Rare De Novo and Inherited Genes in Familial and Nonfamilial Pediatric Attention-Deficit/Hyperactivity Disorder

Anne B Arnett; Elizabeth Harstad; Mia O'Connell; Katheryn Hayes; Stephanie Brewster; William Barbaresi; Ryan N Doan

doi:10.1001/jamapediatrics.2023.4952

Rare De Novo and Inherited Genes in Familial and Nonfamilial Pediatric Attention-Deficit/Hyperactivity Disorder

JAMA Pediatr. 2024 Jan 1;178(1):81-84. doi: 10.1001/jamapediatrics.2023.4952.

Authors

Anne B Arnett^{1

2}, Elizabeth Harstad^{1

2}, Mia O'Connell^{1

3}, Katheryn Hayes^{1

3}, Stephanie Brewster^{1

2

3

4}, William Barbaresi^{1

2}, Ryan N Doan^{1

3}

Affiliations

¹ Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.
² Division of Developmental Medicine, Boston Children's Hospital, Boston, Massachusetts.
³ Division of Genetics & Genomics, Boston Children's Hospital, Boston, Massachusetts.
⁴ Rosamund Stone Zander Translational Neuroscience Center, Boston Children's Hospital, Boston, Massachusetts.

PMID: 37983059
PMCID: PMC10660237 (available on 2024-11-20)
DOI: 10.1001/jamapediatrics.2023.4952

No abstract available

Plain language summary

This case-control study examines the prevalence of rare de novo and inherited sequence variations among children and adolescents with attention-deficit/hyperactivity disorder (ADHD) and siblings and parents without ADHD.

MeSH terms

Attention Deficit Disorder with Hyperactivity* / genetics
Child
Humans
Parents
Siblings

Plain language summary

MeSH terms

Grants and funding