Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

Common genetic variants associated with plasma lipids have been extensively studied for a better understanding of common diseases. Here, the authors use whole-genome sequencing of 16,324 individuals to analyze rare variant associations and to determine their monogenic and polygenic contribution to l...

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Autores principales: Pradeep Natarajan, Gina M. Peloso, Seyedeh Maryam Zekavat, May Montasser, Andrea Ganna, Mark Chaffin, Amit V. Khera, Wei Zhou, Jonathan M. Bloom, Jesse M. Engreitz, Jason Ernst, Jeffrey R. O’Connell, Sanni E. Ruotsalainen, Maris Alver, Ani Manichaikul, W. Craig Johnson, James A. Perry, Timothy Poterba, Cotton Seed, Ida L. Surakka, Tonu Esko, Samuli Ripatti, Veikko Salomaa, Adolfo Correa, Ramachandran S. Vasan, Manolis Kellis, Benjamin M. Neale, Eric S. Lander, Goncalo Abecasis, Braxton Mitchell, Stephen S. Rich, James G. Wilson, L. Adrienne Cupples, Jerome I. Rotter, Cristen J. Willer, Sekar Kathiresan, NHLBI TOPMed Lipids Working Group
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Lenguaje:EN
Publicado: Nature Portfolio 2018
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Acceso en línea:https://doaj.org/article/9e3763d9201a473097a59d1dfd1ef3d8
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spelling oai:doaj.org-article:9e3763d9201a473097a59d1dfd1ef3d82021-12-02T14:40:08ZDeep-coverage whole genome sequences and blood lipids among 16,324 individuals10.1038/s41467-018-05747-82041-1723https://doaj.org/article/9e3763d9201a473097a59d1dfd1ef3d82018-08-01T00:00:00Zhttps://doi.org/10.1038/s41467-018-05747-8https://doaj.org/toc/2041-1723Common genetic variants associated with plasma lipids have been extensively studied for a better understanding of common diseases. Here, the authors use whole-genome sequencing of 16,324 individuals to analyze rare variant associations and to determine their monogenic and polygenic contribution to lipid traits.Pradeep NatarajanGina M. PelosoSeyedeh Maryam ZekavatMay MontasserAndrea GannaMark ChaffinAmit V. KheraWei ZhouJonathan M. BloomJesse M. EngreitzJason ErnstJeffrey R. O’ConnellSanni E. RuotsalainenMaris AlverAni ManichaikulW. Craig JohnsonJames A. PerryTimothy PoterbaCotton SeedIda L. SurakkaTonu EskoSamuli RipattiVeikko SalomaaAdolfo CorreaRamachandran S. VasanManolis KellisBenjamin M. NealeEric S. LanderGoncalo AbecasisBraxton MitchellStephen S. RichJames G. WilsonL. Adrienne CupplesJerome I. RotterCristen J. WillerSekar KathiresanNHLBI TOPMed Lipids Working GroupNature PortfolioarticleScienceQENNature Communications, Vol 9, Iss 1, Pp 1-12 (2018)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Pradeep Natarajan
Gina M. Peloso
Seyedeh Maryam Zekavat
May Montasser
Andrea Ganna
Mark Chaffin
Amit V. Khera
Wei Zhou
Jonathan M. Bloom
Jesse M. Engreitz
Jason Ernst
Jeffrey R. O’Connell
Sanni E. Ruotsalainen
Maris Alver
Ani Manichaikul
W. Craig Johnson
James A. Perry
Timothy Poterba
Cotton Seed
Ida L. Surakka
Tonu Esko
Samuli Ripatti
Veikko Salomaa
Adolfo Correa
Ramachandran S. Vasan
Manolis Kellis
Benjamin M. Neale
Eric S. Lander
Goncalo Abecasis
Braxton Mitchell
Stephen S. Rich
James G. Wilson
L. Adrienne Cupples
Jerome I. Rotter
Cristen J. Willer
Sekar Kathiresan
NHLBI TOPMed Lipids Working Group
Deep-coverage whole genome sequences and blood lipids among 16,324 individuals
description Common genetic variants associated with plasma lipids have been extensively studied for a better understanding of common diseases. Here, the authors use whole-genome sequencing of 16,324 individuals to analyze rare variant associations and to determine their monogenic and polygenic contribution to lipid traits.
format article
author Pradeep Natarajan
Gina M. Peloso
Seyedeh Maryam Zekavat
May Montasser
Andrea Ganna
Mark Chaffin
Amit V. Khera
Wei Zhou
Jonathan M. Bloom
Jesse M. Engreitz
Jason Ernst
Jeffrey R. O’Connell
Sanni E. Ruotsalainen
Maris Alver
Ani Manichaikul
W. Craig Johnson
James A. Perry
Timothy Poterba
Cotton Seed
Ida L. Surakka
Tonu Esko
Samuli Ripatti
Veikko Salomaa
Adolfo Correa
Ramachandran S. Vasan
Manolis Kellis
Benjamin M. Neale
Eric S. Lander
Goncalo Abecasis
Braxton Mitchell
Stephen S. Rich
James G. Wilson
L. Adrienne Cupples
Jerome I. Rotter
Cristen J. Willer
Sekar Kathiresan
NHLBI TOPMed Lipids Working Group
author_facet Pradeep Natarajan
Gina M. Peloso
Seyedeh Maryam Zekavat
May Montasser
Andrea Ganna
Mark Chaffin
Amit V. Khera
Wei Zhou
Jonathan M. Bloom
Jesse M. Engreitz
Jason Ernst
Jeffrey R. O’Connell
Sanni E. Ruotsalainen
Maris Alver
Ani Manichaikul
W. Craig Johnson
James A. Perry
Timothy Poterba
Cotton Seed
Ida L. Surakka
Tonu Esko
Samuli Ripatti
Veikko Salomaa
Adolfo Correa
Ramachandran S. Vasan
Manolis Kellis
Benjamin M. Neale
Eric S. Lander
Goncalo Abecasis
Braxton Mitchell
Stephen S. Rich
James G. Wilson
L. Adrienne Cupples
Jerome I. Rotter
Cristen J. Willer
Sekar Kathiresan
NHLBI TOPMed Lipids Working Group
author_sort Pradeep Natarajan
title Deep-coverage whole genome sequences and blood lipids among 16,324 individuals
title_short Deep-coverage whole genome sequences and blood lipids among 16,324 individuals
title_full Deep-coverage whole genome sequences and blood lipids among 16,324 individuals
title_fullStr Deep-coverage whole genome sequences and blood lipids among 16,324 individuals
title_full_unstemmed Deep-coverage whole genome sequences and blood lipids among 16,324 individuals
title_sort deep-coverage whole genome sequences and blood lipids among 16,324 individuals
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/9e3763d9201a473097a59d1dfd1ef3d8
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