Author details

Full Name

Lili Milani

Affiliation

ORCID

Career Start Year

2006

Papers

150

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36662581	Harnessing the Power of Electronic Health Records and Genomics for Drug Discovery.		2023
36325912	Pharmacogenomics in Stroke and Cardiovascular Disease: State of the Art.	Stroke	2023
36192438	Lessons learned during the process of reporting individual genomic results to participants of a population-based biobank.	European Journal of Human Genetics	2023
37924579	The role of depression and antidepressant treatment in antihypertensive medication adherence and persistence: Utilising electronic health record data.		2023
37923823	HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases.	Commun Biol	2023
37794016	European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation.	Nat Commun	2023
37790435	Complexities of cerebral small vessel disease, blood pressure, and dementia relationship: new insights from genetics.	medRxiv	2023
37954898	Pharmacologic and Genetic Downregulation of Proprotein Convertase Subtilisin/Kexin Type 9 and Survival From Sepsis.	Crit Care Explor	2023
36653562	FinnGen provides genetic insights from a well-phenotyped isolated population.	Nature	2023
36829046	Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.	Nature	2023
36653479	Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases.	Nat Med	2023
36653343	Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure.	Nat Commun	2023
36966315	Common clinical blood and urine biomarkers for ischemic stroke: an Estonian Electronic Health Records database study.	Eur J Med Res	2023
37425374	Psychiatric disorders and subsequent risk of cardiovascular disease: a longitudinal matched cohort study across three countries.	EClinicalMedicine	2023
35287021	The 1<sup>st</sup> year of the COVID-19 epidemic in Estonia: a population-based nationwide sequential/consecutive cross-sectional study.	Public Health	2022
35396580	Mapping genomic loci implicates genes and synaptic biology in schizophrenia.	Nature	2022
35396579	Rare coding variants in ten genes confer substantial risk for schizophrenia.	Nature	2022
35709192	Clinical characteristics and risk factors for COVID-19 infection and disease severity: A nationwide observational study in Estonia.	PLoS ONE	2022
35504910	DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases.	Nat Commun	2022
35978133	Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis.	Commun Biol	2022
34099189	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	Biol Psychiatry	2022
35020900	Cohort Profile: COVIDMENT: COVID-19 cohorts on mental health across six nations.	Int J Epidemiol	2022
34475573	Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression.	Nat Genet	2021
33972266	Stratification of Type 2 Diabetes by Age of Diagnosis in the UK Biobank Reveals Subgroup-Specific Genetic Associations and Causal Risk Profiles.		2021
33859359	Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure.	Mol Psychiatry	2021
34279044	Genomic Insights into Myasthenia Gravis Identify Distinct Immunological Mechanisms in Early and Late Onset Disease.	Ann Neurol	2021
34002096	Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.	Nat Genet	2021
34000646	Hybrid modelling for stroke care: Review and suggestions of new approaches for risk assessment and simulation of scenarios.	Neuroimage Clin	2021
32989287	Genome-wide association study identifies 48 common genetic variants associated with handedness.	Nat Hum Behav	2021
32535895	Global Frequencies of Clinically Important HLA Alleles and Their Implications For the Cost-Effectiveness of Preemptive Pharmacogenetic Testing.	Clinical Pharmacology and Therapeutics	2021
34465810	Genetic regulation of spermine oxidase activity and cancer risk: a Mendelian randomization study.	Scientific Reports	2021
34516913	Rare genetic variability in human drug target genes modulates drug response and can guide precision medicine.	Science advances	2021
34851696	Response to comment on "Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics".	Sci Transl Med	2021
34493871	Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation.	Nat Genet	2021
34887417	Meta-analyses identify DNA methylation associated with kidney function and damage.	Nat Commun	2021
34887389	Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus.	Nat Commun	2021
32520614	Identification, Heritability, and Relation With Gene Expression of Novel DNA Methylation Loci for Blood Pressure.	Hypertension	2020
31588999	Variation near MTNR1A associates with early development and interacts with seasons.	Journal of Sleep Research	2020
32107839	Monocytes present age-related changes in phospholipid concentration and decreased energy metabolism.	Aging Cell	2020
32712624	Differences in local population history at the finest level: the case of the Estonian population.	European Journal of Human Genetics	2020
32978407	A data-driven medication score predicts 10-year mortality among aging adults.	Sci Rep	2020
32581134	Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics.	Sci Transl Med	2020
33239708	An epigenome-wide association study of metabolic syndrome and its components.	Scientific Reports	2020
33239683	Longitudinal proteomic profiling reveals increased early inflammation and sustained apoptosis proteins in severe COVID-19.	Sci Rep	2020
30718923	A distinctive DNA methylation pattern in insufficient sleep.	Scientific Reports	2019
30031151	Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant.	European Journal of Medical Genetics	2019
30420678	Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records.	Eur J Hum Genet	2019
30327539	Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions.	Genet Med	2019
31455423	Translating pharmacogenomics into clinical decisions: do not let the perfect be the enemy of the good.	Human Genomics	2019
31127295	A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure.	Hum Mol Genet	2019