Publikationer forskningsmiljön Biomedicin

Publikationer i forskningsportalen

Till publikationer i högskolans forskningsportal.

Se även publikationer från år 2015 och tidigare nedan

2015

Henmyr V, Lind-Halldén C, Carlberg D, Halldén C, Melén E, Wickman M, Bergström A, Säll T, Cardell LO (2015) Characterization of genetic variation in TLR8 in relation to allergic rhinitis. Allergy Nov 11. DOI: 10.1111/all.12805.

Mårtensson A, Letelier A, Halldén C and Ljung R (2015) Mutation analysis of Swedish haemophilia B families – high frequency of unique mutations. Haemophilia Nov 27. DOI: 10.1111/hae.12854.

Mårtensson A, Ivarsson S, Letelier A, Manderstedt E, Halldén C and Ljung R (2015) Origin of mutation in Swedish families with severe sporadic haemophilia A. Clinical Genetics Dec 10. DOI: 10.1111/cge.12709.

2014

Sävblom C, Halldén C, Cronin AM, Säll T, Savage C, Vertosick EA, Klein RJ, Giwercman A & Lilja H (2014) Genetic variation in KLK2 and KLK3 is associated with concentrations of hK2 and PSA in serum and seminal plasma in young men. Clin Chem 60:490-499

Henmyr V, Vandeplas G, Halldén C, Säll T, Olze H, Bachert C & Cardell LO (2014) Replication study of genetic variants associated with chronic rhinosinusitis and nasal polyposis. J Allergy Clin Immunol 133:273

Nilsson D, Henmyr V, Halldén C, Säll T, Kull I, Wickman M, Melén E & Cardell LO (2014) Replication of genome-wide associations with allergic sensitization and allergic rhinitis. Allergy 69:1506-1514

2013

Halldén C, Mårtensson A, Nilsson D, Säll T, Lind-Halldén C, Lidén AC & Ljung R (2013). Origin of Swedish hemophilia B mutations. J Thromb Haemost 11:2001-2008

Nilsson D, Andiappan AK, Halldén C, Tim CF, Säll T, De Yun W & Cardell LO (2013) Poor reproducibility of allergic rhinitis SNP associations. PLoS ONE 8: e53975
Andiappan AK, Nilsson D, Halldén C, De Yun W, Säll T, Tim CF & Cardell LO (2013) Investigating highly replicated asthma genes and their association with allergic rhinitis. BMC Med Genet 14:51

Lindahl P, Säll T, Bjartell A, Johansson AM, Lilja H & Halldén C (2013) Copy number variants in the kallikrein gene cluster. PLoS ONE 8:e69097
Halldén C, Mårtensson A, Nilsson D, Säll T, Lind-Halldén C, Lidén AC & Ljung R (2013) Origin of Swedish hemophilia B mutations. J Thromb Haemost 11:2001-2008

2012

Klein RJ, Halldén C, Gupta A, Savage CJ, Dahlin A, Bjartell A, Manjer J, Scardina PT, Ulmert D, Wallström P, Vickers AJ & Lilja H (2012) Evaluation of multiple risk-associated single nucleotide polymorphisms versus prostate-specific antigen at baseline to predict prostate cancer in unscreened men. Eur Urol 61:471-477

Halldén C, Knobe KE, Sjörin E, Nilsson D & Ljung R (2012) Investigation of disease-associated factors in hemophilia A patients without detectable mutations. Haemophilia 18:e132-137

Lind-Halldén C, Dahlén A, Hillarp A, Zöller B, Dahlbäck B & Halldén C (2012) Small and large PROS1 deletions but no other types of rearrangements detected in patients with protein S deficiency. Thromb Haemost 108:94-100

Nilsson D, Andiappan AK, Hallden C, Yun WD, Sall T, Tim CF, Cardell LO (2012) Toll-like receptor gene polymorphisms are associated with allergic rhinitis: a case control study. BMC Med Genet 13:66

Halldén C, Nilsson D, Säll T, Lind-Halldén C, Lidén AC & Ljung R (2012) Origin of Swedish hemophilia A mutations. J Thromb Haemost 10:2503-2511

2011

Johansson AM, Lanke E, Säll T, Lethagen S & Halldén C (2011) A large deletion identified in a Swedish family with type 1 VWD. Thromb Haemost 105:733-734

