Padhraig Gormley

Medicine · Health Sciences

41h-index12.1kcitations89works1.62yr avg
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Research Topics

Migraine and Headache Studies(32), Genomics and Rare Diseases(17), Neuroscience of respiration and sleep(15), Genetic Associations and Epidemiology(13), Genetics and Neurodevelopmental Disorders(10)

Publications71 total

Diagnosing migraine from genome-wide genotype data: a machine learning analysis
Brain·2025· 1 citedOpen Access
Patient stratification by genetic risk in Alzheimer’s disease is only effective in the presence of phenotypic heterogeneity
PLoS ONE·2025· 2 citedOpen Access
The genetic architecture of gene expression in individuals of African and European ancestry
2024Open Access
Genetic evidence supports therapeutic hypothesis of increasing progranulin levels for Alzheimer’s Disease
Alzheimer s & Dementia·2024Open Access
HMG-CoA reductase is a potential therapeutic target for migraine: a mendelian randomization study
Scientific Reports·2024· 5 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
Causal relationships between migraine and microstructural white matter: a Mendelian randomization study
The Journal of Headache and Pain·2023· 29 citedOpen Access
Elucidating the relationship between migraine risk and brain structure using genetic data
Brain·2022· 32 citedOpen Access
Migraine, Stroke, and Cervical Arterial Dissection
Neurology Genetics·2022· 44 citedOpen Access
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
Nature Genetics·2022· 357 citedOpen Access
Abstract 9674: Stroke, Migraine, and Cervical Arterial Dissection: Shared Genetics Reveals Concordant and Opposing Risk Mechanisms
Circulation·2021
Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families
Cephalalgia·2021· 14 citedOpen Access
Phenotypic and Genotypic Associations Between Migraine and Lipoprotein Subfractions
Neurology·2021· 75 citedOpen Access
Association of the <i>MYOC</i> p.(Gln368Ter) Variant With Glaucoma in a Finnish Population
JAMA Ophthalmology·2021· 9 citedOpen Access
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
2021· 32 citedOpen Access
An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease
European Journal of Human Genetics·2020· 26 citedOpen Access
A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine
Nature Communications·2020· 76 citedOpen Access
Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders
Genome Medicine·2020· 70 citedOpen Access
Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache
International Journal of Epidemiology·2020· 83 citedOpen Access
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Frequent Co-authors

Aarno Palotie(32), Mikko Kallela(23), Verneri Anttila(21), Ville Artto(21), Eija Hämäläinen(21), Bendik S. Winsvold(19), Tobias Kurth(19), Terho Lehtimäki(19), Maija Wessman(19), Priit Palta(18), Tobias Freilinger(18), Hreinn Stefánsson(18), Mari Kaunisto(17), Rainer Malik(16), Gisela M. Terwindt(16), Martin Dichgans(16), Jaakko Kaprio(15), Cornelia M. van Duijn(14), M. Arfan Ikram(14), Marjo‐Riitta Järvelin(14)