about
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disabilityFunctional impact of global rare copy number variation in autism spectrum disordersMicroduplications of 16p11.2 are associated with schizophreniaRecurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypesGait deviations in children with autism spectrum disorders: a reviewSynaptic, transcriptional and chromatin genes disrupted in autismAn investigation of mitochondrial haplogroups in autismConfirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31Genetic relationship between five psychiatric disorders estimated from genome-wide SNPsCNVs leading to fusion transcripts in individuals with autism spectrum disorderIndividual common variants exert weak effects on the risk for autism spectrum disordersA genome-wide scan for common alleles affecting risk for autismEnhancing studies of the connectome in autism using the autism brain imaging data exchange II.Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.Exploration of empirical Bayes hierarchical modeling for the analysis of genome-wide association study data.Bio-collections in autism research.Preferential transmission of paternal alleles at risk genes in attention-deficit/hyperactivity disorder.The autism brain imaging data exchange: towards a large-scale evaluation of the intrinsic brain architecture in autism.The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses.Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism.Copy-number variants in neurodevelopmental disorders: promises and challenges.Autism Spectrum Disorder (ASD) and Fragile X Syndrome (FXS): Two Overlapping Disorders Reviewed through Electroencephalography-What Can be Interpreted from the Available Information?A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.Dissociation in performance of children with ADHD and high-functioning autism on a task of sustained attention.Mental health problems in children with prader-willi syndromeSocial and monetary reward processing in autism spectrum disorders.The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.Abnormal functional connectivity during visuospatial processing is associated with disrupted organisation of white matter in autism.Dopaminergic-neuropeptide interactions in the social brain.Psychosis, affective disorders and anxiety in autistic spectrum disorder: prevalence and nosological considerations.Genetic influences on social cognition.The cognitive genetics of neuropsychiatric disorders.Abnormal fronto-parietal white matter organisation in the superior longitudinal fasciculus branches in autism spectrum disorders.Lack of effect of vitamin D3 supplementation in autism: a 20-week, placebo-controlled RCT.Artificial milk-feeding women׳s views of their feeding choice in Ireland.Disrupted prediction errors index social deficits in autism spectrum disorder.A genome-wide investigation into parent-of-origin effects in autism spectrum disorder identifies previously associated genes including SHANK3.Widespread Disrupted White Matter Microstructure in Autism Spectrum Disorders.Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.Assessing problem based learning in child and adolescent psychiatry at the trinity college dublin, ireland.
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P50
description
hulumtuese
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researcher
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հետազոտող
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Louise Gallagher
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Louise Gallagher
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Louise Gallagher
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Louise Gallagher
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Louise Gallagher
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Louise Gallagher
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Louise Gallagher
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Louise Gallagher
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Louise Gallagher
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Louise Gallagher
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Louise Gallagher
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Louise Gallagher
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Louise Gallagher
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Louise Gallagher
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Louise Wain
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Louise Gallagher
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Louise Gallagher
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Louise Gallagher
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Louise Gallagher
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Louise Gallagher
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Louise Gallagher
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Louise Gallagher
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7005393044
P21
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0000-0001-9462-2836