Works by Halldén, Christer

Results: 26

A Unique Recent Origin of the Allotetraploid Species Arabidopsis suecica: Evidence from Nuclear DNA Markers.

Published in:

Molecular Biology & Evolution, 2006, v. 23, n. 6, p. 1217, doi. 10.1093/molbev/msk006

By:

Jakobsson, Mattias;
Hagenblad, Jenny;
Tavaré, Simon;
Säll, Torbjörn;
Halldén, Christer;
Lind-Halldén, Christina;
Nordborg, Magnus

Publication type:

Article

Mode of reproduction inArabidopsis suecica.

Published in:

Hereditas, 2004, v. 141, n. 3, p. 313, doi. 10.1111/j.1601-5223.2004.01833.x

By:

Säll, Torbjörn;
Lind-Halldén, Christina;
Jakobsson, Mattias;
Halldén, Christer

Publication type:

Article

Molecular characterization of UV-treated sugar beet somaclones using RFLP markers.

Published in:

Physiologia Plantarum, 1994, v. 90, n. 1, p. 216, doi. 10.1111/j.1399-3054.1994.tb02214.x

By:

Levall, Mats W.;
Bengtsson, Karina;
Nilsson, Nils-Otto;
Hjerdin, Annika;
Halldén, Christer

Publication type:

Article

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

Published in:

Physiologia Plantarum, 1991, v. 83, n. 1, p. 7, doi. 10.1111/j.1399-3054.1991.tb01274.x

By:

Lind, Christina;
Halldén, Christer;
Møller, Ian M.

Publication type:

Article

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

Published in:

Annals of Human Genetics, 2011, v. 75, n. 4, p. 447, doi. 10.1111/j.1469-1809.2011.00652.x

By:

Johansson, Anna M.;
Halldén, Christer;
Säll, Torbjörn;
Lethagen, Stefan

Publication type:

Article

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

Published in:

Journal of Diabetes, 2023, v. 15, n. 9, p. 799, doi. 10.1111/1753-0407.13452

By:

Zöller, Bengt;
Manderstedt, Eric;
Lind‐Halldén, Christina;
Halldén, Christer

Publication type:

Article

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

Published in:

Human Heredity, 2005, v. 60, n. 1, p. 26, doi. 10.1159/000087541

By:

Johansson, Anna M.;
Halldén, Christer;
Säll, Torbjörn

Publication type:

Article

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

Published in:

Molecular Human Reproduction, 2003, v. 9, n. 6, p. 345, doi. 10.1093/molehr/gag049

By:

Lundwall, Åke;
Giwercman, Aleksander;
Ruhayel, Yasir;
Giwercman, Yvonne;
Lilja, Hans;
Halldén, Christer;
Malm, Johan

Publication type:

Article

Chronic Rhinosinusitis Patients Show Accumulation of Genetic Variants in PARS2.

Published in:

PLoS ONE, 2016, v. 11, n. 6, p. 1, doi. 10.1371/journal.pone.0158202

By:

Henmyr, Viktor;
Lind-Halldén, Christina;
Halldén, Christer;
Säll, Torbjörn;
Carlberg, Daniel;
Bachert, Claus;
Cardell, Lars-Olaf

Publication type:

Article

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

Published in:

PLoS ONE, 2018, v. 13, n. 2, p. 1, doi. 10.1371/journal.pone.0192024

By:

Manderstedt, Eric;
Lind-Halldén, Christina;
Lethagen, Stefan;
Halldén, Christer

Publication type:

Article

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

Published in:

Amyloid, 2023, v. 30, n. 4, p. 442, doi. 10.1080/13506129.2023.2226299

By:

Zöller, Bengt;
Manderstedt, Eric;
Lind-Halldén, Christina;
Halldén, Christer

Publication type:

Article

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

Published in:

2022

By:

Manderstedt, Eric;
Halldén, Christina Lind;
Halldén, Christer;
Elf, Johan;
Svensson, Peter J.;
Dahlbäck, Björn;
Engström, Gunnar;
Melander, Olle;
Baras, Aris;
Lotta, Luca A.;
Zöller, Bengt;
Lind-Halldén, Christina;
Regeneron Genetics Center 4 [Link]

Publication type:

journal article

The role of fibrinolysis in vascular diseases in UK biobank.

Published in:

2023

By:

Zöller, Bengt;
Manderstedt, Eric;
Lind-Halldén, Christina;
Halldén, Christer

Publication type:

Letter

A quality assessment survey of SNP genotyping laboratories.

