Marie-Paule Roth



    Alumni: Bioinformatics Research In Disease Genomics (BRIDGe)
    marie-paule.roth@inserm.fr



    Publications

    Article type:

    Co‐Occurring Non‐Cardiac Congenital Anomalies Among Cases With Congenital Heart Defects. Claude Stoll, Yves Alembik, Marie‐Paule Roth, American Journal of Medical Genetics Part A 2026. DOI: 10.1002/ajmga.70002

    Co-occurring non-urinary congenital anomalies among cases with congenital anomalies of the kidney and urinary tract. Claude Stoll, Béatrice Dott, ..., Marie‐Paule Roth, European Journal of Medical Genetics 2025. DOI: 10.1016/j.ejmg.2025.105000

    A human anti-matriptase-2 antibody limits iron overload, α-globin aggregates, and splenomegaly in β-thalassemic mice. Matthew Wake, Anaïs Palin, Audrey Belot, Mathieu Berger, ..., Céline Besson‐Fournier, Chloé Latour, ..., Hélène Coppin, Marie‐Paule Roth, ..., Delphine Meynard, Blood Advances 2024. DOI: 10.1182/bloodadvances.2023012010

    Associated Anomalies in Radial Ray Deficiency. Claude Stoll, Yves Alembik, Marie‐Paule Roth, American Journal of Medical Genetics Part A 2024. DOI: 10.1002/ajmg.a.63874

    Associated anomalies inPierre Robin sequence. Claude Stoll, Yves Alembick, Marie‐Paule Roth, American Journal of Medical Genetics Part A 2023. DOI: 10.1002/ajmg.a.63344

    Regulators of hepcidin expression. Marie‐Paule Roth, Delphine Meynard, Hélène Coppin, Vitamins and Hormones 2019. DOI: 10.1016/bs.vh.2019.01.005

    Associated anomalies in cases with agenesis of the corpus callosum. Claude Stoll, Béatrice Dott, Marie‐Paule Roth, American Journal of Medical Genetics Part A 2019. DOI: 10.1002/ajmg.a.61330

    Shift in skin microbiota of Western European women across aging. Romain Jugé, Pauline Rouaud, ..., Marie‐Paule Roth, Hélène Coppin, et al., Journal of Applied Microbiology 2018. DOI: 10.1111/jam.13929

    Deletion of BMP6 worsens the phenotype of HJV-deficient mice and attenuates hepcidin levels reached after LPS challenge. Chloé Latour, Céline Besson‐Fournier, ..., Delphine Meynard, Marie‐Paule Roth, Hélène Coppin, Blood 2017. DOI: 10.1182/blood-2017-07-795658

    Associated anomalies in cases with esophageal atresia. Claude Stoll, Yves Alembik, ..., Marie‐Paule Roth, American Journal of Medical Genetics Part A 2017. DOI: 10.1002/ajmg.a.38303

    Hepcidin upregulation by inflammation is independent of Smad1/5/8 signaling by activin B. Céline Besson‐Fournier, Aurélie Gineste, Chloé Latour, ..., Delphine Meynard, ..., Éric Oswald, Hélène Coppin, Marie‐Paule Roth, Blood 2016. DOI: 10.1182/blood-2016-10-748541

    Decreased Bone Formation Explains Osteoporosis in a Genetic Mouse Model of Hemochromatosiss. Mathilde Doyard, Daniel Chappard, ..., Marie‐Paule Roth, et al., PLOS ONE 2016. DOI: 10.1371/journal.pone.0148292