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Items: 1 to 50 of 68

1.

Next-Generation Sequencing of 17 Genes Associated with Venous Thromboembolism Reveals a Deficit of Non-Synonymous Variants in Procoagulant Genes.

Manderstedt E, Lind-Halldén C, Svensson P, Zöller B, Halldén C.

Thromb Haemost. 2019 Sep;119(9):1441-1450. doi: 10.1055/s-0039-1693130. Epub 2019 Jul 28.

PMID:
31352677
2.

Targeted re-sequencing of F8, F9 and VWF: Characterization of Ion Torrent data and clinical implications for mutation screening.

Manderstedt E, Nilsson R, Lind-Halldén C, Ljung R, Astermark J, Halldén C.

PLoS One. 2019 Apr 26;14(4):e0216179. doi: 10.1371/journal.pone.0216179. eCollection 2019.

3.

The common VWF single nucleotide variants c.2365A>G and c.2385T>C modify VWF biosynthesis and clearance.

Mufti AH, Ogiwara K, Swystun LL, Eikenboom JCJ, Budde U, Hopman WM, Halldén C, Goudemand J, Peake IR, Goodeve AC, Lillicrap D, Hampshire DJ; European Group on von Willebrand disease (EU-VWD) and Zimmerman Program for the Molecular and Clinical Biology of von Willebrand disease (ZPMCB-VWD) Study Groups.

Blood Adv. 2018 Jul 10;2(13):1585-1594. doi: 10.1182/bloodadvances.2017011643.

4.

Genetic Variation in the Syntaxin-Binding Protein STXBP5 in Type 1 von Willebrand Disease Patients.

Lind-Halldén C, Manderstedt E, Carlberg D, Lethagen S, Halldén C.

Thromb Haemost. 2018 Aug;118(8):1382-1389. doi: 10.1055/s-0038-1661352. Epub 2018 Jul 4.

PMID:
29972863
5.

Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients.

Manderstedt E, Lind-Halldén C, Lethagen S, Halldén C.

PLoS One. 2018 Feb 1;13(2):e0192024. doi: 10.1371/journal.pone.0192024. eCollection 2018.

6.

Genetic Variation in the von Willebrand Factor Gene in Swedish von Willebrand Disease Patients.

Manderstedt E, Lind-Halldén C, Lethagen S, Halldén C.

TH Open. 2018 Jan 30;2(1):e39-e48. doi: 10.1055/s-0037-1618571. eCollection 2018 Jan.

7.

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.

8.

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.

9.

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.

PMID:
26661908
10.

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.

PMID:
26612714
11.

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.

PMID:
26556310
12.

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.

PMID:
25066275
13.

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.

14.

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.

15.

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.

PMID:
24074519
16.

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.

17.

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.

18.

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.

19.

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.

20.

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.

21.

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.

PMID:
22627709
22.

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.

PMID:
22221887
23.

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.

24.

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.

25.

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.

26.

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.

PMID:
21430602
27.

A large deletion identified in a Swedish family with type 1 VWD.

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

Thromb Haemost. 2011 Apr;105(4):733-4. doi: 10.1160/TH10-08-0556. Epub 2011 Jan 12. No abstract available.

PMID:
21225094
28.

Polymorphisms at the Microseminoprotein-beta locus associated with physiologic variation in beta-microseminoprotein and prostate-specific antigen levels.

Xu X, Valtonen-André C, Sävblom C, Halldén C, Lilja H, Klein RJ.

Cancer Epidemiol Biomarkers Prev. 2010 Aug;19(8):2035-42. doi: 10.1158/1055-9965.EPI-10-0431.

29.

Effect of androgen deprivation therapy on the expression of prostate cancer biomarkers MSMB and MSMB-binding protein CRISP3.

Dahlman A, Edsjö A, Halldén C, Persson JL, Fine SW, Lilja H, Gerald W, Bjartell A.

Prostate Cancer Prostatic Dis. 2010 Dec;13(4):369-75. doi: 10.1038/pcan.2010.25. Epub 2010 Aug 3.

PMID:
20680031
30.

Susceptibility loci associated with prostate cancer progression and mortality.

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.

Clin Cancer Res. 2010 May 15;16(10):2819-32. doi: 10.1158/1078-0432.CCR-10-0028. Epub 2010 May 11.

31.

Blood biomarker levels to aid discovery of cancer-related single-nucleotide polymorphisms: kallikreins and prostate cancer.

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.

