Browsing Centre for Genomics and Child Health by Author "Luan, J"
Now showing items 1-8 of 8
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Associations of autozygosity with a broad range of human phenotypes
Clark, DW; Okada, Y; Moore, KHS; Mason, D; Pirastu, N; Gandin, I; Mattsson, H; Barnes, CLK; Lin, K; Zhao, JH (2019-10-31) -
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology.
Suzuki, K; Hatzikotoulas, K; Southam, L; Taylor, HJ; Yin, X; Lorenz, KM; Mandla, R; Huerta-Chagoya, A; Melloni, GEM; Kanoni, S (Nature Research, 2024-02-19)Type 2 diabetes (T2D) is a heterogeneous disease that develops through diverse pathophysiological processes1,2 and molecular mechanisms that are often specific to cell type3,4. Here, to characterize the genetic contribution ... -
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Lu, Y; Day, FR; Gustafsson, S; Buchkovich, ML; Na, J; Bataille, V; Cousminer, DL; Dastani, Z; Drong, AW; Esko, T (2016-02) -
The power of genetic diversity in genome-wide association studies of lipids
Graham, SE; Clarke, SL; Wu, K-HH; Kanoni, S; Zajac, GJM; Ramdas, S; Surakka, I; Ntalla, I; Vedantam, S; Winkler, TW (2021) -
The power of genetic diversity in genome-wide association studies of lipids (vol 600, pg 675, 2021)
Graham, SE; Clarke, SL; Wu, K-HH; Kanoni, S; Zajac, GJM; Ramdas, S; Surakka, I; Ntalla, I; Vedantam, S; Winkler, TW (2023) -
Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis
Yang, Y; van der Klaauw, AA; Zhu, L; Cacciottolo, TM; He, Y; Stadler, LKJ; Wang, C; Xu, P; Saito, K; Hinton, A (2019-04-12) -
The UK10K project identifies rare variants in health and disease
Walter, K; Min, JL; Huang, J; Crooks, L; Memari, Y; McCarthy, S; Perry, JRB; Xu, C; Futema, M; Lawson, D (2015-10-01) -
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits
Tachmazidou, I; Suveges, D; Min, JL; Ritchie, GRS; Steinberg, J; Walter, K; Iotchkova, V; Schwartzentruber, J; Huang, J; Memari, Y (2017-06-01)