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BMC Medical Genomics|January 20, 2025
Visualization using NIPTviewer support the clinical interpretation of noninvasive prenatal testing resultsPatrik Smeds, Izabella Baranowska Körberg, Malin Melin, et al.Virology|January 13, 2026
Twist-ONT: Combining nanopore sequencing with the twist comprehensive viral research panelJonathan Haars, Tomas Cumlin, Claes Ladenvall, et al.Stroke|June 4, 2005
Family history in ischemic stroke before 70 years of age: the Sahlgrenska Academy Study on Ischemic StrokeKatarina Jood, Claes Ladenvall, Annika Rosengren, et al.Stroke|July 1, 2006
Serum C-reactive protein concentration and genotype in relation to ischemic stroke subtypeClaes Ladenvall, Katarina Jood, Christian Blomstrand, et al.Journal of Neurosurgery|December 9, 2008
Association between factor XIII single nucleotide polymorphisms and aneurysmal subarachnoid hemorrhageClaes Ladenvall, Ludvig Csajbok, Karin Nylén, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|February 3, 2007
Thrombin activatable fibrinolysis inhibitor activation peptide shows association with all major subtypes of ischemic stroke and with TAFI gene variationClaes Ladenvall, Ann Gils, Katarina Jood, et al.European Journal of Endocrinology|February 18, 2011
Two common genetic variants near nuclear-encoded OXPHOS genes are associated with insulin secretion in vivoAnders H Olsson, Tina Rönn, Claes Ladenvall, et al.Journal of Medical Genetics|August 14, 2023
Integrating a Polygenic Risk Score into a clinical setting would impact risk predictions in familial breast cancerPanagiotis Baliakas, Arielle R Munters, Anders Kämpe, et al.Hemasphere|August 8, 2022
Five Percent Variant Allele Frequency Is a Reliable Reporting Threshold for TP53 Variants Detected by Next Generation Sequencing in Chronic Lymphocytic Leukemia in the Clinical SettingTatjana Pandzic, Claes Ladenvall, Marie Engvall, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 6, 2023
Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid LeukemiaAnna Eriksson, Marie Engvall, Lucy Mathot, et al.Pageof 6