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Hits 1 – 3 of 3
1
The trans-ancestral genomic architecture of glycemic traits
Chen, J
;
Spracklen, CN
;
Marenne, G
. - : Nature Research, 2021
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2
The trans-ancestral genomic architecture of glycemic traits.
Chen, J
;
Spracklen, CN
;
Marenne, G
;
Varshney, A
;
Corbin, LJ
;
Luan, J
;
Willems, SM
;
Wu, Y
;
Zhang, X
;
Horikoshi, M
;
Boutin, TS
;
Mägi, R
;
Waage, J
;
Li-Gao, R
;
Chan, KHK
;
Yao, J
;
Anasanti, MD
;
Chu, AY
;
Claringbould, A
;
Heikkinen, J
;
Hong, J
;
Hottenga, J-J
;
Huo, S
;
Kaakinen, MA
;
Louie, T
;
März, W
;
Moreno-Macias, H
;
Ndungu, A
;
Nelson, SC
;
Nolte, IM
;
North, KE
;
Raulerson, CK
;
Ray, D
;
Rohde, R
;
Rybin, D
;
Schurmann, C
;
Sim, X
;
Southam, L
;
Stewart, ID
;
Wang, CA
;
Wang, Y
;
Wu, P
;
Zhang, W
;
Ahluwalia, TS
;
Appel, EVR
;
Bielak, LF
;
Brody, JA
;
Burtt, NP
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Cabrera, CP
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Cade, BE
;
Chai, JF
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Chai, X
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Chang, L-C
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Chen, C-H
;
Chen, BH
;
Chitrala, KN
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Chiu, Y-F
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de Haan, HG
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Delgado, GE
;
Demirkan, A
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Duan, Q
;
Engmann, J
;
Fatumo, SA
;
Gayán, J
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Giulianini, F
;
Gong, JH
;
Gustafsson, S
;
Hai, Y
;
Hartwig, FP
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He, J
;
Heianza, Y
;
Huang, T
;
Huerta-Chagoya, A
;
Hwang, MY
;
Jensen, RA
;
Kawaguchi, T
;
Kentistou, KA
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Kim, YJ
;
Kleber, ME
;
Kooner, IK
;
Lai, S
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Lange, LA
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Langefeld, CD
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Lauzon, M
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Li, M
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Ligthart, S
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Liu, J
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Loh, M
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Long, J
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Lyssenko, V
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Mangino, M
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Marzi, C
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Montasser, ME
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Nag, A
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Nakatochi, M
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Noce, D
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Noordam, R
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Pistis, G
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Preuss, M
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Raffield, L
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Rasmussen-Torvik, LJ
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Rich, SS
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Robertson, NR
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Rueedi, R
;
Ryan, K
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Sanna, S
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Saxena, R
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Schraut, KE
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Sennblad, B
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Setoh, K
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Smith, AV
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Sparsø, T
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Strawbridge, RJ
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Takeuchi, F
;
Tan, J
;
Trompet, S
