The impact of low-frequency and rare variants on lipid levels

Ida Surakka, Momoko Horikoshi, Reedik Magi, Antti-Pekka Sarin, Anubha Mahajan, Vasiliki Lagou, Letizia Marullo, Teresa Ferreira, Benjamin Miraglio, Sanna Timonen, Johannes Kettunen, Matti Pirinen, Julia Karjalainen, Gudmar Thorleifsson, Sara Hagg, Jouke-Jan Hottenga, Aaron Isaacs, Claes Ladenvall, Marian Beekman, Tonu EskoJanina S. Ried, Christopher P. Nelson, Christina Willenborg, Stefan Gustafsson, Harm-Jan Westra, Matthew Blades, Anton J. M. de Craen, Eco J. de Geus, Joris Deelen, Harald Grallert, Anders Hamsten, Aki S. Havulinna, Christian Hengstenberg, Jeanine J. Houwing-Duistermaat, Elina Hypponen, Lennart C. Karssen, Terho Lehtimaki, Valeriya Lyssenko, Patrik K. E. Magnusson, Evelin Mihailov, John-Patrick Mpindi, Markus Perola, Jaakko Kaprio, Leif Groop, Johan G. Eriksson, Elina Ikonen, Olli Kallioniemi, Vilja Pietiainen, Aarno Palotie, Samuli Ripatti, ENGAGE Consortium

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalNature Genetics
Volume47
Issue number6
Pages (from-to)589-597
Number of pages9
ISSN1061-4036
DOIs
Publication statusPublished - Jun 2015
MoE publication typeA1 Journal article-refereed

Fields of Science

  • GENOME-WIDE ASSOCIATION
  • IN-VITRO
  • HETEROGENEITY
  • EXPRESSION
  • SIALOMUCIN
  • SEQUENCE
  • DISEASE
  • GLUCOSE
  • GENES
  • LIVER
  • 3111 Biomedicine
  • 1184 Genetics, developmental biology, physiology
  • 3142 Public health care science, environmental and occupational health

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