Vasiliki Lagou
Leuven, VLG, Belgium
Last Updated: 09/26/2026
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Found 48 publications
Impact of flavan-3-ols on blood pressure and endothelial function in diverse populations: a systematic review and meta-analysis of randomized controlled trials.
Journal: European journal of preventive cardiology
Published: November 11, 2024
Machine Learning to Advance Human Genome-Wide Association Studies.
Journal: Genes
Published: November 16, 2023
Homozygous DBF4 mutation as a cause of severe congenital neutropenia.
Journal: The Journal of allergy and clinical immunology
Published: September 08, 2022
Astrocyte-targeted gene delivery of interleukin 2 specifically increases brain-resident regulatory T cell numbers and protects against pathological neuroinflammation.
Journal: Nature immunology
Published: March 01, 2022
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention.
Journal: Nature genetics
Published: November 30, 2021
Integrative genomic analyses in adipocytes implicate DNA methylation in human obesity and diabetes.
Journal: Nature communications
Published: October 13, 2021
GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification.
Journal: Nature genetics
Published: September 18, 2021
Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Journal: Nature communications
Published: February 09, 2021
Author Correction: The cellular composition of the human immune system is shaped by age and cohabitation.
Journal: Nature immunology
Published: November 26, 2020
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Journal: Nature communications
Published: January 23, 2020
Heterogeneous Effects of Calorie Content and Nutritional Components Underlie Dietary Influence on Pancreatic Cancer Susceptibility.
Journal: Cell reports
Published: November 18, 2019
Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia.
Journal: The Journal of allergy and clinical immunology
Published: October 21, 2019
Last Updated: 09/26/2026