Mathilde Doyard

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

Mathilde Doyard, Séverine Bacrot, Céline Huber et al. · Journal of Medical Genetics · 2018 · 79 citations

Medicine, Genetics, Molecular Genetics +16

Bone status in a mouse model of genetic hemochromatosis

Pascal Guggenbuhl, Patricia Fergelot, Mathilde Doyard et al. · Osteoporosis International · 2010 · 76 citations

Medicine, Genetics, Hematology +15

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

Mathilde Doyard, Daniel Chappard, Patricia Leroyer et al. · PLoS ONE · 2016 · 64 citations · Full text

Medicine, Genetics, Hematology +17

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 · 58 citations

Medicine, Genetics, Bone Metabolism +9

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 · 58 citations · Full text

Medicine, Genetics, Molecular Genetics +17