C. Halldén

发表

Variation in the VWF Gene in Swedish Patients with Type 1 von Willebrand Disease

A. Johansson, C. Halldén, T. Säll, 2011, Annals of human genetics.

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

K. V. Subbarao, Bryan C. Carstens, Emily S. Davis, 2009, Molecular ecology resources.

Genetic risk factors for venous thromboembolism

B. Dahlbäck, C. Halldén, P. Svensson, 2020, Expert review of hematology.

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

C. Halldén, P. Svensson, Bengt Zöller, 2019, Thrombosis and Haemostasis.

Distribution and evolution of a tandemly repeated DNA sequence in the family brassicaceae

C. Halldén, T. Säll, T. Bryngelsson, 1987, Journal of Molecular Evolution.

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

D. Hampshire, J. Goudemand, C. Halldén, 2018, Blood advances.

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).

J. Goudemand, C. Halldén, S. Lethagen, 2007, Blood.

Detection of F8 int22h inversions using digital droplet PCR and mile‐post assays

J. Astermark, R. Ljung, C. Halldén, 2020, Journal of thrombosis and haemostasis : JTH.

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

C. Halldén, T. Säll, N. Nilsson, 1997, Genome.

Error Rates and Polymorphism Frequencies for Three RAPD Protocols

C. Halldén, M. Hansen, Torbjörn Sãll, 1998, Plant Molecular Biology Reporter.

Common and Rare Variants in Genes Associated with von Willebrand Factor Level Variation: No Accumulation of Rare Variants in Swedish von Willebrand Disease Patients

C. Halldén, S. Lethagen, C. Lind‐Halldén, 2020, TH Open.

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

J. Astermark, R. Ljung, C. Halldén, 2019, PloS one.

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

C. Halldén, S. Lethagen, C. Lind‐Halldén, 2018, TH Open.

Large deletions of the PROS 1 gene in a large fraction of mutation-negative patients with protein S deficiency

B. Dahlbäck, A. Johansson, C. Halldén, 2018 .

Marker-assisted selection of restored male-fertile Brassica napus plants using a set of dominant RAPD markers

C. Halldén, T. Säll, N. Nilsson, 1997, Molecular Breeding.

A frequent allele codes for a truncated variant of semenogelin I, the major protein component of human semen coagulum.

H. Lilja, A. Giwercman, J. Malm, 2003, Molecular human reproduction.

Tandemly repeated DNA sequences in Brassicaceae: a characterization of the sequences in Cochlearia officinalis and Isatis tinctoria.

C. Halldén, C. Lind, T. Bryngelsson, 2008, Hereditas.

Primer mixtures in RAPD analysis.

C. Halldén, T. Säll, C. Lind‐Halldén, 2004, Hereditas.

Protein synthesis in mitochondria purified from roots, leaves and flowers of sugar beet

C. Halldén, I. Møller, C. Lind, 1991 .

Identification of F8 rearrangements in carrier and non‐carrier mothers of haemophilia A patients

J. Astermark, R. Ljung, C. Halldén, 2021, Haemophilia : the official journal of the World Federation of Hemophilia.

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

R. Ljung, C. Halldén, E. Manderstedt, 2016, Clinical genetics.

Origin of Swedish hemophilia B mutations

D. Nilsson, R. Ljung, C. Halldén, 2013, Journal of thrombosis and haemostasis : JTH.

Origin of Swedish hemophilia A mutations

D. Nilsson, R. Ljung, C. Halldén, 2012, Journal of thrombosis and haemostasis : JTH.

Genetic analysis of 31 Swedish type 1 von Willebrand disease families reveals incomplete linkage to the von Willebrand factor gene and a high frequency of a certain disease haplotype

A. Johansson, C. Halldén, S. Lethagen, 2005, Journal of thrombosis and haemostasis : JTH.

Detection of mosaics in hemophilia A by deep Ion Torrent sequencing and droplet digital PCR

J. Astermark, R. Ljung, C. Halldén, 2020, Research and practice in thrombosis and haemostasis.

Diploid Brassica napus somatic hybrids: characterization of nuclear and organellar DNA

