Mathilde Doyard

Bone status in a mouse model of genetic hemochromatosis

Pascal Guggenbuhl, Patricia Fergelot, Mathilde Doyard et al. · Osteoporosis International · 2010 · 75 citations

Hematology, Osteoporosis, Bone Homeostasis +6

<i>FAM46A</i> mutations are responsible for autosomal recessive osteogenesis imperfecta

Mathilde Doyard, Séverine Bacrot, Céline Huber et al. · Journal of Medical Genetics · 2018 · 74 citations

Decreased Bone Formation Explains Osteoporosis in a Genetic Mouse Model of Hemochromatosiss

Mathilde Doyard, Daniel Chappard, Patricia Leroyer et al. · PLoS ONE · 2016 · 62 citations · Full text

Iron excess limits HHIPL-2 gene expression and decreases osteoblastic activity in human MG-63 cells

Mathilde Doyard, Nadia Fatih, Annabelle Monnier et al. · Osteoporosis International · 2012 · 57 citations

Bone Morphogenic Protein, Iron Metabolism, Osteoarthritis +8

Homozygous Loss-of-Function Mutations in CCDC134 Are Responsible for a Severe Form of Osteogenesis Imperfecta

Johanne Dubail, Perrine Brunelle, Geneviève Baujat et al. · Journal of Bone and Mineral Research · 2020 · 55 citations · Full text

Bone Disease, Sclerostin, Developmental Biology +15