Lista de obras - Louise Gallagher - Dominio Público Uruguay

A framework for an evidence-based gene list relevant to autism spectrum disorder

artículo científico publicado en 2020

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

artículo científico publicado en 2016

A genome-wide scan for common alleles affecting risk for autism

scientific journal article

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

artículo científico publicado en 2011

A profile of mental health and behaviour in Prader-Willi syndrome

artículo científico publicado en 2019

A review of neuropsychological and neuroimaging research in autistic spectrum disorders: Attention, inhibition and cognitive flexibility

article

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

artículo científico publicado en 2017

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

artículo científico publicado en 2013

Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets

scientific article published on 31 October 2019

Altered structural brain asymmetry in autism spectrum disorder: large-scale analysis via the ENIGMA Consortium

An evaluation of the appropriateness and effectiveness of structured reflection for midwifery students in Ireland.

artículo científico publicado en 2016

An investigation of mitochondrial haplogroups in autism

artículo científico publicado en 2008

Artificial milk-feeding women׳s views of their feeding choice in Ireland

artículo científico publicado en 2015

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

artículo científico publicado en 2012

Association of the alpha4 integrin subunit gene (ITGA4) with autism

artículo científico publicado en 2009

Atypical visuospatial processing in autism: insights from functional connectivity analysis

artículo científico publicado en 2012

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

artículo científico publicado en 2015

Autism in a recently arrived immigrant population

artículo científico publicado en 2013

Bio-collections in autism research

artículo científico publicado en 2017

Brief report: A case of autism associated with del(2)(q32.1q32.2) or (q32.2q32.3).

artículo científico publicado en 2003

CNVs leading to fusion transcripts in individuals with autism spectrum disorder

artículo científico publicado en 2012

Child Health Care in Ireland. ⬇️

artículo científico publicado en 2016

Complexity based measures of postural stability provide novel evidence of functional decline in fragile X premutation carriers

scientific article published on 12 July 2019

Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31

artículo científico publicado en 2005

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

artículo científico publicado en 2014

Copy-number variants in neurodevelopmental disorders: promises and challenges

artículo científico publicado en 2009

Cortical and Subcortical Brain Morphometry Differences Between Patients With Autism Spectrum Disorder and Healthy Individuals Across the Lifespan: Results From the ENIGMA ASD Working Group

artículo científico publicado en 2017

Derivation of familial iPSC lines from three ASD patients carrying NRXN1α+/- and two controls (NUIGi022-A, NUIGi022-B; NUIGi023-A, NUIGi023-B; NUIGi025-A, NUIGi025-B; NUIGi024-A, NUIGi024-B; NUIGi026-A, NUIGi026-B)

artículo científico publicado en 2019

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

artículo científico publicado en 2010

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

artículo científico publicado en 2014

Disrupted prediction errors index social deficits in autism spectrum disorder

artículo científico publicado en 2017

Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability

artículo científico publicado en 2010

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

artículo científico publicado en 2007

Dopaminergic-neuropeptide interactions in the social brain

artículo científico publicado en 2008

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

artículo científico publicado en 2017

Evidence of Assortative Mating in Autism Spectrum Disorder

artículo científico publicado en 2019

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

artículo científico publicado en 2013

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

artículo científico publicado en 2011

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

artículo científico publicado en 2009

Functional and structural connectivity of frontostriatal circuitry in Autism Spectrum Disorder

artículo científico publicado en 2013

Functional impact of global rare copy number variation in autism spectrum disorders

artículo científico publicado en 2010

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

artículo científico publicado en 2011

Gaining Insights into Aggressive Behaviour in Autism Spectrum Disorder Using Latent Profile Analysis

scientific article published on 01 October 2019

Gait deviations in children with autism spectrum disorders: a review

artículo científico publicado en 2015

Genetic influences on social cognition

artículo científico publicado en 2011

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

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

scientific article published on 01 March 2019

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

artículo científico publicado en 2014

Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort study

artículo científico publicado en 2020

Increased BDNF levels and NTRK2 gene association suggest a disruption of BDNF/TrkB signaling in autism.

