Kates, Wendy R.

Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome

Schneider, M., Debbané, M., Bassett, A. S., Chow, E. W. C., Fung, W. L. A., van den Bree, M. B. M., Owen, M., Murphy, K. C., Niarchou, M., Kates, W. R., et al. (2014) · American Journal of Psychiatry

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 779

Smaller prefrontal and premotor volumes in boys with attention-deficit/hyperactivity disorder

Mostofsky, S. H., Cooper, K. L., Kates, W. R., Denckla, M. B., & Kaufmann, W. E. (2002) · Biological Psychiatry

Attention Deficit Hyperactivity DisorderNeural and Behavioral Psychology Studies

Cited by 379

Autistic Spectrum Disorders in Velo-cardio Facial Syndrome (22q11.2 Deletion)

Antshel, K. M., Aneja, A., Strunge, L., Peebles, J., Fremont, W. P., Stallone, K., AbdulSabur, N., Higgins, A. M., Shprintzen, R. J., & Kates, W. R. (2007) · Journal of Autism and Developmental Disorders

Autism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalities

Cited by 183

MRI parcellation of the frontal lobe in boys with attention deficit hyperactivity disorder or Tourette syndrome

Kates, W. R., Frederikse, M., Mostofsky, S. H., Folley, B. S., Cooper, K., Mazur-Hopkins, P., Kofman, O., Singer, H. S., Denckla, M. B., Pearlson, G. D., et al. (2002) · Psychiatry Research: Neuroimaging

Attention Deficit Hyperactivity DisorderObsessive-Compulsive Spectrum Disorders

Cited by 179

Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome

International 22q11.2 Brain and Behavior Consortium, Davies, R. W., Fiksinski, A. M., Breetvelt, E. J., Williams, N. M., Hooper, S. R., Monfeuga, T., Bassett, A. S., Owen, M. J., Gur, R. E., et al. (2020) · Nature Medicine

Schizophrenia research and treatmentGenomic variations and chromosomal abnormalities

Cited by 139

Neuroanatomic Variation in Monozygotic Twin Pairs Discordant for the Narrow Phenotype for Autism

Kates, W. R., Burnette, C. P., Eliez, S., Strunge, L. A., Kaplan, D., Landa, R., Reiss, A. L., & Pearlson, G. D. (2004) · American Journal of Psychiatry

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 137

A comparison of FreeSurfer-generated data with and without manual intervention

McCarthy, C. S., Ramprashad, A., Thompson, C., Botti, J.-A., Coman, I. L., & Kates, W. R. (2015) · Frontiers in Neuroscience

Medical Image Segmentation TechniquesAdvanced Neuroimaging Techniques and Applications

Cited by 122

A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants

Chawner, S. J. R. A., Doherty, J. L., Anney, R. J. L., Antshel, K. M., Bearden, C. E., Bernier, R., Chung, W. K., Clements, C. C., Curran, S. R., Cuturilo, G., et al. (2021) · American Journal of Psychiatry

Autism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalities

Cited by 95

Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome

Mlynarski, E. E., Sheridan, M. B., Xie, M., Guo, T., Racedo, S. E., McDonald-McGinn, D. M., Gai, X., Chow, E. W. C., Vorstman, J., Swillen, A., et al. (2015) · The American Journal of Human Genetics

Genomic variations and chromosomal abnormalitiesCongenital heart defects research

Cited by 74

Is child intelligence associated with parent and sibling intelligence in individuals with developmental disorders? An investigation in youth with 22q11.2 deletion (velo-cardio-facial) syndrome

Olszewski, A. K., Radoeva, P. D., Fremont, W., Kates, W. R., & Antshel, K. M. (2014) · Research in Developmental Disabilities

Genomic variations and chromosomal abnormalitiesDown syndrome and intellectual disability research

Cited by 37