Nuala Sykes
Centre for Human Genetics(GB)University of Oxford(GB)
Publications by Year
Research Areas
Autism Spectrum Disorder Research, Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, Congenital heart defects research, Parkinson's Disease Mechanisms and Treatments
Most-Cited Works
- → Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits(2005)415 cited
- → Individual common variants exert weak effects on the risk for autism spectrum disorders(2012)374 cited
- → A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder(2011)202 cited
- → Candidate-Gene Screening and Association Analysis at the Autism-Susceptibility Locus on Chromosome 16p: Evidence of Association at GRIN2A and ABAT(2005)181 cited
- → High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility(2009)143 cited
- → MET and autism susceptibility: family and case–control studies(2008)90 cited
- → Mutation screening and association analysis of six candidate genes for autism on chromosome 7q(2004)79 cited
- → Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection(2009)71 cited
- → Autism: the quest for the genes(2007)55 cited
- → CNVs leading to fusion transcripts in individuals with autism spectrum disorder(2012)36 cited