The UK10K project identifies rare variants in health and disease

UK10K Consortium, UCLEB Consortium

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

Originalspråkengelska
TidskriftNature
Volym526
Utgåva7571
Sidor (från-till)82-+
Antal sidor21
ISSN0028-0836
DOI
StatusPublicerad - 1 okt 2015
MoE-publikationstypA1 Tidskriftsartikel-refererad

Bibliografisk information

M. Kivimäki työryhmäjäsen.
Volume:
Proceeding volume:

Vetenskapsgrenar

  • 3141 Hälsovetenskap

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UK10K Consortium ; UCLEB Consortium. / The UK10K project identifies rare variants in health and disease. I: Nature. 2015 ; Vol. 526, Nr. 7571. s. 82-+.
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title = "The UK10K project identifies rare variants in health and disease",
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author = "Klaudia Walter and Min, {Josine L.} and Jie Huang and Lucy Crooks and Yasin Memari and Shane McCarthy and Perry, {John R. B.} and ChangJiang Xu and Marta Futema and Daniel Lawson and Valentina Iotchkova and Stephan Schiffels and Hendricks, {Audrey E.} and Petr Danecek and Rui Li and James Floyd and Wain, {Louise V.} and Ines Barroso and Humphries, {Steve E.} and Hurles, {Matthew E.} and Eleftheria Zeggini and Barrett, {Jeffrey C.} and Vincent Plagnol and Richards, {J. Brent} and Greenwood, {Celia M. T.} and Timpson, {Nicholas J.} and Richard Durbin and Nicole Soranzo and Senduran Bala and Peter Clapham and Guy Coates and Tony Cox and Allan Daly and Petr Danecek and Yuanping Du and Richard Durbin and Sarah Edkins and Peter Ellis and Paul Flicek and Xiaosen Guo and Xueqin Guo and Liren Huang and Jackson, {David K.} and Chris Joyce and Thomas Keane and Anja Kolb-Kokocinski and Tiina Paunio and Olli Pietil{\"a}inen and Aarno Palotie and {UK10K Consortium} and {UCLEB Consortium} and Mika Kivim{\"a}ki",
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UK10K Consortium & UCLEB Consortium 2015, 'The UK10K project identifies rare variants in health and disease', Nature, vol. 526, nr. 7571, s. 82-+. https://doi.org/10.1038/nature14962

The UK10K project identifies rare variants in health and disease. / UK10K Consortium; UCLEB Consortium.

I: Nature, Vol. 526, Nr. 7571, 01.10.2015, s. 82-+.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

TY - JOUR

T1 - The UK10K project identifies rare variants in health and disease

AU - Walter, Klaudia

AU - Min, Josine L.

AU - Huang, Jie

AU - Crooks, Lucy

AU - Memari, Yasin

AU - McCarthy, Shane

AU - Perry, John R. B.

AU - Xu, ChangJiang

AU - Futema, Marta

AU - Lawson, Daniel

AU - Iotchkova, Valentina

AU - Schiffels, Stephan

AU - Hendricks, Audrey E.

AU - Danecek, Petr

AU - Li, Rui

AU - Floyd, James

AU - Wain, Louise V.

AU - Barroso, Ines

AU - Humphries, Steve E.

AU - Hurles, Matthew E.

AU - Zeggini, Eleftheria

AU - Barrett, Jeffrey C.

AU - Plagnol, Vincent

AU - Richards, J. Brent

AU - Greenwood, Celia M. T.

AU - Timpson, Nicholas J.

AU - Durbin, Richard

AU - Soranzo, Nicole

AU - Bala, Senduran

AU - Clapham, Peter

AU - Coates, Guy

AU - Cox, Tony

AU - Daly, Allan

AU - Danecek, Petr

AU - Du, Yuanping

AU - Durbin, Richard

AU - Edkins, Sarah

AU - Ellis, Peter

AU - Flicek, Paul

AU - Guo, Xiaosen

AU - Guo, Xueqin

AU - Huang, Liren

AU - Jackson, David K.

AU - Joyce, Chris

AU - Keane, Thomas

AU - Kolb-Kokocinski, Anja

AU - Paunio, Tiina

AU - Pietiläinen, Olli

AU - Palotie, Aarno

AU - UK10K Consortium

AU - UCLEB Consortium

AU - Kivimäki, Mika

N1 - M. Kivimäki työryhmäjäsen. Volume: Proceeding volume:

PY - 2015/10/1

Y1 - 2015/10/1

KW - GENOME-WIDE ASSOCIATION

KW - OF-FUNCTION MUTATIONS

KW - LOW-FREQUENCY

KW - INCIDENTAL FINDINGS

KW - SEQUENCE VARIATION

KW - COMPLEX TRAITS

KW - POPULATION

KW - COMMON

KW - HERITABILITY

KW - APOC3

KW - 3141 Health care science

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SP - 82-+

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