Detalhe da pesquisa
1.
NCOR2 is a novel candidate gene for migraine-epilepsy phenotype.
Cephalalgia
; 42(7): 631-644, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35166138
2.
The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families.
Cephalalgia
; 38(12): 1849-1863, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29486580
3.
Multi-ethnic GWAS and meta-analysis of sleep quality identify MPP6 as a novel gene that functions in sleep center neurons.
Sleep
; 44(3)2021 03 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33034629
4.
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families.
Neuron
; 98(4): 743-753.e4, 2018 05 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-29731251
5.
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families.
Neuron
; 99(5): 1098, 2018 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30189203