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Publications

Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.

Lagou V. et al, (2021), Nat Commun, 12

Large-scale association analyses identify host factors influencing human gut microbiome composition.

Kurilshikov A. et al, (2021), Nat Genet

Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.

Lagou V. et al, (2021), Nat Commun, 12

Genome-wide association study identifies 48 common genetic variants associated with handedness.

Cuellar-Partida G. et al, (2021), Nat Hum Behav, 5, 59 - 70

Identification of Biomarkers for the Prevention of Chronic Disease

Boccia S. et al, (2021), SpringerBriefs in Public Health, 9 - 32

Association of common genetic variants with brain microbleeds: A genome-wide association study.

Knol MJ. et al, (2020), Neurology, 95, e3331 - e3343

Cerebral small vessel disease genomics and its implications across the lifespan.

Sargurupremraj M. et al, (2020), Nat Commun, 11

Association of lysophosphatidic acids with cerebrospinal fluid biomarkers and progression to Alzheimer's disease.

Ahmad S. et al, (2020), Alzheimers Res Ther, 12

Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation.

Weng L-C. et al, (2020), Circ Genom Precis Med, 13, 387 - 395

Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study

Jones E. et al, (2020), The Lancet Neurology, 19, 840 - 848

Metabolic Age Based on the BBMRI-NL 1H-NMR Metabolomics Repository as Biomarker of Age-related Disease.

van den Akker EB. et al, (2020), Circ Genom Precis Med, 13, 541 - 547

Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults.

Hofer E. et al, (2020), Nat Commun, 11

Serum fatty acid chain length associates with prevalent symptomatic end-stage osteoarthritis, independent of BMI.

Meessen JMTA. et al, (2020), Sci Rep, 10

Refining Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Genetic Loci by Integrating Summary Data From Genome-wide Association, Gene Expression, and DNA Methylation Studies

Byrne E. et al, (2020), Biological Psychiatry

Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.

Yaghootkar H. et al, (2020), Diabetes

Circulating metabolites are associated with brain atrophy and white matter hyperintensities.

de Leeuw FA. et al, (2020), Alzheimers Dement

Genetic Predisposition to Coronary Artery Disease in Type 2 diabetes

van Zuydam NR. et al, (2020), Circulation: Genomic and Precision Medicine

Many roads lead to Rome: molecular pathways leading to high myopia

Tedja MS. et al, (2020), ACTA OPHTHALMOLOGICA, 98, 23 - 23

A cross-omics integrative study of metabolic signatures of chronic obstructive pulmonary disease.

Prokić I. et al, (2020), BMC Pulm Med, 20

Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities.

Armstrong NJ. et al, (2020), Stroke, 51, 2111 - 2121

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