about
IFITM3 restricts the morbidity and mortality associated with influenzaA high-density association screen of 155 ion transport genes for involvement with common migraineGenetic relationship between five psychiatric disorders estimated from genome-wide SNPsGenome-Wide Meta-Analysis of Sciatica in Finnish PopulationGenome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohortsGenome-wide association analysis identifies susceptibility loci for migraine without aura.Genome-wide meta-analysis identifies new susceptibility loci for migraine.Integrating common and rare genetic variation in diverse human populationsShared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants.Genome-wide association study reveals three susceptibility loci for common migraine in the general population.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.Serum calcium and risk of migraine: a Mendelian randomization studySelectivity in genetic association with sub-classified migraine in women.European lactase persistence genotype shows evidence of association with increase in body mass indexA visual migraine aura locus maps to 9q21-q22Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging.Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene.Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.A potential novel spontaneous preterm birth gene, AR, identified by linkage and association analysis of X chromosomal markers.Trait components provide tools to dissect the genetic susceptibility of migraine.The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort.Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorderPartitioning heritability by functional annotation using genome-wide association summary statistics.Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas.An atlas of genetic correlations across human diseases and traitsConsistently replicating locus linked to migraine on 10q22-q23Genetic analysis for a shared biological basis between migraine and coronary artery disease.Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of conceptGenetic risk for autism spectrum disorders and neuropsychiatric variation in the general populationHigh risk population isolate reveals low frequency variants predisposing to intracranial aneurysms.ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties.In silico phenotyping via co-training for improved phenotype prediction from genotype.Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies.Candidate-gene association study searching for genetic factors involved in migraine chronification.Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa.Gene-based pleiotropy across migraine with aura and migraine without aura patient groups.Involvement of astrocyte and oligodendrocyte gene sets in migraine.Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies.
P50
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P50
description
hulumtues
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հետազոտող
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name
Verneri Anttila
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Verneri Anttila
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Verneri Anttila
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Verneri Anttila
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Verneri Anttila
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Verneri Anttila
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Verneri Anttila
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Verneri Anttila
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Verneri Anttila
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Verneri Anttila
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prefLabel
Verneri Anttila
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Verneri Anttila
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Verneri Anttila
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Verneri Anttila
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Verneri Anttila
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P108
P106
P2038
Verneri_Anttila
P21
P31
P496
0000-0002-0073-4675
P569
2000-01-01T00:00:00Z