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Publications by Kelly Schoch
Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome With Intellectual Disability and Developmental Delay
American Journal of Human Genetics
Genetics
IRF2BPL Is Associated With Neurological Phenotypes
American Journal of Human Genetics
Genetics
De Novo Variants in WDR37 Are Associated With Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia
American Journal of Human Genetics
Genetics
Bi-Allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes
American Journal of Human Genetics
Genetics
Characteristics of Undiagnosed Diseases Network Applicants: Implications for Referring Providers
BMC Health Services Research
Health Policy
COMT and Anxiety and Cognition in Children With Chromosome 22q11.2 Deletion Syndrome
Psychiatry Research
Psychiatry
Mental Health
Biological Psychiatry
Assessment of Parental Disclosure of a 22q11.2 Deletion Syndrome Diagnosis and Implications for Clinicians
Journal of Genetic Counseling
Genetics
A Longitudinal Examination of the Psychoeducational, Neurocognitive, and Psychiatric Functioning in Children With 22q11.2 Deletion Syndrome
Research in Developmental Disabilities
Clinical Psychology
Educational Psychology
Developmental
Discrepancies in Parent and Teacher Ratings of Social-Behavioral Functioning of Children With Chromosome 22q11.2 Deletion Syndrome: Implications for Assessment
American Journal on Intellectual and Developmental Disabilities
Developmental
Arts
Pediatrics
Neuropsychology
Educational Psychology
Humanities
Mental Health
Physiological Psychology
Perinatology
Psychiatry
Neurology
Medicine
Child Health
