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

Ida Surakka; Momoko Horikoshi; Reedik Mägi; Antti‐Pekka Sarin; Anubha Mahajan; Vasiliki Lagou; Letizia Marullo; Teresa Ferreira; Benjamin Miraglio; Sanna Timonen; Johannes Kettunen; Matti Pirinen; Juha Karjalainen; Guðmar Þorleifsson; Sara Hägg; Jouke‐Jan Hottenga; Aaron Isaacs; Claes Ladenvall; Marian Beekman; Tõnu Esko; Janina S. Ried; Christopher P. Nelson; Christina Willenborg; Stefan Gustafsson; Harm-Jan Westra; Matthew Blades; Anton J. M. de Craen; Eco J. C. de Geus; Joris Deelen; Harald Grallert; Anders Hamsten; Aki S. Havulinna; Christian Hengstenberg; Jeanine J. Houwing‐Duistermaat; Elina Hyppönen; Lennart C. Karssen; Terho Lehtimäki; Valeriya Lyssenko; Patrik K. E. Magnusson; Evelin Mihailov; Martina Müller‐Nurasyid; John-Patrick Mpindi; Nancy L. Pedersen; Brenda W.J.H. Penninx; Markus Perola; Tune H. Pers; Annette Peters; Johan Rung; Johannes H. Smit; Valgerður Steinthórsdóttir; Martin D. Tobin; Natalia Tšernikova; Elisabeth M van Leeuwen; Jorma Viikari; Sara M. Willems; Gonneke Willemsen; Heribert Schunkert; Jeanette Erdmann; Nilesh J. Samani; Jaakko Kaprio; Lars Lind; Christian Gieger; Andres Metspalu; P. Eline Slagboom; Leif Groop; Cornelia M. van Duijn; Johan G. Eriksson; Antti Jula; Veikko Salomaa; Dorret I. Boomsma; Christopher Power; Olli T. Raitakari; Erik Ingelsson; Marjo‐Riitta Järvelin; Unnur Þorsteinsdóttir; Lude Franke; Elina Ikonen; Olli Kallioniemi; Vilja Pietiäinen; Cecilia M. Lindgren; Kari Stefansson; Aarno Palotie; Mark I. McCarthy; Andrew P. Morris; Inga Prokopenko; Samuli Ripatti

doi:10.1038/ng.3300

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

Ida Surakka(University of Helsinki), Momoko Horikoshi(Centre for Human Genetics), Reedik Mägi(University of Tartu), Antti‐Pekka Sarin(University of Helsinki), Anubha Mahajan(Centre for Human Genetics), Vasiliki Lagou(Centre for Human Genetics), Letizia Marullo(University of Ferrara), Teresa Ferreira(Centre for Human Genetics), Benjamin Miraglio(University of Helsinki), Sanna Timonen(University of Helsinki), Johannes Kettunen(University of Helsinki), Matti Pirinen(University of Helsinki), Juha Karjalainen(University Medical Center Groningen), Guðmar Þorleifsson(deCODE Genetics (Iceland)), Sara Hägg(Science for Life Laboratory), Jouke‐Jan Hottenga(Amsterdam Public Health), Aaron Isaacs(Erasmus MC), Claes Ladenvall(Lund University), Marian Beekman(Leiden University Medical Center), Tõnu Esko(Boston Children's Hospital), Janina S. Ried(Helmholtz Zentrum München), Christopher P. Nelson(University of Leicester), Christina Willenborg(Institute for Integrative and Experimental Genomics), Stefan Gustafsson(Science for Life Laboratory), Harm-Jan Westra(University Medical Center Groningen), Matthew Blades(Imperial College London), Anton J. M. de Craen(Leiden University Medical Center), Eco J. C. de Geus(Amsterdam Public Health), Joris Deelen(Leiden University Medical Center), Harald Grallert(Helmholtz Zentrum München), Anders Hamsten(Karolinska Institutet), Aki S. Havulinna(Finnish Institute for Health and Welfare), Christian Hengstenberg(German Centre for Cardiovascular Research), Jeanine J. Houwing‐Duistermaat(Leiden University Medical Center), Elina Hyppönen(University of South Australia), Lennart C. Karssen(Erasmus MC), Terho Lehtimäki(Tampere University), Valeriya Lyssenko(Steno Diabetes Centers), Patrik K. E. Magnusson(Karolinska Institutet), Evelin Mihailov(University of Tartu), Martina Müller‐Nurasyid(Helmholtz Zentrum München), John-Patrick Mpindi(University of Helsinki), Nancy L. Pedersen(Karolinska Institutet), Brenda W.J.H. Penninx(Amsterdam UMC Location Vrije Universiteit Amsterdam), Markus Perola(Institute for Molecular Medicine Finland), Tune H. Pers(Boston Children's Hospital), Annette Peters(Helmholtz Zentrum München), Johan Rung(European Bioinformatics Institute), Johannes H. Smit(Amsterdam UMC Location Vrije Universiteit Amsterdam), Valgerður Steinthórsdóttir(deCODE Genetics (Iceland)), Martin D. Tobin(University of Leicester), Natalia Tšernikova(University of Tartu), Elisabeth M van Leeuwen(Erasmus MC), Jorma Viikari(University of Turku), Sara M. Willems(Erasmus MC), Gonneke Willemsen(Amsterdam Public Health), Heribert Schunkert(German Centre for Cardiovascular Research), Jeanette Erdmann(Institute for Integrative and Experimental Genomics), Nilesh J. Samani(University of Leicester), Jaakko Kaprio(Finnish Institute for Health and Welfare), Lars Lind(Uppsala University Hospital), Christian Gieger(Helmholtz Zentrum München), Andres Metspalu(University of Tartu), P. Eline Slagboom(Leiden University Medical Center), Leif Groop(Lund University), Cornelia M. van Duijn(Erasmus MC), Johan G. Eriksson(Finnish Institute for Health and Welfare), Antti Jula(Finnish Institute for Health and Welfare), Veikko Salomaa(Finnish Institute for Health and Welfare), Dorret I. Boomsma(Amsterdam Public Health), Christopher Power(University College London), Olli T. Raitakari(University of Turku), Erik Ingelsson(Uppsala University), Marjo‐Riitta Järvelin(Oulu University Hospital), Unnur Þorsteinsdóttir(deCODE Genetics (Iceland)), Lude Franke(University Medical Center Groningen), Elina Ikonen(University of Helsinki), Olli Kallioniemi(University of Helsinki), Vilja Pietiäinen(University of Helsinki), Cecilia M. Lindgren(Broad Institute), Kari Stefansson(deCODE Genetics (Iceland)), Aarno Palotie(Broad Institute), Mark I. McCarthy(Centre for Human Genetics), Andrew P. Morris(Centre for Human Genetics), Inga Prokopenko(Hammersmith Hospital), Samuli Ripatti(University of Helsinki)

Nature Genetics

May 11, 2015

10.1038/ng.3300

Cited by 408Open Access

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