Last Posted: Jun 30, 2017
- From 0 to 60 in 10 years - After a decade of fast-paced discovery, researchers are racing toward bigger datasets, more genes and a deeper understanding of the biology of autism.
S Makin, The Spectrum, June 27, 2017
- The interplay of common, rare variation in autism
M Daly, Spectrum, June 27, 2017
- Genes, Ozone and Autism
Science Mag, June 23, 2017
- Do the data really support ordering fragile X testing as a first-tier test without clinical features?
Weinstein Veronique et al. Genetics in medicine : official journal of the American College of Medical Genetics 2017 May
- Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined Immunodeficiency.
Barry Jessica C et al. Journal of clinical immunology 2017 May
- Parents' Attitudes toward Clinical Genetic Testing for Autism Spectrum Disorder-Data from a Norwegian Sample.
Johannessen Jarle et al. International journal of molecular sciences 2017 May 18(5)
- Public-Private Partnerships in Cloud-Computing Services in the Context of Genomic Research.
Granados Moreno Palmira et al. Frontiers in medicine 2017 43
- The joint effect of air pollution exposure and copy number variation on risk for autism.
Kim Dokyoon et al. Autism research : official journal of the International Society for Autism Research 2017 Apr
- Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
DJ Weiner et al, Nature, May 15, 2017
- A microcosting and cost-consequence analysis of clinical genomic testing strategies in autism spectrum disorder.
Tsiplova Kate et al. Genetics in medicine : official journal of the American College of Medical Genetics 2017 May
- Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy.
Fry Andrew E et al. BMC medical genetics 2016 Apr 17(1) 34
- Pharmacogenomics and Efficacy of Risperidone Long-Term Treatment in Thai Autistic Children and Adolescents.
Nuntamool Nopphadol et al. Basic & clinical pharmacology & toxicology 2017 May
- Recurrent copy number variations as risk factors for autism spectrum disorders: analysis of the clinical implications.
Oikonomakis V et al. Clinical genetics 2016 Jun 89(6) 708-18
- A microcosting and costconsequence analysis of clinical genomic testing strategies in autism spectrum disorder
K Tsiplova et al, Genetics in Medicine, May 4, 2017
- Missed Opportunities: Unidentified genetic risk factors in prenatal care.
McClatchey Trissa et al. Prenatal diagnosis 2017 Apr
- Autism: Why Act Early?
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