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Markus Perola

Finnish Institute for Health and Welfare
H指数:138
被引数:9.3万

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Low prevalence of CWH43 variants among Finnish and Norwegian idiopathic normal pressure hydrocephalus patients: a cohort-based observational study
2025-02-130
OAAI
Risk Variants Associated With Normal Pressure Hydrocephalus Genome-Wide Association Study in the FinnGen Cohort
2024-09-102
OAAI
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction

不宁腿综合征的全基因组荟萃分析可深入了解遗传结构,疾病生物学和风险预测

2024-06-053
OAAI
Markers of imminent myocardial infarction
2024-02-123
OAAI
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements

X染色体和肾功能: 来自908,697个体的多性状遗传分析的证据揭示了雄激素反应元件调节的基因中的性别特异性和性别差异发现

2024-01-184
OAAI
Risk factors for severe respiratory syncytial virus infection during the first year of life: development and validation of a clinical prediction model
2023-11-0111
OAAI
A FinnGen pilot clinical recall study for Alzheimer's disease
2023-08-031
OAAI