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Items: 1 to 20 of 62


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

Henmyr V, Carlberg D, Manderstedt E, Lind-Halldén C, Säll T, Cardell LO, Halldén C.

BMC Med Genet. 2017 Feb 23;18(1):18. doi: 10.1186/s12881-017-0379-6.


Chronic Rhinosinusitis Patients Show Accumulation of Genetic Variants in PARS2.

Henmyr V, Lind-Halldén C, Halldén C, Säll T, Carlberg D, Bachert C, Cardell LO.

PLoS One. 2016 Jun 27;11(6):e0158202. doi: 10.1371/journal.pone.0158202. eCollection 2016.


Origin of mutation in sporadic cases of severe haemophilia A in Sweden.

Mårtensson A, Ivarsson S, Letelier A, Manderstedt E, Halldén C, Ljung R.

Clin Genet. 2016 Jul;90(1):63-8. doi: 10.1111/cge.12709. Epub 2016 Jan 20.


Mutation analysis of Swedish haemophilia B families - high frequency of unique mutations.

Mårtensson A, Letelier A, Halldén C, Ljung R.

Haemophilia. 2016 May;22(3):440-5. doi: 10.1111/hae.12854. Epub 2015 Nov 27.


Characterization of genetic variation in TLR8 in relation to allergic rhinitis.

Henmyr V, Lind-Halldén C, Carlberg D, Halldén C, Melén E, Wickman M, Bergström A, Säll T, Cardell LO.

Allergy. 2016 Mar;71(3):333-41. doi: 10.1111/all.12805. Epub 2015 Dec 2.


Replication of genomewide associations with allergic sensitization and allergic rhinitis.

Nilsson D, Henmyr V, Halldén C, Säll T, Kull I, Wickman M, Melén E, Cardell LO.

Allergy. 2014 Nov;69(11):1506-14. doi: 10.1111/all.12495. Epub 2014 Sep 6.


Genetic variation in KLK2 and KLK3 is associated with concentrations of hK2 and PSA in serum and seminal plasma in young men.

Sävblom C, Halldén C, Cronin AM, Säll T, Savage C, Vertosick EA, Klein RJ, Giwercman A, Lilja H.

Clin Chem. 2014 Mar;60(3):490-9. doi: 10.1373/clinchem.2013.211219. Epub 2013 Nov 22.


Origin of Swedish hemophilia B mutations.

Halldén C, Mårtensson A, Nilsson D, Säll T, Lind-Halldén C, Lidén AC, Ljung R.

J Thromb Haemost. 2013 Nov;11(11):2001-8. doi: 10.1111/jth.12410.


Replication study of genetic variants associated with chronic rhinosinusitis and nasal polyposis.

Henmyr V, Vandeplas G, Halldén C, Säll T, Olze H, Bachert C, Cardell LO.

J Allergy Clin Immunol. 2014 Jan;133(1):273-5. doi: 10.1016/j.jaci.2013.08.011. Epub 2013 Sep 26. No abstract available.


Copy number variants in the kallikrein gene cluster.

Lindahl P, Säll T, Bjartell A, Johansson AM, Lilja H, Halldén C.

PLoS One. 2013 Jul 22;8(7):e69097. doi: 10.1371/journal.pone.0069097. Print 2013.


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

Andiappan AK, Nilsson D, Halldén C, Yun WD, Säll T, Cardell LO, Tim CF.

BMC Med Genet. 2013 May 10;14:51. doi: 10.1186/1471-2350-14-51.


Poor reproducibility of allergic rhinitis SNP associations.

Nilsson D, Andiappan AK, Halldén C, Tim CF, Säll T, Wang de Y, Cardell LO.

PLoS One. 2013;8(1):e53975. doi: 10.1371/journal.pone.0053975. Epub 2013 Jan 30.


Origin of Swedish hemophilia A mutations.

Halldén C, Nilsson D, Säll T, Lind-Halldén C, Lidén AC, Ljung R.

J Thromb Haemost. 2012 Dec;10(12):2503-11. doi: 10.1111/jth.12010.


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

Nilsson D, Andiappan AK, Halldén C, De Yun W, Säll T, Tim CF, Cardell LO.

BMC Med Genet. 2012 Aug 2;13:66.


Small and large PROS1 deletions but no other types of rearrangements detected in patients with protein S deficiency.

Lind-Halldén C, Dahlen A, Hillarp A, Zöller B, Dahlbäck B, Halldén C.

Thromb Haemost. 2012 Jul;108(1):94-100. doi: 10.1160/TH12-01-0040. Epub 2012 May 25.


Investigation of disease-associated factors in haemophilia A patients without detectable mutations.

Halldén C, Knobe KE, Sjörin E, Nilsson D, Ljung R.

Haemophilia. 2012 May;18(3):e132-7. doi: 10.1111/j.1365-2516.2011.02737.x. Epub 2012 Jan 4.


Evaluation of multiple risk-associated single nucleotide polymorphisms versus prostate-specific antigen at baseline to predict prostate cancer in unscreened men.

Klein RJ, Hallden C, Gupta A, Savage CJ, Dahlin A, Bjartell A, Manjer J, Scardino PT, Ulmert D, Wallström P, Vickers AJ, Lilja H.

Eur Urol. 2012 Mar;61(3):471-7. doi: 10.1016/j.eururo.2011.10.047. Epub 2011 Nov 7.


Variation in the VWF gene in Swedish patients with type 1 von Willebrand Disease.

Johansson AM, Halldén C, Säll T, Lethagen S.

Ann Hum Genet. 2011 Jul;75(4):447-55. doi: 10.1111/j.1469-1809.2011.00652.x. Epub 2011 Apr 28.


A systematic study of gene mutations in urothelial carcinoma; inactivating mutations in TSC2 and PIK3R1.

Sjödahl G, Lauss M, Gudjonsson S, Liedberg F, Halldén C, Chebil G, Månsson W, Höglund M, Lindgren D.

PLoS One. 2011 Apr 14;6(4):e18583. doi: 10.1371/journal.pone.0018583.


Estrogen receptor α single nucleotide polymorphism modifies the risk of azoospermia in childhood cancer survivors.

Romerius P, Giwercman A, Moëll C, Relander T, Cavallin-Ståhl E, Wiebe T, Halldén C, Giwercman YL.

Pharmacogenet Genomics. 2011 May;21(5):263-9. doi: 10.1097/FPC.0b013e328343a132.


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