Heidi M. Hautakangas

Helsinki, Finland

Last Updated: 09/26/2026

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Found 8 publications

Fine-mapping a genome-wide meta-analysis of 98,374 migraine cases identifies 181 sets of candidate causal variants.

Fine-mapping a genome-wide meta-analysis of 98,374 migraine cases identifies 181 sets of candidate causal variants.

Journal: medRxiv : the preprint server for health sciences
Published: October 07, 2024

Fine-mapping a genome-wide meta-analysis of 98,374 migraine cases identifies 181 sets of candidate causal variants.

Fine-mapping a genome-wide meta-analysis of 98,374 migraine cases identifies 181 sets of candidate causal variants.

Journal: Nature communications
Published: May 06, 2024

Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor.

Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor.

Journal: Annals of neurology
Published: March 01, 2023

NCOR2 is a novel candidate gene for migraine-epilepsy phenotype.

NCOR2 is a novel candidate gene for migraine-epilepsy phenotype.

Journal: Cephalalgia : an international journal of headache
Published: February 15, 2022

Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation.

Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation.

Journal: Nature communications
Published: June 24, 2021

Dissecting the shared genetic basis of migraine and mental disorders using novel statistical tools.

Dissecting the shared genetic basis of migraine and mental disorders using novel statistical tools.

Journal: Brain : a journal of neurology
Published: March 03, 2021

Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles.

Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles.

Journal: Nature genetics
Published: January 12, 2021

Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure.

Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure.

Journal: Nature communications
Published: November 02, 2020
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Last Updated: 09/26/2026