artículo científico publicado en 2010

Increased Ca2+ signaling in NRXN1α +/- neurons derived from ASD induced pluripotent stem cells

artículo científico publicado en 2019

Individual common variants exert weak effects on the risk for autism spectrum disorders

scientific journal article

Intragenic CAMTA1 rearrangements cause non-progressive congenital ataxia with or without intellectual disability.

artículo científico publicado en 2012

Lack of association between markers in the ITGA3, ITGAV, ITGA6 and ITGB3 and autism in an Irish sample

artículo científico publicado en 2010

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

artículo científico publicado en 2017

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

scientific article published on 23 January 2020

Mental health aspects of autistic spectrum disorders in children

artículo científico publicado en 2011

Mental health problems in children with prader-willi syndrome

artículo científico publicado en 2012

Microduplications of 16p11.2 are associated with schizophrenia

artículo científico publicado en 2009

Molecular Pathways in Autistic Spectrum Disorders

scholarly article

Molecular and genetic influences on the neural substrate of social cognition in humans

Monitoring of prolactin levels in children and adolescents prescribed antipsychotic medication: a complete audit cycle

NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families

article by Maryam Al Shehhi et al published March 2019 in European Journal of Medical Genetics

No evidence that common genetic risk variation is shared between schizophrenia and autism

artículo científico publicado en 2012

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

article

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

artículo científico publicado en 2010

Parental age, birth order and neurodevelopmental disorders

artículo científico publicado en 2015

Preferential transmission of paternal alleles at risk genes in attention-deficit/hyperactivity disorder

artículo científico publicado en 2005

Problem-based learning in child and adolescent psychiatry at Trinity College, Dublin, Ireland

artículo científico publicado en 2012

Protein kinase C-beta 1 gene variants are not associated with autism in the Irish population

artículo científico publicado en 2007

Psychosis, affective disorders and anxiety in autistic spectrum disorder: prevalence and nosological considerations

artículo científico publicado en 2009

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

artículo científico publicado en 2008

Regulation and postsynaptic binding of neurexins — drug targets for neurodevelopmental and neuropsychiatric disorders

Serotonin transporter gene and autism: a haplotype analysis in an Irish autistic population

artículo científico publicado en 2004

Social and monetary reward processing in autism spectrum disorders

artículo científico publicado en 2012

Synaptic, transcriptional and chromatin genes disrupted in autism

artículo científico publicado en 2014

The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses

artículo científico publicado en 2014

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

artículo científico publicado en 2013

The clinical relevance of intragenic NRXN1 deletions

artículo científico publicado en 2020

The cognitive genetics of neuropsychiatric disorders

artículo científico publicado en 2012

The phenotypic manifestations of rare CNVs in schizophrenia

artículo científico publicado en 2014

The phenotypic manifestations of rare genic CNVs in autism spectrum disorder

artículo científico publicado en 2014

The role of rare compound heterozygous events in autism spectrum disorder

artículo científico publicado en 2020

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

artículo científico publicado en 2015

Virtual Ontogeny of Cortical Growth Preceding Mental Illness

scientific article published in 2022

White matter and visuospatial processing in autism: a constrained spherical deconvolution tractography study

artículo científico publicado en 2013

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

artículo científico publicado en 2017

Widespread Disrupted White Matter Microstructure in Autism Spectrum Disorders.

artículo científico publicado en 2016

Lista de obras de Louise Gallagher

A framework for an evidence-based gene list relevant to autism spectrum disorder

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

A genome-wide scan for common alleles affecting risk for autism

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

A profile of mental health and behaviour in Prader-Willi syndrome

A review of neuropsychological and neuroimaging research in autistic spectrum disorders: Attention, inhibition and cognitive flexibility

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

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

Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets

Altered structural brain asymmetry in autism spectrum disorder: large-scale analysis via the ENIGMA Consortium

An evaluation of the appropriateness and effectiveness of structured reflection for midwifery students in Ireland.

