Dr Gillian Rice

Research Fellow

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Publications

  1. Published

    Sine causa tetraparesis: A pilot study on its possible relationship with interferon signature analysis and Aicardi Goutières syndrome related genes analysis

    AGS study group, Dec 2018, In : Medicine (Philadelphia). 97, 52, p. e13893

    Research output: Contribution to journalArticle

  2. Published

    Chilblains as a diagnostic sign of aicardi-goutiéres syndrome

    Abdel-Salam, G. M. H., El-Kamah, G. Y., Rice, G. I., El-Darouti, M., Gornall, H., Szynkiewicz, M., Aymard, F., Zaki, M. S., Abdel-Aleem, A. K., Lebon, P. & Crow, Y. J., 2010, In : Neuropediatrics. 41, 1, p. 18-23 5 p.

    Research output: Contribution to journalArticle

  3. Published

    A child with severe juvenile dermatomyositis treated with ruxolitinib

    Aeschlimann, F. A., Frémond, M., Duffy, D., Rice, G. I., Charuel, J., Bondet, V., Saire, E., Neven, B., Bodemer, C., Balu, L., Gitiaux, C., Crow, Y. J. & Bader-meunier, B., 1 Nov 2018, In : Brain. 141, 11, p. e80

    Research output: Contribution to journalArticle

  4. Published

    A child with severe juvenile dermatomyositis treated with ruxolitinib (vol 141, pg e80, 2018)

    Aeschlimann, F. A., Fremond, M-L., Duffy, D., Rice, G. I., Charuel, J-L., Bondet, V., Saire, E., Neven, B., Bodemer, C., Balu, L., Gitiaux, C., Crow, Y. J. & Bader-Meunier, B., Jan 2019, In : Brain. 142, p. e3-e3

    Research output: Contribution to journalArticle

  5. Published

    Tartrate-Resistant Acid Phosphatase Deficiency in the Predisposition to Systemic Lupus Erythematosus

    An, J., Briggs, T., Dumax-Vorzet, A., Alarcón-Riquelme, M. E., Belot, A., Beresford, M., Bruce, I., Carvalho, C., Chaperot, L., Frostegård, J., Plumas, J., Rice, G., Vyse, T. J., Wiedeman, A., Crow, Y. & Elkon, K. B., 2017, In : Arthritis and Rheumatology. 69, 1, p. 131-142

    Research output: Contribution to journalArticle

  6. Published

    Expression of Cyclic GMP-AMP Synthase in Patients With Systemic Lupus Erythematosus

    An, J., Durcan, L., Karr, R. M., Briggs, T. A., Rice, G. I., Teal, T. H., Woodward, J. J. & Elkon, K. B., Apr 2017, In : Arthritis & rheumatology (Hoboken, N.J.). 69, 4, p. 800-807

    Research output: Contribution to journalArticle

  7. Published

    Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus

    Anderson, B., Kasher, P. R., Mayer, J., Szynkiewicz, M., Jenkinson, E. M., Bhaskar, S. S., Urquhart, J. E., Daly, S. B., Dickerson, J. E., O'Sullivan, J., Leibundgut, E. O., Muter, J., Abdel-Salem, G. M. H., Babul-Hirji, R., Baxter, P., Berger, A., Bonafé, L., Brunstom-Hernandez, J. E., Buckard, J. A., Chitayat, D. & 45 othersChong, W. K., Cordelli, D. M., Ferreira, P., Fluss, J., Forrest, E. H., Franzoni, E., Garone, C., Hammans, S. R., Houge, G., Hughes, I., Jacquemont, S., Jeannet, P. Y., Jefferson, R. J., Kumar, R., Kutschke, G., Lundberg, S., Loureno, C. M., Mehta, R., Naidu, S., Nischal, K. K., Nunes, L., Ounap, K., Philippart, M., Prabhakar, P., Risen, S. R., Schiffmann, R., Soh, C., Stephenson, J. B. P., Stewart, H., Stone, J., Tolmie, J. L., Van Der Knaap, M. S., Vieira, J. P., Vilain, C. N., Wakeling, E. L., Wermenbol, V., Whitney, A., Lovell, S. C., Meyer, S., Livingston, J. H., Baerlocher, G. M., Black, G. C. M., Rice, G. I., Yanick, J. & Lourenço, C. M., Mar 2012, In : Nature Genetics. 44, 3, p. 338-342 4 p.

    Research output: Contribution to journalArticle

  8. Published

    Identification and characterization of an inborn error of metabolism caused by dihydrofolate reductase deficiency

    Banka, S., Blom, H. J., Walter, J., Aziz, M., Urquhart, J., Clouthier, C. M., Rice, G. I., De Brouwer, A. P. M., Hilton, E., Vassallo, G., Will, A., Smith, D. E. C., Smulders, Y. M., Wevers, R. A., Steinfeld, R., Heales, S., Crow, Y. J., Pelletier, J. N., Jones, S. & Newman, W. G., 11 Feb 2011, In : American Journal of Human Genetics. 88, 2, p. 216-225 9 p.

    Research output: Contribution to journalArticle

  9. Published

    Protein kinase cδ deficiency causes mendelian systemic lupus erythematosus with B cell-defective apoptosis and hyperproliferation.

    Belot, A., Kasher, P. R., Trotter, E. W., Foray, A-P., Debaud, A-L., Rice, G. I., Szynkiewicz, M., Zabot, M-T., Rouvet, I., Bhaskar, S. S., Daly, S. B., Dickerson, J. E., Mayer, J., O'Sullivan, J., Juillard, L., Urquhart, J. E., Fawdar, S., Marusiak, A. A., Stephenson, N., Waszkowycz, B. & 15 othersW Beresford, M., Biesecker, L. G., C M Black, G., René, C., Eliaou, J-F., Fabien, N., Ranchin, B., Cochat, P., Gaffney, P. M., Rozenberg, F., Lebon, P., Malcus, C., Crow, Y. J., Brognard, J. & Bonnefoy, N., Aug 2013, In : Arthritis Care & Research. 65, 8, p. 2161-2171 10 p.

    Research output: Contribution to journalArticle

  10. Published

    Mutations in CECR1 associated with a neutrophil signature in peripheral blood

    Belot, A., Wassmer, E., Twilt, M., Lega, J. C., Zeef, L. A. H., Oojageer, A., Kasher, P. R., Mathieu, A. L., Malcus, C., Demaret, J., Fabien, N., Collardeau-Frachon, S., Mechtouff, L., Derex, L., Walzer, T., Rice, G. I., Durieu, I. & Crow, Y. J., 24 Sep 2014, In : Pediatric Rheumatology. 12, 1, 44.

    Research output: Contribution to journalArticle

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