G. Audry

Frequent <i>hSNF5/INI1</i> Germline Mutations in Patients with Rhabdoid Tumor

Franck Bourdeaut, Delphine Lequin, Laurence Brugières et al. · Clinical Cancer Research · 2011 · 222 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith–Wiedemann syndrome

Véronique Gaston, Yves Le Bouc, V. Soupre et al. · European Journal of Human Genetics · 2001 · 173 citations

Life Sciences, Genetics, Molecular Genetics +8

Beckwith-Wiedemann Syndrome: Growth Pattern and Tumor Risk according to Molecular Mechanism, and Guidelines for Tumor Surveillance

Frédéric Brioude, Alix M.B. Lacoste, Irène Netchine et al. · Hormone Research in Paediatrics · 2013 · 157 citations

Life Sciences, Genetics, Molecular Genetics +16

Nephron sparing surgery (NSS) for unilateral wilms tumor (UWT): The SIOP 2001 experience

Jim C. H. Wilde, Daniël C. Aronson, Beata Sznajder et al. · Pediatric Blood & Cancer · 2014 · 113 citations · Full text

Medicine, Oncology, Surgery +16

Outcome of suprarenal localized masses diagnosed during the perinatal period

Frédérique Sauvat, Sabine Sarnacki, Hervé J. Brisse et al. · Cancer · 2002 · 111 citations · Full text

Medicine, Oncology, Surgery +9