BMC Medical Genetics, 1471-2350

Tidskrift

Fler filtreringsmöjligheter
  1. 2017
  2. Association of common genetic variants related to atrial fibrillation and the risk of ventricular fibrillation in the setting of first ST-elevation myocardial infarction

    Jabbari, R., Jabbari, J., Glinge, C., Risgaard, B., Sattler, S., Winkel, B. G., Terkelsen, C. J., Tilsted, H. H., Jensen, L. O., Hougaard, M., Haunsø, S., Thomas Engstrøm, Albert, C. M. & Tfelt-Hansen, J., 2017 nov 21, I : BMC Medical Genetics. 18, 1, 138.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  3. Genetic variation of the Toll-like receptors in a Swedish allergic rhinitis case population

    Henmyr, V., Carlberg, D., Manderstedt, E., Lind-Halldén, C., T. Säll, Cardell, L. O. & Halldén, C., 2017 feb 23, I : BMC Medical Genetics. 18, 1, 18.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  4. 2016
  5. Association of CD247 (CD3ζ) gene polymorphisms with T1D and AITD in the population of northern Sweden

    Dan Holmberg, Ruikka, K., Lindgren, P., Eliasson, M. & Mayans, S., 2016 okt 4, I : BMC Medical Genetics. 17, 1, 70.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  6. 2015
  7. Genes involved in muscle contractility and nutrient signaling pathways within celiac disease risk loci show differential mRNA expression

    Caroline Montén, Gudjonsdottir, A. H., Browaldh, L., Arnell, H., Nilsson, S., Daniel Agardh & Naluai, A. T., 2015, I : BMC Medical Genetics. 16, 44.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  8. Physical activity, smoking, and genetic predisposition to obesity in people from Pakistan: the PROMIS study.

    Shafqat Ahmad, Zhao, W., Frida Renström, Rasheed, A., Samuel, M., Zaidi, M., Shah, N., Mallick, N. H., Zaman, K. S., Ishaq, M., Rasheed, S. Z., Memon, F-U-R., Hanif, B., Lakhani, M. S., Ahmed, F., Kazmi, S. U., Frossard, P., Paul Franks & Saleheen, D., 2015, I : BMC Medical Genetics. 16, 1, 114.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  9. 2014
  10. 2013
  11. DNA methylation of the glucagon-like peptide 1 receptor (GLP1R) in human pancreatic islets.

    Hall, E., Dayeh, T., Kirkpatrick, C. L., Claes Wollheim, Dekker Nitert, M. & Charlotte Ling, 2013, I : BMC Medical Genetics. 14, Jul,23, 76.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  12. Heterozygous FA2H mutations in autism spectrum disorders

    Scheid, I., Maruani, A., Huguet, G., Leblond, C. S., Nygren, G., Anckarsäter, H., Beggiato, A., Maria Råstam, Amsellem, F., Gillberg, I. C., Elmaleh, M., Leboyer, M., Gillberg, C., Betancur, C., Coleman, M., Hama, H., Cook, E. H., Bourgeron, T. & Delorme, R., 2013, I : BMC Medical Genetics. 14, 124.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  13. Investigating highly replicated asthma genes as candidate genes for allergic rhinitis

    Andiappan, A. K., Nilsson, D., Hallden, C., De Yun, W., Torbjörn Säll, Cardell, L. O. & Tim, C. F., 2013, I : BMC Medical Genetics. 14, 51.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  14. 2012
  15. Polymorphisms in the mitochondrial oxidative phosphorylation chain genes as prognostic markers for colorectal cancer

    Lascorz, J., Bevier, M., Schoenfels, W. V., Kalthoff, H., Aselmann, H., Beckmann, J., Egberts, J., Buch, S., Becker, T., Schreiber, S., Hampe, J., Kari Hemminki, Asta Försti & Schafmayer, C., 2012, I : BMC Medical Genetics. 13

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  16. Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases

    Huhn, S., Bevier, M., Rudolph, A., Pardini, B., Naccarati, A., Hein, R., Hoffmeister, M., Vodickova, L., Novotny, J., Brenner, H., Chang-Claude, J., Kari Hemminki, Vodicka, P. & Asta Försti, 2012, I : BMC Medical Genetics. 13, 94

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  17. Toll-like receptor gene polymorphisms are associated with allergic rhinitis: a case control study

    Nilsson, D., Andiappan, A. K., Halldén, C., Yun, W. D., Torbjörn Säll, Tim, C. F. & Cardell, L-O., 2012, I : BMC Medical Genetics. 13, 66

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  18. 2011
  19. A validation of the first genome-wide association study of calcaneus ultrasound parameters in the European Male Ageing Study

    Roshandel, D., Thomson, W., Pye, S. R., Boonen, S., Borghs, H., Vanderschueren, D., Huhtaniemi, I. T., Adams, J. E., Ward, K. A., Bartfai, G., Casanueva, F., Finn, J. D., Forti, G., Giwercman, A., Han, T. S., Kula, K., Lean, M. E., Pendleton, N., Punab, M., Silman, A. J. & 3 andraWu, F. C., Holliday, K. L. & O'Neill, T. W., 2011, I : BMC Medical Genetics. 12

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  20. 2009
  21. An investigation of ribosomal protein L10 gene in autism spectrum disorders

    Gong, X., Delorme, R., Fauchereau, F., Durand, C. M., Chaste, P., Betancur, C., Goubran-Botros, H., Nygren, G., Anckarsäter, H., Maria Råstam, Gillberg, I. C., Kopp, S., Mouren-Simeoni, M-C., Gillberg, C., Leboyer, M. & Bourgeron, T., 2009, I : BMC Medical Genetics. 10, 7

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  22. 2008
  23. 2007
  24. A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study

    Kathiresan, S., Manning, A. K., Demissie, S., D'Agostino, R. B., Surti, A., Guiducci, C., Gianniny, L., Burtt, N. P., Olle Melander, Marju Orho-Melander, Arnett, D. K., Peloso, G. M., Ordovas, J. M. & Cupples, L. A., 2007, I : BMC Medical Genetics. 8

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  25. CT60 genotype does not affect CTLA-4 isoform expression despite association to TID and AITD in northern Sweden

    Mayans, S., Lackovic, K., Bolmeson, C., Lindgren, P., Ruikka, K., Eliasson, M., Corrado Cilio & Holmberg, D., 2007, I : BMC Medical Genetics. 8

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  26. Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephaly

    Buxbaum, J. D., Cai, G., Nygren, G., Chaste, P., Delorme, R., Goldsmith, J., Maria Råstam, Silverman, J. M., Hollander, E., Gillberg, C., Leboyer, M. & Betancur, C., 2007, I : BMC Medical Genetics. 8, 68

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  27. 2006