about
Functional impact of global rare copy number variation in autism spectrum disordersReview of statistical methodologies for the detection of parent-of-origin effects in family trio genome-wide association data with binary disease traits.Reconstruction of transcriptional dynamics from gene reporter data using differential equations.Exploration of empirical Bayes hierarchical modeling for the analysis of genome-wide association study data.Genetic classification of populations using supervised learningThe phenotypic manifestations of rare genic CNVs in autism spectrum disorder.No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association dataset.Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders.Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility.The phenotypic manifestations of rare CNVs in schizophrenia.Bayesian inference for dynamic transcriptional regulation; the Hes1 system as a case study.Mauling of the "Celtic Tiger": clinical characteristics and outcome of first-episode depression secondary to the economic recession in Ireland.Parental age, birth order and neurodevelopmental disorders.The SNP ratio test: pathway analysis of genome-wide association datasets
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P50
description
researcher ORCID ID = 0000-0003-2219-4005
@en
wetenschapper
@nl
name
Elizabeth A Heron
@ast
Elizabeth A Heron
@en
Elizabeth A Heron
@es
Elizabeth A Heron
@nl
type
label
Elizabeth A Heron
@ast
Elizabeth A Heron
@en
Elizabeth A Heron
@es
Elizabeth A Heron
@nl
altLabel
Elizabeth Heron
@en
prefLabel
Elizabeth A Heron
@ast
Elizabeth A Heron
@en
Elizabeth A Heron
@es
Elizabeth A Heron
@nl
P106
P21
P31
P496
0000-0003-2219-4005