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van den Akker, E
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van der Most, PJ
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Verweij, N
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Vogel, M
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Wang, H
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Wang, C
;
Wang, N
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Warren, HR
;
Wen, W
;
Wilsgaard, T
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Wong, A
;
Wood, AR
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Xie, T
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Zafarmand, MH
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Zhao, J-H
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Zhao, W
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Amin, N
;
Arzumanyan, Z
;
Astrup, A
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Bakker, SJL
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Baldassarre, D
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Beekman, M
;
Bergman, RN
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Bertoni, A
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Blüher, M
;
Bonnycastle, LL
;
Bornstein, SR
;
Bowden, DW
;
Cai, Q
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Campbell, A
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Campbell, H
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Chang, YC
;
de Geus, EJC
;
Dehghan, A
;
Du, S
;
Eiriksdottir, G
;
Farmaki, AE
;
Frånberg, M
;
Fuchsberger, C
;
Gao, Y
;
Gjesing, AP
;
Goel, A
;
Han, S
;
Hartman, CA
;
Herder, C
;
Hicks, AA
;
Hsieh, C-H
;
Hsueh, WA
;
Ichihara, S
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Igase, M
;
Ikram, MA
;
Johnson, WC
;
Jørgensen, ME
;
Joshi, PK
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Kalyani, RR
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Kandeel, FR
;
Katsuya, T
;
Khor, CC
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Kiess, W
;
Kolcic, I
;
Kuulasmaa, T
;
Kuusisto, J
;
Läll, K
;
Lam, K
;
Lawlor, DA
;
Lee, NR
;
Lemaitre, RN
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Li, H
;
Lifelines Cohort Study
;
Lin, S-Y
;
Lindström, J
;
Linneberg, A
;
Lorenzo, C
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Matsubara, T
;
Matsuda, F
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Mingrone, G
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Mooijaart, S
;
Moon, S
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Nabika, T
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Nadkarni, GN
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Nadler, JL
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Nelis, M
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Neville, MJ
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Norris, JM
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Ohyagi, Y
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Peters, A
;
Peyser, PA
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Polasek, O
;
Qi, Q
;
Raven, D
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Reilly, DF
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Reiner, A
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Rivideneira, F
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Roll, K
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Rudan, I
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Sabanayagam, C
;
Sandow, K
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Sattar, N
;
Schürmann, A
;
Shi, J
;
Stringham, HM
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Taylor, KD
;
Teslovich, TM
;
Thuesen, B
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Timmers, PRHJ
;
Tremoli, E
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Tsai, MY
;
Uitterlinden, A
;
van Dam, RM
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van Heemst, D
;
van Hylckama Vlieg, A
;
van Vliet-Ostaptchouk, JV
;
Vangipurapu, J
;
Vestergaard, H
;
Wang, T
;
