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Publications by V. Pillonel
Whole-Exome-Sequencing of Nodal Marginal Zone Lymphomas Identifies Recurrent Molecular Lesions in Genes Involved in Chromatin Remodelling and Notch Signalling
Hematological Oncology
Medicine
Cancer Research
Oncology
Hematology
Related publications
Whole-Exome Sequencing Identifies a Recurrent NAB2-STAT6 Fusion in Solitary Fibrous Tumors
Nature Genetics
Genetics
Exome Sequencing Identifies Recurrent Somatic RAC1 Mutations in Melanoma
Nature Genetics
Genetics
Whole-Exome Sequencing Reveals Frequent Mutations in Chromatin Remodeling Genes in Mammary and Extramammary Paget’s Diseases
Journal of Investigative Dermatology
Biochemistry
Dermatology
Cell Biology
Molecular Biology
Whole-Exome Sequencing Identifies Somatic ATRX Mutations in Pheochromocytomas and Paragangliomas
Nature Communications
Astronomy
Genetics
Molecular Biology
Biochemistry
Chemistry
Physics
Whole Exome Sequencing Identifies a Novel and a Recurrent Mutation inBBS2Gene in a Family With Bardet-Biedl Syndrome
BioMed Research International
Immunology
Molecular Biology
Biochemistry
Microbiology
Medicine
Genetics
Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease
Arthritis and Rheumatology
Rheumatology
Allergy
Immunology
Whole Exome Sequencing Identifies CRB1 Defect in an Unusual Maculopathy Phenotype
Ophthalmology
Ophthalmology
Whole Exome Sequencing of Microdissected Splenic Marginal Zone Lymphoma: A Study to Discover Novel Tumor-Specific Mutations
BMC Cancer
Cancer Research
Oncology
Genetics
Exome Sequencing Identifies Molecular Diagnosis in Children With Drug-Resistant Epilepsy
Epilepsia Open
Neurology
