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P

Pui-Yan Kwok

Academia Sinica
H指数:89
被引数:3.0万

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The Taiwan Precision Medicine Initiative provides a cohort for large-scale studies

台湾精准医学计划提供了一个队列用于大规模研究

Nature
IF48.5
2025-10-150
PRE
Population-specific polygenic risk scores for people of Han Chinese ancestry

汉族人群特异的多基因风险评分

Nature
IF48.5
2025-10-150
OAAI
Clinical impact of pharmacogenetic risk variants in a large chinese cohort

Wei, C.-Y.; Wen, M.-S.; Cheng, C.-K.; Sheen, Y.-J.; Yao, T.-C.; Lee, S.-L.; Wu, J.-Y.; Tsai, M.-F.; Li, L.-H.; Chen, C.; et al. 药物基因组学风险变异在一个大型中国人群中的临床影响。Nat. Commun. 2025, 16, 6344. [Google Scholar] [CrossRef]

2025-07-090
OAAI
Polygenic height prediction for the Han Chinese in Taiwan

台湾汉族多基因身高预测

2025-02-050
OA
CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods

CAGI,基因组解释的关键评估,建立了计算遗传变异解释方法的进展和前景

2024-02-2210
OAAI
South Asian medical cohorts reveal strong founder effects and high rates of homozygosity
2023-06-088
OAAI
Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia
2022-06-012
OAAI
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder (Jan, 10.1038/s41380-020-01006-9, 2021)
2021-03-050
OAAI
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder
2021-01-2214
OAAI
A Large-Scale Association Study Detects Novel Rare Variants, Risk Genes, Functional Elements, and Polygenic Architecture of Prostate Cancer Susceptibility
2020-12-0815
OAAI
Towards a reference genome that captures global genetic diversity

迈向捕获全球遗传多样性的参考基因组

2020-10-3028
OAAI
The role of exome sequencing in newborn screening for inborn errors of metabolism
2020-08-10137
OAAI