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Genetic markers for PTSD risk and resilience among survivors of the World Trade Center attacks.
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- Disease Markers, 2011, v. 30, n. 2-3, p. 101
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- Article
Comorbidities in autism spectrum disorder and their etiologies.
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- Translational Psychiatry, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41398-023-02374-w
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- Article
Clinical, genetic, and cognitive correlates of seizure occurrences in Phelan-McDermid syndrome.
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- Journal of Neurodevelopmental Disorders, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s11689-024-09541-0
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- Article
Rapid and Objective Assessment of Neural Function in Autism Spectrum Disorder Using Transient Visual Evoked Potentials.
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- PLoS ONE, 2016, v. 11, n. 10, p. 1, doi. 10.1371/journal.pone.0164422
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- Article
Prospective phenotyping of CHAMP1 disorder indicates that coding mutations may not act through haploinsufficiency.
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- Human Genetics, 2023, v. 142, n. 9, p. 1385, doi. 10.1007/s00439-023-02578-6
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- Article
The Alzheimer Amyloid Precursor Protein (APP) and FE65, an APP-binding Protein, Regulate Cell...
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- Journal of Cell Biology, 2001, v. 153, n. 7, p. 1403, doi. 10.1083/jcb.153.7.1403
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- Article
Treatment with controlled-release lovastatin decreases serum concentrations of human ²-amyloid (A²) peptide.
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- International Journal of Neuropsychopharmacology, 2001, v. 4, n. 2, p. 127, doi. 10.1017/S1461145701002310
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- Article
Oxytocin improves behavioral and electrophysiological deficits in a novel Shank3-deficient rat.
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- eLife, 2017, p. 1, doi. 10.7554/eLife.18904
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- Article
Regulatory consequences of neuronal ELAV-like protein binding to coding and non-coding RNAs in human brain.
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- eLife, 2016, p. 1, doi. 10.7554/eLife.10421
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- Article
Reduced axonal caliber and structural changes in a rat model of Fragile X syndrome with a deletion of a K-Homology domain of Fmr1.
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- Translational Psychiatry, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41398-020-00943-x
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- Article
Functional annotation of rare structural variation in the human brain.
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- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-16736-1
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- Article
mTADA is a framework for identifying risk genes from de novo mutations in multiple traits.
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- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-16487-z
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- Article
Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0497-y
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- Article
Integrative network analysis of nineteen brain regions identifies molecular signatures and networks underlying selective regional vulnerability to Alzheimer's disease.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0355-3
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- Article
Calsenilin regulates presenilin γ-secretase-mediated N-cadherin &epsilon-cleavage and β-catenin signaling.
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- FASEB Journal, 2011, v. 25, n. 12, p. 4174, doi. 10.1096/fj.11-185926
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- Article
Somatic comorbidities of mental disorders in pregnancy.
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- European Psychiatry, 2023, v. 66, n. 1, p. 1, doi. 10.1192/j.eurpsy.2023.1
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- Article
Systematic review and meta‐analysis identify significant relationships between clinical anxiety and lower urinary tract symptoms.
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- Brain & Behavior, 2021, v. 11, n. 9, p. 1, doi. 10.1002/brb3.2268
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- Article
HDAC2 regulates atypical antipsychotic responses through the modulation of mGlu2 promoter activity.
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- Nature Neuroscience, 2012, v. 15, n. 9, p. 1245, doi. 10.1038/nn.3181
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- Article
Neuregulin 1-erbB signaling and the molecular/cellular basis of schizophrenia.
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- Nature Neuroscience, 2004, v. 7, n. 6, p. 575, doi. 10.1038/nn1258
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- Article
Brief Report: Assessment of a Caregiver-Implemented Intervention for Improving Social Communication Skills in Toddlers and Young Children with Autism.
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- Journal of Autism & Developmental Disorders, 2024, v. 54, n. 2, p. 794, doi. 10.1007/s10803-022-05587-y
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- Article
The Immersive Theater Experience for Individuals with Autism Spectrum Disorder.
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- Journal of Autism & Developmental Disorders, 2020, v. 50, n. 3, p. 1073, doi. 10.1007/s10803-019-04284-7
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- Article
Parent-reported measure of repetitive behavior in Phelan-McDermid syndrome.
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- Journal of Neurodevelopmental Disorders, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s11689-021-09398-7
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- Article
Social visual attentional engagement and memory in Phelan-McDermid syndrome and autism spectrum disorder: a pilot eye tracking study.
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- Journal of Neurodevelopmental Disorders, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s11689-021-09400-2
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- Article
FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring.
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- Journal of Neurodevelopmental Disorders, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s11689-021-09358-1
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- Article
Family-based association tests for sequence data, and comparisons with population-based association tests.
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- European Journal of Human Genetics, 2013, v. 21, n. 10, p. 1158, doi. 10.1038/ejhg.2012.308
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- Article
Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders.
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- European Journal of Human Genetics, 2011, v. 19, n. 10, p. 1082, doi. 10.1038/ejhg.2011.75
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- Article
PLXNA 4 is associated with Alzheimer disease and modulates tau phosphorylation.
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- Annals of Neurology, 2014, v. 76, n. 3, p. 379, doi. 10.1002/ana.24219
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- Article
PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation.
