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Genetic analyses of diverse populations improves discovery for complex traits.

Authors :
Wojcik, Genevieve
Wojcik, Genevieve
Graff, Mariaelisa
Nishimura, Katherine
Tao, Ran
Haessler, Jeffrey
Gignoux, Christopher
Highland, Heather
Patel, Yesha
Sorokin, Elena
Avery, Christy
Belbin, Gillian
Bien, Stephanie
Cheng, Iona
Cullina, Sinead
Hodonsky, Chani
Hu, Yao
Huckins, Laura
Jeff, Janina
Justice, Anne
Kocarnik, Jonathan
Lim, Unhee
Lin, Bridget
Lu, Yingchang
Nelson, Sarah
Park, Sung-Shim
Poisner, Hannah
Preuss, Michael
Richard, Melissa
Schurmann, Claudia
Setiawan, Veronica
Sockell, Alexandra
Vahi, Karan
Verbanck, Marie
Vishnu, Abhishek
Walker, Ryan
Young, Kristin
Zubair, Niha
Acuña-Alonso, Victor
Ambite, Jose
Barnes, Kathleen
Boerwinkle, Eric
Bottinger, Erwin
Bustamante, Carlos
Caberto, Christian
Canizales-Quinteros, Samuel
Conomos, Matthew
Deelman, Ewa
Do, Ron
Doheny, Kimberly
Fernández-Rhodes, Lindsay
Fornage, Myriam
Hailu, Benyam
Heiss, Gerardo
Hindorff, Lucia
Jackson, Rebecca
Laurie, Cecelia
Laurie, Cathy
Li, Yuqing
Lin, Dan-Yu
Moreno-Estrada, Andres
Nadkarni, Girish
Norman, Paul
Pooler, Loreall
Reiner, Alexander
Romm, Jane
Sabatti, Chiara
Sandoval, Karla
Sheng, Xin
Stahl, Eli
Stram, Daniel
Thornton, Timothy
Wassel, Christina
Wilkens, Lynne
Winkler, Cheryl
Yoneyama, Sachi
Buyske, Steven
Haiman, Christopher
Kooperberg, Charles
Le Marchand, Loic
Loos, Ruth
Matise, Tara
North, Kari
Peters, Ulrike
Kenny, Eimear
Carlson, Christopher
Henn, Brenna
Wojcik, Genevieve
Wojcik, Genevieve
Graff, Mariaelisa
Nishimura, Katherine
Tao, Ran
Haessler, Jeffrey
Gignoux, Christopher
Highland, Heather
Patel, Yesha
Sorokin, Elena
Avery, Christy
Belbin, Gillian
Bien, Stephanie
Cheng, Iona
Cullina, Sinead
Hodonsky, Chani
Hu, Yao
Huckins, Laura
Jeff, Janina
Justice, Anne
Kocarnik, Jonathan
Lim, Unhee
Lin, Bridget
Lu, Yingchang
Nelson, Sarah
Park, Sung-Shim
Poisner, Hannah
Preuss, Michael
Richard, Melissa
Schurmann, Claudia
Setiawan, Veronica
Sockell, Alexandra
Vahi, Karan
Verbanck, Marie
Vishnu, Abhishek
Walker, Ryan
Young, Kristin
Zubair, Niha
Acuña-Alonso, Victor
Ambite, Jose
Barnes, Kathleen
Boerwinkle, Eric
Bottinger, Erwin
Bustamante, Carlos
Caberto, Christian
Canizales-Quinteros, Samuel
Conomos, Matthew
Deelman, Ewa
Do, Ron
Doheny, Kimberly
Fernández-Rhodes, Lindsay
Fornage, Myriam
Hailu, Benyam
Heiss, Gerardo
Hindorff, Lucia
Jackson, Rebecca
Laurie, Cecelia
Laurie, Cathy
Li, Yuqing
Lin, Dan-Yu
Moreno-Estrada, Andres
Nadkarni, Girish
Norman, Paul
Pooler, Loreall
Reiner, Alexander
Romm, Jane
Sabatti, Chiara
Sandoval, Karla
Sheng, Xin
Stahl, Eli
Stram, Daniel
Thornton, Timothy
Wassel, Christina
Wilkens, Lynne
Winkler, Cheryl
Yoneyama, Sachi
Buyske, Steven
Haiman, Christopher
Kooperberg, Charles
Le Marchand, Loic
Loos, Ruth
Matise, Tara
North, Kari
Peters, Ulrike
Kenny, Eimear
Carlson, Christopher
Henn, Brenna
Source :
Nature; vol 570, iss 7762
Publication Year :
2019

Abstract

Genome-wide association studies (GWAS) have laid the foundation for investigations into the biology of complex traits, drug development and clinical guidelines. However, the majority of discovery efforts are based on data from populations of European ancestry1-3. In light of the differential genetic architecture that is known to exist between populations, bias in representation can exacerbate existing disease and healthcare disparities. Critical variants may be missed if they have a low frequency or are completely absent in European populations, especially as the field shifts its attention towards rare variants, which are more likely to be population-specific4-10. Additionally, effect sizes and their derived risk prediction scores derived in one population may not accurately extrapolate to other populations11,12. Here we demonstrate the value of diverse, multi-ethnic participants in large-scale genomic studies. The Population Architecture using Genomics and Epidemiology (PAGE) study conducted a GWAS of 26 clinical and behavioural phenotypes in 49,839 non-European individuals. Using strategies tailored for analysis of multi-ethnic and admixed populations, we describe a framework for analysing diverse populations, identify 27 novel loci and 38 secondary signals at known loci, as well as replicate 1,444 GWAS catalogue associations across these traits. Our data show evidence of effect-size heterogeneity across ancestries for published GWAS associations, substantial benefits for fine-mapping using diverse cohorts and insights into clinical implications. In the United States-where minority populations have a disproportionately higher burden of chronic conditions13-the lack of representation of diverse populations in genetic research will result in inequitable access to precision medicine for those with the highest burden of disease. We strongly advocate for continued, large genome-wide efforts in diverse populations to maximize genetic discovery and reduce health dis

Details

Database :
OAIster
Journal :
Nature; vol 570, iss 7762
Notes :
application/pdf, Nature vol 570, iss 7762
Publication Type :
Electronic Resource
Accession number :
edsoai.on1401032777
Document Type :
Electronic Resource