Lili Milani

Oslo University Hospital — Norway

Biochemistry, Genetics and Molecular Biology · Life Sciences

114h-index80.6kcitations466works12.02yr avg
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Research Topics

Genetic Associations and Epidemiology(159), Epigenetics and DNA Methylation(60), Birth, Development, and Health(33), Genomics and Rare Diseases(26), Genetic Syndromes and Imprinting(22)

Publications326 total

Genome-wide meta-analyses of non-response to antidepressants provide insights into underlying molecular genetics and suggest potential pharmacotherapies
Molecular Psychiatry·2025
Genome-wide association study and polygenic risk prediction of hypothyroidism
Nature Genetics·2025Open Access
Eleição de Mamdani a prefeito de Nova York expõe a crise interna da hegemonia representada por Trump
2025
Development and validation of a risk prediction algorithm for high-risk populations combining genetic and conventional risk factors of cardiovascular disease
PLoS ONE·2025· 1 citedOpen Access
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
UNC Libraries·2025Open Access
Characterization of prevalent genetic variants in the Estonian Biobank body-mass index GWAS
Nature Communications·2025· 1 citedOpen Access
Trans-eQTL mapping prioritises USP18 as a negative regulator of interferon response at a lupus risk locus
Nature Communications·2025· 4 citedOpen Access
LEVERAGING REAL-WORLD DATA FROM HEALTH REGISTRIES TO MEASURE ANTIDEPRESSANT TREATMENT OUTCOMES FOR LARGE-SCALE GENOME-WIDE ASSOCIATION ANALYSES
European Neuropsychopharmacology·2025
A hidden confounder for microbiome studies: medications used years before sample collection
mSystems·2025· 7 citedOpen Access
Hormonal contraceptive drug use trends in the Estonian Biobank
2025Open Access
Review for "HMGB1 and mitochondrial dysfunction: a double-edged sword in ageing"
2025
Parent-of-origin effects on complex traits in up to 236,781 individuals
Nature·2025· 9 citedOpen Access
Genome-wide study of somatic symptom and related disorders identifies novel genomic loci and map genetic architecture
2025· 1 citedOpen Access
Polygenic and pharmacogenomic contributions to medication dosing: a real-world longitudinal biobank study
Journal of Translational Medicine·2025· 2 citedOpen Access
Genetic influences on antidepressant side effects: a CYP2C19 gene variation and polygenic risk study in the Estonian Biobank
European Journal of Human Genetics·2025· 6 citedOpen Access
Proof of principle concept for the analysis and functional prediction of rare genetic variants in the CYP2C19 and CYP2D6 genes
Human Genomics·2025· 7 citedOpen Access
Pleiotropic and sex-specific genetic mechanisms of circulating metabolic markers
Nature Communications·2025· 6 citedOpen Access
The effect of LRRK2 loss-of-function variants in humans
UNC Libraries·2025Open Access
Author Correction: The effect of LRRK2 loss-of-function variants in humans
UNC Libraries·2025Open Access
Discovering age- and sex-specific genetic risk factors in sensorineural hearing loss: genome-wide evidence from large-scale biobank studies
2025Open Access
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Frequent Co-authors

Tōnu Esko(31), Andres Metspalu(19), Dorret I. Boomsma(16), Silva Kasela(16), Reedik Mägi(15), Lude Franke(15), Zoltán Kutalik(13), Grant W. Montgomery(13), Joyce B. J. van Meurs(13), Rick Jansen(12), Peter M. Visscher(12), André G. Uitterlinden(12), Jouke‐Jan Hottenga(11), Katharina Schramm(11), Gibran Hemani(11), Terho Lehtimäki(11), Jian Yang(10), Holger Prokisch(10), Bruce M. Psaty(10), Marc Jan Bonder(10)