Cancer Prev Res (Phila). 2010 May;3(5):611-9. doi: 10.1158/1940-6207.CAPR-09-0206. Epub 2010 Apr 27.

32.

Combined gene expression and genomic profiling define two intrinsic molecular subtypes of urothelial carcinoma and gene signatures for molecular grading and outcome.

Lindgren D, Frigyesi A, Gudjonsson S, Sjödahl G, Hallden C, Chebil G, Veerla S, Ryden T, Månsson W, Liedberg F, Höglund M.

Cancer Res. 2010 May 1;70(9):3463-72. doi: 10.1158/0008-5472.CAN-09-4213. Epub 2010 Apr 20.

33.

Permanent Genetic Resources added to Molecular Ecology Resources Database 1 May 2009-31 July 2009.

Molecular Ecology Resources Primer Development Consortium, Almany GR, DE Arruda MP, Arthofer W, Atallah ZK, Beissinger SR, Berumen ML, Bogdanowicz SM, Brown SD, Bruford MW, Burdine C, Busch JW, Campbell NR, Carey D, Carstens BC, Chu KH, Cubeta MA, Cuda JP, Cui Z, Datnoff LE, Dávila JA, Davis ES, Davis RM, Diekmann OE, Eizirik E, Fargallo JA, Fernandes F, Fukuda H, Gale LR, Gallagher E, Gao Y, Girard P, Godhe A, Gonçalves EC, Gouveia L, Grajczyk AM, Grose MJ, Gu Z, Halldén C, Härnström K, Hemmingsen AH, Holmes G, Huang CH, Huang CC, Hudman SP, Jones GP, Kanetis L, Karunasagar I, Karunasagar I, Keyghobadi N, Klosterman SJ, Klug PE, Koch J, Koopman MM, Köppler K, Koshimizu E, Krumböck S, Kubisiak T, Landis JB, Lasta ML, Lee CY, Li Q, Li SH, Lin RC, Liu M, Liu N, Liu WC, Liu Y, Loiseau A, Luan W, Maruthachalam KK, McCormick HM, Mellick R, Monnahan PJ, Morielle-Versute E, Murray TE, Narum SR, Neufeld K, De Nova PJ, Ojiambo PS, Okamoto N, Othman AS, Overholt WA, Pardini R, Paterson IG, Patty OA, Paxton RJ, Planes S, Porter C, Pratchett MS, Püttker T, Rasic G, Rasool B, Rey O, Riegler M, Riehl C, Roberts JM, Roberts PD, Rochel E, Roe KJ, Rossetto M, Ruzzante DE, Sakamoto T, Saravanan V, Sarturi CR, Schmidt A, Schneider MP, Schuler H, Serb JM, Serrão ET, Shi Y, Silva A, Sin YW, Sommer S, Stauffer C, Strüssmann CA, Subbarao KV, Syms C, Tan F, Tejedor ED, Thorrold SR, Trigiano RN, Trucco MI, Tsuchiya-Jerep MT, Vergara P, Van De Vliet MS, Wadl PA, Wang A, Wang H, Wang RX, Wang X, Wang Y, Weeks AR, Wei F, Werner WJ, Wiley EO, Williams DA, Wilkins RJ, Wisely SM, With KA, Wu D, Yao CT, Yau C, Yeap BK, Zhai BP, Zhan X, Zhang GY, Zhang SY, Zhao R, Zhu L.

Mol Ecol Resour. 2009 Nov;9(6):1460-6. doi: 10.1111/j.1755-0998.2009.02759.x. Epub 2009 Sep 29.

PMID:
21564933
34.

CLC- a novel susceptibility gene for allergic rhinitis?

Bryborn M, Halldén C, Säll T, Cardell LO.

Allergy. 2010 Feb;65(2):220-8. doi: 10.1111/j.1398-9995.2009.02141.x. Epub 2009 Jul 24.

PMID:
19650845
35.

Important research questions in allergy and related diseases: 3-chronic rhinosinusitis and nasal polyposis - a GALEN study.

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.

Allergy. 2009 Apr;64(4):520-33. doi: 10.1111/j.1398-9995.2009.01964.x. Review.

PMID:
19317839
36.

A haplotype in the inducible T-cell tyrosine kinase is a risk factor for seasonal allergic rhinitis.

Benson M, Mobini R, Barrenäs F, Halldén C, Naluai AT, Säll T, Cardell LO.

Allergy. 2009 Sep;64(9):1286-91. doi: 10.1111/j.1398-9995.2009.01991.x. Epub 2009 Feb 13.

