Aarno Palotie

Biochemistry, Genetics and Molecular Biology · Life Sciences

169h-index169.3kcitations1.2kworks10.92yr avg
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Research Topics

Genetic Associations and Epidemiology(312), Genomics and Rare Diseases(153), Genomic variations and chromosomal abnormalities(87), Genetics and Neurodevelopmental Disorders(85), Migraine and Headache Studies(76)

Publications989 total

Multitrait analyses identify genetic variants associated with aortic valve function and aortic stenosis risk
Nature Genetics·2025· 1 citedOpen Access
Cost-effective non-additive GWAS across 2329 diseases in 500,349 individuals
Nature Communications·2025Open Access
Plasma biomarkers of Alzheimer's disease and cognition in a population‐based sample
Alzheimer s & Dementia·2025Open Access
Population-scale multiome immune cell atlas reveals complex disease drivers
2025Open Access
131 genetic loci highlight immunological pathways and tissues in nasal polyposis and asthma
Nature Communications·2025· 1 citedOpen Access
Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk
UNC Libraries·2025Open Access
Validity of telephone-administered word list learning measures for assessment of episodic memory in aging and Alzheimer’s disease.
Neuropsychology·2025
Genetic architecture of 67 oral diseases and their links to systemic diseases
2025Open Access
23. RARE CODING VARIANTS IN SCHIZOPHRENIA HAVE ADDITIVE EFFECTS ON POLYGENIC RISK AND ASSOCIATE WITH COGNITIVE ABILITIES IN INDIVIDUALS WITH PSYCHOTIC DISORDERS
European Neuropsychopharmacology·2025Open Access
68. TRAJECTORY-BASED STRATIFICATION OF PSYCHOTIC DISORDERS REVEALS GENOMIC AND FUNCTIONAL DIFFERENCES ACROSS SEVERITY SUBTYPES
European Neuropsychopharmacology·2025
Correction: Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa
UNC Libraries·2025Open Access
Predicting Alzheimer’s Disease Phenotypes With Aging Clocks: An Exploratory Analysis
2025Open Access
Scalable biological-cognitive profiling for Alzheimer’s disease in the population
2025Open Access
Genetic Architecture and Risk Profile of Alcohol-Related Diseases
2025Open Access
Genetic associations between serotonin receptor 1F (<i>HTR1F</i>) regulatory variation and sleep apnoea in non-obese individuals: insights from GWAS and eQTL analyses
European Respiratory Journal·2025· 1 citedOpen Access
Polygenic Scores for Schizophrenia and Educational Attainment Predict Global Functioning Across Psychiatric Hospitalization Among People with Schizophrenia
2025Open 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
Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucoma
Nature Communications·2025· 7 citedOpen Access
Diagnosing migraine from genome-wide genotype data: a machine learning analysis
Brain·2025· 1 citedOpen Access
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Frequent Co-authors

Mark J. Daly(12), Samuli Ripatti(11), Johan G. Eriksson(11), Cornelia M. van Duijn(9), Veikko Salomaa(9), Terho Lehtimäki(9), Tōnu Esko(7), Markus Perola(7), Christine Stevens(6), Leena Peltonen(6), Michael Inouye(6), Hreinn Stefánsson(6), Jari Lahti(6), Jouke‐Jan Hottenga(6), Dale R. Nyholt(6), Johannes Kettunen(6), Jaakko Kaprio(6), Mitja Kurki(5), David Altshuler(5), Mark I. McCarthy(5)