B. Rosen, C. Halldén, W. Heneen, 1988, Theoretical and Applied Genetics.

Important research questions in allergy and related diseases: 3‐chronic rhinosinusitis and nasal polyposis – a GA2LEN study

N. Zhang, J. Bousquet, T. Zuberbier, 2009, Allergy.

Variation in mitochondrial translation products in fertile and cytoplasmic male-sterile sugar beets

C. Halldén, I. Møller, C. Lind, 1992, Theoretical and Applied Genetics.

Cytoplasmic male sterility inBeta is associated with structural rearrangements of the mitochondrial DNA and is not due to interspecific organelle transfer

N. O. Bosemark, C. Halldén, T. Säll, 1990, Journal of Molecular Evolution.

Two new types of cytoplasmic male sterility found in wild Beta beets

N. O. Bosemark, C. Halldén, T. Bryngelsson, 1988, Theoretical and Applied Genetics.

Microsporogenesis and tapetal development in fertile and cytoplasmic male-sterile sugar beet (Beta vulgaris L.)

C. Halldén, I. Møller, C. Lind, 1991, Sexual Plant Reproduction.

Minicircle variation in Beta mitochondrial DNA

C. Halldén, C. Lind, T. Bryngelsson, 1989, Theoretical and Applied Genetics.

Components of a Cytoplasmic Male Sterility System in Resynthesized and Cultivated Forms of Oilseed Rape (Brassies napus L.)

C. Halldén, W. Heneen, B. Y. Chen, 1990 .

Polymorphisms at the Microseminoprotein-β Locus Associated with Physiologic Variation in β-Microseminoprotein and Prostate-Specific Antigen Levels

R. Klein, H. Lilja, C. Halldén, 2010, Cancer Epidemiology, Biomarkers & Prevention.

Prostate-Specific Antigen Levels

R. Klein, H. Lilja, C. Halldén, 2010 .

Androgen receptor gene GGN and CAG polymorphisms among severely oligozoospermic and azoospermic Swedish men.

A. Giwercman, C. Halldén, Y. Giwercman, 2004, Human reproduction.

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

Mattias Höglund, Srinivas Veerla, Attila Frigyesi, 2010, Cancer research.

Susceptibility Loci Associated with Prostate Cancer Progression and Mortality

P. Scardino, J. Eastham, K. Offit, 2010, Clinical Cancer Research.

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

C. Halldén, S. Lethagen, C. Lind‐Halldén, 2018, Thrombosis and Haemostasis.

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

C. Halldén, S. Lethagen, C. Lind‐Halldén, 2018, PloS one.

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

M. Jakobsson, C. Halldén, T. Säll, 2007, Journal of evolutionary biology.

Evolution of chloroplast mononucleotide microsatellites in Arabidopsis thaliana

M. Jakobsson, C. Halldén, T. Säll, 2006, Theoretical and Applied Genetics.

Chloroplast DNA indicates a single origin of the allotetraploid Arabidopsis suecica

M. Jakobsson, C. Halldén, T. Säll, 2003, Journal of evolutionary biology.

Characterization of large in-frame von Willebrand factor deletions highlights differing pathogenic mechanisms.

D. Hampshire, J. Goudemand, C. Halldén, 2020, Blood advances.

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

Mattias Jakobsson, Simon Tavaré, Jenny Hagenblad, 2006, Molecular biology and evolution.

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

W. Gerald, S. Fine, H. Lilja, 2010, Prostate Cancer and Prostatic Diseases.

Competition as a source of errors in RAPD analysis

C. Halldén, T. Säll, N. Nilsson, 1996, Theoretical and Applied Genetics.

Positive correlation between recombination rates and levels of genetic variation in natural populations of sea beet (Beta vulgaris subsp. maritima).

