Author details

Full Name

Aarno Palotie

Affiliation

ORCID

Career Start Year

1980

Papers

530

H Index

108

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37419095	Response to Li and Hopper.		2023
36253440	Genome-wide association study meta-analysis of suicide death and suicidal behavior.	Molecular Psychiatry	2023
37988105	Association of APOE Haplotypes With Common Age-Related Ocular Diseases in 412,171 Individuals.	Invest Ophthalmol Vis Sci	2023
38076931	Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events.	medRxiv	2023
37965200	TWINGEN - protocol for an observational clinical biobank recall and biomarker study to identify individuals with high risk of Alzheimer's disease.	medRxiv	2023
37965200	TWINGEN - protocol for an observational clinical biobank recall and biomarker study to identify individuals with high risk of Alzheimer's disease.	medRxiv	2023
37697398	Use of electronic health record data mining for heart failure subtyping.		2023
37289866	Taurine deficiency as a driver of aging.		2023
36779498	Functional Characterization of Six (OATP1B1) Variants Observed in Finnish Individuals with a Psychotic Disorder.		2023
36653562	FinnGen provides genetic insights from a well-phenotyped isolated population.	Nature	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
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
36653477	Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population.		2023
36653354	Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation.	Nat Commun	2023
36653343	Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure.	Nat Commun	2023
37464041	Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses.	Nat Med	2023
37079300	Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular Degeneration.	JAMA Ophthalmol	2023
37453564	Genome-Wide Association Study Identifies 4 Novel Risk Loci for Small Intestinal Neuroendocrine Tumors Including a Missense Mutation in LGR5.	Gastroenterology	2023
37179546	Novel patients with NHLRC2 variants expand the phenotypic spectrum of FINCA disease.		2023
37045567	Cohort profile: SUPER-Finland - the Finnish study for hereditary mechanisms of psychotic disorders.	BMJ Open	2023
37503126	Understanding the genetic complexity of puberty timing across the allele frequency spectrum.	medRxiv	2023
37502935	The Cardiovascular Impact and Genetics of Pericardial Adiposity.	medRxiv	2023
34411351	Effects of PNPLA3 I148M on hepatic lipid and very-low-density lipoprotein metabolism in humans.	Journal of Internal Medicine	2022
35396580	Mapping genomic loci implicates genes and synaptic biology in schizophrenia.	Nature	2022
35974141	Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning.	Mol Psychiatry	2022
35591975	Genome-wide risk prediction of common diseases across ancestries in one million people.	Cell Genom	2022
35396579	Rare coding variants in ten genes confer substantial risk for schizophrenia.	Nature	2022
36038634	Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility.	Nat Genet	2022
35760976	The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia.	Nat Commun	2022
36347255	Systematic comparison of family history and polygenic risk across 24 common diseases.	American Journal of Human Genetics	2022
35874969	The relative proportion of comorbidities among rhinitis and rhinosinusitis patients and their impact on visit burden.	Clinical and Translational Allergy	2022
36198465	Recontacting biobank participants to collect lifestyle, behavioural and cognitive information via online questionnaires: lessons from a pilot study within FinnGen.	BMJ Open	2022
36055244	Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk.	Am J Hum Genet	2022
36419110	Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations.	Genome Med	2022
36114182	Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanks.	Nat Commun	2022
35978133	Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis.	Commun Biol	2022
35916366	Integrated analyses of growth differentiation factor-15 concentration and cardiometabolic diseases in humans.	Elife	2022
35301180	A genome-wide association study of outcome from traumatic brain injury.	EBioMedicine	2022
35166138	is a novel candidate gene for migraine-epilepsy phenotype.	Cephalalgia	2022
35130028	How Communicating Polygenic and Clinical Risk for Atherosclerotic Cardiovascular Disease Impacts Health Behavior: an Observational Follow-up Study.	Circulation. Genomic and precision medicine	2022
34648375	Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families.	Cephalalgia	2022
35087184	A novel variant in SMG9 causes intellectual disability, confirming a role for nonsense-mediated decay components in neurocognitive development.	Eur J Hum Genet	2022
35197553	Implementation of CYP2D6 copy-number imputation panel and frequency of key pharmacogenetic variants in Finnish individuals with a psychotic disorder.	Pharmacogenomics J	2022
30848161	Apolipoprotein E4 Polymorphism and Outcomes from Traumatic Brain Injury: A Living Systematic Review and Meta-Analysis.	J Neurotrauma	2021
32064741	Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.	Addict Biol	2021
32346736	The relation of severe malocclusion to patients' mental and behavioral disorders, growth, and speech problems.	European Journal of Orthodontics	2021
33491305	The Role of Inflammatory Cytokines as Intermediates in the Pathway from Increased Adiposity to Disease.	Obesity (Silver Spring)	2021
34240440	Genetics of Cluster Headache Takes a Leap.	Annals of Neurology	2021