Roberts, Wendy

A large data resource of genomic copy number variation across neurodevelopmental disorders

Zarrei, M., Burton, C. L., Engchuan, W., Young, E. J., Higginbotham, E. J., MacDonald, J. R., Trost, B., Chan, A. J. S., Walker, S., Lamoureux, S., et al. (2019) · npj Genomic Medicine

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 187

Autism comes to the hospital: The experiences of patients with autism spectrum disorder, their parents and health-care providers at two Canadian paediatric hospitals

Muskat, B., Burnham Riosa, P., Nicholas, D. B., Roberts, W., Stoddart, K. P., & Zwaigenbaum, L. (2015) · Autism

Autism Spectrum Disorder ResearchPatient-Provider Communication in Healthcare

Cited by 184

Sex Differences in Children with Autism Spectrum Disorder Identified Within a High-Risk Infant Cohort

Zwaigenbaum, L., Bryson, S. E., Szatmari, P., Brian, J., Smith, I. M., Roberts, W., Vaillancourt, T., & Roncadin, C. (2012) · Journal of Autism and Developmental Disorders

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 178

Stability of diagnostic assessment for autism spectrum disorder between 18 and 36 months in a high-risk cohort.

Zwaigenbaum, L., Bryson, S. E., Brian, J., Smith, I. M., Roberts, W., Szatmari, P., Roncadin, C., Garon, N., & Vaillancourt, T. (2016) · Autism Research

Autism Spectrum Disorder ResearchChild Nutrition and Feeding Issues

Cited by 165

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

Lionel, A. C., Tammimies, K., Vaags, A. K., Rosenfeld, J. A., Ahn, J. W., Merico, D., Noor, A., Runke, C. K., Pillalamarri, V. K., Carter, M. T., et al. (2014) · Human Molecular Genetics

Genetics and Neurodevelopmental DisordersGenomic variations and chromosomal abnormalities

Cited by 163

A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism

Celestino-Soper, P. B. S., Violante, S., Crawford, E. L., Luo, R., Lionel, A. C., Delaby, E., Cai, G., Sadikovic, B., Lee, K., Lo, C., et al. (2012) · Proceedings of the National Academy of Sciences

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 139

A Prospective Study of Autistic-Like Traits in Unaffected Siblings of Probands With Autism Spectrum Disorder

Georgiades, S., Szatmari, P., Zwaigenbaum, L., Bryson, S., Brian, J., Roberts, W., Smith, I., Vaillancourt, T., Roncadin, C., & Garon, N. (2013) · JAMA Psychiatry

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 130

Structure of the Autism Symptom Phenotype

GEORGIADES, S., SZATMARI, P., ZWAIGENBAUM, L., DUKU, E., BRYSON, S., ROBERTS, W., GOLDBERG, J., & MAHONEY, W. (2007) · Journal of the American Academy of Child & Adolescent Psychiatry

Autism Spectrum Disorder ResearchChild Nutrition and Feeding Issues

Cited by 119

Auditory evoked fields predict language ability and impairment in children

Oram Cardy, J. E., Flagg, E. J., Roberts, W., & Roberts, T. P. L. (2008) · International Journal of Psychophysiology

Language Development and DisordersNeurobiology of Language and Bilingualism

Cited by 115

Inhibition of motor responses in siblings concordant and discordant for attention deficit hyperactivity disorder

Schachar, R. J., Crosbie, J., Barr, C. L., Ornstein, T. J., Kennedy, J., Malone, M., Roberts, W., Ickowicz, A., Tannock, R., Chen, S., et al. (2005) · American Journal of Psychiatry

Attention Deficit Hyperactivity DisorderNeural and Behavioral Psychology Studies

Cited by 87

Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorder

Carter, M., Nikkel, S., Fernandez, B., Marshall, C., Noor, A., Lionel, A., Prasad, A., Pinto, D., Joseph-George, A., Noakes, C., et al. (2011) · Clinical Genetics

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 77

Experiences of emergency department care from the perspective of families in which a child has autism spectrum disorder

Nicholas, D. B., Zwaigenbaum, L., Muskat, B., Craig, W. R., Newton, A. S., Kilmer, C., Greenblatt, A., Roberts, W., & Cohen-Silver, J. (2016) · Social Work in Health Care

Emergency and Acute Care StudiesPatient Satisfaction in Healthcare

Cited by 74

Type 1 Diabetes and Autism

Freeman, S. J., Roberts, W., & Daneman, D. (2005) · Diabetes Care

Autism Spectrum Disorder ResearchDiabetes and associated disorders

Cited by 47

Positive Affect in Infant Siblings of Children Diagnosed with Autism Spectrum Disorder

Filliter, J. H., Longard, J., Lawrence, M. A., Zwaigenbaum, L., Brian, J., Garon, N., Smith, I. M., Roncadin, C., Roberts, W., & Bryson, S. E. (2015) · Journal of Abnormal Child Psychology

Autism Spectrum Disorder ResearchChild and Animal Learning Development

Cited by 43

Emerging cognitive profiles in high-risk infants with and without autism spectrum disorder

Brian, A. J., Roncadin, C., Duku, E., Bryson, S. E., Smith, I. M., Roberts, W., Szatmari, P., Drmic, I., & Zwaigenbaum, L. (2014) · Research in Autism Spectrum Disorders

Autism Spectrum Disorder ResearchChild Nutrition and Feeding Issues

Cited by 43

Brief Report: Evaluation of the Short Quantitative Checklist for Autism in Toddlers (Q-CHAT-10) as a Brief Screen for Autism Spectrum Disorder in a High-Risk Sibling Cohort

Raza, S., Zwaigenbaum, L., Sacrey, L.-A. R., Bryson, S., Brian, J., Smith, I. M., Reid, K., Roberts, W., Szatmari, P., Vaillancourt, T., et al. (2019) · Journal of Autism and Developmental Disorders

Autism Spectrum Disorder ResearchChild Nutrition and Feeding Issues

Cited by 29

Variability of Creatine Metabolism Genes in Children with Autism Spectrum Disorder

Cameron, J. M., Levandovskiy, V., Roberts, W., Anagnostou, E., Scherer, S., Loh, A., & Schulze, A. (2017) · International Journal of Molecular Sciences

Autism Spectrum Disorder ResearchMetabolism and Genetic Disorders

Cited by 15