C. Halldén, T. Säll, T. Kraft, 1998, Genetics.

Droplet digital PCR and mile‐post analysis for the detection of F8 int1h inversions

J. Astermark, R. Ljung, C. Halldén, 2020, Journal of thrombosis and haemostasis : JTH.

Investigating highly replicated asthma genes as candidate genes for allergic rhinitis

A. Andiappan, D. Nilsson, C. Halldén, 2013, BMC Medical Genetics.

Thrombotic risk determined by protein C receptor (PROCR) variants among middle-aged and older adults: a population-based cohort study

O. Melander, G. Engström, C. Halldén, 2022, Thrombosis and Haemostasis.

Thrombomodulin (THBD) gene variants and thrombotic risk in a population‐based cohort study

O. Melander, G. Engström, C. Halldén, 2021, Journal of thrombosis and haemostasis : JTH.

A Systematic Study of Gene Mutations in Urothelial Carcinoma; Inactivating Mutations in TSC2 and PIK3R1

M. Höglund, M. Lauss, D. Lindgren, 2011, PloS one.

Poor Reproducibility of Allergic Rhinitis SNP Associations

A. Andiappan, D. Nilsson, D. Wang, 2013, PloS one.

The Moraxella catarrhalis Immunoglobulin D-Binding Protein MID Has Conserved Sequences and Is Regulated by a Mechanism Corresponding to Phase Variation

Therése Nordström, A. Forsgren, K. Riesbeck, 2003, Journal of bacteriology.

Detecting Deletions in Families Affected by a Dominant Disease by Use of Marker Data

A. Johansson, C. Halldén, T. Säll, 2005, Human Heredity.

Estrogen receptor &agr; single nucleotide polymorphism modifies the risk of azoospermia in childhood cancer survivors

A. Giwercman, C. Halldén, Y. Giwercman, 2011, Pharmacogenetics and genomics.

A quality assessment survey of SNP genotyping laboratories

C. Lindgren, J. Kere, A. Brookes, 2006, Human mutation.

Genetic variation of the blood coagulation regulator tissue factor pathway inhibitor and venous thromboembolism among middle‐aged and older adults: A population‐based cohort study

O. Melander, G. Engström, C. Halldén, 2022, Research and practice in thrombosis and haemostasis.

Classic Thrombophilias and Thrombotic Risk Among Middle‐Aged and Older Adults: A Population‐Based Cohort Study

O. Melander, G. Engström, B. Dahlbäck, 2022, Journal of the American Heart Association.

The relationship between juvenile laryngeal papillomatosis and maternal condylomata acuminata.

C. Halldén, B. Majmudar, 1986, The Journal of reproductive medicine.

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

A. Johansson, C. Halldén, T. Säll, 2011, Thrombosis and Haemostasis.

Evaluation of RFLP and RAPD markers in a comparison of Brassica napus breeding lines

C. Halldén, T. Säll, N. Nilsson, 1994, Theoretical and Applied Genetics.

Genetic Variation Among Wild and Cultivated Beets of the Section Beta as Revealed by RFLP Analysis

C. Halldén, T. Säll, C. H. Bornman, 1994 .

No conserved homoeologous regions found in the sugar beet genome

D. Ahrén, C. Halldén, T. Säll, 1998 .

A high density RFLP linkage map of sugar beet.

C. Halldén, T. Säll, C. Åkesson, 1996, Genome.

Characterization of genetic variation in TLR8 in relation to allergic rhinitis

M. Wickman, C. Halldén, T. Säll, 2016, Allergy.

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

A. Andiappan, D. Nilsson, C. Halldén, 2012, BMC Medical Genetics.

Characterization of Organellar DNA in Alloplasmic Lines of Brassica napus L.

C. Halldén, T. Säll, C. Lind‐Halldén, 1993 .

Thrombotic risk determined by rare and common SERPINA1 variants in a population‐based cohort study

O. Melander, G. Engström, C. Halldén, 2022, Journal of thrombosis and haemostasis : JTH.

Blood Biomarker Levels to Aid Discovery of Cancer-Related Single-Nucleotide Polymorphisms: Kallikreins and Prostate Cancer

Andrew J. Vickers, Pär Stattin, Fredrik Wiklund, 2010, Cancer Prevention Research.

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

H. Lilja, A. Giwercman, J. Malm, 2009, International journal of andrology.

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

C. Halldén, T. Säll, L. Cardell, 2017, BMC Medical Genetics.

Mode of reproduction in Arabidopsis suecica.