Published in:

Human Mutation, 2006, v. 27, n. 7, p. 711, doi. 10.1002/humu.20346

By:

Lahermo, Päivi;
Liljedahl, Ulrika;
Alnaes, Grethe;
Axelsson, Tomas;
Brookes, Anthony J.;
Ellonen, Pekka;
Groop, Per-Henrik;
Halldén, Christer;
Holmberg, Dan;
Holmberg, Kristina;
Keinänen, Mauri;
Kepp, Katrin;
Kere, Juha;
Kiviluoma, Päivi;
Kristensen, Vessela;
Lindgren, Cecilia;
Odeberg, Jacob;
Osterman, Pia;
Parkkonen, Maija;
Saarela, Janna

Publication type:

Article

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

Published in:

Human Reproduction, 2004, v. 19, n. 9, p. 2076, doi. 10.1093/humrep/deh349

By:

Yasir Ruhayel;
Kristina Lundin;
Yvonne Giwercman;
Christer Halldén;
Marianne Willén;
Aleksander Giwercman

Publication type:

Article

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

Published in:

Haemophilia, 2021, v. 27, n. 5, p. e654, doi. 10.1111/hae.14394

By:

Manderstedt, Eric;
Lind‐Halldén, Christina;
Ljung, Rolf;
Astermark, Jan;
Halldén, Christer

Publication type:

Article

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

Published in:

PLoS ONE, 2019, v. 14, n. 4, p. 1, doi. 10.1371/journal.pone.0216179

By:

Manderstedt, Eric;
Nilsson, Rosanna;
Lind-Halldén, Christina;
Ljung, Rolf;
Astermark, Jan;
Halldén, Christer

Publication type:

Article

Genetic Variation in KLK2 and KLK3 Is Associated with Concentrations of hK2 and PSA in Serum and Seminal Plasma in Young Men.

Published in:

Clinical Chemistry, 2014, v. 60, n. 3, p. 490, doi. 10.1373/clinchem.2013.211219

By:

Sävblom, Charlotta;
Halldén, Christer;
Cronin, Angel M.;
Säll, Torbjörn;
Savage, Caroline;
Vertosick, Emily A.;
Klein, Robert J.;
Giwercman, Aleksander;
Lilja, Hans

Publication type:

Article

Contribution of rare genetic variants to heart failure and cardiomyopathy in the UK Biobank.

Published in:

ESC Heart Failure, 2023, v. 10, n. 5, p. 3234, doi. 10.1002/ehf2.14490

By:

Zöller, Bengt;
Manderstedt, Eric;
Lind‐Halldén, Christina;
Halldén, Christer

Publication type:

Article

Evolution of chloroplast mononucleotide microsatellites in Arabidopsis thaliana.

Published in:

Theoretical & Applied Genetics, 2007, v. 114, n. 2, p. 223, doi. 10.1007/s00122-006-0425-9

By:

Jakobsson, Mattias;
Säll, Torbjörn;
Lind-Halldén, Christina;
Halldén, Christer

Publication type:

Article

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

Published in:

BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-51

By:

Andiappan, Anand Kumar;
Nilsson, Daniel;
Halldén, Christer;
De Yun, Wang;
Säll, Torbjörn;
Cardell, Lars Olaf;
Tim, Chew Fook

Publication type:

Article

Copy Number Variants in the Kallikrein Gene Cluster.

Published in:

PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0069097

By:

Lindahl, Pernilla;
Säll, Torbjörn;
Bjartell, Anders;
Johansson, Anna M.;
Lilja, Hans;
Halldén, Christer

Publication type:

Article

Poor Reproducibility of Allergic Rhinitis SNP Associations.

Published in:

PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0053975

By:

Nilsson, Daniel;
Andiappan, Anand Kumar;
Halldén, Christer;
Tim, Chew Fook;
Säll, Torbjörn;
De Yun Wang;
Cardell, Lars-Olaf

Publication type:

Article

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

Published in:

PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0018583

By:

Sjödahl, Gottfrid;
Lauss, Martin;
Gudjonsson, Sigurdur;
Liedberg, Fredrik;
Halldén, Christer;
Chebil, Gunilla;
Månsson, Wiking;
Höglund, Mattias;
Lindgren, David

Publication type:

Article

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

Published in:

2008

By:

Bryborn M;
Halldén C;
Säll T;
Adner M;
Cardell LO;
Bryborn, Malin;
Halldén, Christer;
Säll, Torbjörn;
Adner, Mikael;
Cardell, Lars Olaf

Publication type:

journal article

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

Published in:

Respiratory Research, 2008, v. 9, p. 1, doi. 10.1186/1465-9921-9-29

By:

Bryborn, Malin;
Halldén, Christer;
Säll, Torbjörn;
Adner, Mikael;
Cardell, Lars Olaf

Publication type:

Article