Maija Wessman
Helsinki, Finland
Last Updated: 09/26/2026
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Found 23 publications
NCOR2 is a novel candidate gene for migraine-epilepsy phenotype.
Journal: Cephalalgia : an international journal of headache
Published: February 15, 2022
Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families.
Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families.
Journal: Cephalalgia : an international journal of headache
Published: October 14, 2021
High-resolution population-specific recombination rates and their effect on phasing and genotype imputation.
Journal: European journal of human genetics : EJHG
Published: May 27, 2020
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families.
Journal: Neuron
Published: September 07, 2018
The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families.
Journal: Cephalalgia : an international journal of headache
Published: March 01, 2018
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families.
Journal: Neuron
Published: November 30, 2017
Molecular genetic overlap between migraine and major depressive disorder.
Journal: European journal of human genetics : EJHG
Published: October 24, 2017
Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.
Journal: Nature genetics
Published: September 30, 2016
Effect of endocannabinoid degradation on pain: role of FAAH polymorphisms in experimental and postoperative pain in women treated for breast cancer.
Journal: Pain
Published: January 26, 2016
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.
Journal: Nature genetics
Published: October 27, 2015
Last Updated: 09/26/2026