Browsing Centre for Genomics and Child Health by Author "Mahajan, A"
Now showing items 1-7 of 7
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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 ... -
Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci
Thurner, M; van de Bunt, M; Torres, JM; Mahajan, A; Nylander, V; Bennett, AJ; Gaulton, KJ; Barrett, A; Burrows, C; Bell, CG (2018-02-07) -
Mapping the human genetic architecture of COVID-19
Niemi, MEK; Karjalainen, J; Daly, M; Ganna, A; Mehtonen, J; Cordioli, M; Kaunisto, M; Pigazzini, S; Donner, K; Kivinen, K (2021) -
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)