Associated Papers
Whole Exome Sequencing of Hemiplegic Migraine Patients Shows an Increased Burden of Missense Variants in CACNA1H and CACNA1I Genes.
Maksemous N et al.
Molecular Neurobiology, 2023
36786913 (PubMed )
Supplement: 12035_2023_3255_MOESM1_ESM.xlsx › Supplementary_Table_1
Analysing an allelic series of rare missense variants of CACNA1I in a Swedish schizophrenia cohort.
Baez-Nieto D et al.
Brain : a Journal of Neurology, 2022
A review of migraine genetics: gathering genomic and transcriptomic factors.
Dias A et al.
Human Genetics, 2022
Investigation of CACNA1I Cav3.3 Dysfunction in Hemiplegic Migraine.
Maksemous N et al.
Frontiers in Molecular Neuroscience, 2022
Exploring Neuronal Vulnerability to Head Trauma Using a Whole Exome Approach.
Ibrahim O et al.
Journal of Neurotrauma, 2020
Select a paper to view details