Willems van Dijk, K
;
Zemunik, T
;
Abecasis, GR
;
Adair, LS
;
Aguilar-Salinas, CA
;
Alarcón-Riquelme, ME
;
An, P
;
Aviles-Santa, L
;
Becker, DM
;
Beilin, LJ
;
Bergmann, S
;
Bisgaard, H
;
Black, C
;
Boehnke, M
;
Boerwinkle, E
;
Böhm, BO
;
Bønnelykke, K
;
Boomsma, DI
;
Bottinger, EP
;
Buchanan, TA
;
Canouil, M
;
Caulfield, MJ
;
Chambers, JC
;
Chasman, DI
;
Chen, Y-DI
;
Cheng, C-Y
;
Collins, FS
;
Correa, A
;
Cucca, F
;
de Silva, HJ
;
Dedoussis, G
;
Elmståhl, S
;
Evans, MK
;
Ferrannini, E
;
Ferrucci, L
;
Florez, JC
;
Franks, PW
;
Frayling, TM
;
Froguel, P
;
Gigante, B
;
Goodarzi, MO
;
Gordon-Larsen, P
;
Grallert, H
;
Grarup, N
;
Grimsgaard, S
;
Groop, L
;
Gudnason, V
;
Guo, X
;
Hamsten, A
;
Hansen, T
;
Hayward, C
;
Heckbert, SR
;
Horta, BL
;
Huang, W
;
Ingelsson, E
;
James, PS
;
Jarvelin, M-R
;
Jonas, JB
;
Jukema, JW
;
Kaleebu, P
;
Kaplan, R
;
Kardia, SLR
;
Kato, N
;
Keinanen-Kiukaanniemi, SM
;
Kim, B-J
;
Kivimaki, M
;
Koistinen, HA
;
Kooner, JS
;
Körner, A
;
Kovacs, P
;
Kuh, D
;
Kumari, M
;
Kutalik, Z
;
Laakso, M
;
Lakka, TA
;
Launer, LJ
;
Leander, K
;
Lin, X
;
Lind, L
;
Lindgren, C
;
Liu, S
;
Loos, RJF
;
Magnusson, PKE
;
Mahajan, A
;
Metspalu, A
;
Mook-Kanamori, DO
;
Mori, TA
;
Munroe, PB
;
Njølstad, I
;
O'Connell, JR
;
Oldehinkel, AJ
;
Ong, KK
;
Padmanabhan, S
;
Palmer, CNA
;
Palmer, ND
;
Pedersen, O
;
Pennell, CE
;
Porteous, DJ
;
Pramstaller, PP
;
Province, MA
;
Psaty, BM
;
Qi, L
;
Raffel, LJ
;
Rauramaa, R
;
Redline, S
;
Ridker, PM
;
Rosendaal, FR
;
Saaristo, TE
;
Sandhu, M
;
Saramies, J
;
Schneiderman, N
;
Schwarz, P
;
Scott, LJ
;
Selvin, E
;
Sever, P
;
Shu, X-O
;
Slagboom, PE
;
Small, KS
;
Smith, BH
;
Snieder, H
;
Sofer, T
;
Sørensen, TIA
;
Spector, TD
;
Stanton, A
;
Steves, CJ
;
Stumvoll, M
;
Sun, L
;
Tabara, Y
;
Tai, ES
;
Timpson, NJ
;
Tönjes, A
;
Tuomilehto, J
;
Tusie, T
;
Uusitupa, M
;
van der Harst, P
;
van Duijn, C
;
Vitart, V
;
Vollenweider, P
;
Vrijkotte, TGM
;
Wagenknecht, LE
;
Walker, M
;
Wang, YX
;
Wareham, NJ
;
Watanabe, RM
;
Watkins, H
;
Wei, WB
;
Wickremasinghe, AR
;
Willemsen, G
;
Wilson, JF
;
Wong, T-Y
;
Wu, J-Y
;
Xiang, AH
;
Yanek, LR
;
Yengo, L
;
Yokota, M
;
Zeggini, E
;
Zheng, W
;
Zonderman, AB
;
Rotter, JI
;
Gloyn, AL
;
McCarthy, MI
;
Dupuis, J
;
Meigs, JB
;
Scott, RA
;
Prokopenko, I
;
Leong, A
;
Liu, C-T
;
Parker, SCJ
;
Mohlke, KL
;
Langenberg, C
;
Wheeler, E
;
Morris, AP
;
Barroso, I
;
Meta-Analysis of Glucose and Insulin-related Traits Consortium
(MAGIC). - 2021
Abstract:
Glycemic traits are used to diagnose and monitor type 2 diabetes and cardiometabolic health. To date, most genetic studies of glycemic traits have focused on individuals of European ancestry. Here we aggregated genome-wide association studies comprising up to 281,416 individuals without diabetes (30% non-European ancestry) for whom fasting glucose, 2-h glucose after an oral glucose challenge, glycated hemoglobin and fasting insulin data were available. Trans-ancestry and single-ancestry meta-analyses identified 242 loci (99 novel; P < 5 × 10-8), 80% of which had no significant evidence of between-ancestry heterogeneity. Analyses restricted to individuals of European ancestry with equivalent sample size would have led to 24 fewer new loci. Compared with single-ancestry analyses, equivalent-sized trans-ancestry fine-mapping reduced the number of estimated variants in 99% credible sets by a median of 37.5%. Genomic-feature, gene-expression and gene-set analyses revealed distinct biological signatures for each trait, highlighting different underlying biological pathways. Our results increase our understanding of diabetes pathophysiology by using trans-ancestry studies for improved power and resolution.
URL:
https://doi.org/10.1038/s41588-021-00852-9
https://qmro.qmul.ac.uk/xmlui/handle/123456789/72348
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3
The trans-ancestral genomic architecture of glycemic traits.
Chen, J.
;
Spracklen, C.N.
;
Marenne, G.
...
In: Nature genetics, vol. 53, no. 6, pp. 840-860 (2021)
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