Sandrine-Hélène Lefèvre

Molecular structure of double-minute chromosomes bearing amplified copies of the epidermal growth factor receptor gene in gliomas

Nicolas Vogt, Sandrine-Hélène Lefèvre, Françoise Apiou et al. · Proceedings of the National Academy of Sciences · 2004 · 174 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Novel <i>FH</i> mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma

Betty Gardie, Audrey Remenieras, Darouna Kattygnarath et al. · Journal of Medical Genetics · 2011 · 142 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Mutations in BHD and TP53 genes, but not in HNF1β gene, in a large series of sporadic chromophobe renal cell carcinoma

Sophie Gad, Sandrine-Hélène Lefèvre, Sok Kean Khoo et al. · British Journal of Cancer · 2006 · 73 citations · Full text

Medicine, Genetics, Oncology +13

Genome instability in secondary solid tumors developing after radiotherapy of bilateral retinoblastoma

Sandrine-Hélène Lefèvre, Nicolas Vogt, Anne‐Marie Dutrillaux et al. · Oncogene · 2001 · 28 citations

Medicine, Genetics, Oncology +16