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L. Milani

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Open access Sep 2026

Body mass index modifies symptom-specific metabolomic associations with depressive symptoms in the Estonian Biobank

Circulating metabolic correlates of depressive symptoms are heterogeneous and strongly dependent on symptom phenotype and BMI-related metabolic context, suggesting that metabolic biomarkers in depression should be interpreted in relation to both symptom presentation and metabolic state rather than as uniform correlates...

S. Kurvits, N. Taba, Estonian biobank research team et al. · 0 citations
Open access Aug 2026

Side effects in hypertension treatment: a pharmacogenomic analysis.

BACKGROUND AND AIMS Up to half of patients switch or discontinue antihypertensive medications within the first year, but underlying mechanisms remain elusive. This study aimed to identify genetic predictors of antihypertensive medication use trajectories within the first year. METHODS Using longitudinal medication da...

F. Vaura, Kristi Krebs, T. Kiiskinen et al. · 0 citations
Open access Jul 2026

Psychiatric genetic liability is associated with the severity of COVID-19 and other acute respiratory infections: an observational study across five Northern European countries

The results underscore the role of psychiatric genetic liability, beyond diagnosed psychiatric disorders, in contributing to both COVID-19 and other respiratory infection severity, and provide insights that may improve future risk stratification and public health strategies targeting respiratory viruses.

K. Kõiv, R. Askeland, L. N. Christoffersen et al. · 0 citations
Open access Aug 2026

Detecting CYP2C19 deletions from genotyping array signals using neural networks

This work developed a neural network model, nnCNV, to predict deletions in the CYP2C19 pharmacogene region from array intensity signals and demonstrated that long-range information, which cannot be utilized by hidden Markov models, can improve CNV calling.

Burak Yelmen, R. Hofmeister, Viido Kaur Lutsar et al. · 0 citations

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