People / Staff

Daniel Raúl Grinberg Vaisman

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Publications

  • Urreizti R, Garcia-Giralt N, Riancho JA, González-Macías J, Civit S, Güerri R, Yoskovitz G, Sarrion P, Mellivobsky L, Díez-Pérez A, Nogués X, Balcells S and Grinberg-Vaisman DR.

    COL1A1 haplotypes and hip fracture.

    JOURNAL OF BONE AND MINERAL RESEARCH . 27(4): 950-953. Number of citations: 18

    [doi:10.1002/jbmr.1536]

  • Rodríguez-Pascau L, Coll MJ, Casas J, Vilageliu L and Grinberg-Vaisman DR.

    Generation of a human neuronal stable cell model for niemann-pick C disease by RNA interference.

    JIMD Reports . 4: 29-37. Number of citations: 6

    [doi:10.1007/8904_2011_64]

  • Cozar M, Urreizti R, Vilarinho L, Grosso C, Dodelson de Kremer R, Asteggiano CG, Dalmau J, García AM, Vilaseca MA, Grinberg-Vaisman DR and Balcells S.

    Identification and functional analyses of CBS alleles in Spanish and Argentinian homocystinuric patients.

    HUMAN MUTATION . 32(7): 835-842. Number of citations: 13

    [doi:10.1002/humu.21514]

  • Agueda L, Velázquez-Cruz R, Urreizti R, Yoskovitz G, Sarrión P, Jurado S, Güerri R, Garcia-Giralt N, Nogués X, Mellibovsky L, Díez-Pérez A, Marie PJ, Balcells S and Grinberg-Vaisman DR.

    Functional relevance of the BMD-associated polymorphism rs312009: novel involvement of RUNX2 in LRP5 transcriptional regulation.

    JOURNAL OF BONE AND MINERAL RESEARCH . 26(5): 1133-1144. Number of citations: 12

    [doi:10.1002/jbmr.293]

  • Cozar M, Bembi B, Dominissini S, Zampieri S, Vilageliu L, Grinberg-Vaisman DR and Dardis A.

    Molecular characterization of a new deletion of the GBA1 gene due to an inter Alu recombination event.

    MOLECULAR GENETICS AND METABOLISM . 102(2): 226-228. Number of citations: 10

    [doi:10.1016/j.ymgme.2010.10.004]

  • Sánchez-Ollé G, Duque J, Egido-Gabás M, Casas J, Lluch-Canut T, Chabás A, Grinberg-Vaisman DR and Vilageliu L.

    Promising results of the chaperone effect caused by imino sugars and aminocyclitol derivatives on mutant glucocerebrosidases causing Gaucher disease.

    BLOOD CELLS MOLECULES AND DISEASES . 42(2): 159-166. Number of citations: 37

    [doi:10.1016/j.bcmd.2008.11.002]

  • Grinberg-Vaisman DR.

    Recent patents relating to siRNAs and therapeutic strategies for genetic diseases.

    Recent Patents on DNA and Gene Sequences . 2(1): 40-43.

    [doi:10.2174/187221508783406530]

  • Pintó X, Vilaseca MA, Balcells S, Artuch-Iriberri R, Corbella E, Meco JF, Vila R, Pujol R and Grinberg-Vaisman DR.

    A folate-rich diet is as effective as folic acid from supplements in decreasing plasma homocysteine concentrations.

    INTERNATIONAL JOURNAL OF MEDICAL SCIENCES . 2(2): 58-63. Number of citations: 21

    [doi:10.7150/ijms.2.58]

  • Mainou Cid C, García Giralt N, Vilaseca MA, Ferrer I, Meco López JF, Mainou Pintó A, Pintó Sala X, Grinberg-Vaisman DR and Balcells S.

    Hiperhomocistinemia y polimorfismo 677C T de la 5,10-metilenotetrahidrofolato reductasa en hijos de pacientes con enfermedad coronaria prematura.

    Anales espanoles de pediatria . 56(5): 402-408.

  • Bayés M, Goldaracena B, Martínez-Mir A, Iragui-Madoz MI, Solans T, Chivelet P, Bussaglia E, Ramos-Arroyo MA, Baiget M, Vilageliu L, Balcells S, Gonzalez R and Grinberg-Vaisman DR.

    A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2q31-q33.

    JOURNAL OF MEDICAL GENETICS . 35(2): 141-145. Number of citations: 29

    [doi:10.1136/jmg.35.2.141]