|
| 34994928 | Brief Report: Evaluating the Diagnostic Yield of Commercial Gene Panels in Autism. | Journal of Autism and Developmental Disorders | 2023 |
| 37031194 | A review of the cognitive impact of neurodevelopmental and neuropsychiatric associated copy number variants. | | 2023 |
| 36747038 | Sex and gender in neurodevelopmental conditions. | | 2023 |
| 37441676 | Bridging the translational gap: what can synaptopathies tell us about autism? | Front Mol Neurosci | 2023 |
| 36788583 | CRISIS AFAR: an international collaborative study of the impact of the COVID-19 pandemic on mental health and service access in youth with autism and neurodevelopmental conditions. | Mol Autism | 2023 |
| 34364706 | How does genetic variation modify ND-CNV phenotypes? | Trends in Genetics | 2022 |
| 36106582 | Establishing an Irish autism research network. | | 2022 |
| 36368308 | Genomic architecture of autism from comprehensive whole-genome sequence annotation. | Cell | 2022 |
| 35965061 | Autism spectrum disorders: current issues and future directions. | | 2022 |
| 32420680 | Consortium neuroscience of attention deficit/hyperactivity disorder and autism spectrum disorder: The ENIGMA adventure. | Hum Brain Mapp | 2022 |
| 35250672 | Maternal Immune Activation and Interleukin 17A in the Pathogenesis of Autistic Spectrum Disorder and Why It Matters in the COVID-19 Era. | Frontiers in Psychiatry | 2022 |
| 35250452 | The Synaptic Gene Study: Design and Methodology to Identify Neurocognitive Markers in Phelan-McDermid Syndrome and <i>NRXN1</i> Deletions. | Front Neurosci | 2022 |
| 34823622 | Can stratification biomarkers address the heterogeneity of autism spectrum disorder? | | 2022 |
| 34525970 | NRXN1α<sup>+/-</sup> is associated with increased excitability in ASD iPSC-derived neurons. | BMC Neurosci | 2021 |
| 33631419 | Derivation of four iPSC lines from a male ASD patient carrying a deletion in the middle coding region of NRXN1α gene (NUIGi039-A and NUIGi039-B) and a male sibling control (NUIGi040-A and NUIGi040-B). | Stem Cell Res | 2021 |
| 33578364 | Derivation of iPSC lines from two patients with autism spectrum disorder carrying NRXN1α deletion (NUIGi041-A, NUIG041-B; NUIGi045-A) and one sibling control (NUIGi042-A, NUIGi042-B). | Stem Cell Res | 2021 |
| 34001500 | COVID-19 health and social care access for autistic people: European policy review. | BMJ Open | 2021 |
| 33571692 | 'More than a box of puzzles': Understanding the parental experience of having a child with a rare genetic condition". | European Journal of Medical Genetics | 2021 |
| 33941482 | A novel non-viral delivery method that enables efficient engineering of primary human T cells for ex vivo cell therapy applications. | Cytotherapy | 2021 |
| 34148559 | Behavioral features in Prader-Willi syndrome (PWS): consensus paper from the International PWS Clinical Trial Consortium. | Journal of Neurodevelopmental Disorders | 2021 |
| 33866895 | Parental stress and adjustment in the context of rare genetic syndromes: A scoping review. | Journal of Intellectual Disabilities | 2021 |
| 33384013 | A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants. | Am J Psychiatry | 2021 |
| 34880244 | Author Correction: Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets. | Nat Commun | 2021 |
| 33321999 | Rare Pathogenic Copy Number Variation in the 16p11.2 (BP4-BP5) Region Associated with Neurodevelopmental and Neuropsychiatric Disorders: A Review of the Literature. | International Journal of Environmental Research and Public Health | 2020 |
| 32317787 | A framework for an evidence-based gene list relevant to autism spectrum disorder. | Nat Rev Genet | 2020 |
| 31964429 | Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort study. | Br J Psychiatry | 2020 |
| 31849130 | A profile of mental health and behaviour in Prader-Willi syndrome. | Journal of Intellectual Disability Research | 2020 |
| 31932357 | The clinical relevance of intragenic deletions. | Journal of Medical Genetics | 2020 |
| 32097875 | Derivation of two iPSC lines from a sporadic ASD patient (NUIGi033-A) and a paternal control (NUIGi034-A). | Stem Cell Research | 2020 |
| 32539527 | Subcortical Brain Volume, Regional Cortical Thickness, and Cortical Surface Area Across Disorders: Findings From the ENIGMA ADHD, ASD, and OCD Working Groups. | Am J Psychiatry | 2020 |
| 33370872 | Derivation of iPSC lines from three young healthy donors of Caucasian origin (NUIGi035-A; NUIGi036-A; NUIGi037-A). | Stem Cell Research | 2020 |
| 32572023 | The role of rare compound heterozygous events in autism spectrum disorder. | Transl Psychiatry | 2020 |
| 33338084 | Coupling of autism genes to tissue-wide expression and dysfunction of synapse, calcium signalling and transcriptional regulation. | PLoS ONE | 2020 |
| 32941983 | Autism spectrum disorder genomics: The progress and potential of genomic technologies. | Genomics | 2020 |
| 27207090 | Widespread Disrupted White Matter Microstructure in Autism Spectrum Disorders. | Journal of Autism and Developmental Disorders | 2019 |
| 31893021 | Increased Ca<sup>2+</sup> signaling in <i>NRXN1α</i><sup><i>+/-</i></sup> neurons derived from ASD induced pluripotent stem cells. | Mol Autism | 2019 |
| 31673008 | Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets. | Nat Commun | 2019 |
| 31759289 | Derivation of familial iPSC lines from three ASD patients carrying NRXN1α<sup>+/-</sup> and two controls (NUIGi022-A, NUIGi022-B; NUIGi023-A, NUIGi023-B; NUIGi025-A, NUIGi025-B; NUIGi024-A, NUIGi024-B; NUIGi026-A, NUIGi026-B). | Stem Cell Res | 2019 |
| 30031152 | NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families. | Eur J Med Genet | 2019 |
| 30823851 | He said, she said: Autism spectrum diagnosis and gender differentially affect relationships between executive functions and social communication. | Autism | 2019 |
| 31200929 | Evidence of Assortative Mating in Autism Spectrum Disorder. | Biological Psychiatry | 2019 |
| 31299981 | Complexity based measures of postural stability provide novel evidence of functional decline in fragile X premutation carriers. | Journal of NeuroEngineering and Rehabilitation | 2019 |
| 31292900 | Gaining Insights into Aggressive Behaviour in Autism Spectrum Disorder Using Latent Profile Analysis. | Journal of Autism and Developmental Disorders | 2019 |
| 29145754 | 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. | Am J Psychiatry | 2018 |
| 28741714 | Abnormal fronto-parietal white matter organisation in the superior longitudinal fasciculus branches in autism spectrum disorders. | European Journal of Neuroscience | 2018 |
| 28291247 | Enhancing studies of the connectome in autism using the autism brain imaging data exchange II. | Sci Data | 2017 |
| 28626020 | Lack of effect of vitamin D supplementation in autism: a 20-week, placebo-controlled RCT. | Archives of Disease in Childhood | 2017 |
| 28702161 | Bio-collections in autism research. | Molecular Autism | 2017 |
| 28358921 | Vector-free intracellular delivery by reversible permeabilization. | PLoS ONE | 2017 |
| 30115169 | Monitoring of prolactin levels in children and adolescents prescribed antipsychotic medication: a complete audit cycle. | | 2017 |