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  1. Article

    Open Access

    Author Correction: DNA damage in circulating leukocytes measured with the comet assay may predict the risk of death

    Stefano Bonassi, Marcello Ceppi, Peter Møller, Amaya Azqueta in Scientific Reports (2021)

  2. Article

    Open Access

    DNA damage in circulating leukocytes measured with the comet assay may predict the risk of death

    The comet assay or single cell gel electrophoresis, is the most common method used to measure strand breaks and a variety of other DNA lesions in human populations. To estimate the risk of overall mortality, m...

    Stefano Bonassi, Marcello Ceppi, Peter Møller, Amaya Azqueta in Scientific Reports (2021)

  3. Article

    Open Access

    Mixed logistic regression in genome-wide association studies

    Mixed linear models (MLM) have been widely used to account for population structure in case-control genome-wide association studies, the status being analyzed as a quantitative phenotype. Chen et al. proved in...

    Jacqueline Milet, David Courtin, André Garcia, Hervé Perdry in BMC Bioinformatics (2020)

  4. No Access

    Article

    First genome-wide association study of non-severe malaria in two birth cohorts in Benin

    Recent research efforts to identify genes involved in malaria susceptibility using genome-wide approaches have focused on severe malaria. Here, we present the first GWAS on non-severe malaria designed to ident...

    Jacqueline Milet, Anne Boland, Pierre Luisi, Audrey Sabbagh in Human Genetics (2019)

  5. Article

    Open Access

    Detecting the dominance component of heritability in isolated and outbred human populations

    Inconsistencies between published estimates of dominance heritability between studies of human genetic isolates and human outbred populations incite investigation into whether such differences result from part...

    Anthony F. Herzig, Teresa Nutile, Daniela Ruggiero, Marina Ciullo in Scientific Reports (2018)

  6. Article

    Open Access

    Accuracy of heritability estimations in presence of hidden population stratification

    The heritability of a trait is the proportion of its variance explained by genetic factors; it has historically been estimated using familial data. However, new methods have appeared for estimating heritabilit...

    Claire Dandine-Roulland, Céline Bellenguez, Stéphanie Debette in Scientific Reports (2016)

  7. Article

    Open Access

    A novel tree-based procedure for deciphering the genomic spectrum of clinical disease entities

    Dissecting the genomic spectrum of clinical disease entities is a challenging task. Recursive partitioning (or classification trees) methods provide powerful tools for exploring complex interplay among genomic...

    Cyprien Mbogning, Hervé Perdry, Wilson Toussile in Journal of Clinical Bioinformatics (2014)

  8. No Access

    Article

    Space alternating penalized Kullback proximal point algorithms for maximizing likelihood with nondifferentiable penalty

    The EM algorithm is a widely used methodology for penalized likelihood estimation. Provable monotonicity and convergence are the hallmarks of the EM algorithm and these properties are well established for smoo...

    Stéphane Chrétien, Alfred Hero, Hervé Perdry in Annals of the Institute of Statistical Mat… (2012)

  9. No Access

    Protocol

    Modeling the Effect of Susceptibility Factors (HLA and PTPN22) in Rheumatoid Arthritis

    Numerous genome-wide analyses on common multifactorial diseases have been recently published in providing, for each associated Single Nucleotide Polymorphism (SNP), an Odds Ratio (OR), either for one of the su...

    Hervé Perdry, Françoise Clerget-Darpoux in Genetic Epidemiology (2011)

  10. Article

    Open Access

    An ordered subset approach to including covariates in the transmission disequilibrium test

    Clinical heterogeneity of a disease may reflect an underlying genetic heterogeneity, which may hinder the detection of trait loci. Consequently, many statistical methods have been developed that allow for the ...

    Hervé Perdry, Brion S Maher, Marie-Claude Babron, Toby McHenry in BMC Proceedings (2007)

  11. Article

    Open Access

    Modeling the effect of PTPN22in rheumatoid arthritis

    In order to model the effect of PTPN22 on rheumatoid arthritis (RA), we determined the combination of single-nucleotide-polymorphisms (SNPs) showing the strongest association with RA. Three SNPs (rs2476601-rs1273...

    Mathieu Bourgey, Hervé Perdry, Françoise Clerget-Darpoux in BMC Proceedings (2007)