Human Molecular Genetics, 0964-6906

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  1. Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

    Philippe, A., Martinez, M., Guilloud-Bataille, M., Gillberg, C., Maria Råstam, Sponheim, E., Coleman, M., Zappella, M., Aschauer, H., Van Maldergem, L., Penet, C., Feingold, J., Brice, A. & Leboyer, M., 1999, I : Human Molecular Genetics. 8, 5, s. 805-812

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  2. High-resolution mapping of a complex disease, a model for rheumatoid arthritis, using heterogeneous stock mice

    Emma Ahlqvist, Ekman, D., Lindvall, T., Popovic, M., Förster, M., Hultqvist, M., Klaczkowska, D., Teneva, I., Johannesson, M., Flint, J., Valdar, W., Kutty Selva, N. & Holmdahl, R., 2011, I : Human Molecular Genetics. 20, 15, s. 3031-3041

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  3. High resolution mapping of an arthritis susceptibility locus on rat chromosome 4, and characterization of regulated phenotypes

    Ribbhammar, U., Flornes, L., Backdahl, L., Holger Luthman, Fossum, S. & Lorentzen, JC., 2003, I : Human Molecular Genetics. 12, 17, s. 2087-2096

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  4. Hsa-miR-34b is a plasma-stable microRNA that is elevated in pre-manifest Huntington's disease

    Gaughwin, P., Ciesla, M., Lahiri, N., Tabrizi, S. J., Brundin, P. & Maria Björkqvist, 2011, I : Human Molecular Genetics. 20, 11, s. 2225-2237

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  5. IDENTIFICATION OF BTK MUTATIONS IN 20 UNRELATED PATIENTS WITH X-LINKED AGAMMAGLOBULINEMIA (XLA)

    JIN, H., WEBSTER, ADB., Mauno Vihinen, SIDERAS, P., VORECHOVSKY, I., HAMMARSTROM, L., BERNATOWSKAMATUSZKIEWICZ, E., SMITH, CIE., BOBROW, M. & VETRIE, D., 1995, I : Human Molecular Genetics. 4, 4, s. 693-700

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  6. Identification of novel genes for glucose metabolism based upon expression pattern in human islets and effect on insulin secretion and glycemia.

    Taneera, J., Fadista, J., Emma Ahlqvist, Grubich Atac, D., Ottosson Laakso, E., Claes Wollheim & Leif Groop, 2015, I : Human Molecular Genetics. 24, 7, s. 1945-1955

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  7. Impact of age, BMI and HbA1c levels on the genome-wide DNA methylation and mRNA expression patterns in human adipose tissue and identification of epigenetic biomarkers in blood.

    Tina Rönn, Petr Volkov, Gillberg, L., Kokosar, M., Alexander Perfilyev, Jacobsen, A. L., Jørgensen, S. W., Brøns, C., Jansson, P-A., Karl-Fredrik Eriksson, Pedersen, O., Hansen, T., Leif Groop, Stener-Victorin, E., Allan Vaag, Emma A Nilsson & Charlotte Ling, 2015, I : Human Molecular Genetics. 24, 13, s. 3792-3813

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  8. Impaired dopamine storage resulting from alpha-synuclein mutations may contribute to the pathogenesis of Parkinson's disease.

    Lotharius, J. & Brundin, P., 2002, I : Human Molecular Genetics. 11, 20, s. 2395-2407

    Forskningsoutput: TidskriftsbidragÖversiktsartikel