Showing results (91-100 of 109) with videos related to
Sort By:
Pageof 11
Nature Genetics|July 13, 2010
Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarctionConnie R Bezzina, Raha Pazoki, Abdennasser Bardai, et al.Pediatric Nephrology (Berlin, Germany)|January 14, 2026
APOL1 kidney risk variants and outcomes in children with congenital anomalies of the kidney and urinary tractLisanne M Vendrig, Juntao Ke, Michael W T Tanck, et al.Journal of Human Genetics|January 4, 2023
Familial multiple discoid fibromas is linked to a locus on chromosome 5 including the FNIP1 geneIrma van de Beek, Iris E Glykofridis, Michael W T Tanck, et al.Molecular Vision|April 18, 2012
Multicenter cohort association study of SLC2A1 single nucleotide polymorphisms and age-related macular degenerationDominique C Baas, Lintje Ho, Michael W T Tanck, et al.International Journal of Cancer|April 27, 2026
Transcriptome-Based Classification of Resected Pancreatic Ductal Adenocarcinoma Enhances Prognostic Modelling Accuracy of Overall Survival Following Adjuvant TreatmentMarjolein F Lansbergen, Vincent R Lanting, Paul Manoukian, et al.Heart Rhythm|July 4, 2020
Common and rare susceptibility genetic variants predisposing to Brugada syndrome in ThailandPattarapong Makarawate, Charlotte Glinge, Apichai Khongphatthanayothin, et al.Frontiers in Pediatrics|August 11, 2020
Biomarkers for the Discrimination of Acute Kawasaki Disease From Infections in ChildhoodJudith Zandstra, Annemarie van de Geer, Michael W T Tanck, et al.Frontiers in Immunology|April 6, 2019
Extensive Ethnic Variation and Linkage Disequilibrium at the FCGR2/3 Locus: Different Genetic Associations Revealed in Kawasaki DiseaseSietse Q Nagelkerke, Carline E Tacke, Willemijn B Breunis, et al.European Heart Journal|May 3, 2018
A common co-morbidity modulates disease expression and treatment efficacy in inherited cardiac sodium channelopathyMathilde R Rivaud, John A Jansen, Pieter G Postema, et al.European Heart Journal|May 15, 2024
Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk lociTaisuke Ishikawa, Tatsuo Masuda, Tsuyoshi Hachiya, et al.Pageof 11