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Carl FeinsteinAcademic Appointments
Appointment
Organization
Professor - Med Center Line
Professor - Med Center Line (By courtesy)
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Administrative Appointments
Title
Organization
Start Year
End Year
Director, Division of Child and Adolescent Psychiatry
Department of Psychiatry and Behavioral Sciences
2005
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Research Interests
Autism and Asperger's Disorder.
Genetically-based neurodevelopmental disorder, including Velocardiofacial Syndrome, Smith-Magenis Syndrome, Williams Syndrome, and Fragile X Syndrome.
Intellectual Disability (mental retardation) and psychiatric disorders.
Developmental Language Disorder and Learning Disabilities.
Sensory impairment in children, including visual and hearing impairment.
Psychiatric aspects of medical illness and disability in children.
Genetically-based neurodevelopmental disorder, including Velocardiofacial Syndrome, Smith-Magenis Syndrome, Williams Syndrome, and Fragile X Syndrome.
Intellectual Disability (mental retardation) and psychiatric disorders.
Developmental Language Disorder and Learning Disabilities.
Sensory impairment in children, including visual and hearing impairment.
Psychiatric aspects of medical illness and disability in children.
Publications
- Feinstein C, Singh S "Social phenotypes in neurogenetic syndromes." Child Adolesc Psychiatr Clin N Am 2007; 16: 3: 631-47 More »
- Gothelf D, Feinstein C, Thompson T, Gu E, Penniman L, Van Stone E, Kwon H, Eliez S, Reiss AL "Risk factors for the emergence of psychotic disorders in adolescents with 22q11.2 deletion syndrome." Am J Psychiatry 2007; 164: 4: 663-9 More »
- C. Morris, H. Lenhoff & P. Wang, Feinstein, C. & Reiss, A. "The Neurobiology of Williams-Beuren Syndrome" Williams-Beuren syndrome : research, evaluation, and treatment 2006; More »
- Debbané M, Glaser B, David MK, Feinstein C, Eliez S "Psychotic symptoms in children and adolescents with 22q11.2 deletion syndrome: Neuropsychological and behavioral implications." Schizophr Res 2006; 84: 2-3: 187-93 More »
- Gothelf D, Eliez S, Thompson T, Hinard C, Penniman L, Feinstein C, Kwon H, Jin S, Jo B, Antonarakis SE, Morris MA, Reiss AL "COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome." Nat Neurosci 2005; 8: 11: 1500-2 More »
76 publications: view full list