Romerius P, Giwercman A, Moëll C, Relander T, Cavallin-Ståhl E, Wiebe T, Halldén C & Giwercman, YL (2011) Estrogen receptor α single nucleotide polymorphism modifies the risk of azoospermia in childhood cancer survivors. Pharmacogenet Genomics 21:263-269

Johansson AM, Halldén C, Säll T & Lethagen S (2011) Variation in the VWF gene in Swedish patients with type 1 von Willebrand disease. Annals Hum Genet 75:447-455

Sjödahl G, Lauss M, Gudjonsson S, Liedberg F, Halldén C, Chebil G, Månsson W, Höglund M & Lindgren D (2011) A Systematic Study of Gene Mutations in Urothelial Carcinoma; Inactivating Mutations in TSC2 and PIK3R1.PLoS One. 2011;6;e18583. PMID: 21533174 DOI: 10.1371/journal.pone.0018583

2010

Bryborn M, Halldén C, Säll T & Cardell LO (2010) CLC- a novel susceptibility gene for allergic rhinitis? Allergy 65:220-228

Lindgren D, Frigyesi A, Gudjonsson S, Sjödahl G, Hallden C, Chebil G, Veerla S, Ryden T, Månsson W, Liedberg F & Höglund M (2010) Combined gene expression and genomic profiling define two intrinsic molecular subtypes of urothelial carcinoma and gene signatures for molecular grading and outcome. Cancer Res 70:3463-3472

Klein RJ, Halldén C, Cronin AM, Ploner A, Wiklund F, Bjartell AS, Stattin P, Xu J, Scardino PT, Offit K, Vickers AJ, Grönberg H & Lilja H (2010) Blood biomarker levels to aid discovery of cancer-related single-nucleotide polymorphisms: kallikreins and prostate cancer. Cancer Prev Res (Phila Pa) 3:611-619

Gallagher DJ, Vijai J, Cronin AM, Bhatia J, Vickers AJ, Gaudet MM, Fine S, Reuter V, Scher HI, Halldén C, Dutra-Clarke A, Klein RJ, Scardino PT, Eastham JA, Lilja H, Kirchhoff T & Offit K (2010) Susceptibility loci associated with prostate cancer progression and mortality. Clin Cancer Res 16:2819-2832

Dahlman A, Edsjö A, Halldén C, Persson JL, Fine SW, Lilja H, Gerald W & Bjartell A (2010) Effect of androgen deprivation therapy on the expression of prostate cancer biomarkers MSMB and MSMB-binding protein CRISP3. Prostate Cancer Prostatic Dis 13:369-375

Xu X, Valtonen-André C, Sävblom C, Halldén C, Lilja H & Klein RJ (2010) Polymorphisms at the microseminoprotein-beta (MSMB) locus associated with physiological variation in beta-microseminoprotein (β-MSP) and prostate specific antigen (PSA) levels. Cancer Epidemiol Biomarkers Prev 19:2035-2042

2009

Sävblom C, Giwercman A, Malm J, Halldén C, Lundin K, Lilja H & Giwercman Y (2009) Association between polymorphisms in the prostate-specific antigen (PSA) promoter and release of PSA. Int J Androl 32:479-485

Bachert C, Van Bruaene N, Toskala E, Zhang N, Olze H, Scadding G, Van Drunen CM, Mullol J, Cardell L, Gevaert P, Van Zele T, Claeys S, Halldén C, Kostamo K, Foerster U, Kowalski M, Bieniek K, Olszewska-Ziaber A, Nizankowska-Mogilnicka E, Szczeklik A, Swierczynska M, Arcimowicz M, Lund V, Fokkens W, Zuberbier T, Akdis C, Canonica G, Van Cauwenberge P, Burney P & Bousquet J (2009) Important research questions in allergy and related diseases: 3-chronic rhinosinusitis and nasal polyposis - a GALEN study. Allergy 64:520-533

Benson M, Mobini R, Barrenäs F, Halldén C, Naluai AT, Säll T & Cardell LO (2009) A haplotype in the inducible T-cell tyrosine kinase is a risk factor for seasonal allergic rhinitis. Allergy 64:1286-1291

Almany GR, De Arruda MP, Arthofer W et al. (2009) Permanent Genetic Resources added to Molecular Ecology Resources Database 1 May 2009 – 31 July 2009. Mol Ecol Res 9:1460-1559.