M’Hamed Lajmi Lakhal Chaieb

Chiu CY, Yuan F, Zhang BS, Yuan A, Li X, Fang HB, Lange K, Weeks DE, Wilson AF, Bailey-Wilson JE, Musolf AM, Stambolian D, Lakhal-Chaieb ML, Cook RJ, McMahon FJ, Amos CI, Xiong M, Fan R

Linear mixed models for association analysis of quantitative traits with next-generation sequencing data.

Genet Epidemiol, 43 (2), p. 189-206, 2019, ISSN: 0741-0395.

Résumé | Liens:

Sun JP, Oualkacha K, Greenwood CMT, Lakhal-Chaieb L

Multivariate association test for rare variants controlling for cryptic

Can J Stat, 47 (1 (Special issue)), p. 90-107, 2019, ISSN: 0319-5724.

| Liens:

Lakhal-Chaieb L, Simard J, Bull S

Sequence kernel association test for survival outcomes in the presence of a non-susceptible fraction.

Biostatistics, 2018, ISSN: 1465-4644.

Résumé | Liens:

Choi YH, Lakhal-Chaieb L, Krol A, Yu B, Buchanan D, Ahnen D, Le Marchand L, Newcomb PA, Win AK, Jenkins M, Lindor NM, Briollais L

Risks of Colorectal Cancer and Cancer-Related Mortality in Familial Colorectal Cancer Type X and Lynch Syndrome Families.

J Natl Cancer Inst, 2018, ISSN: 0027-8874.

Résumé | Liens:

Lakhal-Chaieb L, Greenwood CMT, Ouhourane M, Zhao K, Abdous B, Oualkacha K

A smoothed EM-algorithm for DNA methylation profiles from sequencing-based methods in cell lines or for a single cell type.

Stat Appl Genet Mol Biol, 16 (5-6), p. 333-347, 2017.

Résumé | Liens:

Lakhal-Chaieb L, Duchesne T

Association measures for bivariate failure times in the presence of a cure fraction.

Lifetime Data Anal, 23 (4), p. 517-532, 2017, ISSN: 1380-7870.

Résumé | Liens:

Choi YH, Briollais L, Win AK, Hopper J, Buchanan D, Jenkins M, Lakhal-Chaieb L

Modeling of successive cancer risks in Lynch syndrome families in the presence of competing risks using copulas.

Biometrics, 73 (1), p. 271-282, 2017, ISSN: 0006-341X.

Résumé | Liens:

Lakhal-Chaieb L, Oualkacha K, Richards BJ, Greenwood CM

A rare variant association test in family-based designs and non-normal quantitative traits.

Stat Med, 35 (6), p. 905-21, 2016, ISSN: 0277-6715.

Résumé | Liens:

Oualkacha K, Lakhal-Chaieb L, Greenwood CM

Software Application Profile: RVPedigree: a suite of family-based rare variant association tests for normally and non-normally distributed quantitative traits.

Int J Epidemiol, 45 (2), p. 402-7, 2016, ISSN: 0300-5771.

Résumé | Liens:

Samb R, Khadraoui K, Belleau P, Deschenes A, Lakhal-Chaieb L, Droit A

Using informative Multinomial-Dirichlet prior in a t-mixture with reversible jump estimation of nucleosome positions for genome-wide profiling.

Stat Appl Genet Mol Biol, 14 (6), p. 517-32, 2015.

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