Josiane Grosgeorge
Centre Antoine Lacassagne(FR)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Genomics and Chromatin Dynamics, Sarcoma Diagnosis and Treatment, Chromosomal and Genetic Variations, Chronic Myeloid Leukemia Treatments
Most-Cited Works
- → Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy(2000)1,421 cited
- → Deregulation of the platelet-derived growth factor β-chain gene via fusion with collagen gene COL1A1 in dermatof ibrosarcoma protuberans and giant-cell fibroblastoma(1997)528 cited
- → Fusion of TEL, the ETS-Variant Gene 6 (ETV6), to the Receptor-Associated Kinase JAK2 as a Result of t(9; 12) in a Lymphoid and t(9; 15; 12) in a Myeloid Leukemia(1997)481 cited
- → The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia(1996)251 cited
- → The gene encoding the mouse homologue of the human osteoclast-specific 116-kDa V-ATPase subunit bears a deletion in osteosclerotic (oc/oc) mutants(2000)202 cited
- → Detailed map of a region commonly amplified at 11q13→q14 in human breast carcinoma(1997)151 cited
- → Expanded range of 11q13 breakpoints with differing patterns of cyclin D1 expression in B‐cell malignancies(1993)105 cited
- → Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): a recurring chromosomal abnormality involving the TEL gene (ETV6) in myelodysplastic syndromes(1996)91 cited
- Definition of the Minimal MEN1 Candidate Area Based on a 5-Mb Integrated Map of Proximal 11q13(1996)