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- 2014
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- Publication type:
- journal article
The ACMSD gene, involved in tryptophan metabolism, is mutated in a family with cortical myoclonus, epilepsy, and parkinsonism.
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- Journal of Molecular Medicine, 2013, v. 91, n. 12, p. 1399, doi. 10.1007/s00109-013-1075-4
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- Article
Reduced engagement of visual attention in children with autism spectrum disorder.
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- Autism: The International Journal of Research & Practice, 2021, v. 25, n. 7, p. 2064, doi. 10.1177/13623613211010072
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- Article
Grandma knows best: Family structure and age of diagnosis of autism spectrum disorder.
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- Autism: The International Journal of Research & Practice, 2018, v. 22, n. 3, p. 368, doi. 10.1177/1362361316679632
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- Article
Advancing paternal age and simplex autism.
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- Autism: The International Journal of Research & Practice, 2012, v. 16, n. 4, p. 367, doi. 10.1177/1362361311427154
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- Publication type:
- Article
Systematic review and meta-analysis: relationships between attention-deficit/hyperactivity disorder and urinary symptoms in children.
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- European Child & Adolescent Psychiatry, 2022, v. 31, n. 4, p. 663, doi. 10.1007/s00787-021-01736-3
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- Article
Phenotypic Impact of Rare Potentially Damaging Copy Number Variation in Obsessive-Compulsive Disorder and Chronic Tic Disorders.
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- Genes, 2022, v. 13, n. 10, p. N.PAG, doi. 10.3390/genes13101796
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- Article
Sensory Reactivity Phenotype in Phelan–McDermid Syndrome Is Distinct from Idiopathic ASD.
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- Genes, 2021, v. 12, n. 7, p. 977, doi. 10.3390/genes12070977
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- Article
Sensory Reactivity Symptoms Are a Core Feature of ADNP Syndrome Irrespective of Autism Diagnosis.
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- Genes, 2021, v. 12, n. 3, p. 351, doi. 10.3390/genes12030351
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- Article
Information Avoidance and Information Seeking Among Parents of Children With ASD.
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- 2021
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- Publication type:
- journal article
Calsenilin: A calcium-binding protein that interacts with the presenilins and regulates the levels of a presenilin fragment.
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- Nature Medicine, 1998, v. 4, n. 10, p. 1177, doi. 10.1038/2673
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- Article
Generation and Regulation of β-Amyloid Peptide Variants by Neurons.
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- Journal of Neurochemistry, 1998, v. 71, n. 5, p. 1920, doi. 10.1046/j.1471-4159.1998.71051920.x
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- Article
Regulation of Secretion of Alzheimer Amyloid Precursor Protein by the Mitogen-Activated Protein Kinase Cascade.
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- Journal of Neurochemistry, 1998, v. 70, n. 2, p. 524, doi. 10.1046/j.1471-4159.1998.70020524.x
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- Article
In Vitro Protein Phosphorylation in Head Preparations from Normal and Mutant Drosophila melanogaster.
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- Journal of Neurochemistry, 1987, v. 49, n. 4, p. 1161, doi. 10.1111/j.1471-4159.1987.tb10007.x
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- Article
Identification of Rare Causal Variants in Sequence-Based Studies: Methods and Applications to VPS13B, a Gene Involved in Cohen Syndrome and Autism.
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- PLoS Genetics, 2014, v. 10, n. 12, p. 1, doi. 10.1371/journal.pgen.1004729
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- Article
Integrated Model of <i>De Novo</i> and Inherited Genetic Variants Yields Greater Power to Identify Risk Genes.
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- PLoS Genetics, 2013, v. 9, n. 8, p. 1, doi. 10.1371/journal.pgen.1003671
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- Article
Network Topologies and Convergent Aetiologies Arising from Deletions and Duplications Observed in Individuals with Autism.
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- PLoS Genetics, 2013, v. 9, n. 6, p. 1, doi. 10.1371/journal.pgen.1003523
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- Article
Overexpression of Calsenilin in Sporadic Alzheimer's Disease Brain.
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- Annals of the New York Academy of Sciences, 2001, v. 928, n. 1, p. 373, doi. 10.1111/j.1749-6632.2001.tb05692.x
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- Article
Increased Expression of Calsenilin in the Brains of Scrapie-infected Mice.
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- Annals of the New York Academy of Sciences, 2001, v. 928, n. 1, p. 363, doi. 10.1111/j.1749-6632.2001.tb05682.x
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- Article
AnnTools: a comprehensive and versatile annotation toolkit for genomic variants.
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- Bioinformatics, 2012, v. 28, n. 5, p. 724, doi. 10.1093/bioinformatics/bts032
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- Article
Association of Genetic and Environmental Factors With Autism in a 5-Country Cohort.
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- 2019
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- Publication type:
- journal article
Association of Autism Spectrum Disorder With Prenatal Exposure to Medication Affecting Neurotransmitter Systems.
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- 2018
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- Publication type:
- journal article
Familial Clustering of Tic Disorders and Obsessive-Compulsive Disorder.
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- JAMA Psychiatry, 2015, v. 72, n. 4, p. 359, doi. 10.1001/jamapsychiatry.2014.2656
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- Article