Found: 29
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Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.
- Published in:
- Translational Psychiatry, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41398-019-0402-0
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- Publication type:
- Article
Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability.
- Published in:
- Frontiers in Psychiatry, 2024, p. 1, doi. 10.3389/fpsyt.2024.1369767
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- Publication type:
- Article
Single-cell analysis reveals inflammatory interactions driving macular degeneration.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37025-7
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- Publication type:
- Article
Bayonet-shaped language development in autism with regression: a retrospective study.
- Published in:
- Molecular Autism, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13229-021-00444-8
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- Publication type:
- Article
Copy Number Variant Risk Scores Associated With Cognition, Psychopathology, and Brain Structure in Youths in the Philadelphia Neurodevelopmental Cohort.
- Published in:
- 2022
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- Publication type:
- journal article
Deletion of Loss-of-Function-Intolerant Genes and Risk of 5 Psychiatric Disorders.
- Published in:
- 2022
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- Publication type:
- journal article
Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples.
- Published in:
- 2018
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- Publication type:
- journal article
Effects of eight neuropsychiatric copy number variants on human brain structure.
- Published in:
- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01490-9
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- Publication type:
- Article
Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 4, p. 1686, doi. 10.1093/brain/awac315
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- Publication type:
- Article
Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway.
- Published in:
- Journal of Pineal Research, 2013, v. 54, n. 1, p. 46, doi. 10.1111/j.1600-079X.2012.01020.x
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- Publication type:
- Article
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.
- Published in:
- Journal of Pineal Research, 2011, v. 51, n. 4, p. 394, doi. 10.1111/j.1600-079X.2011.00902.x
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- Publication type:
- Article
The emerging role of SHANK genes in neuropsychiatric disorders.
- Published in:
- Developmental Neurobiology (19328451), 2014, v. 74, n. 2, p. 113, doi. 10.1002/dneu.22128
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- Publication type:
- Article
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 9, p. 1, doi. 10.1371/journal.pgen.1004580
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- Publication type:
- Article
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders.
- Published in:
- PLoS Genetics, 2012, v. 8, n. 2, p. 1, doi. 10.1371/journal.pgen.1002521
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- Publication type:
- Article
Using developmental regression to reorganize the clinical importance of autistic atypicalities.
- Published in:
- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-02263-8
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- Publication type:
- Article
Investigating the contributions of circadian pathway and insomnia risk genes to autism and sleep disturbances.
- Published in:
- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-02188-2
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- Publication type:
- Article
Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-18997-2
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- Publication type:
- Article
Heterogeneous Pattern of Selective Pressure for PRRT2 in Human Populations, but No Association with Autism Spectrum Disorders.
- Published in:
- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0088600
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- Publication type:
- Article
Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders.
- Published in:
- Human Genetics, 2014, v. 133, n. 6, p. 781, doi. 10.1007/s00439-013-1416-y
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- Publication type:
- Article
Zinc deficiency and low enterocyte zinc transporter expression in human patients with autism related mutations in SHANK3.
- Published in:
- Scientific Reports, 2017, p. 45190, doi. 10.1038/srep45190
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- Publication type:
- Article
Author Correction: Using rare genetic mutations to revisit structural brain asymmetry.
- Published in:
- 2024
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- Publication type:
- Correction Notice
Using rare genetic mutations to revisit structural brain asymmetry.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-46784-w
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- Publication type:
- Article
Heterozygous FA2H mutations in autism spectrum disorders.
- Published in:
- BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-124
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- Publication type:
- Article
Estimating the effects of copy‐number variants on intelligence using hierarchical Bayesian models.
- Published in:
- Genetic Epidemiology, 2020, v. 44, n. 8, p. 825, doi. 10.1002/gepi.22344
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- Publication type:
- Article
Both rare and common genetic variants contribute to autism in the Faroe Islands.
- Published in:
- NPJ Genomic Medicine, 2019, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41525-018-0075-2
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- Publication type:
- Article
Both rare and common genetic variants contribute to autism in the Faroe Islands.
- Published in:
- NPJ Genomic Medicine, 2019, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41525-018-0075-2
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- Publication type:
- Article
11q24.2-25 Micro-Rearrangements in Autism Spectrum Disorders: Relation to Brain Structures.
- Published in:
- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 12, p. 3019, doi. 10.1002/ajmg.a.37345
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- Publication type:
- Article
Effects of Alzheimer's disease genetic risk on brain morphometric development in three multiple‐ancestry pediatric datasets.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.080302
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- Publication type:
- Article
Effects of Alzheimer's disease genetic risk on brain morphometric development in three multiple‐ancestry pediatric datasets.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, n. 10, p. 1, doi. 10.1002/alz.081996
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- Publication type:
- Article