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New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries

Shrine, Nick; Guyatt, Anna L.; Erzurumluoglu, A. Mesut; Jackson, Victoria E.; Hobbs, Brian D.; Melbourne, Carl A.; Batini, Chiara; Fawcett, Katherine A.; Song, Kijoung; Sakornsakolpat, Phuwanat; Li, Xingnan; Boxall, Ruth; Reeve, Nicola F.; Obeidat, Ma'en; Zhao, Jing Hua; Wielscher, Matthias; Weiss, Stefan; Kentistou, Katherine A.; Cook, James P.; Sun, Benjamin B.; Zhou, Jian; Hui, Jennie; Karrasch, Stefan; Imboden, Medea; Harris, Sarah E.; Marten, Jonathan; Enroth, Stefan; Kerr, Shona M.; Surakka, Ida; Vitart, Veronique; Lehtimäki, Terho; Allen, Richard J.; Bakke, Per S.; Beaty, Terri H.; Bleecker, Eugene R.; Bosse, Yohan; Brandsma, Corry-Anke; Chen, Zhengming; Crapo, James D.; Danesh, John; DeMeo, Dawn L.; Dudbridge, Frank; Ewert, Ralf; Gieger, Christian; Gulsvik, Amund; Hansell, Anna L.; Hao, Ke; Hoffman, Joshua D.; Hokanson, John E.; Homuth, Georg; Joshi, Peter K.; Joubert, Philippe; Langenberg, Claudia; Li, Xuan; Li, Liming; Lin, Kuang; Lind, Lars; Locantore, Nicholas; Luan, Jian'an; Mahajan, Anubha; Maranville, Joseph C.; Murray, Alison; Nickle, David C.; Packer, Richard; Parker, Margaret M.; Paynton, Megan L.; Porteous, David J.; Prokopenko, Dmitry; Qiao, Dandi; Rawal, Rajesh; Runz, Heiko; Sayers, Ian; Sin, Don D.; Smith, Blair H.; Artigas, Maria Soler; Sparrow, David; Tal-Singer, Ruth; Timmers, Paul R. H. J.; Van den Berge, Maarten; Whittaker, John C.; Woodruff, Prescott G.; Verges-Armstrong, Laura M.; Troyanskaya, Olga G.; Raitakari, Olli T.; Kähönen, Mika; Polasek, Ozren; Gyllensten, Ulf; Rudan, Igor; Deary, Ian J.; Probst-Hensch, Nicole M.; Schulz, Holger; James, Alan L.; Wilson, James F.; Stubbe, Beate; Zeggini, Eleftheria; Järvelin, Marjo-Riitta; Wareham, Nick; Silverman, Edwin K.; Hayward, Caroline; Morris, Andrew P.; Butterworth, Adam S.; Scott, Robert A.; Walters, Robin G.; Meyers, Deborah A.; Cho, Michael H.; Strachan, David P.; Hall, Ian P.; Tobin, Martin D.; Wain, Louise, V (2019-02-25)

 
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URL:
https://doi.org/10.1038/s41588-018-0321-7

Shrine, Nick
Guyatt, Anna L.
Erzurumluoglu, A. Mesut
Jackson, Victoria E.
Hobbs, Brian D.
Melbourne, Carl A.
Batini, Chiara
Fawcett, Katherine A.
Song, Kijoung
Sakornsakolpat, Phuwanat
Li, Xingnan
Boxall, Ruth
Reeve, Nicola F.
Obeidat, Ma'en
Zhao, Jing Hua
Wielscher, Matthias
Weiss, Stefan
Kentistou, Katherine A.
Cook, James P.
Sun, Benjamin B.
Zhou, Jian
Hui, Jennie
Karrasch, Stefan
Imboden, Medea
Harris, Sarah E.
Marten, Jonathan
Enroth, Stefan
Kerr, Shona M.
Surakka, Ida
Vitart, Veronique
Lehtimäki, Terho
Allen, Richard J.
Bakke, Per S.
Beaty, Terri H.
Bleecker, Eugene R.
Bosse, Yohan
Brandsma, Corry-Anke
Chen, Zhengming
Crapo, James D.
Danesh, John
DeMeo, Dawn L.
Dudbridge, Frank
Ewert, Ralf
Gieger, Christian
Gulsvik, Amund
Hansell, Anna L.
Hao, Ke
Hoffman, Joshua D.
Hokanson, John E.
Homuth, Georg
Joshi, Peter K.
Joubert, Philippe
Langenberg, Claudia
Li, Xuan
Li, Liming
Lin, Kuang
Lind, Lars
Locantore, Nicholas
Luan, Jian'an
Mahajan, Anubha
Maranville, Joseph C.
Murray, Alison
Nickle, David C.
Packer, Richard
Parker, Margaret M.
Paynton, Megan L.
Porteous, David J.
Prokopenko, Dmitry
Qiao, Dandi
Rawal, Rajesh
Runz, Heiko
Sayers, Ian
Sin, Don D.
Smith, Blair H.
Artigas, Maria Soler
Sparrow, David
Tal-Singer, Ruth
Timmers, Paul R. H. J.
Van den Berge, Maarten
Whittaker, John C.
Woodruff, Prescott G.
Verges-Armstrong, Laura M.
Troyanskaya, Olga G.
Raitakari, Olli T.
Kähönen, Mika
Polasek, Ozren
Gyllensten, Ulf
Rudan, Igor
Deary, Ian J.
Probst-Hensch, Nicole M.
Schulz, Holger
James, Alan L.
Wilson, James F.
Stubbe, Beate
Zeggini, Eleftheria
Järvelin, Marjo-Riitta
Wareham, Nick
Silverman, Edwin K.
Hayward, Caroline
Morris, Andrew P.
Butterworth, Adam S.
Scott, Robert A.
Walters, Robin G.
Meyers, Deborah A.
Cho, Michael H.
Strachan, David P.
Hall, Ian P.
Tobin, Martin D.
Wain, Louise, V
Springer Nature
25.02.2019

Shrine, N., Guyatt, A. L., Erzurumluoglu, A. M., Jackson, V. E., Hobbs, B. D., … Wain, L. V. (2019). New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. Nature Genetics, 51(3), 481–493. https://doi.org/10.1038/s41588-018-0321-7

https://rightsstatements.org/vocab/InC/1.0/
© The Author(s), under exclusive licence to Springer Nature America, Inc. 2019. Published in this repository with the kind permission of the publisher.
https://rightsstatements.org/vocab/InC/1.0/
doi:https://doi.org/10.1038/s41588-018-0321-7
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Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi-fe2019091928792
Tiivistelmä

Abstract

Reduced lung function predicts mortality and is key to the diagnosis of chronic obstructive pulmonary disease (COPD). In a genome-wide association study in 400,102 individuals of European ancestry, we define 279 lung function signals, 139 of which are new. In combination, these variants strongly predict COPD in independent populations. Furthermore, the combined effect of these variants showed generalizability across smokers and never smokers, and across ancestral groups. We highlight biological pathways, known and potential drug targets for COPD and, in phenome-wide association studies, autoimmune-related and other pleiotropic effects of lung function–associated variants. This new genetic evidence has potential to improve future preventive and therapeutic strategies for COPD.

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