Edinburgh Research Explorer

Nerea Alonso Lopez

Research Fellow / Laboratory manager

  1. 2020
  2. Loss‐of‐function mutations in the ALPL gene presenting with adult onset osteoporosis and low serum concentrations of total alkaline phosphatase

    Alonso, N., Larraz‐Prieto, B., Berg, K., Lambert, Z., Redmond, P., Harris, S. E., Deary, I. J., Pugh, C., Prendergast, J. & Ralston, S. H., 8 Apr 2020, In: Journal of Bone and Mineral Research. 35, 4, p. 657-661 4 p.

    Research output: Contribution to journalArticlepeer-review

  3. 2018
  4. Identification of a novel locus on chromosome 2q13 which predisposes to clinical vertebral fractures independently of bone density

    Alonso, N., Estrada, K., Albagha, O. M. E., Herrera, L., Reppe, S., Olstad, O. K., Gautvik, K. M., Ryan, N. M., Evans, K. L., Nielson, C. M., Hsu, Y-H., Kiel, D. P., Markozannes, G., Ntzani, E. E., Evangelou, E., Feenstra, B., Liu, X., Melbye, M., Masi, L., Brandi, M. L. & 41 others, Riches, P., Daroszewska, A., Olmos, J. M., Valero, C., Castillo, J., Riancho, J. A., Husted, L. B., Langdahl, B. L., Brown, M. A., Duncan, E. L., Kaptoge, S., Khaw, K-T., Usategui-Martín, R., del Pino Montes, J., Gonzalez-Sarmiento, R., Lewis, J. R., Prince, R. L., D'Amelio, P., Garcia-Giralt, N., Nogues, X., Mencej-Bedrac, S., Marc, J., Wolstein, O., Eisman, J. A., Oei, L., Medina-Gomez, C., Schraut, K., Navarro, P., Wilson, J. F., Davies, G., Starr, J., Deary, I., Tanaka, T., Ferrucci, L., Gianfrancesco, F., Gennari, L., Lucas, G., Elosua, R., Uitterlinden, A. G., Rivadeneira, F. & Ralston, S. H., Mar 2018, In: Annals of the Rheumatic Diseases. 77, 3, p. 378-385 8 p.

    Research output: Contribution to journalArticlepeer-review

  5. 2016
  6. Clinical and Genetic Advances in Paget’s Disease of Bone: a Review

    Alonso Lopez, N., Calero-Paniagua, I. & del Pino Montes, J., 19 Dec 2016, In: Clinical Reviews in Bone and Mineral Metabolism. 15, 1

    Research output: Contribution to journalLiterature reviewpeer-review

  7. Novel Genetic Variants are Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SCL1A3 and EPHB2

    Nielson, C. M., Liu, C-T., Smith, A. V., Ackert-Bicknell, C. L., Reppe, S., Johanna, J., Wassel, C., Register, T. C., Oei, L., Alonso Lopez, N., Oei, E. H., Parimi, N., Samelson, E. J., Nalls, M. A., Zmuda, J., Lang, T., Bouxsein, M., Latourelle, J., Claussnitzer, M., Siggeirsdottir, K. & 31 others, Srikanth, P., Lorentzen, E., Vandenput, L., Langefeld, C., Raffield, L., Terry, G., Cox, A. J., Allison, M. A., Criqui, M. H., Bowden, D., Ikram, M. A., Mellström, D., Karlsson, M. K., Carr, J., Budoff, M., Phillips, C., Cupples, L. A., Chou, W-C., Myers, R. H., Ralston, S. H., Gautvik, K. M., Cawthon, P. M., Cummings, S., Karasik, D., Rivadeneira, F., Gudnason, V., Orwoll, E. S., Harris, T. B., Ohlsson, C., Kiel, D. P. & Hsu, Y-H., Dec 2016, In: Journal of Bone and Mineral Research. 31, 12

    Research output: Contribution to journalArticlepeer-review

  8. 2015
  9. Atypical Femoral Fracture in Osteoporosis Pseudoglioma Syndrome Associated With Two Novel Compound Heterozygous Mutations in LRP5

    Alonso, N., Soares, D. C., McCloskey, E., Summers, G. D., Ralston, S. H. & Gregson, C. L., Apr 2015, In: Journal of Bone and Mineral Research. 30, 4, p. 615-620

    Research output: Contribution to journalArticlepeer-review

  10. 2010
  11. Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone

    Albagha, O. M. E., Visconti, M. R., Alonso, N., Langston, A. L., Cundy, T., Dargie, R., Dunlop, M. G., Fraser, W. D., Hooper, M. J., Isaia, G., Nicholson, G. C., del Pino Montes, J., Gonzalez-Sarmiento, R., di Stefano, M., Tenesa, A., Walsh, J. P. & Ralston, S. H., Jun 2010, In: Nature Genetics. 42, 6, p. 520-524 5 p.

    Research output: Contribution to journalArticlepeer-review