Detalhe da pesquisa
1.
Tiered analysis of whole-exome sequencing for epilepsy diagnosis.
Mol Genet Genomics
; 295(3): 751-763, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-32146541
2.
The NRP1 migraine risk variant shows evidence of association with menstrual migraine.
J Headache Pain
; 19(1): 31, 2018 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-29671086
3.
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene.
Hum Mol Genet
; 22(18): 3654-66, 2013 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23686279
4.
Investigation of brain-derived neurotrophic factor (BDNF) gene variants in migraine.
Headache
; 54(7): 1184-93, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24708359
5.
Association of oestrogen-receptor gene (ESR1) polymorphisms with migraine in the large Norfolk Island pedigree.
Cephalalgia
; 33(14): 1139-47, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23674830
6.
Association of a GRIA3 gene polymorphism with migraine in an Australian case-control cohort.
Headache
; 53(8): 1245-9, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23772601
7.
Genetic variation in cytokine-related genes and migraine susceptibility.
Twin Res Hum Genet
; 16(6): 1079-86, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24054031
8.
Identification of molecular genetic factors that influence migraine.
Mol Genet Genomics
; 285(6): 433-46, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21519858
9.
An X chromosome association scan of the Norfolk Island genetic isolate provides evidence for a novel migraine susceptibility locus at Xq12.
PLoS One
; 7(5): e37903, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22666411