about
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibilityRare and low-frequency coding variants alter human adult heightCoding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals.Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis.Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.Association analyses based on false discovery rate implicate new loci for coronary artery disease.Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions.Exome-wide association study of plasma lipids in >300,000 individuals.Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.Lifestyle may modify the glucose-raising effect of genetic loci. A study in the Greek populationRefining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 DiabetesPROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTIONCombination therapy as a potential risk factor for the development of type 2 diabetes in patients with schizophrenia: the GOMAP studyEvidence for genetic contribution to the increased risk of type 2 diabetes in schizophreniaMeta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestryMeta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic lociMendelian randomisation analyses find pulmonary factors mediate the effect of height on coronary artery diseaseEpigenome-Wide Association Study (EWAS) of Blood Lipids in Healthy Population from STANISLAS Family Study (SFS)Gender Specificity of a Genetic Variant of Androgen Receptor and Risk of Coronary Artery Disease
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P50
description
researcher ORCID ID = 0000-0001-6179-1609
@en
wetenschapper
@nl
name
Eirini Marouli
@ast
Eirini Marouli
@en
Eirini Marouli
@es
Eirini Marouli
@nl
type
label
Eirini Marouli
@ast
Eirini Marouli
@en
Eirini Marouli
@es
Eirini Marouli
@nl
prefLabel
Eirini Marouli
@ast
Eirini Marouli
@en
Eirini Marouli
@es
Eirini Marouli
@nl
P106
P21
P31
P496
0000-0001-6179-1609