Mari Kaunisto

University of Helsinki — Finland

Medicine · Health Sciences

49h-index17.7kcitations154works5.32yr avg
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Research Topics

Migraine and Headache Studies(47), Neuroscience of respiration and sleep(24), Genetic Associations and Epidemiology(17), Pain Management and Opioid Use(11), Pain Mechanisms and Treatments(8)

Publications118 total

Diagnosing migraine from genome-wide genotype data: a machine learning analysis
Brain·2025· 1 citedOpen Access
<scp>HLA</scp> ‐Region Genetic Association Analysis of Breast Cancer Patients With and Without Persistent Postsurgical Neuropathic Pain
European Journal of Pain·2025· 1 citedOpen Access
Genome-wide Study on Propofol Requirements: Reply
Anesthesiology·2025Open Access
Transforming science communication through storytelling
FEBS Letters·2024Open Access
HMG-CoA reductase is a potential therapeutic target for migraine: a mendelian randomization study
Scientific Reports·2024· 5 citedOpen Access
Influence of Clinical and Genetic Factors on Propofol Dose Requirements: A Genome-wide Association Study
Anesthesiology·2024· 8 citedOpen Access
A FinnGen pilot clinical recall study for Alzheimer’s disease
Scientific Reports·2023· 8 citedOpen Access
A causal effects of gut microbiota in the development of migraine
The Journal of Headache and Pain·2023· 42 citedOpen Access
Migraine, chronic kidney disease and kidney function: observational and genetic analyses
Human Genetics·2023· 10 citedOpen Access
Clinical and genetic factors associated with post‐operative nausea and vomiting after propofol anaesthesia
Acta Anaesthesiologica Scandinavica·2023· 6 citedOpen Access
Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population
Nature·2023· 109 citedOpen Access
Causal relationships between migraine and microstructural white matter: a Mendelian randomization study
The Journal of Headache and Pain·2023· 29 citedOpen Access
FinnGen provides genetic insights from a well-phenotyped isolated population
Nature·2023· 3.8k citedOpen Access
Elucidating the relationship between migraine risk and brain structure using genetic data
Brain·2022· 32 citedOpen Access
FinnGen: Unique genetic insights from combining isolated population and national health register data
2022· 412 citedOpen Access
Implementation of CYP2D6 copy-number imputation panel and frequency of key pharmacogenetic variants in Finnish individuals with a psychotic disorder
The Pharmacogenomics Journal·2022· 13 citedOpen Access
<i>NCOR2</i> is a novel candidate gene for migraine-epilepsy phenotype
Cephalalgia·2022· 11 citedOpen Access
Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families
Cephalalgia·2021· 14 citedOpen Access
A Randomized, Sham-Controlled Trial of Repetitive Transcranial Magnetic Stimulation Targeting M1 and S2 in Central Poststroke Pain: A Pilot Trial
Neuromodulation Technology at the Neural Interface·2021· 42 citedOpen Access
Mapping the human genetic architecture of COVID-19
Nature·2021· 1.1k citedOpen Access
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Frequent Co-authors

Maija Wessman(25), Mikko Kallela(23), Aarno Palotie(22), Eija Hämäläinen(21), Martti Färkkilâ(18), Jaakko Kaprio(18), Verneri Anttila(18), Ville Artto(15), Priit Palta(13), Terho Lehtimäki(13), Gisela M. Terwindt(12), Tobias Freilinger(12), Mitja Kurki(11), Martin Dichgans(11), Risto Kajanne(10), Padhraig Gormley(10), Cornelia M. van Duijn(10), Christian Kubisch(10), Arn M. J. M. van den Maagdenberg(10), Kalle Pärn(9)