Bodemer, Christine

Chronic Mucocutaneous Candidiasis in Humans with Inborn Errors of Interleukin-17 Immunity

Puel, A., Cypowyj, S., Bustamante, J., Wright, J. F., Liu, L., Lim, H. K., Migaud, M., Israel, L., Chrabieh, M., Audry, M., et al. (2011) · Science

Immunodeficiency and Autoimmune DisordersAntifungal resistance and susceptibility

Cited by 1,056

Pediatric mastocytosis is a clonal disease associated with D816V and other activating c-KIT mutations

Bodemer, C., Hermine, O., Palmérini, F., Yang, Y., Grandpeix-Guyodo, C., Leventhal, P. S., Hadj-Rabia, S., Nasca, L., Georgin-Lavialle, S., Cohen-Akenine, A., et al. (2010) · Journal of Investigative Dermatology

Mast cells and histamineGastrointestinal Tumor Research and Treatment

Cited by 397

Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases

Cluzeau, C., Hadj-Rabia, S., Jambou, M., Mansour, S., Guigue, P., Masmoudi, S., Bal, E., Chassaing, N., Vincent, M.-C., Viot, G., et al. (2011) · Human Mutation

dental development and anomaliesGenetic and rare skin diseases.

Cited by 311

Human lipodystrophies linked to mutations in A-type lamins and to HIV protease inhibitor therapy are both associated with prelamin A accumulation, oxidative stress and premature cellular senescence

Caron, M., Auclair, M., Donadille, B., Béréziat, V, Guerci, B., Laville, M., Narbonne, H., Bodemer, C., Lascols, O., Capeau, J., et al. (2007) · Cell Death & Differentiation

Nuclear Structure and FunctionTelomeres, Telomerase, and Senescence

Cited by 226

Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus

Bal, E., Baala, L., Cluzeau, C., El Kerch, F., Ouldim, K., Hadj-Rabia, S., Bodemer, C., Munnich, A., Courtois, G., Sefiani, A., et al. (2007) · Human Mutation

dental development and anomaliesGenetic and rare skin diseases.

Cited by 100

Multidisciplinary consensus recommendations from a European network for the diagnosis and practical management of patients with incontinentia pigmenti

Bodemer, C., Diociaiuti, A., Hadj‐Rabia, S., Robert, M. P., Desguerre, I., Manière, M. ‐., de la Dure‐Molla, M., De Liso, P., Federici, M., Galeotti, A., et al. (2020) · Journal of the European Academy of Dermatology and Venereology

Genetic and rare skin diseases.Dermatology and Skin Diseases

Cited by 59

Clinical and histologic features of incontinentia pigmenti in adults with nuclear factor-κB essential modulator gene mutations

Hadj-Rabia, S., Rimella, A., Smahi, A., Fraitag, S., Hamel-Teillac, D., Bonnefont, J.-P., de Prost, Y., & Bodemer, C. (2011) · Journal of the American Academy of Dermatology

Genetic and rare skin diseases.Skin and Cellular Biology Research

Cited by 57

Paediatric mastocytosis: long-term follow-up of 53 patients with whole sequencing of KIT. A prospective study

Meni, C., Georgin-Lavialle, S., Le Saché de Peufeilhoux, L., Jais, J. P., Hadj-Rabia, S., Bruneau, J., Fraitag, S., Hanssens, K., Dubreuil, P., Hermine, O., et al. (2018) · British Journal of Dermatology

Mast cells and histamineHistiocytic Disorders and Treatments

Cited by 34

Improvement of epidermal covering on AEC patients with severe skin erosions by PRIMA-1MET/APR-246

Aberdam, E., Roux, L. N., Secrétan, P.-H., Boralevi, F., Schlatter, J., Morice-Picard, F., Sol, S., Bodemer, C., Missero, C., Cisternino, S., et al. (2020) · Cell Death & Disease

Genetic and rare skin diseases.Skin and Cellular Biology Research

Cited by 26