José A. Caparrós‐Martín

Identification of a Frameshift Mutation in Osterix in a Patient with Recessive Osteogenesis Imperfecta

Pablo Lapunzina, Mona Aglan, Samia A. Temtamy et al. · The American Journal of Human Genetics · 2010 · 283 citations · Full text

Bone Disease, Recessive Osteogenesis Imperfecta, Developmental Biology +7

Mutations in WNT1 Cause Different Forms of Bone Fragility

Katharina Keupp, Filippo Beleggia, Hülya Kayserili et al. · The American Journal of Human Genetics · 2013 · 277 citations · Full text

Bone Disease, Bone Fragility, Bone Morphogenic Protein +4

Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta

Víctor Martínez‐Glez, José A. Caparrós‐Martín, Mona Aglan et al. · Human Mutation · 2011 · 213 citations · Full text

Sclerostin, Genetics, Bone Repair +20

Statin therapy causes gut dysbiosis in mice through a PXR-dependent mechanism

José A. Caparrós‐Martín, Ricky R. Lareu, Joshua P. Ramsay et al. · Microbiome · 2017 · 207 citations · Full text

The ciliary Evc/Evc2 complex interacts with Smo and controls Hedgehog pathway activity in chondrocytes by regulating Sufu/Gli3 dissociation and Gli3 trafficking in primary cilia

José A. Caparrós‐Martín, Edel Reytor, María Pacheco et al. · Human Molecular Genetics · 2012 · 109 citations · Full text

Cellular Physiology, Hh Pathway, Signaling Pathway +17