Personas / Equipo Humano

Daniel Raúl Grinberg Vaisman

Buscador de publicaciones

Publicaciones

  • Roca N, Martinez-Gil N, Cozar M, Gerousi M, Garcia-Giralt N, Ovejero D, Mellibovsky L, Nogués X, Díez-Pérez A, Grinberg-Vaisman DR and Balcells S.

    Functional characterization of the C7ORF76 genomic region, a prominent GWAS signal for osteoporosis in 7q21.3.

    Bone . 123: 39-47. Nº de citas: 10

    [doi:10.1016/j.bone.2019.03.014]

  • Mason S, Castilla-Vallmanya L, James C, Andrews PI, Balcells S, Grinberg-Vaisman DR, Kirk EP and Urreizti R.

    Case report of a child bearing a novel deleterious splicing variant in PIGT

    Medicine . 98(8): . Nº de citas: 7

    [doi:10.1097/MD.0000000000014524]

  • Roca 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-Vaisman DR, Balcells S and 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 . 33(12): 2091-2098. Nº de citas: 24

    [doi:10.1002/jbmr.3580]

  • De-Ugarte L, Balcells S, Nogues X, Grinberg-Vaisman DR, Diez-Perez A and Garcia-Giralt N.

    Pro-osteoporotic miR-320a impairs osteoblast function and induces oxidative stress.

    PLoS One . 13(11): . Nº de citas: 23

    [doi:10.1371/journal.pone.0208131]

  • Trajanoska K, Morris JA, Oei L, Zheng HF, Evans DM, Kiel DP, Ohlsson C, Richards JB, Rivadeneira F and GEFOS/GENOMOS consortium and the 23andMe research team.

    Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study.

    BMJ (Clinical research ed.) . 362: . Nº de citas: 190

    [doi:10.1136/bmj.k3225]

  • Urreizti R, Gürsoy S, Castilla-Vallmanya L, Cunill G, Rabionet-Janssen R, Erçal D, Grinberg-Vaisman DR and Balcells S.

    The ASXL1 mutation p.Gly646Trpfs*12 found in a Turkish boy with Bohring-Opitz Syndrome.

    clinical case reports . 6(8): 1452-1456. Nº de citas: 4

    [doi:10.1002/ccr3.1603]

  • Martinez-Gil N, Roca N, Monistrol-Mula A, García-Giralt N, Díez-Pérez A, Nogués X, Mellibovsky L, Grinberg-Vaisman DR and Balcells S.

    Common and rare variants of WNT16, DKK1 and SOST and their relationship with bone mineral density.

    SCIENTIFIC REPORTS . 8(1): 10951-10951. Nº de citas: 15

    [doi:10.1038/s41598-018-29242-8]

  • Cammarata-Scalisi F, Stock F, Avendaño A, Cozar M, Balcells S and Grinberg-Vaisman DR.

    Estudio clínico y molecular en una familia con osteocondromatosis mltiple.

    Acta ortopédica mexicana . 32(2): 108-111.

  • Urreizti R, Damanti S, Esteve-Matanza C, Franco-Valls H, Castilla-Vallmanya L, Tonda R, Cormand B, Vilageliu L, Opitz JM, Neri G, Grinberg-Vaisman DR and Balcells S.

    A De Novo FOXP1 Truncating Mutation in a Patient Originally Diagnosed as C Syndrome

    SCIENTIFIC REPORTS . 8: 694-694. Nº de citas: 11

    [doi:10.1038/s41598-017-19109-9]

  • De-Ugarte L, Serra-Vinardell J, Nonell L, Balcells S, Arnal M, Nogues X, Mellibovsky L, Grinberg-Vaisman DR, Diez-Perez A and Garcia-Giralt N.

    Expression profiling of microRNAs in human bone tissue from postmenopausal women.

    Human Cell . 31(1): 33-41. Nº de citas: 12

    [doi:10.1007/s13577-017-0181-y]