An investigation of mitochondrial haplogroups in autism

Artificial milk-feeding women׳s views of their feeding choice in Ireland

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

Association of the alpha4 integrin subunit gene (ITGA4) with autism

Atypical visuospatial processing in autism: insights from functional connectivity analysis

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

Autism in a recently arrived immigrant population

Bio-collections in autism research

Brief report: A case of autism associated with del(2)(q32.1q32.2) or (q32.2q32.3).

CNVs leading to fusion transcripts in individuals with autism spectrum disorder

Child Health Care in Ireland. ⬇️

Complexity based measures of postural stability provide novel evidence of functional decline in fragile X premutation carriers

Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

Copy-number variants in neurodevelopmental disorders: promises and challenges

Cortical and Subcortical Brain Morphometry Differences Between Patients With Autism Spectrum Disorder and Healthy Individuals Across the Lifespan: Results From the ENIGMA ASD Working Group

Derivation of familial iPSC lines from three ASD patients carrying NRXN1α+/- and two controls (NUIGi022-A, NUIGi022-B; NUIGi023-A, NUIGi023-B; NUIGi025-A, NUIGi025-B; NUIGi024-A, NUIGi024-B; NUIGi026-A, NUIGi026-B)

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

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

Disrupted prediction errors index social deficits in autism spectrum disorder

Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability

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

Dopaminergic-neuropeptide interactions in the social brain

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

Evidence of Assortative Mating in Autism Spectrum Disorder

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

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

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

Functional and structural connectivity of frontostriatal circuitry in Autism Spectrum Disorder

Functional impact of global rare copy number variation in autism spectrum disorders

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

Gaining Insights into Aggressive Behaviour in Autism Spectrum Disorder Using Latent Profile Analysis

Gait deviations in children with autism spectrum disorders: a review

Genetic influences on social cognition

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

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

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

Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort study

Increased BDNF levels and NTRK2 gene association suggest a disruption of BDNF/TrkB signaling in autism.

Increased Ca2+ signaling in NRXN1α +/- neurons derived from ASD induced pluripotent stem cells

Individual common variants exert weak effects on the risk for autism spectrum disorders

Intragenic CAMTA1 rearrangements cause non-progressive congenital ataxia with or without intellectual disability.

Lack of association between markers in the ITGA3, ITGAV, ITGA6 and ITGB3 and autism in an Irish sample

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

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

Mental health aspects of autistic spectrum disorders in children

Mental health problems in children with prader-willi syndrome

Microduplications of 16p11.2 are associated with schizophrenia

Molecular Pathways in Autistic Spectrum Disorders

Molecular and genetic influences on the neural substrate of social cognition in humans

Monitoring of prolactin levels in children and adolescents prescribed antipsychotic medication: a complete audit cycle

NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families

No evidence that common genetic risk variation is shared between schizophrenia and autism

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

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

Parental age, birth order and neurodevelopmental disorders

Preferential transmission of paternal alleles at risk genes in attention-deficit/hyperactivity disorder

Problem-based learning in child and adolescent psychiatry at Trinity College, Dublin, Ireland

Protein kinase C-beta 1 gene variants are not associated with autism in the Irish population

Psychosis, affective disorders and anxiety in autistic spectrum disorder: prevalence and nosological considerations

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

Regulation and postsynaptic binding of neurexins — drug targets for neurodevelopmental and neuropsychiatric disorders

Serotonin transporter gene and autism: a haplotype analysis in an Irish autistic population

Social and monetary reward processing in autism spectrum disorders

Synaptic, transcriptional and chromatin genes disrupted in autism

The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses

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

The clinical relevance of intragenic NRXN1 deletions