about
A high-density association screen of 155 ion transport genes for involvement with common migraineKinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2Genome-wide association analysis identifies susceptibility loci for migraine without aura.Genome-wide meta-analysis identifies new susceptibility loci for migraine.Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants.Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraineSystematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set.Low birth weight does not increase the risk of nephropathy in Finnish type 1 diabetic patients.Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect.Novel susceptibility locus at 22q11 for diabetic nephropathy in type 1 diabetes.Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.The molecular genetics of migraine.Comorbidity in Finnish migraine families.Consistently replicating locus linked to migraine on 10q22-q23Genetic analysis for a shared biological basis between migraine and coronary artery disease.Migraine: a complex genetic disorder.WNT1 mutations in early-onset osteoporosis and osteogenesis imperfecta.Elevated MBL concentrations are not an indication of association between the MBL2 gene and type 1 diabetes or diabetic nephropathy.A susceptibility locus for migraine with aura, on chromosome 4q24.A novel splice mutation in PLS3 causes X-linked early onset low-turnover osteoporosis.Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies.Gene-based pleiotropy across migraine with aura and migraine without aura patient groups.Premonitory symptoms in migraine: A cross-sectional study in 2714 persons.Towards an understanding of genetic predisposition to migraine.
P50
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P50
description
onderzoeker
@nl
name
Maija Wessman
@ast
Maija Wessman
@en
Maija Wessman
@es
Maija Wessman
@nl
Maija Wessman
@sl
type
label
Maija Wessman
@ast
Maija Wessman
@en
Maija Wessman
@es
Maija Wessman
@nl
Maija Wessman
@sl
prefLabel
Maija Wessman
@ast
Maija Wessman
@en
Maija Wessman
@es
Maija Wessman
@nl
Maija Wessman
@sl