Browsing Centre for Genomics and Child Health by Author "Ntalla, I"
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Association analyses based on false discovery rate implicate new loci for coronary artery disease
Nelson, CP; Goel, A; Butterworth, AS; Kanoni, S; Webb, TR; Marouli, E; Zeng, L; Ntalla, I; Lai, FY; Hopewell, JC (2017-09) -
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 ... -
Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease.
Williams, AT; Chen, J; Coley, K; Batini, C; Izquierdo, A; Packer, R; Abner, E; Kanoni, S; Shepherd, DJ; Free, RC (2023-10-23)Thyroid hormones play a critical role in regulation of multiple physiological functions and thyroid dysfunction is associated with substantial morbidity. Here, we use electronic health records to undertake a genome-wide ... -
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) -
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)