Nuala Sykes

Functional impact of global rare copy number variation in autism spectrum disorders

Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei et al. · Nature · 2010 · 2K citations · Full text

Autism Spectrum Disorders, Syndromic Autism, Genetics +4

Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits

Kay MacDermot, Elena Bonora, Nuala Sykes et al. · The American Journal of Human Genetics · 2005 · 414 citations · Full text

Neurolinguistics, Language Development, Atypical Language Development +16

Individual common variants exert weak effects on the risk for autism spectrum disorders

Richard Anney, Lambertus Klei, Dalila Pinto et al. · Human Molecular Genetics · 2012 · 372 citations · Full text

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

Jillian P. Casey, Tiago R. Magalhães, Judith Conroy et al. · Human Genetics · 2011 · 200 citations · Full text

Candidate-Gene Screening and Association Analysis at the Autism-Susceptibility Locus on Chromosome 16p: Evidence of Association at GRIN2A and ABAT

Gabrielle Barnby, Aaron Abbott, Nuala Sykes et al. · The American Journal of Human Genetics · 2005 · 179 citations · Full text

Genome-wide Association Study, Association Analysis, Syndromic Autism +5