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Louise Gallagher

Institution

Trinity College Dublin

Contact

Subjects

Psychiatry

Details
Publications 61
As first author 14
As last author 24
Unique topics 310
Collaborations 51
Sources 12
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2019
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2012
2011
Earlier
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2019
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2011
Earlier

2019

He said, she said: Autism spectrum diagnosis and gender differentially affect relationships between executive functions and social communication
2019

Low-frequency variation in TP53 has large effects on head circumference and intracranial volume
2018

NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families
2018

Typography and Narrative Voice in Children's Literature: Relationships, Interactions, and Symbiosis
2017

Bio-collections in autism research.
2017

Enhancing studies of the connectome in autism using the autism brain imaging data exchange II
2017

Lack of effect of vitamin D3 supplementation in autism: a 20-week, placebo-controlled RCT.
2017

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.
2017

Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity
2017

Vector-free intracellular delivery by reversible permeabilization
2016

A genome-wide investigation into parent-of-origin effects in autism spectrum disorder identifies previously associated genes including SHANK3.
2016

Abnormal fronto-parietal white matter organisation in the superior longitudinal fasciculus branches in autism spectrum disorders.
2016

Disrupted prediction errors index social deficits in autism spectrum disorder.
2016

Enhancing studies of the connectome in autism using the autism brain imaging data exchange II.
2016

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
2016

Widespread Disrupted White Matter Microstructure in Autism Spectrum Disorders.
2015

Autism Spectrum Disorder (ASD) and Fragile X Syndrome (FXS): Two Overlapping Disorders Reviewed through Electroencephalography-What Can be Interpreted from the Available Information?
2015

Parental age, birth order and neurodevelopmental disorders.
2015

The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.
2015

Use of early intervention for young children with autism spectrum disorder across Europe.
2014

Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
2014

Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders.
2014

Gait deviations in children with autism spectrum disorders: a review.
2014

Holistic processing of faces as measured by the Thatcher illusion is intact in autism spectrum disorders.
2014

Synaptic, transcriptional and chromatin genes disrupted in autism.
2014

The autism brain imaging data exchange: Towards a large-scale evaluation of the intrinsic brain architecture in autism
2014

The phenotypic manifestations of rare CNVs in schizophrenia.
2014

The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.
2013

Abnormal functional connectivity during visuospatial processing is associated with disrupted organisation of white matter in autism.
2013

Abnormal functional connectivity in autism spectrum disorder is associated with disrupted white matter microstructural organisation
2013

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
2013

Disrupted functional connectivity in dorsal and ventral attention networks during attention orienting in autism spectrum disorders.
2013

Functional and structural connectivity of frontostriatal circuitry in Autism Spectrum Disorder.
2012

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
2012

Assessing Problem based learning in Child and Adolescent Psychiatry at the Trinity College Dublin Ireland
2012

Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders.
2012

Individual common variants exert weak effects on the risk for autism spectrum disorderspi.
2012

Mental health problems in children with prader-willi syndrome.
2012

The Cognitive Genetics of Neuropsychiatric Disorders
2012

The autism brain imaging data exchange: towards a large-scale evaluation of the intrinsic brain architecture in autism.
2012

The cognitive genetics of neuropsychiatric disorders.
2011

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
2011

Assessing problem based learning in child and adolescent psychiatry at the trinity college dublin, ireland.
2011

Exploration of empirical Bayes hierarchical modeling for the analysis of genome-wide association study data.
2011

Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for Autism.
2011

Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders.
2011

Mental health aspects of autistic spectrum disorders in children.
2011

Mental health problems in children with prader-willi syndrome.
2010

A genomewide scan for common alleles affecting risk for autism.
2010

Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism.
2009

A genome-wide linkage and association scan reveals novel loci for autism.
2009

Detecting subtle facial emotion recognition deficits in high-functioning Autism using dynamic stimuli of varying intensities.
2009

Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: genetic and molecular studies.
2008

Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32.
2008

Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
2008

Serial Post-mortem Relaxometry in the Normal Rat Brain and Following Stroke
2007

Dissociation in performance of children with ADHD and autism on a task of sustained attention
2007

Dissociation in performance of children with ADHD and high-functioning autism on a task of sustained attention.
2006

Dissociation in performance of children with ADHD and high-functioning autism on a task of sustained attention.
2005

Preferential Transmission of Paternal Alleles at Risk Genes in Attention Deficit/Hyperactivity Disorder
2004

Molecular genetics investigations in autism

These arethe12 unique sources for Louise Gallagher's 61 publications. A single publication may appear in multiple sources. Click on a name or publication count to see the publications for a particular source.

Source #
Ireland -> Maynooth University 1
Ireland -> National College Ireland 1
Ireland -> National College of Ireland 2
Ireland -> National University of Ireland Galway 1
Ireland -> National University of Ireland Galway -> PubMed 1
Ireland -> Royal College of Surgeons in Ireland 1
Ireland -> Royal College of Surgeons in Ireland -> PubMed 1
Ireland -> TU Dublin 1
Ireland -> Trinity College Dublin 57
Ireland -> Trinity College Dublin -> PubMed 24
Ireland -> University College Dublin 3
Ireland -> University College Dublin -> PubMed 1

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