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
firstname.lastname@univ-evry.fr

Publications

2023
[1]	Obry, L. & Dalmasso, C. Weighted multiple testing procedures in genome-wide association studies. PeerJ, 11:e15369, PeerJ, 2023.
2022
[2]	Courbariaux, M., De Santiago, K., Dalmasso, C., Danjou, F., Bekadar, S., Corvol, J.C., Martinez, M., Szafranski, M. & Ambroise, C. A Sparse Mixture-of-Experts Model With Screening of Genetic Associations to Guide Disease Subtyping. Frontiers in Genetics, 13, Frontiers, 2022.
2021
[3]	Bianco, B., Francois-Garret, B., Butin, M., Dalmasso, C., Casagrande, F., Mokhtari, M. & Eleni Dit Trolli, S. Procalcitonin in Preterm Neonates: A Different Threshold and Prolonged Interpretation. Frontiers in Pediatrics, 9, Frontiers, 2021.
[4]	Dalmasso, C., Derbois, C., Veyssiere, M., Olaso, R., Lamacchia, C., Alpizar-rodriguez, D., Deleuze, J.f., Finckh, A. & Petit-Teixeira, E. Identification of biological pathways specific to phases preceding rheumatoid arthritis development through gene expression profiling. International Journal of Immunogenetics, Wiley, 2021.
2019
[5]	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.
2017
[6]	Becu, J.M., Grandvalet, Y., Ambroise, C. & Dalmasso, C. Beyond support in two-stage variable selection. Statistics and Computing, 27(1):169-179, Springer Verlag (Germany), 2017.
[7]	Stanislas, V., Dalmasso, C. & Ambroise, C. Eigen-Epistasis for detecting Gene-Gene interactions. BMC Bioinformatics, 18:54, BioMed Central, 2017.
[8]	Stanislas, V., Dalmasso, C. & Ambroise, C. Eigen-Epistasis for detecting gene-gene interactions. BMC Bioinformatics, 18:np, BioMed Central, 2017.
2016
[9]	Aubouin, N., Coblence, E., Dalmasso, C. & Kletz, F. Transformation des organisations culturelles et des métiers : quelles formes de reconnaissance ? . In STP\&A, 2016.
2015
[10]	Dalmasso, C., Carpentier, W., Guettier, C., Camilleri-Broet, S., Vendramini Borelli, W., Campos dos Santos, C.R., Castaing, D., Duclos-Vallee, J.C. & Broet, P. Patterns of chromosomal copy-number alterations in intrahepatic cholangiocarcinoma. BMC Cancer, 15:126, BioMed Central, 2015.
[11]	Becu, J.M., Grandvalet, Y., Ambroise, C. & Dalmasso, C. Significance testing for variable selection in high-dimension. In Conference on Computational Intelligence in Bioinformatics and Computational Biology (CIBCB), pages 1-8, IEEE, 2015.
[12]	Becu, J.M., Grandvalet, Y., Ambroise, C. & Dalmasso, C. Beyond Support in Two-Stage Variable Selection. , 2015., (working paper or preprint).
2012
[13]	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.
2011
[14]	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.
[15]	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.
[16]	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.
[17]	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.
2010
[18]	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.
[19]	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.
2009
[20]	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.
2008
[21]	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.
[22]	Dalmasso, C., Genin, E. & Tregouet, D. A weighted-Holm procedure accounting for allele frequencies in genomewide association studies.. Genetics, 180(1):697-702, 2008.
[23]	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.
2007
[24]	Dalmasso, C., Bar-Hen, A. & Broet, P. A constrained polynomial regression procedure for estimating the local False Discovery Rate.. BMC Bioinformatics, 8():229, 2007.
[25]	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.
[26]	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.
2006
[27]	Bar-Hen, A., Broet, P., Dalmasso, C., Daudin, J. & Robin, S. False discovery rate.. Encyclopedia of Biopharmaceutical Statistics: Second Edition., 1():1-9, 2006.
2005
[28]	Dalmasso, C., Broet, P. & Moreau, T. A simple procedure for estimating the false discovery rate.. Bioinformatics, 21(5):660-668, 2005.
[29]	Dalmasso, C. & Broet, P. Procédures destimation du false discovery rate basées sur la distribution des degrés de signification.. Journal de la Société française de Statistique, 146(1):, 2005.
2004
[30]	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.
[31]	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.