|
1
|
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.
|
Nat Genet
|
2010
|
2.35
|
|
2
|
Mutations in DEPDC5 cause familial focal epilepsy with variable foci.
|
Nat Genet
|
2013
|
2.10
|
|
3
|
Migraine is not associated with enhanced atherosclerosis.
|
Cephalalgia
|
2012
|
1.49
|
|
4
|
PRRT2 mutation causes benign familial infantile convulsions.
|
Neurology
|
2012
|
0.98
|
|
5
|
Dynamin 2 homozygous mutation in humans with a lethal congenital syndrome.
|
Eur J Hum Genet
|
2012
|
0.95
|
|
6
|
Stepwise web-based questionnaires for diagnosing cluster headache: LUCA and QATCH.
|
Cephalalgia
|
2013
|
0.76
|
|
7
|
Cluster-tic syndrome: a cross-sectional study of cluster headache patients.
|
Headache
|
2013
|
0.75
|