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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2011
Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21Holly N Cukier, Daria Salyakina, Sarah F Blankstein, et al.Molecular Autism|January 21, 2011
A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autismJohn P Hussman, Ren-Hua Chung, Anthony J Griswold, et al.Molecular Autism|November 5, 2011
An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in malesRen-Hua Chung, Deqiong Ma, Kai Wang, et al.Plos One|October 22, 2011
Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism riskDaria Salyakina, Holly N Cukier, Joycelyn M Lee, et al.Autism Research : Official Journal of the International Society for Autism Research|October 12, 2012
The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1Holly N Cukier, Joycelyn M Lee, Deqiong Ma, et al.Human Molecular Genetics|May 1, 2012
Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathwaysAnthony J Griswold, Deqiong Ma, Holly N Cukier, et al.Molecular Autism|April 5, 2012
Evidence of novel fine-scale structural variation at autism spectrum disorder candidate lociDale J Hedges, Kara L Hamilton-Nelson, Stephanie J Sacharow, et al.Annals of Human Genetics|May 22, 2009
A genome-wide association study of autism reveals a common novel risk locus at 5p14.1Deqiong Ma, Daria Salyakina, James M Jaworski, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 6, 2023
Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working GroupRyan J Schmidt, Marcie Steeves, Pinar Bayrak-Toydemir, et al.Nature|May 1, 2009
Common genetic variants on 5p14.1 associate with autism spectrum disordersKai Wang, Haitao Zhang, Deqiong Ma, et al.Pageof 3