Chudley, Albert E.

Comorbidity of fetal alcohol spectrum disorder: a systematic review and meta-analysis

Popova, S., Lange, S., Shield, K., Mihic, A., Chudley, A. E., Mukherjee, R. A. S., Bekmuradov, D., & Rehm, J. (2016) · The Lancet

Prenatal Substance Exposure EffectsFetal and Pediatric Neurological Disorders

Cited by 541

TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone.

Huang, L., Szymanska, K., Jensen, V. L., Janecke, A. R., Innes, A. M., Davis, E. E., Frosk, P., Li, C., Willer, J. R., Chodirker, B. N., et al. (2011) · The American Journal of Human Genetics

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 194

Disruption at the PTCHD1 Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability

Noor, A., Whibley, A., Marshall, C. R., Gianakopoulos, P. J., Piton, A., Carson, A. R., Orlic-Milacic, M., Lionel, A. C., Sato, D., Pinto, D., et al. (2010) · Science Translational Medicine

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 193

Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype

Prasad, C., Prasad, A. N., Chodirker, B. N., Lee, C., Dawson, A. K., Jocelyn, L. J., & Chudley, A. E. (2000) · Clinical Genetics

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 103

Outcomes of Genetic Evaluation in Children with Pervasive Developmental Disorder

CHUDLEY, A. E., GUTIERREZ, E., JOCELYN, L. J., & CHODIRKER, B. N. (1998) · Journal of Developmental & Behavioral Pediatrics

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 68

Correlates of age at diagnosis of autism spectrum disorders in six Canadian regions

Coo, H., Ouellette-Kuntz, H., Lam, M., Yu, C. T., Dewey, D., Bernier, F. P., Chudley, A. E., Hennessey, P. E., Breitenbach, M. M., Noonan, A. L., et al. (2012) · Chronic Diseases and Injuries in Canada

Autism Spectrum Disorder ResearchFamily and Disability Support Research

Cited by 56

Clinical genetics and the Hutterite population: a review of Mendelian disorders.

Boycott, K. M., Parboosingh, J. S., Chodirker, B. N., Lowry, R. B., McLeod, D. R., Morris, J., Greenberg, C. R., Chudley, A. E., Bernier, F. P., Midgley, J., et al. (2008) · American Journal of Medical Genetics Part A

Genomics and Rare DiseasesGenetic Associations and Epidemiology

Cited by 50

Prevalence of pervasive developmental disorders in two Canadian provinces

Ouellette‐Kuntz, H., Coo, H., Yu, C. T., Chudley, A. E., Noonan, A., Breitenbach, M., Ramji, N., Prosick, T., Bedard, A., & Holden, J. J. A. (2006) · Journal of Policy and Practice in Intellectual Disabilities

Autism Spectrum Disorder ResearchFamily and Disability Support Research

Cited by 39

Functional magnetic resonance imaging of facial information processing in children with autistic disorder, attention deficit hyperactivity disorder and typically developing controls

Malisza, K. L., Clancy, C., Shiloff, D., Holden, J., Jones, C., Paulson, K., Yu, D. C. T., Summers, R., & Chudley, A. E. (2011) · ijamh

Autism Spectrum Disorder ResearchFace Recognition and Perception

Cited by 32

Eye movement defects in KO zebrafish reveals SRPK3 as a causative gene for an X‐linked intellectual disability

Kim, C.-H., Lee, Y.-R., Thomas, M., Roychaudhury, A., Skinner, C., Maconachie, G., Crosier, M., Horak, H., Constantinescu, C., Choi, T.-I., et al. (2023) · Research Square

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 3