Maija Wessman
occupation: researcher
Articles 29
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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
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Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
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Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants.
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Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set.
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Genetic analysis for a shared biological basis between migraine and coronary artery disease
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A novel splice mutation in PLS3 causes X-linked early onset low-turnover osteoporosis
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Gene-based pleiotropy across migraine with aura and migraine without aura patient groups
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Premonitory symptoms in migraine: A cross-sectional study in 2714 persons
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Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies
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Genome-wide meta-analysis identifies new susceptibility loci for migraine
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WNT1 mutations in early-onset osteoporosis and osteogenesis imperfecta
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Genome-wide association analysis identifies susceptibility loci for migraine without aura
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Novel susceptibility locus at 22q11 for diabetic nephropathy in type 1 diabetes
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Towards an understanding of genetic predisposition to migraine
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Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.
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Association of the SLC22A1, SLC22A2, and SLC22A3 genes encoding organic cation transporters with diabetic nephropathy and hypertension.
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Elevated MBL concentrations are not an indication of association between the MBL2 gene and type 1 diabetes or diabetic nephropathy
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A high-density association screen of 155 ion transport genes for involvement with common migraine
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Consistently replicating locus linked to migraine on 10q22-q23
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Migraine: a complex genetic disorder
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A functional polymorphism in the manganese superoxide dismutase gene and diabetic nephropathy.
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Low birth weight does not increase the risk of nephropathy in Finnish type 1 diabetic patients
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Comorbidity in Finnish migraine families
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Glu298Asp and NOS4ab polymorphisms in diabetic nephropathy.
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Kinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2
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The molecular genetics of migraine
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Birth weight is inversely correlated to adult systolic blood pressure and pulse pressure in type 1 diabetes.
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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
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A susceptibility locus for migraine with aura, on chromosome 4q24.
Human - wd:Q42539403