Neus Roca-Ayats
Affiliations: | Department of Genetics, Microbiology and Statistics | Universitat de Barcelona, Barcelona, Cataluña, Spain |
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"Neus Roca-Ayats"
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| Garcia-Giralt N, Roca-Ayats N, Abril JF, et al. (2022) Gene Network of Susceptibility to Atypical Femoral Fractures Related to Bisphosphonate Treatment. Genes. 13 |
| Ugartondo N, Martínez-Gil N, Esteve M, et al. (2021) Functional Analyses of Four Missense Mutations Present in Patients with Atypical Femoral Fractures. International Journal of Molecular Sciences. 22 |
| Martínez-Gil N, Roca-Ayats N, Cozar M, et al. (2021) Genetics and Genomics of : Functional Analysis of Variants and Genomic Regulation in Osteoblasts. International Journal of Molecular Sciences. 22 |
| Martínez-Gil N, Roca-Ayats N, Atalay N, et al. (2020) Functional Assessment of Coding and Regulatory Variants From the Locus. Jbmr Plus. 4: e10423 |
| Serra-Vinardell J, Roca-Ayats N, De-Ugarte L, et al. (2019) Bone development and remodeling in metabolic disorders. Journal of Inherited Metabolic Disease |
| Roca-Ayats N, Martínez-Gil N, Cozar M, et al. (2019) Functional characterization of the C7ORF76 genomic region, a prominent GWAS signal for osteoporosis in 7q21.3. Bone. 123: 39-47 |
| Roca-Ayats N, Ng PY, Garcia-Giralt N, et al. (2018) Functional characterization of a GGPPS variant identified in atypical femoral fracture patients and delineation of the role of GGPPS in bone-relevant cell types. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research |
| Martínez-Gil N, Roca-Ayats N, Monistrol-Mula A, et al. (2018) Common and rare variants of WNT16, DKK1 and SOST and their relationship with bone mineral density. Scientific Reports. 8: 10951 |
| Roca-Ayats N, Balcells S, Garcia-Giralt N, et al. (2017) GGPS1 Mutation and Atypical Femoral Fractures with Bisphosphonates. The New England Journal of Medicine. 376: 1794-1795 |
| Urreizti R, Cueto-Gonzalez AM, Franco-Valls H, et al. (2017) A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C Syndromes. Scientific Reports. 7: 44138 |