Novel 6p21.3 Risk Haplotype Predisposes to Acute Coronary Syndrome

Juha Sinisalo, Efthymia Vlachopoulou, Marja Marchesani, Johanna Nokelainen, Mikko I. Mayranpaa, Jani Lappalainen, Riitta Paakkanen, Annika Wennerstrom, Krista Salli, Heikki J. Niemi, Satu Mannisto, Perttu Salo, Juhani Junttila, Markku Eskola, Kjell Nikus, T. Petteri Arstila, Markus Perola, Heikki Huikuri, Pekka J. Karhunen, Petri T KovanenAarno Palotie, Aki S. Havulinna, Carla Lluis-Ganella, Jaume Marrugat, Roberto Elosua, Veikko Salomaa, Markku S. Nieminen, Marja-Liisa Lokki

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalCirculation. Cardiovascular genetics
Volume9
Issue number1
Pages (from-to)55-63
Number of pages9
ISSN1942-325X
DOIs
Publication statusPublished - Feb 2016
MoE publication typeA1 Journal article-refereed

Fields of Science

  • expression experiments
  • human leukocyte antigen
  • BTNL2
  • single nucleotide polymorphism
  • MHC
  • genetics
  • association studies
  • haplotype
  • regulatory T cell
  • acute coronary syndrome
  • GENOME-WIDE ASSOCIATION
  • MAJOR HISTOCOMPATIBILITY COMPLEX
  • ACUTE MYOCARDIAL-INFARCTION
  • SPLICE-SITE MUTATION
  • ARTERY-DISEASE
  • SUSCEPTIBILITY LOCI
  • FINNISH POPULATION
  • HLA-ANTIGEN
  • HUMAN MHC
  • GENOTYPE
  • 3111 Biomedicine
  • 3121 General medicine, internal medicine and other clinical medicine

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