M. Jakobsson, C. Halldén, T. Säll, 2005, Hereditas.

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

C. Bachert, C. Halldén, T. Säll, 2014, The Journal of allergy and clinical immunology.

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

C. Halldén, T. Säll, L. Cardell, 2008, Respiratory research.

Rare-variant collapsing analyses of arterial hypertension in the UK biobank.

C. Halldén, Bengt Zöller, C. Lind‐Halldén, 2023, Journal of human hypertension.

Contribution of rare and common coding variants to haematological malignancies in the UK biobank

C. Halldén, Bengt Zöller, C. Lind‐Halldén, 2023, Leukemia research reports.

Replication of genomewide associations with allergic sensitization and allergic rhinitis

M. Wickman, D. Nilsson, C. Halldén, 2014, Allergy.

Thrombotic Risk Determined by STAB 2 Variants in a Population-Based Cohort Study.

Alexander E. Lopez, Andrew L Blumenfeld, G. Abecasis, 2021, Circulation. Genomic and precision medicine.

CLC– a novel susceptibility gene for allergic rhinitis?

C. Halldén, T. Säll, L. Cardell, 2010, Allergy.

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

P. Scardino, R. Klein, A. Vickers, 2012, European urology.

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

R. Klein, H. Lilja, A. Giwercman, 2014, Clinical chemistry.

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

B. Dahlbäck, C. Halldén, A. Dahlén, 2012, Thrombosis and Haemostasis.

Genetic variation in Arabidopsis suecica and its parental species A. arenosa and A. thaliana.

C. Halldén, T. Säll, C. Lind‐Halldén, 2002, Hereditas.

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

B. Dahlbäck, A. Johansson, C. Halldén, 2004, Journal of thrombosis and haemostasis : JTH.

Chronic Rhinosinusitis Patients Show Accumulation of Genetic Variants in PARS2

C. Bachert, C. Halldén, T. Säll, 2016, PloS one.

Copy Number Variants in the Kallikrein Gene Cluster

H. Lilja, A. Bjartell, A. Johansson, 2013, PloS one.

Bioinformatic and rare-variant collapsing analyses for type 1 and type 2 diabetes in the UK Biobank reveal novel pleiotropic susceptibility loci.

C. Halldén, Bengt Zöller, C. Lind‐Halldén, 2023, Journal of Diabetes.

The use of bulked segregant analysis to accumulate RAPD markers near a locus for beet cyst nematode resistance in Beta vulgaris

K. Olsson, C. Halldén, T. Säll, 1997 .

Mutation analysis of Swedish haemophilia B families – high frequency of unique mutations

R. Ljung, C. Halldén, A. Letelier, 2016, Haemophilia : the official journal of the World Federation of Hemophilia.

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

F. Barrenäs, M. Benson, R. Mobini, 2009, Allergy.

RFLP markers in the genus Beta: characterization of DNA sequences from a Beta vulgaris library

C. Halldén, T. Säll, A. Hjerdin, 2004, Genetica.

Rare-variant collapsing analyses reveal novel risk genes for arterial and venous cardiovascular diseases in the UK biobank.

C. Halldén, Bengt Zöller, C. Lind‐Halldén, 2023, Thrombosis research.

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

C. Halldén, S. Lethagen, C. Lind‐Halldén, 2018, Thrombosis and Haemostasis.

Rare-variant collapsing and bioinformatic analyses for amyloidosis, dementia and Parkinson's disease in the UK biobank reveal novel susceptibility loci.

C. Halldén, Bengt Zöller, C. Lind‐Halldén, 2023, Amyloid: Journal of Protein Folding Disorders.

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

C. Halldén, S. Lethagen, B. Friberg, 2008, Thrombosis and Haemostasis.

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

A. Johansson, C. Halldén, T. Säll, 2011, Thrombosis and Haemostasis.

Estimating genetic variation in sugar beets and wild beets using pools of individuals.

C. Halldén, T. Säll, T. Kraft, 1997, Genome.