| Year |
Citation |
Score |
| 2022 |
Garcia-Giralt N, Roca-Ayats N, Abril JF, Martinez-Gil N, Ovejero D, Castañeda S, Nogues X, Grinberg D, Balcells S, Rabionet R. Gene Network of Susceptibility to Atypical Femoral Fractures Related to Bisphosphonate Treatment. Genes. 13. PMID 35052486 DOI: 10.3390/genes13010146 |
0.79 |
|
| 2021 |
Ugartondo N, Martínez-Gil N, Esteve M, Garcia-Giralt N, Roca-Ayats N, Ovejero D, Nogués X, Díez-Pérez A, Rabionet R, Grinberg D, Balcells S. Functional Analyses of Four Missense Mutations Present in Patients with Atypical Femoral Fractures. International Journal of Molecular Sciences. 22. PMID 34299011 DOI: 10.3390/ijms22147395 |
0.782 |
|
| 2021 |
Martínez-Gil N, Roca-Ayats N, Cozar M, Garcia-Giralt N, Ovejero D, Nogués X, Grinberg D, Balcells S. Genetics and Genomics of : Functional Analysis of Variants and Genomic Regulation in Osteoblasts. International Journal of Molecular Sciences. 22. PMID 33419004 DOI: 10.3390/ijms22020489 |
0.787 |
|
| 2020 |
Martínez-Gil N, Roca-Ayats N, Atalay N, Pineda-Moncusí M, Garcia-Giralt N, Van Hul W, Boudin E, Ovejero D, Mellibovsky L, Nogués X, Díez-Pérez A, Grinberg D, Balcells S. Functional Assessment of Coding and Regulatory Variants From the Locus. Jbmr Plus. 4: e10423. PMID 33354644 DOI: 10.1002/jbm4.10423 |
0.803 |
|
| 2019 |
Serra-Vinardell J, Roca-Ayats N, De-Ugarte L, Vilageliu L, Balcells S, Grinberg D. Bone development and remodeling in metabolic disorders. Journal of Inherited Metabolic Disease. PMID 30942483 DOI: 10.1002/Jimd.12097 |
0.763 |
|
| 2019 |
Roca-Ayats N, Martínez-Gil N, Cozar M, Gerousi M, Garcia-Giralt N, Ovejero D, Mellibovsky L, Nogués X, Díez-Pérez A, Grinberg D, Balcells S. Functional characterization of the C7ORF76 genomic region, a prominent GWAS signal for osteoporosis in 7q21.3. Bone. 123: 39-47. PMID 30878523 DOI: 10.1016/J.Bone.2019.03.014 |
0.792 |
|
| 2018 |
Roca-Ayats N, Ng PY, Garcia-Giralt N, Falcó-Mascaró M, Cozar M, Abril JF, Quesada Gómez JM, Prieto-Alhambra D, Nogués X, Dunford JE, Russell RG, Baron R, Grinberg D, Balcells S, Díez-Pérez A. 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. PMID 30184270 DOI: 10.1002/Jbmr.3580 |
0.706 |
|
| 2018 |
Martínez-Gil N, Roca-Ayats N, Monistrol-Mula A, García-Giralt N, Díez-Pérez A, Nogués X, Mellibovsky L, Grinberg D, Balcells S. Common and rare variants of WNT16, DKK1 and SOST and their relationship with bone mineral density. Scientific Reports. 8: 10951. PMID 30026596 DOI: 10.1038/S41598-018-29242-8 |
0.798 |
|
| 2017 |
Roca-Ayats N, Balcells S, Garcia-Giralt N, Falcó-Mascaró M, Martínez-Gil N, Abril JF, Urreizti R, Dopazo J, Quesada-Gómez JM, Nogués X, Mellibovsky L, Prieto-Alhambra D, Dunford JE, Javaid MK, Russell RG, et al. GGPS1 Mutation and Atypical Femoral Fractures with Bisphosphonates. The New England Journal of Medicine. 376: 1794-1795. PMID 28467865 DOI: 10.1056/Nejmc1612804 |
0.733 |
|
| 2017 |
Urreizti R, Cueto-Gonzalez AM, Franco-Valls H, Mort-Farre S, Roca-Ayats N, Ponomarenko J, Cozzuto L, Company C, Bosio M, Ossowski S, Montfort M, Hecht J, Tizzano EF, Cormand B, Vilageliu L, et al. 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. PMID 28281571 DOI: 10.1038/Srep44138 |
0.761 |
|
| 2017 |
Roca-Ayats N, Cozar Morillo M, Gerousi M, Czwan E, Urreizti R, Martínez-Gil N, García-Giralt N, Mellibovsky L, Nogués X, Díez-Pérez A, Balcells S, Grinberg D. Identificación de variantes genéticas asociadas con la densidad mineral ósea (DMO) en el gen FLJ42280 Revista De Osteoporosis Y Metabolismo Mineral. 9: 28-34. DOI: 10.4321/S1889-836X2017000100005 |
0.745 |
|
| 2016 |
Urreizti R, Roca-Ayats N, Trepat J, Garcia-Garcia F, Aleman A, Orteschi D, Marangi G, Neri G, Opitz JM, Dopazo J, Cormand B, Vilageliu L, Balcells S, Grinberg D. Screening of CD96 and ASXL1 in 11 patients with Opitz C or Bohring-Opitz syndromes. American Journal of Medical Genetics. Part A. 170: 24-31. PMID 26768331 DOI: 10.1002/Ajmg.A.37418 |
0.75 |
|
| 2016 |
Martinez-Gil N, Roca-Ayats N, Urreizti R, Franco-Valls H, Garcia-Giralt N, Mellibovsky L, Nogues X, Diez-Perez A, Grinberg D, Balcells S. Search for BMD-related variants of DKK1 and SOST by resequencing in the BARCOS cohort Bone Abstracts. DOI: 10.1530/Boneabs.5.P239 |
0.73 |
|
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