AUTISM & GENOMICS || Public Health Genomics Knowledge Base (v1.2)

Public Health Genomics Knowledge Base (v1.2)

AUTISM & GENOMICS

Last Updated: Aug 29, 2016

• Genome-wide, integrative analysis implicates microRNA dysregulation in autism spectrum disorder
  YE WU et al, Nature Neurosci, August 2016
• Impact of Maternal Serotonin Transporter Genotype on Placental Serotonin, Fetal Forebrain Serotonin, and Neurodevelopment.
  Muller Christopher L, et al. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2016 8
• Oxytocin efficacy is modulated by dosage and oxytocin receptor genotype in young adults with high-functioning autism: a 24-week randomized clinical trial.
  Kosaka H, et al. Translational psychiatry 2016 0 (8) e872
• Genetic testing and counseling in the case of an autism diagnosis: A caregivers perspective.
  Hens Kristien et al. European journal of medical genetics 2016 Aug
• The Clinical Spectrum of Female Epilepsy Patients with PCDH19 Mutations in a Chinese Population.
  Liu Aijie, et al. Clinical genetics 2016 8
• Copy number variation analysis in adults with catatonia confirms haploinsufficiency of SHANK3 as a predisposing factor.
  Breckpot Jeroen, et al. European journal of medical genetics 2016 8
• Genome-wide characteristics of de novo mutations in autism.
  Yuen Ryan K C, et al. NPJ genomic medicine 2016 8 160271-1602710
• Prenatal stress exposure, oxytocin receptor gene (OXTR) methylation and child autistic traits: The moderating role of OXTR rs53576 genotype.
  Rijlaarsdam Jolien, et al. Autism research : official journal of the International Society for Autism Research 2016 8
• Association between IRS1 Gene Polymorphism and Autism Spectrum Disorder: A Pilot Case-Control Study in Korean Males.
  Park Hae Jeong, et al. International journal of molecular sciences 2016 0 (8)
• Genome-wide prediction and functional characterization of the genetic basis of autism spectrum disorder.
  Krishnan Arjun, et al. Nature neuroscience 2016 8
• A sneak peek at personalized medicine in autism?
  LF Kung, Science Translational Medicine, July 27, 2016
• Utilization of genetic testing among children with developmental disabilities in the United States.
  Kiely Bridget et al. The application of clinical genetics 2016 993-100
• Whole Exome Sequencing Reveals a BSCL2 Mutation Causing Progressive Encephalopathy with Lipodystrophy (PELD) in an Iranian Pediatric Patient.
  Alaei Mohammad Reza, et al. Iranian biomedical journal 2016 7
• Glycan susceptibility factors in autism spectrum disorders.
  Dwyer Chrissa A, et al. Molecular aspects of medicine 2016 7
• Lack of replication of previous autism spectrum disorder GWAS hits in European populations.
  Torrico Bàrbara, et al. Autism research : official journal of the International Society for Autism Research 2016 7

• CDC Information (6)
• CDC-Authored Pub (1)

• Human (25)
• Pathogen (0)

• Human (801)
• Pathogen (0)

• Human (33)
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• Guidelines (1)
• Tier Table (2)
• Synthesis (5)

• Huamn (3)
• Pathogen (0)

Relevant Resources

• Cancer Genomics and Epidemiology Navigator (CGEN)
• Genetics and Genomics Competencies Center (G2C2)
• NIH Genetic Testing Registry
• NIH MedGen Database
• Online Mendelian Inheritance in Man (OMIM)
• PharmGKB