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Shared and divergent mental health characteristics of ADNP-, CHD8- and DYRK1A-related neurodevelopmental conditions.
- Published in:
- Journal of Neurodevelopmental Disorders, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s11689-024-09532-1
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- Publication type:
- Article
Resting state EEG in youth with ASD: age, sex, and relation to phenotype.
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- Journal of Neurodevelopmental Disorders, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s11689-021-09390-1
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- Publication type:
- Article
A computer-generated animated face stimulus set for psychophysiological research.
- Published in:
- Behavior Research Methods, 2015, v. 47, n. 2, p. 562, doi. 10.3758/s13428-014-0491-x
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- Publication type:
- Article
Erratum to: A computer-generated animated face stimulus set for psychophysiological research.
- Published in:
- 2015
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- Publication type:
- Erratum
Excess of rare, inherited truncating mutations in autism.
- Published in:
- Nature Genetics, 2015, v. 47, n. 6, p. 582, doi. 10.1038/ng.3303
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- Publication type:
- Article
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
- Published in:
- 2012
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- Publication type:
- Correction Notice
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
- Published in:
- Nature Genetics, 2011, v. 43, n. 6, p. 585, doi. 10.1038/ng.835
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- Publication type:
- Article
Educational and therapeutic behavioral approaches to providing dental care for patients with Autism Spectrum Disorder.
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- Special Care in Dentistry, 2015, v. 35, n. 3, p. 105, doi. 10.1111/scd.12101
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- Publication type:
- Article
Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes.
- Published in:
- Human Genetics, 2015, v. 134, n. 10, p. 1055, doi. 10.1007/s00439-015-1585-y
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- Publication type:
- Article
Comorbid symptoms of inattention, autism, and executive cognition in youth with putative genetic risk.
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- Journal of Child Psychology, 2018, v. 59, n. 3, p. 268, doi. 10.1111/jcpp.12815
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- Publication type:
- Article
Sleep Problems in Children with ASD and Gene Disrupting Mutations.
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- Journal of Genetic Psychology, 2021, v. 182, n. 5, p. 317, doi. 10.1080/00221325.2021.1922869
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- Publication type:
- Article
Long-term Risk of Neuropsychiatric Disease After Exposure to Infection In Utero.
- Published in:
- 2019
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- Publication type:
- journal article
The phenotypic spectrum and genotype-phenotype correlations in 106 patients with variants in major autism gene CHD8.
- Published in:
- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-02189-1
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- Publication type:
- Article
The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2014, v. 166C, n. 3, p. 315, doi. 10.1002/ajmg.c.31413
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- Article
Language characterization in 16p11.2 deletion and duplication syndromes.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2020, v. 183, n. 6, p. 380, doi. 10.1002/ajmg.b.32809
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- Publication type:
- Article
Developmental trajectories for young children with 16p11.2 copy number variation.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 4, p. 367, doi. 10.1002/ajmg.b.32525
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- Publication type:
- Article
Face processing among twins with and without autism: social correlates and twin concordance.
- Published in:
- Social Cognitive & Affective Neuroscience, 2016, v. 11, n. 1, p. 44, doi. 10.1093/scan/nsv085
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- Publication type:
- Article
Developmental changes in mu suppression to observed and executed actions in autism spectrum disorders.
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- Social Cognitive & Affective Neuroscience, 2013, v. 8, n. 3, p. 300, doi. 10.1093/scan/nsr097
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- Publication type:
- Article
Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes.
- Published in:
- PLoS Genetics, 2011, v. 7, n. 11, p. 1, doi. 10.1371/journal.pgen.1002334
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- Publication type:
- Article
BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorder.
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- Human Mutation, 2020, v. 41, n. 5, p. 921, doi. 10.1002/humu.23992
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- Publication type:
- Article
Co-occurring medical conditions among individuals with ASD-associated disruptive mutations.
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- Children's Health Care, 2020, v. 49, n. 4, p. 361, doi. 10.1080/02739615.2020.1741361
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- Publication type:
- Article
Family-based exome sequencing and case-control analysis implicate CEP41 as an ASD gene.
- Published in:
- Translational Psychiatry, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41398-018-0343-z
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- Publication type:
- Article
Psychiatric disorders in children with 16p11.2 deletion and duplication.
- Published in:
- Translational Psychiatry, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41398-018-0339-8
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- Publication type:
- Article
Identifying Age Based Maturation in the ERP Response to Faces in Children With Autism: Implications for Developing Biomarkers for Use in Clinical Trials.
- Published in:
- Frontiers in Psychiatry, 2022, v. 13, p. 1, doi. 10.3389/fpsyt.2022.841236
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- Publication type:
- Article
α7 Nicotinic Acetylcholine Receptor Signaling Modulates Ovine Fetal Brain Astrocytes Transcriptome in Response to Endotoxin.
- Published in:
- Frontiers in Immunology, 2019, p. N.PAG, doi. 10.3389/fimmu.2019.01063
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- Publication type:
- Article
The Autism Biomarkers Consortium for Clinical Trials: evaluation of a battery of candidate eye-tracking biomarkers for use in autism clinical trials.
- Published in:
- Molecular Autism, 2022, v. 13, n. 1, p. 1, doi. 10.1186/s13229-021-00482-2
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- Publication type:
- Article
The autism biomarkers consortium for clinical trials: evaluation of a battery of candidate eye-tracking biomarkers for use in autism clinical trials.
- Published in:
- Molecular Autism, 2022, v. 13, n. 1, p. 1, doi. 10.1186/s13229-021-00482-2
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- Publication type:
- Article
Clinical phenotype of ASD-associated DYRK1A haploinsufficiency.
