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Philip R. Jansen

vu amsterdam
H指数:34
被引数:1.1万

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Genetic testing of common and rare variants in dementia patients from a memory clinic

痴呆患者中常见和罕见变异的遗传检测:来自记忆诊所的研究

2025-10-150
OAAI
Genome-Wide Analyses of Vocabulary Size in Infancy and Toddlerhood: Associations With Attention-De fi cit/Hyperactivity Disorder, Literacy, and Cognition-Related Traits

婴儿期和学步期词汇量的全基因组分析: 与注意力/多动症,识字和认知相关特征的关联

2024-05-013
OAAI
Clinical and functional heterogeneity associated with the disruption of retinoic acid receptor beta
2023-08-014
OAAI
Genetic Burden of TNNI3K in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular Arrhythmias

TNNI3K在扩张型心肌病和室上性心律失常患者诊断测试中的遗传负担

2023-08-013
OAAI
Correspondence on Frequency of truncating FLCN variants and Birt-Hogg-Dub acute accent e-associated phenotypes in a health care system population by Savatt et al

Savatt等人在医疗保健系统人群中截断FLCN变体和birt-hogg-dub急性重音e相关表型的频率的对应关系

2023-01-012
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
Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis

通过全基因组关联研究荟萃分析揭示广泛反社会行为的遗传结构

2022-10-2524
OA
The phenotypic spectrum and genotype-phenotype correlations in 106 patients with variants in major autism gene CHD8

主要自闭症基因CHD8变异的106患者的表型谱和基因型-表型相关性

2022-10-0116
OAAI
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

对多达34,000人的阅读和语言相关技能进行定量评估的个体差异的全基因组分析

2022-08-2346
OA
Genetic variants associated with longitudinal changes in brain structure across the lifespan

与整个生命周期中脑结构纵向变化相关的遗传变异

2022-04-050
PREAI