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 Internal medicine

Cite this

Sinisalo, Juha ; Vlachopoulou, Efthymia ; Marchesani, Marja ; Nokelainen, Johanna ; Mayranpaa, Mikko I. ; Lappalainen, Jani ; Paakkanen, Riitta ; Wennerstrom, Annika ; Salli, Krista ; Niemi, Heikki J. ; Mannisto, Satu ; Salo, Perttu ; Junttila, Juhani ; Eskola, Markku ; Nikus, Kjell ; Arstila, T. Petteri ; Perola, Markus ; Huikuri, Heikki ; Karhunen, Pekka J. ; Kovanen, Petri T ; Palotie, Aarno ; Havulinna, Aki S. ; Lluis-Ganella, Carla ; Marrugat, Jaume ; Elosua, Roberto ; Salomaa, Veikko ; Nieminen, Markku S. ; Lokki, Marja-Liisa. / Novel 6p21.3 Risk Haplotype Predisposes to Acute Coronary Syndrome. In: Circulation. Cardiovascular genetics. 2016 ; Vol. 9, No. 1. pp. 55-63.
@article{ca922c03609b41b5b3750f9bbe0b99fe,
title = "Novel 6p21.3 Risk Haplotype Predisposes to Acute Coronary Syndrome",
keywords = "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 Internal medicine",
author = "Juha Sinisalo and Efthymia Vlachopoulou and Marja Marchesani and Johanna Nokelainen and Mayranpaa, {Mikko I.} and Jani Lappalainen and Riitta Paakkanen and Annika Wennerstrom and Krista Salli and Niemi, {Heikki J.} and Satu Mannisto and Perttu Salo and Juhani Junttila and Markku Eskola and Kjell Nikus and Arstila, {T. Petteri} and Markus Perola and Heikki Huikuri and Karhunen, {Pekka J.} and Kovanen, {Petri T} and Aarno Palotie and Havulinna, {Aki S.} and Carla Lluis-Ganella and Jaume Marrugat and Roberto Elosua and Veikko Salomaa and Nieminen, {Markku S.} and Marja-Liisa Lokki",
year = "2016",
month = "2",
doi = "10.1161/CIRCGENETICS.115.001226",
language = "English",
volume = "9",
pages = "55--63",
journal = "Circulation. Cardiovascular genetics",
issn = "1942-325X",
publisher = "LIPPINCOTT WILLIAMS & WILKINS",
number = "1",

}

Sinisalo, J, Vlachopoulou, E, Marchesani, M, Nokelainen, J, Mayranpaa, MI, Lappalainen, J, Paakkanen, R, Wennerstrom, A, Salli, K, Niemi, HJ, Mannisto, S, Salo, P, Junttila, J, Eskola, M, Nikus, K, Arstila, TP, Perola, M, Huikuri, H, Karhunen, PJ, Kovanen, PT, Palotie, A, Havulinna, AS, Lluis-Ganella, C, Marrugat, J, Elosua, R, Salomaa, V, Nieminen, MS & Lokki, M-L 2016, 'Novel 6p21.3 Risk Haplotype Predisposes to Acute Coronary Syndrome', Circulation. Cardiovascular genetics, vol. 9, no. 1, pp. 55-63. https://doi.org/10.1161/CIRCGENETICS.115.001226

Novel 6p21.3 Risk Haplotype Predisposes to Acute Coronary Syndrome. / Sinisalo, Juha; Vlachopoulou, Efthymia; Marchesani, Marja; Nokelainen, Johanna; Mayranpaa, Mikko I.; Lappalainen, Jani; Paakkanen, Riitta; Wennerstrom, Annika; Salli, Krista; Niemi, Heikki J.; Mannisto, Satu; Salo, Perttu; Junttila, Juhani; Eskola, Markku; Nikus, Kjell; Arstila, T. Petteri; Perola, Markus; Huikuri, Heikki; Karhunen, Pekka J.; Kovanen, Petri T; Palotie, Aarno; Havulinna, Aki S.; Lluis-Ganella, Carla; Marrugat, Jaume; Elosua, Roberto; Salomaa, Veikko; Nieminen, Markku S.; Lokki, Marja-Liisa.

In: Circulation. Cardiovascular genetics, Vol. 9, No. 1, 02.2016, p. 55-63.

Research output: Contribution to journalArticleScientificpeer-review

TY - JOUR

T1 - Novel 6p21.3 Risk Haplotype Predisposes to Acute Coronary Syndrome

AU - Sinisalo, Juha

AU - Vlachopoulou, Efthymia

AU - Marchesani, Marja

AU - Nokelainen, Johanna

AU - Mayranpaa, Mikko I.

AU - Lappalainen, Jani

AU - Paakkanen, Riitta

AU - Wennerstrom, Annika

AU - Salli, Krista

AU - Niemi, Heikki J.

AU - Mannisto, Satu

AU - Salo, Perttu

AU - Junttila, Juhani

AU - Eskola, Markku

AU - Nikus, Kjell

AU - Arstila, T. Petteri

AU - Perola, Markus

AU - Huikuri, Heikki

AU - Karhunen, Pekka J.

AU - Kovanen, Petri T

AU - Palotie, Aarno

AU - Havulinna, Aki S.

AU - Lluis-Ganella, Carla

AU - Marrugat, Jaume

AU - Elosua, Roberto

AU - Salomaa, Veikko

AU - Nieminen, Markku S.

AU - Lokki, Marja-Liisa

PY - 2016/2

Y1 - 2016/2

KW - expression experiments

KW - human leukocyte antigen

KW - BTNL2

KW - single nucleotide polymorphism

KW - MHC

KW - genetics

KW - association studies

KW - haplotype

KW - regulatory T cell

KW - acute coronary syndrome

KW - GENOME-WIDE ASSOCIATION

KW - MAJOR HISTOCOMPATIBILITY COMPLEX

KW - ACUTE MYOCARDIAL-INFARCTION

KW - SPLICE-SITE MUTATION

KW - ARTERY-DISEASE

KW - SUSCEPTIBILITY LOCI

KW - FINNISH POPULATION

KW - HLA-ANTIGEN

KW - HUMAN MHC

KW - GENOTYPE

KW - 3111 Biomedicine

KW - 3121 Internal medicine

U2 - 10.1161/CIRCGENETICS.115.001226

DO - 10.1161/CIRCGENETICS.115.001226

M3 - Article

VL - 9

SP - 55

EP - 63

JO - Circulation. Cardiovascular genetics

JF - Circulation. Cardiovascular genetics

SN - 1942-325X

IS - 1

ER -