Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism

Frank Ruehle, Anika Witten, Andrei Barysenka, Andreas Huge, Astrid Arning, Christine Heller, Anne Kruempel, Rolf Mesters, Andre Franke, Wolfgang Lieb, Mona Riemenschneider, Milan Hiersche, Verena Limperger, Ulrike Nowak-Goettl, Monika Stoll*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)783-790
Number of pages8
JournalBlood
Volume129
Issue number6
DOIs
Publication statusPublished - 9 Feb 2017

Keywords

  • GENOME-WIDE ASSOCIATION
  • ARTERIAL ISCHEMIC-STROKE
  • DNA-SEQUENCING DATA
  • FAMILY-BASED TESTS
  • THROMBOPHILIA
  • RISK
  • METAANALYSIS
  • RELEASE
  • LINKAGE
  • DISEQUILIBRIUM

Cite this

Ruehle, F., Witten, A., Barysenka, A., Huge, A., Arning, A., Heller, C., Kruempel, A., Mesters, R., Franke, A., Lieb, W., Riemenschneider, M., Hiersche, M., Limperger, V., Nowak-Goettl, U., & Stoll, M. (2017). Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism. Blood, 129(6), 783-790. https://doi.org/10.1182/blood-2016-07-728840