Associated Papers
Exome-based cancer predisposition gene testing can provide a genetic diagnosis for individuals with heterogeneous tumor phenotypes.
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Preclinical NCI-MPACT: prospective modeling of the mutation-based NCI-MPACT clinical trial therapeutic strategy in patient-derived xenograft models.
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Transcriptome meta-analysis of lung cancer reveals recurrent aberrations in NRG1 and Hippo pathway genes.
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Neurofibromatosis type 1-associated tumours: their somatic mutational spectrum and pathogenesis.
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Molecular diagnosis of neurofibromatosis type 1: 2 years experience.
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Familial Cancer, 2007
Comprehensive NF1 screening on cultured Schwann cells from neurofibromas.
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Human Mutation, 2006
Somatic NF1 mutational spectrum in benign neurofibromas: mRNA splice defects are common among point mutations.
Serra E et al.
Human Genetics, 2001
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