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Updated: Jan 8, 2026

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异常新生儿动脉缺血性中风:一个基于三组的全外体序列测序研究

Jonathan Olival1, Janet Hoenicka1,2, Gemma Arca3,4

  • 1Laboratory of Neurogenetics and Genomic Medicine, Center for Genomic Sciences in Medicine, Institut de Recerca Sant Joan de Déu and Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain.

Archives of disease in childhood. Fetal and neonatal edition
|December 18, 2025
PubMed
概括

罕见的遗传变异似乎不会导致异常新生儿动脉缺血性中风 (NAIS). 整体外因子测序发现没有共同的遗传原因,这表明其他因素可能参与NAIS.

关键词:
遗传学 遗传学 是一个分子生物学分子生物学新生儿科学 新生儿科学儿科 儿科 儿科

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Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
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