Research group - Lennart Hammarström
Genetic basis of immunodeficiency diseases
Hyper IgM syndrome (HIGM)
Common variable immunodeficiency (CVID)
IgA deficiency (IgAD)
Expression of antibody encoding genes in
Lactobacilli (Rotavirus, Clostridium difficile, HIV)
Cytokines (IL-10, IL-21)
Research group leader Lennart Hammarström
|Hassan Abolhassani||PhD student|
|Kerstin Bergman||Laboratory technician|
|Mingyan Fang||Graduate Student|
|Jovanka King||PhD student|
|Harold Marcotte||Senior researcher|
Swedish Research Council, EU, National Institutes of Health, ALF
BMA, study programme in medicine, study programme in medicine
Rice-based oral antibody fragment prophylaxis and therapy against rotavirus infection.
J. Clin. Invest. 2013 Sep;123(9):3829-38
Impact of Down syndrome on the performance of neonatal screening assays for severe primary immunodeficiency diseases.
J. Allergy Clin. Immunol. 2014 Apr;133(4):1208-11
The dog as a genetic model for immunoglobulin A (IgA) deficiency: identification of several breeds with low serum IgA concentrations.
Vet. Immunol. Immunopathol. 2014 Aug;160(3-4):255-9
Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia.
Science 2013 May;340(6135):976-8
Neonatal screening for severe primary immunodeficiency diseases using high-throughput triplex real-time PCR.
Blood 2012 Mar;119(11):2552-5
Selective IgA deficiency in autoimmune diseases.
Mol. Med. 2011 ;17(11-12):1383-96
Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.
Nat. Genet. 2010 Sep;42(9):777-80
Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases.
Proc. Natl. Acad. Sci. U.S.A. 2009 Nov;106(44):18680-5