- Published in:
- Molecular Autism, 2017, v. 8, p. 1, doi. 10.1186/s13229-017-0173-5
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- Publication type:
- Article
Prospective investigation of FOXP1 syndrome.
- Published in:
- Molecular Autism, 2017, v. 8, p. 1, doi. 10.1186/s13229-017-0172-6
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- Publication type:
- Article
Do Biological Sex and Early Developmental Milestones Predict the Age of First Concerns and Eventual Diagnosis in Autism Spectrum Disorder?
- Published in:
- Autism Research: Official Journal of the International Society for Autism Research, 2021, v. 14, n. 1, p. 156, doi. 10.1002/aur.2446
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- Publication type:
- Article
Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriers.
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- Autism Research: Official Journal of the International Society for Autism Research, 2020, v. 13, n. 8, p. 1300, doi. 10.1002/aur.2332
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- Publication type:
- Article
Concentrations of Cortical GABA and Glutamate in Young Adults With Autism Spectrum Disorder.
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- Autism Research: Official Journal of the International Society for Autism Research, 2020, v. 13, n. 7, p. 1111, doi. 10.1002/aur.2300
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- Publication type:
- Article
The diagnosis conundrum: Comparison of crowdsourced and expert assessments of toddlers with high and low risk of autism spectrum disorder.
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- Autism Research: Official Journal of the International Society for Autism Research, 2018, v. 11, n. 12, p. 1629, doi. 10.1002/aur.2030
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- Publication type:
- Article
The autism spectrum phenotype in ADNP syndrome.
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- Autism Research: Official Journal of the International Society for Autism Research, 2018, v. 11, n. 9, p. 1300, doi. 10.1002/aur.1980
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- Publication type:
- Article
Child and family characteristics moderate agreement between caregiver and clinician report of autism symptoms.
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- Autism Research: Official Journal of the International Society for Autism Research, 2018, v. 11, n. 3, p. 476, doi. 10.1002/aur.1907
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- Publication type:
- Article
Next Generation Sequencing Mitochondrial DNA Analysis in Autism Spectrum Disorder.
- Published in:
- Autism Research: Official Journal of the International Society for Autism Research, 2017, v. 10, n. 8, p. 1338, doi. 10.1002/aur.1792
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- Publication type:
- Article
Severity of ASD symptoms and their correlation with the presence of copy number variations and exposure to first trimester ultrasound.
- Published in:
- Autism Research: Official Journal of the International Society for Autism Research, 2017, v. 10, n. 3, p. 472, doi. 10.1002/aur.1690
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- Publication type:
- Article
Executive function predicts the development of play skills for verbal preschoolers with autism spectrum disorders.
- Published in:
- Autism Research: Official Journal of the International Society for Autism Research, 2016, v. 9, n. 12, p. 1274, doi. 10.1002/aur.1608
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- Publication type:
- Article
Children with Autism Show Altered Autonomic Adaptation to Novel and Familiar Social Partners.
- Published in:
- Autism Research: Official Journal of the International Society for Autism Research, 2016, v. 9, n. 5, p. 579, doi. 10.1002/aur.1543
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- Publication type:
- Article
Electrodermal Response to Reward and Non-Reward Among Children With Autism.
- Published in:
- Autism Research: Official Journal of the International Society for Autism Research, 2015, v. 8, n. 4, p. 357, doi. 10.1002/aur.1451
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- Publication type:
- Article
Evidence for broader autism phenotype characteristics in parents from multiple-incidence autism families.
- Published in:
- Autism Research: Official Journal of the International Society for Autism Research, 2012, v. 5, n. 1, p. 13, doi. 10.1002/aur.226
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- Publication type:
- Article
Infants' grip strength predicts mu rhythm attenuation during observation of lifting actions with weighted blocks.
- Published in:
- Developmental Science, 2016, v. 19, n. 2, p. 195, doi. 10.1111/desc.12308
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- Publication type:
- Article
Correction: Long-term real-life outcomes of the Clareon® hydrophobic intraocular lens: the Clarte study in 191 eyes: 3-years real-life outcomes of the Clareon® intraocular lens.
- Published in:
- 2024
- By:
- Publication type:
- Correction Notice
Long-term real-life outcomes of the Clareon® hydrophobic intraocular lens: the Clarte study in 191 eyes: 3-years real-life outcomes of the Clareon® intraocular lens.
- Published in:
- BMC Ophthalmology, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12886-024-03393-x
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- Publication type:
- Article
Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16.
- Published in:
- Human Genetics, 2011, v. 129, n. 1, p. 59, doi. 10.1007/s00439-010-0899-z
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- Publication type:
- Article
Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.
- Published in:
- 2016
- By:
- Publication type:
- journal article
The Role of Parental Cognitive, Behavioral, and Motor Profiles in Clinical Variability in Individuals With Chromosome 16p11.2 Deletions.
- Published in:
- JAMA Psychiatry, 2015, v. 72, n. 2, p. 119, doi. 10.1001/jamapsychiatry.2014.2147
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- Publication type:
- Article
Neural responsivity to social rewards in autistic female youth.
- Published in:
- Translational Psychiatry, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41398-020-0824-8
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- Publication type:
- Article
Imaging-genetics of sex differences in ASD: distinct effects of OXTR variants on brain connectivity.
- Published in:
- Translational Psychiatry, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41398-020-0750-9
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- Publication type:
- Article
Correction: Psychiatric disorders in children with 16p11.2 deletion and duplication.
- Published in:
- Translational Psychiatry, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41398-019-0441-6
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- Publication type:
- Article