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Zdenka Pausová

University of Toronto
H指数:72
被引数:2.3万

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Genetic risk factors underlying white matter hyperintensities and cortical atrophy

白质高信号和皮质萎缩的遗传危险因素

2024-11-040
OAAI
Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability

拷贝数变异和智力的多基因风险赋予自闭症谱系障碍的风险,而不管它们对认知能力的影响如何

2024-05-010
OAAI
Beyond the Global Brain Differences: Intraindividual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion Carriers

超越全局大脑差异: 1 q21.1远端和15 q11.2 BP1-BP2缺失携带者的个体内变异性差异

2024-01-010
OAAI
Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

假设驱动的全基因组关联研究为阅读障碍的遗传学提供了新的见解

2022-11-297
OAAI
Intake of mother's milk by very-low-birth-weight infants and variation in DNA methylation of genes involved in neurodevelopment at 5.5 years of age

极低出生体重婴儿的母乳摄入量和5.5岁时参与神经发育的基因的DNA甲基化变化

2022-10-017
OAAI