenetic characterization.
Journal: Current research in translational medicine
Published: July 10, 2023
Cytogenetics in the management of mature T-cell and NK-cell neoplasms: Guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH).
Journal: Current research in translational medicine
Published: July 04, 2023
Antenatal ultrasound features of isolated recurrent copy number variation in 7q11.23 (Williams syndrome and 7q11.23 duplication syndrome).
Journal: Prenatal diagnosis
Published: December 14, 2022
AnnotSV and knotAnnotSV: a web server for human structural variations annotations, ranking and analysis.
Journal: Nucleic acids research
Published: March 11, 2021
Clinical and biological features of B-cell neoplasms with CDK6 translocations: an association with a subgroup of splenic marginal zone lymphomas displaying frequent CD5 expression, prolymphocytic cells, and TP53 abnormalities.
Journal: British journal of haematology
Published: June 12, 2020
Disruption of chromatin organisation causes MEF2C gene overexpression in intellectual disability: a case report.
Journal: BMC medical genomics
Published: January 23, 2019
Mosaic complete tetrasomy 21 in a fetus with complete atrioventricular septal defect and minor morphological variations.
Journal: Molecular genetics & genomic medicine
Published: January 21, 2019
Poor prognosis of chromosome 7 clonal aberrations in Philadelphia-negative metaphases and relevance of potential underlying myelodysplastic features in chronic myeloid leukemia.
Journal: Haematologica
Published: October 08, 2018
Last Updated: 09/26/2026