Christine Bodemer

CEMARA an information system for rare diseases

Mohamed Ben Saïd, Paul Landais, Jean Philippe Jaïs, 2010, MedInfo.

CEMARA: a Web Dynamic Application Within a N-tier Architecture for Rare Diseases

Mohamed Ben Saïd, Paul Landais, Jean Philippe Jaïs, 2008, MIE.

Phenotypic and Genotypic Characteristics of Mastocytosis According to the Age of Onset

Olivier Hermine, Felipe Suarez, Christine Bodemer, 2008, PloS one.

BRAF Mutation Correlates With High-Risk Langerhans Cell Histiocytosis and Increased Resistance to First-Line Therapy.

Valérie Rigau, Valérie Taly, Christine Bodemer, 2016, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Infantile myofibromatosis: a series of 28 cases.

Christine Bodemer, C. Bodemer, A. Harroche, 2014, Journal of the American Academy of Dermatology.

Heterozygous PDGFRB Mutation in a Three-generation Family with Autosomal Dominant Infantile Myofibromatosis.

Christine Bodemer, C. Bodemer, S. Hadj-Rabia, 2017, Acta dermato-venereologica.

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

Yang Liu, Sen Yang, Miao Sun, 2009, Nature Genetics.