PMID:
19222422
37.

Distribution of von Willebrand factor levels in young women with and without bleeding symptoms: influence of ABO blood group and promoter haplotypes.

Lethagen S, Hillarp A, Ekholm C, Mattson E, Halldén C, Friberg B.

Thromb Haemost. 2008 Jun;99(6):1013-8. doi: 10.1160/TH07-06-0419.

PMID:
18521502
38.

Comparing the distribution of RAPD and RFLP markers in a high density linkage map of sugar beet.

Nilsson NO, Halldén C, Hansen M, Hjerdin A, Säll T.

Genome. 1997 Oct;40(5):644-51.

PMID:
18464855
39.

Comprehensive evaluation of genetic variation in S100A7 suggests an association with the occurrence of allergic rhinitis.

Bryborn M, Halldén C, Säll T, Adner M, Cardell LO.

Respir Res. 2008 Mar 28;9:29. doi: 10.1186/1465-9921-9-29.

40.

Association between polymorphisms in the prostate-specific antigen (PSA) promoter and release of PSA.

Sävblom C, Giwercman A, Malm J, Halldén C, Lundin K, Lilja H, Giwercman Y.

Int J Androl. 2009 Oct;32(5):479-85. doi: 10.1111/j.1365-2605.2008.00882.x. Epub 2008 Mar 10.

PMID:
18336535
41.

The evolutionary history of the common chloroplast genome of Arabidopsis thaliana and A. suecica.

Jakobsson M, Säll T, Lind-Halldén C, Halldén C.

J Evol Biol. 2007 Jan;20(1):104-21.

42.

Evolution of chloroplast mononucleotide microsatellites in Arabidopsis thaliana.

Jakobsson M, Säll T, Lind-Halldén C, Halldén C.

Theor Appl Genet. 2007 Jan;114(2):223-35. Epub 2006 Nov 23.

PMID:
17123063
43.

Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD).

Goodeve A, Eikenboom J, Castaman G, Rodeghiero F, Federici AB, Batlle J, Meyer D, Mazurier C, Goudemand J, Schneppenheim R, Budde U, Ingerslev J, Habart D, Vorlova Z, Holmberg L, Lethagen S, Pasi J, Hill F, Hashemi Soteh M, Baronciani L, Hallden C, Guilliatt A, Lester W, Peake I.

Blood. 2007 Jan 1;109(1):112-21. Epub 2006 Sep 19. Erratum in: Blood. 2008 Mar 15;111(6):3299-300.

PMID:
16985174
44.

A quality assessment survey of SNP genotyping laboratories.

Lahermo P, Liljedahl U, Alnaes G, Axelsson T, Brookes AJ, Ellonen P, Groop PH, Halldén C, Holmberg D, Holmberg K, Keinänen M, Kepp K, Kere J, Kiviluoma P, Kristensen V, Lindgren C, Odeberg J, Osterman P, Parkkonen M, Saarela J, Sterner M, Strömqvist L, Talas U, Wessman M, Palotie A, Syvänen AC.

Hum Mutat. 2006 Jul;27(7):711-4.

PMID:
16786507
45.

A unique recent origin of the allotetraploid species Arabidopsis suecica: Evidence from nuclear DNA markers.

Jakobsson M, Hagenblad J, Tavaré S, Säll T, Halldén C, Lind-Halldén C, Nordborg M.

Mol Biol Evol. 2006 Jun;23(6):1217-31. Epub 2006 Mar 20.

PMID:
16549398
46.

Large deletions of the PROS1 gene in a large fraction of mutation-negative patients with protein S deficiency.

Johansson AM, Hillarp A, Säll T, Zöller B, Dahlbäck B, Halldén C.

Thromb Haemost. 2005 Nov;94(5):951-7.

PMID:
16363235
48.

Detecting deletions in families affected by a dominant disease by use of marker data.

Johansson AM, Halldén C, Sall T.

Hum Hered. 2005;60(1):26-35. Epub 2005 Aug 23.

PMID:
16118504
49.

Mode of reproduction in Arabidopsis suecica.

Säll T, Lind-Halldén C, Jakobsson M, Halldén C.

Hereditas. 2004;141(3):313-7.

50.

Co-segregation of the PROS1 locus and protein S deficiency in families having no detectable mutations in PROS1.

Lanke E, Johansson AM, Hillarp A, Lethagen S, Zöller B, Dahlbäck B, Halldén C.

J Thromb Haemost. 2004 Nov;2(11):1918-23.

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