Nasséra Abermil

SDH Mutations Establish a Hypermethylator Phenotype in Paraganglioma

Éric Letouzé, Cosimo Martinelli, Céline Loriot et al. · Cancer Cell · 2013 · 758 citations · Full text

Sdh Mutations Establish, Tumor Heterogeneity, Pathology +3

<i>MAX</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

Nelly Burnichon, Alberto Cascón, Francesca Schiavi et al. · Clinical Cancer Research · 2012 · 321 citations · Full text

Somatic NF1 inactivation is a frequent event in sporadic pheochromocytoma

Nelly Burnichon, Alexandre Buffet, Béatrice Parfait et al. · Human Molecular Genetics · 2012 · 146 citations · Full text

Endocrine Oncology, Nf1 Expression, Somatic Variant +14

<i>TMEM127</i>Screening in a Large Cohort of Patients with Pheochromocytoma and/or Paraganglioma

Nasséra Abermil, Marine Guillaud-Bataille, Nelly Burnichon et al. · The Journal of Clinical Endocrinology & Metabolism · 2012 · 63 citations · Full text

Precision and prognostic value of clone-specific minimal residual disease in acute myeloid leukemia

Pierre Hirsch, Ruoping Tang, Nasséra Abermil et al. · Haematologica · 2017 · 46 citations · Full text