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Cyril Dalmasso

Maître de conférence (UEVE)
Université d'Évry Val d'Essonne
Laboratoire de Mathématiques et Modélisation d'Évry (UMR 8071)
I.B.G.B.I., 23 Bd. de France, 91037 Évry Cedex
☎ +33 (0) 1 64 85 35 30


COURBARIAUX, M., Szafranski, M., Dalmasso, C., Danjou, F., Bekadar, S., Corvol, J.C., Martinez, M. & Ambroise, C. A sparse logistic mixture model for disease subtyping with clinical and genetic data. , 2021., (working paper or preprint). implementation
Palomares, M.A., Dalmasso, C., Bonnet, E., Derbois, C., Brohard-Julien, S., Ambroise, C., Battail, C., Deleuze, J.F. & Olaso, R.E. Systematic analysis of TruSeq, SMARTer and SMARTer Ultra-Low RNA-seq kits for standard, low and ultra-low quantity samples.. Scientific Reports, 9:1-12, Nature Publishing Group, 2019. implementation
Guergnon, J., Dalmasso, C., Broet, P., Meyer, L., Westrop, S., Imami, N., Vicenzi, E., Morsica, G., Tinelli, M., Poma, B., Goujard, C., Potard, V., Gotch, F., Casoli, C., Cossarizza, A. & others, O. Single Nucleotide Polymorphism-defined Class-I and Class-III MHC genetic subregions contribute to natural long-term non progression in HIV infection. Journal of Infectious Diseases, 205(5):718-24, 2012.
Broet, P., Dalmasso, C., Tan, E., Alifano, M., Zhang, S., Wu, J., Lee, M., Regnard, J., Lim, W., Koong, H., Agasthian, T., Miller, L., Camilleri-Broet, S. & Tan, P. Genomic Profiles Specific to Patient Ethnicity in Lung Adenocarcinoma. Clinical Cancer Research, 17(11):3542-50, 2011.
Dalmasso, C. & Broet, P. Detection of chromosomal abnormalities using high resolution arrays in clinical cancer research. Journal of Biomedical Informatics, (doi:10.1016/j.jbi.2011.06.003):, 2011. implementation
Ruggiero, D., Dalmasso, C., Nutile, T., Sorice, R., Dionisi, L., Aversano, M., Broet, P., Leutenegger, A., Bourgain, C. & Ciullo, M. Genetics of VEGF Serum Variation in Human Isolated Populations of Cilento: Importance of VEGF Polymorphisms.. PLoS One, 6(2):e16982, 2011. implementation
Soon, W., Miller, L., Black, M., Dalmasso, C., Chan, X., Pang, B., Ong, C., Salto-Tellez, M., Desai, K. & Liu, E. Combined genomic and phenotype screening reveals secretory factor SPINK1 as an invasion and survival factor associated with patient prognosis in breast cancer. EMBO Molecular Medicine, x(x):, 2011. implementation
Ahmed, I., Dalmasso, C., Haramburu, F., Thiessard, F., Broet, P. & Tubert-Bitter, P. False discovery rate estimation for frequentist pharmacovigilance signal detection methods.. Biometrics, 66(1):301-309, 2010. implementation
Idbaih, A., Dalmasso, C., Kouwenhoven, M., Jeuken, J., Carpentier, C., Gorlia, T., Kros, J., French, P., Teepen, J., Broet, P., Delattre, O., Mokhtari, K., Sanson, M., Delattre, J., Van den Bent, M. & oang-, . Genomic aberrations associated with outcome in anaplastic oligodendroglial tumors treated within the EORTC phase III trial 26951.. J Neurooncol, [Epub ahead of print]():, 2010. implementation
Marenne, G., Dalmasso, C., Perdry, H., Genin, E. & Broet, P. Impaired performance of FDR-based strategies in whole-genome association studies when SNPs are excluded prior to the analysis.. Genet Epidemiol, 33(1):45-53, 2009. implementation
Ciullo, M., Nutile, T., Dalmasso, C., Sorice, R., Bellenguez, C., Colonna, V., Persico, M. & Bourgain, C. Identification and replication of a novel obesity locus on chromosome 1q24 in isolated populations of Cilento.. Diabetes, 57(3):783-790, 2008. implementation
Dalmasso, C., Genin, E. & Tregouet, D. A weighted-Holm procedure accounting for allele frequencies in genomewide association studies.. Genetics, 180(1):697-702, 2008. implementation
Dalmasso, C., Carpentier, W., Meyer, L., Rouzioux, C., Goujard, C., Chaix, M., Lambotte, O., Avettand-Fenoel, V., Le Clerc, S., Denis de Senneville, L., Deveau, C., Boufassa, F., Debre, P., Delfraissy, J. & ro, . Distinct genetic loci control plasma HIV-RNA and cellular HIV-DNA levels in HIV-1 infection: the ANRS Genome Wide Association 01 study.. PLoS One, 3(12):e3907, 2008. implementation
Dalmasso, C., Bar-Hen, A. & Broet, P. A constrained polynomial regression procedure for estimating the local False Discovery Rate.. BMC Bioinformatics, 8():229, 2007. implementation
Dalmasso, C., Pickrell, J., Tuefferd, M., Genin, E., Bourgain, C. & Broet, P. A mixture model approach to multiple testing for the genetic analysis of gene expression.. BMC Proc, 1 Suppl 1():S141, 2007. implementation
Martin, L., Woo, J., Avery, C., Chen, H., North, K., Au, K., Broet, P., Dalmasso, C., Guedj, M., Holmans, P., Huang, B., Kuo, P., Lam, A., Li, H., Manning, A., Nikolov, I., Sinha, R. & Shi, J. Multiple testing in the genomics era: findings from Genetic Analysis Workshop 15, Group 15.. Genet Epidemiol, 31 Suppl 1():S124-S131, 2007. implementation
Bar-Hen, A., Broet, P., Dalmasso, C., Daudin, J. & Robin, S. False discovery rate.. Encyclopedia of Biopharmaceutical Statistics: Second Edition., 1():1-9, 2006.
Dalmasso, C., Broet, P. & Moreau, T. A simple procedure for estimating the false discovery rate.. Bioinformatics, 21(5):660-668, 2005. implementation
Dalmasso, C. & Broet, P. Procédures d’estimation du false discovery rate basées sur la distribution des degrés de signification.. Journal de la Société française de Statistique, 146(1):, 2005.
Broet, P., Lewin, A., Richardson, S., Dalmasso, C. & Magdelenat, H. A mixture model-based strategy for selecting sets of genes in multiclass response microarray experiments.. Bioinformatics, 20(16):2562-2571, 2004. implementation
Dalmasso, C., Broet, P. & Moreau, T. [Multiple comparison procedures: principles, limits. Applications to microarray phenotype-genotype analysis].. Rev Epidemiol Sante Publique, 52(6):523-537, 2004.
members/cdalmasso/welcome.txt · Last modified: 2021/01/20 13:15 by Cyril Dalmasso

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