Articles


Diagnosis and Prevalence





Autism Spectrum Disorder Prevalence

Diagnosis

Intellectual Developmental Disorder

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Articles


Co-Occuring Conditions





Prevalence & Epidemiology

Anxiety & Depression

Suicidality & Self-Harm

Irritability

Psychosis, Bipolar Disorder, and Catatonia

Sleep & Circadian Issues

Substance Use & Risk Behaviors

ADHD

Repetitive Behavior and OCD

Seizures

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Articles


Psychopharmacology





General and Common Co-occurring Conditions

Catatonia

Alternative Treatments

Pharmacotherapy in Intellectual Developmental Disorder (IDD)

Seminal Articles

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Articles


Genetics





Resources to Understand Unique Genetic Conditions

  • Gene Reviews
    Useful for in-depth expert reviews of specific genetic conditions and phenotypes.
  • Online Catalog of Human Genes and Genetics (Online Mendelian Inheritance in Man or OMIM)
    Database of human genes, detailing relevant research and associated phenotypes, with links to additional resources such as ClinVar.
  • Unique
    Non-profit charity based in the UK that produces printable pamphlets for families detailing the molecular changes, lived experience of families caring for those with these changes, and a summary of the associated symptoms.
  • Simons
    Simons Searchlight aims to recruit individuals with changes in particular genes associated with autism, and information on characteristics of people with those changes who have enrolled in their study.

ASD

IDD

Down Syndrome

22q11.2 Deletion Syndrome (DiGeorge syndrome)

Williams Syndrome

Fragile X Syndrome

Prader-Willi Syndrome

  • Prader-Willi syndrome: consensus diagnostic criteria. Holm VA, Cassidy SB, Butler MG, et al. Pediatrics. 1993.
    This article established the foundational clinical diagnostic criteria still used today and created the scoring system that remains the clinical standard.
  • Prader-Willi syndrome. Cassidy SB, Schwartz S, Miller JL, et al. Genet Med. 2012.
    Comprehensive review of genetics, phenotype, and management; authoritative reference for understanding molecular mechanisms and clinical care.
  • Neuropsychiatric features of Prader–Willi syndrome. Shelkowitz E, Gantz MG, Ridenour TA, et al. Am J Med Genet A. 2022.
    A research study investigating the behavioral and psychiatric manifestations of Prader-Willi syndrome.

Angelman Syndrome

  • Angelman syndrome 2005: updated consensus for diagnostic criteria.Williams CA, Beaudet AL, Clayton-Smith J, et al. Am J Med Genet A. 2006.
    Current gold standard for clinical diagnostic criteria; updated and refined the original 1995 criteria with molecular testing integration.
  • Angelman Syndrome. Dagli AI, Mueller J, Williams CA. GeneReviews®. 1993.
    Most comprehensive and current clinical reference; regularly updated authoritative source for diagnosis, management, and genetic counseling.

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Articles


Behavioral Therapy





Cognitive Behavioral Therapy

Social Skills Training

PCIT: Parent-Child Interaction Therapy

ABA: Applied Behavioral Analysis

ESDM: Early Start Denver Model

EIBI: Early Intensive Behavioral Intervention

PRT: Pivotal Response Treatment

JASPER: Joint Attention Symbolic Play and Engagement Regulation

Other Therapies

TEACCH: Treatment and Education of Autistic and Related Communication-handicapped Children

RUBI: Research Unit on Behavioral Interventions

OT/Sensory

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Articles


Diversity and Inclusion





Racial and Gender Disparities in ASD/IDD

Gender Differences

Gender Diversity/Sexuality

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