Collins, Julianne S.
Greenwood Genetic Center
3 papers on CoChat
Most cited papers
- Verified
Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders
Boccuto, L., Lauri, M., Sarasua, S. M., Skinner, C. D., Buccella, D., Dwivedi, A., Orteschi, D., Collins, J. S., Zollino, M., Visconti, P., et al. (2013) · European Journal of Human Genetics
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 240
- Verified
Folic acid supplementation and neural tube defect recurrence prevention
Grosse, S. D., & Collins, J. S. (2007) · Birth Defects Research Part A: Clinical and Molecular Teratology
Folate and B Vitamins ResearchSpinal Dysraphism and Malformations
Cited by 69
- Verified
Further evidence that the rs1858830 C variant in the promoter region of the MET gene is associated with autistic disorder
Jackson, P. B., Boccuto, L., Skinner, C., Collins, J. S., Neri, G., Gurrieri, F., & Schwartz, C. E. (2009) · Autism Research
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 65
Go further with a free account
Verify every reference, keep papers in a library, and ask questions across them.
Sign up - it is free