Accès ouvert
2026
article
OpenAlex
Alicia Huerta‐Chagoya, Joohyun Kim, Ravi Mandla, Yingchang Lu et autres
BACKGROUND: Polygenic risk scores (PRSs) improve prediction of the development of type 2 diabetes over the use of clinical risk factors alone; however, they perform poorly in populations of non-European ancestry, limiting their global clinical utility. We aimed to deliver comprehensive and …
us, gb, jp, sg, kr, mx, si, ca, cn, de, in, tw, lk, bd, fr
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Accès ouvert
2024
article
OpenAlex
Véronique Vitart, Stefan Weiß, Jeanette Erdmann, Kristian Hveem et autres
us
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Accès ouvert
2024
article
OpenAlex
Victor Lim, Donald W. Bowden, Ko Willems van Dijk, Lars Lind et autres
us
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Accès ouvert
2024
erratum
OpenAlex
Jirong Long, Ketian Yu, Alaitz Poveda, Shweta Ramdas et autres
us
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Accès ouvert
2024
article
OpenAlex
Jette Bork‐Jensen, Joel N. Hirschhorn, Zoltán Kutalik, Sanni Ruotsalainen et autres
us
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Accès ouvert
2024
article
OpenAlex
Ken Suzuki, Konstantinos Hatzikotoulas, Lorraine Southam, Henry J. Taylor et autres
Abstract Type 2 diabetes (T2D) is a heterogeneous disease that develops through diverse pathophysiological processes 1,2 and molecular mechanisms that are often specific to cell type 3,4 . Here, to characterize the genetic contribution to these processes across ancestry groups, we aggregate …
gb, jp, de, us, cn, ee, kr, ca, sg, is, dk, nl, in, hk, tw, ir, se, mx, fr
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Accès ouvert
2023
erratum
OpenAlex
Sarah E. Graham, Shoa L. Clarke, Kuan-Han H. Wu, Stavroula Kanoni et autres
us, gb, de, kr, jp, Afrique du Sud, is, no, fi, qa, pk, se, nl, cn, sg, dk, es, it, ch
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Accès ouvert
2023
preprint
OpenAlex
Ken Suzuki, Konstantinos Hatzikotoulas, Lorraine Southam, Henry J. Taylor et autres
Type 2 diabetes (T2D) is a heterogeneous disease that develops through diverse pathophysiological processes. To characterise the genetic contribution to these processes across ancestry groups, we aggregate genome-wide association study (GWAS) data from 2,535,601 individuals (39.7% non-European ancestry), including 428,452 T2D cases. …
gb, jp, de, us, cn, mx, ee, kr, ca, sg, is, dk, nl, in, hk, tw, ir, fr, lk
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Accès ouvert
2022
article
OpenAlex
Stavroula Kanoni, Sarah E. Graham, Yuxuan Wang, Ida L. Surakka et autres
BACKGROUND: Genetic variants within nearly 1000 loci are known to contribute to modulation of blood lipid levels. However, the biological pathways underlying these associations are frequently unknown, limiting understanding of these findings and hindering downstream translational efforts such as drug target discovery. …
gb, us, cn, de, is, kr, jp, no, fi, pk, qa, Afrique du Sud, se, nl, Égypte, sg, dk, tw, es, it
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Accès ouvert
2022
article
OpenAlex
Shweta Ramdas, Jonathan Judd, Sarah E. Graham, Stavroula Kanoni et autres
us, gb, cn, de, is, kr, jp, no, fi, pk, qa, Afrique du Sud, se, nl, sg, dk, tw, es
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2022
article
OpenAlex
Anubha Mahajan, Cassandra Nichole Spracklen, Weihua Zhang, Maggie C. Y. Ng et autres
), which were delineated to 338 distinct association signals. Fine-mapping of these signals was enhanced by the increased sample size and expanded population diversity of the multi-ancestry meta-analysis, which localized 54.4% of T2D associations to a single variant with >50% posterior probability. …
gb, fr, us, jp, fi, kr, de, sg, es, nl, ca, mx, is, ee, dk, in, hk, cn, tw
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Accès ouvert
2021
preprint
OpenAlex
Stavroula Kanoni, Sarah E. Graham, Yuxuan Wang, Ida L. Surakka et autres
ABSTRACT Genetic variants within nearly 1,000 loci are known to contribute to modulation of blood lipid levels. However, the biological pathways underlying these associations are frequently unknown, limiting understanding of these findings and hindering downstream translational efforts such as drug target discovery. …
gb, us, de, is, kr, jp, no, fi, pk, qa, Afrique du Sud, se, nl, cn, sg, dk, tw, es, it
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