Thrombomodulin (THBD) gene variants and thrombotic risk in a population‐based cohort study von Manderstedt, Eric, Halldén, Christer, Lind‐Halldén, Christina, Elf, Johan, Svensson, Peter J., Engström, Gunnar, Melander, Olle, Baras, Aris, Lotta, Luca A., Zöller, Bengt

Volltext

Droplet digital PCR and mile‐post analysis for the detection of F8 int1h inversions von Manderstedt, Eric, Lind‐Halldén, Christina, Ljung, Rolf, Astermark, Jan, Halldén, Christer

Volltext

Detection of F8 int22h inversions using digital droplet PCR and mile‐post assays von Manderstedt, Eric, Lind‐Halldén, Christina, Ljung, Rolf, Astermark, Jan, Halldén, Christer

Volltext

Identification of F8 rearrangements in carrier and non‐carrier mothers of haemophilia A patients von Manderstedt, Eric, Lind‐Halldén, Christina, Ljung, Rolf, Astermark, Jan, Halldén, Christer

Volltext

Bioinformatic and rare-variant collapsing analyses for type 1 and type 2 diabetes in the UK Biobank reveal novel pleiotropic susceptibility loci von Zöller, Bengt, Manderstedt, Eric, Lind-Halldén, Christina, Halldén, Christer

Volltext

Genetic risk factors for venous thromboembolism von Zöller, Bengt, Svensson, Peter J, Dahlbäck, Björn, Lind-Halldén, Christina, Halldén, Christer, Elf, Johan

Volltext

Thrombotic risk determined by rare and common SERPINA1 variants in a population‐based cohort study von Manderstedt, Eric, Halldén, Christer, Lind‐Halldén, Christina, Elf, Johan, Svensson, Peter J., Engström, Gunnar, Melander, Olle, Baras, Aris, Lotta, Luca A., Zöller, Bengt, Abecasis, Goncalo, Cantor, Michael, Coppola, Giovanni, Economides, Aris, Overton, John D., Reid, Jeffrey G., Shuldiner, Alan, Beechert, Christina, Forsythe, Caitlin, Fuller, Erin D., Gu, Zhenhua, Lattari, Michael, Lopez, Alexander, Manoochehri, Kia, Overton, John D., Padilla, Maria Sotiropoulos, Pradhan, Manasi, Schleicher, Thomas D., Ulloa, Ricardo H., Widom, Louis, Wolf, Sarah E., Bai, Xiaodong, Balasubramanian, Suganthi, Blumenfeld, Andrew, Boutkov, Boris, Eom, Gisu, Habegger, Lukas, Hawes, Alicia, Khalid, Shareef, Krasheninina, Olga, Lanche, Rouel, Mansfield, Adam J., Maxwell, Evan K., Nafde, Mrunali, O’Keeffe, Sean, Orelus, Max, Panea, Razvan, Polanco, Tommy, Rasool, Ayesha, Reid, Jeffrey G., Salerno, William, Staples, Jeffrey C., Jones, Marcus B., Mighty, Jason, Mitnaul, Lyndon J.

Volltext

Contribution of rare genetic variants to heart failure and cardiomyopathy in the UK Biobank von Zöller, Bengt, Manderstedt, Eric, Lind-Halldén, Christina, Halldén, Christer

Volltext

Classic Thrombophilias and Thrombotic Risk Among Middle-Aged and Older Adults: A Population-Based Cohort Study von Manderstedt, Eric, Lind-Halldén, Christina, Halldén, Christer, Elf, Johan, Svensson, Peter J, Dahlbäck, Björn, Engström, Gunnar, Melander, Olle, Baras, Aris, Lotta, Luca A, Zöller, Bengt

Volltext

Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients von Manderstedt, Eric, Lind-Halldén, Christina, Lethagen, Stefan, Halldén, Christer

Volltext

Targeted re-sequencing of F8, F9 and VWF: Characterization of Ion Torrent data and clinical implications for mutation screening von Manderstedt, Eric, Nilsson, Rosanna, Lind-Halldén, Christina, Ljung, Rolf, Astermark, Jan, Halldén, Christer

Volltext

Contribution of rare and common coding variants to haematological malignancies in the UK biobank von Zöller, Bengt, Manderstedt, Eric, Lind-Halldén, Christina, Halldén, Christer

Volltext

Detection of mosaics in hemophilia A by deep Ion Torrent sequencing and droplet digital PCR von Manderstedt, Eric, Nilsson, Rosanna, Ljung, Rolf, Lind‐Halldén, Christina, Astermark, Jan, Halldén, Christer

Volltext

Chronic Rhinosinusitis Patients Show Accumulation of Genetic Variants in PARS2 von Henmyr, Viktor, Lind-Halldén, Christina, Halldén, Christer, Säll, Torbjörn, Carlberg, Daniel, Bachert, Claus, Cardell, Lars-Olaf

Volltext

A unique recent origin of the allotetraploid species Arabidopsis suecica: Evidence from nuclear DNA markers von Jakobsson, Mattias, Hagenblad, Jenny, Tavaré, Simon, Säll, Torbjörn, Halldén, Christer, Lind-Halldén, Christina, Nordborg, Magnus

Volltext

Rare-variant collapsing analyses reveal novel risk genes for arterial and venous cardiovascular diseases in the UK biobank von Zöller, Bengt, Manderstedt, Eric, Lind-Halldén, Christina, Halldén, Christer

Volltext

Rare-variant collapsing analyses of arterial hypertension in the UK biobank von Zöller, Bengt, Manderstedt, Eric, Lind-Halldén, Christina, Halldén, Christer

Volltext

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... von Manderstedt, Eric, Lind‐Halldén, Christina, Halldén, Christer, Elf, Johan, Svensson, Peter J., Engström, Gunnar, Melander, Olle, Baras, Aris, Lotta, Luca A., Zöller, Bengt, Abecasis, Goncalo, Baras, Aris, Cantor, Michael, Coppola, Giovanni, Economides, Aris, Lotta, Luca A., Overton, John D., Reid, Jeffrey G., Shuldiner, Alan, Beechert, Christina, Forsythe, Caitlin, Fuller, Erin D., Gu, Zhenhua, Lattari, Michael, Lopez, Alexander, Schleicher, Thomas D., Padilla, Maria Sotiropoulos, Widom, Louis, Wolf, Sarah E., Pradhan, Manasi, Manoochehri, Kia, Ulloa, Ricardo H., Bai, Xiaodong, Balasubramanian, Suganthi, Blumenfeld, Andrew, Boutkov, Boris, Eom, Gisu, Habegger, Lukas, Hawes, Alicia, Khalid, Shareef, Krasheninina, Olga, Lanche, Rouel, Mansfield, Adam J., Maxwell, Evan K., Nafde, Mrunali, O’Keeffe, Sean, Orelus, Max, Panea, Razvan, Polanco, Tommy, Rasool, Ayesha, Salerno, William, Staples, Jeffrey C., Jones, Marcus B., Mighty, Jason, Mitnaul, Lyndon J.

Volltext

Ventricular catheter placement accuracy in non-stereotactic shunt surgery for hydrocephalus von Lind, Christopher R.P, Tsai, Amy M.C, Lind, Christina J, Law, Andrew J.J

Volltext

The role of fibrinolysis in vascular diseases in UK biobank von Zöller, Bengt, Manderstedt, Eric, Lind-Halldén, Christina, Halldén, Christer

Volltext