Eric Manderstedt

Sökresultat

• 2024

  Tissue factor (F3) gene variants and thrombotic risk among middle-aged and older adults: A population-based cohort study

  Manderstedt, E., Lind-Halldén, C., Halldén, C., Elf, J., Svensson, P. J., Engström, G., Melander, O., Baras, A., Lotta, L. A., Zöller, B. & Regeneron Genetics Center, 2024 dec., I: Thrombosis Update. 17, 100190.

  Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review

  Öppen tillgång

  • Cohort Study 100%
  • Missense 100%
  • Exon 66%
  • Minor Allele Frequency 33%
  • Prevalence 33%

• Origin of pathogenic variant and mosaicism in families with a sporadic case of haemophilia B

  Mårtensson, A., Letelier, A., Manderstedt, E., Glosli, H. & Ljung, R., 2024, I: Haemophilia. 30, 3, s. 774-779

  Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review

  Öppen tillgång

  • Mothers 100%
  • Family 100%
  • Sequencing 50%
  • Droplet 50%
  • Sanger Sequencing 33%

• Rare-variant collapsing and bioinformatic analyses for different types of cardiac arrhythmias in the UK Biobank reveal novel susceptibility loci and candidate amyloid-forming proteins

  Zöller, B., Manderstedt, E., Lind-Halldén, C. & Halldén, C., 2024, I: Cardiovascular Digital Health Journal. 5, 1, s. 15-18 4 s.

  Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review

  Öppen tillgång

  • Protein 100%
  • Arrhythmia 100%
  • UK Biobank 100%
  • Heart Arrhythmia 100%
  • Heart Muscle Conduction Disturbance 37%

• SERPINH1 variants and thrombotic risk among middle-aged and older adults: a population-based cohort study

  Manderstedt, E., Lind-Halldén, C., Halldén, C., Elf, J., Svensson, P. J., Engström, G., Melander, O., Baras, A., Lotta, L. A., Zöller, B. & Regeneron Genetics Center, 2024, I: Journal of Thrombosis and Haemostasis. 22, 3, s. 869-873 5 s.

  Forskningsoutput: Tidskriftsbidrag › Letter › Peer review
• 2023

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

  Zöller, B., Manderstedt, E., Lind-Halldén, C. & Halldén, C., 2023 nov., I: Journal of Human Hypertension. 37, 11, s. 1040–1042 3 s.

  Forskningsoutput: Tidskriftsbidrag › Letter › Peer review

  Öppen tillgång

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

  Zöller, B., Manderstedt, E., Lind-Halldén, C. & Halldén, C., 2023 okt., I: ESC Heart Failure. 10, 5, s. 3234-3235 2 s.

  Forskningsoutput: Tidskriftsbidrag › Letter › Peer review

  Öppen tillgång

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

  Zöller, B., Manderstedt, E., Lind-Halldén, C. & Halldén, C., 2023 jan., I: Leukemia Research Reports. 19, 100362.

  Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review

  Öppen tillgång

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

  Zöller, B., Manderstedt, E., Lind-Halldén, C. & Halldén, C., 2023, I: Journal of Diabetes. 15, 9, s. 799-802 4 s.

  Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review

  Öppen tillgång

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

  Zöller, B., Manderstedt, E., Lind-Halldén, C. & Halldén, C., 2023, I: Thrombosis Research. 229, s. 86-89 4 s.

  Forskningsoutput: Tidskriftsbidrag › Letter › Peer review

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

  Zöller, B., Manderstedt, E., Lind-Halldén, C. & Halldén, C., 2023, I: Amyloid. 30, 4, s. 442-444

  Forskningsoutput: Tidskriftsbidrag › Letter › Peer review

• The role of fibrinolysis in vascular diseases in UK biobank

  Zöller, B., Manderstedt, E., Lind-Halldén, C. & Halldén, C., 2023, I: Journal of Thrombosis and Thrombolysis. 56, 4, s. 635-638 4 s.

  Forskningsoutput: Tidskriftsbidrag › Letter › Peer review
• 2019

  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., 2019, I: Thrombosis and Haemostasis. 119, 09, s. 1441-1450

  Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review

  • Next Generation Sequencing 100%
  • Gene 100%
  • Patient 62%
  • Anticoagulant Agent 42%
  • Antithrombotic 37%