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  • Showing 1-6 of 6 Results
2016
Meta-analysis of the DRD5 VNTR in persistent ADHD.Klein, M., Berger S., Hoogman M., Dammers J., Makkinje R., Heister AJ, Galesloot TE, Kiemeney LA, Weber H., Kittel-Schneider S., Lesch KP, Reif A., Ribasés M., Ramos-Quiroga JA, Cormand B., Zayats T., Hegvik TA, Jacobsen KK, Johansson S., Haavik J., et al. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 2016/07/29, (2016) Read More / View Supplemental Materials
Abstract
Common and rare forms of diabetes mellitus: towards a continuum of diabetes subtypes.Flannick, J., Johansson S., and Njølstad PR Nature reviews. Endocrinology, 2016/04/15, (2016) Read More / View Supplemental Materials
Abstract
2014
Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder.Jacobsen, KK, Nievergelt CM, Zayats T., Greenwood TA, Anttila V., Akiskal HS, BiGS Consortium, IHG Consortium, include: BiGS Consortium Co-Authors, include: IHG Consortium Co-Authors, Haavik J., Bernt Fasmer O., Kelsoe JR, Johansson S., Oedegaard KJ, include BiGS Consortium Co-Authors, and include IHG Consortium Co-Authors Journal of affective disorders, 2014/10/12, Volume 172C, p.453-461, (2014) Read More / View Supplemental Materials
Abstract
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.Flannick, J., Thorleifsson G., Beer NL, Jacobs SB, Grarup N., Burtt NP, Mahajan A., Fuchsberger C., Atzmon G., Benediktsson R., Blangero J., Bowden DW, Brandslund I., Brosnan J., Burslem F., Chambers J., Cho YS, Christensen C., Douglas DA, Duggirala R., et al. Nature genetics, 2014/04/01, Volume 46, Issue 4, p.357-63, (2014) Read More / View Supplemental Materials
Abstract
2013
A novel GATA6 mutation in a child with congenital heart malformation and neonatal diabetes.Eifes, S., Chudasama KK, Molnes J., Wagner K., Hoang T., Schierloh U., Rocour-Brumioul D., Johansson S., Njølstad PR, and de Beaufort C. Clinical case reports, 2013/12/01, Volume 1, Issue 2, p.86-90, (2013) Read More / View Supplemental Materials
Abstract
Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes.Flannick, J., Beer NL, Bick AG, Agarwala V., Molnes J., Gupta N., Burtt NP, Florez JC, Meigs JB, Taylor H., Lyssenko V., Irgens H., Fox E., Burslem F., Johansson S., Brosnan MJ, Trimmer JK, Newton-Cheh C., Tuomi T., Molven A., et al. Nature genetics, 2013/11/01, Volume 45, Issue 11, p.1380-5, (2013) Read More / View Supplemental Materials
Abstract
  • Showing 1-6 of 6 Results