Padhraig Gormley
educated at: Queen's University Belfast
occupation: researcher
Articles 25
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Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland
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Analysis of shared heritability in common disorders of the brain
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Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families
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Contribution of rare and common variants to intellectual disability in a high-risk population sub-isolate of Northern Finland
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The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families
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Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies
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Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants
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Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathy.
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Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide Signaling.
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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
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Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes
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Pitfalls in genetic testing: the story of missed SCN1A mutations
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Migraine genetics: from genome-wide association studies to translational insights
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Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
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Analysis of shared heritability in common disorders of the brain
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Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathy
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Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy
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Genetic analysis for a shared biological basis between migraine and coronary artery disease
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Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia.
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De novo mutations in HCN1 cause early infantile epileptic encephalopathy
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De novo mutations in schizophrenia implicate synaptic networks
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De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome
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Genome-wide meta-analysis identifies new susceptibility loci for migraine
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Reverse Engineering of Biochemical Reaction Networks Using Co-evolution with Eng-Genes
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Modelling molecular interaction pathways using a two-stage identification algorithm.
Human - wd:Q55473311