Found: 17
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Mosaic trisomy 20 and mitigation in capital crimes sentencing: A review and case report.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Forging the path for PRecISion Medicine in Autism: The PRISMA Neurogenetic Psychiatry Consultation Service.
- Published in:
- Brown University Child & Adolescent Behavior Letter, 2018, v. 34, n. 2, p. 1, doi. 10.1002/cbl.30270
- By:
- Publication type:
- Article
Clinical Genetic Testing in Autism Spectrum Disorder in a Large Community-Based Population Sample.
- Published in:
- 2020
- By:
- Publication type:
- journal article
21st-Century Genetics in Psychiatric Residency Training: How Do We Get There?
- Published in:
- 2019
- 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
- By:
- Publication type:
- Article
Behavioral and neuroanatomical analyses in a genetic mouse model of 2q13 duplication.
- Published in:
- Genes to Cells, 2017, v. 22, n. 5, p. 436, doi. 10.1111/gtc.12487
- By:
- Publication type:
- Article
Autism Heterogeneity in a Densely Sampled U.S. Population: Results From the First 1,000 Participants in the RI‐CART Study.
- Published in:
- Autism Research: Official Journal of the International Society for Autism Research, 2020, v. 13, n. 3, p. 474, doi. 10.1002/aur.2261
- By:
- Publication type:
- Article
Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15 q11.2, Specifically Breakpoints 1 to 2.
- Published in:
- Autism Research: Official Journal of the International Society for Autism Research, 2014, v. 7, n. 3, p. 355, doi. 10.1002/aur.1378
- By:
- Publication type:
- Article
Chiari I malformation, delayed gross motor skills, severe speech delay, and epileptiform discharges in a child with FOXP1 haploinsufficiency.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 11, p. 1216, doi. 10.1038/ejhg.2010.96
- By:
- Publication type:
- Article
Common genetic variants, acting additively, are a major source of risk for autism.
- Published in:
- Molecular Autism, 2012, v. 3, n. 1, p. 1, doi. 10.1186/2040-2392-3-9
- By:
- Publication type:
- Article
Trains and Outer Space-The Unique Worlds Within Autism.
- Published in:
- JAMA: Journal of the American Medical Association, 2020, v. 324, n. 16, p. 1591, doi. 10.1001/jama.2020.19051
- By:
- Publication type:
- Article
Loss of δ-catenin function in severe autism.
- Published in:
- Nature, 2015, v. 520, n. 7545, p. 51, doi. 10.1038/nature14186
- By:
- Publication type:
- Article
Actionable Genomics in Clinical Practice: Paradigmatic Case Reports of Clinical and Therapeutic Strategies Based upon Genetic Testing.
- Published in:
- Genes, 2022, v. 13, n. 2, p. 323, doi. 10.3390/genes13020323
- By:
- Publication type:
- Article
Tyrosine Hydroxylase and DOPA Decarboxylase Gene Variants in Personality Traits.
- Published in:
- Neuropsychobiology, 2009, v. 59, n. 1, p. 23, doi. 10.1159/000202826
- By:
- Publication type:
- Article
Copy Number Variants: A New Molecular Frontier in Clinical Psychiatry.
- Published in:
- Current Psychiatry Reports, 2011, v. 13, n. 2, p. 129, doi. 10.1007/s11920-011-0183-5
- By:
- Publication type:
- Article
Leveraging neuroscience education to address stigma related to opioid use disorder in the community: a pilot study.
- Published in:
- Frontiers in Psychiatry, 2024, p. 1, doi. 10.3389/fpsyt.2024.1360356
- By:
- Publication type:
- Article
Search for copy number variants in chromosomes15q11-q13 and 22q11.2 in obsessive compulsivedisorder.
- Published in:
- BMC Medical Genetics, 2010, v. 11, p. 100, doi. 10.1186/1471-2350-11-100
- By:
- Publication type:
- Article