Menu
Currency
GWAS Study

A Protective Role of Low Polygenic Risk Score in Healthy Individuals Carrying Attention-Deficit/Hyperactivity Disorder-Associated Copy Number Variations.

Chang X, Qu H, Liu Y et al.

37865391 PubMed ID
GWAS Study Type
4800 Participants
62 Views
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

CX
Chang X
QH
Qu H
LY
Liu Y
GJ
Glessner J
HH
Hakonarson H
Chapter II

Abstract

Summary of the research findings

Previous studies have implicated both rare copy number variations (CNVs) and common variants in liability for attention-deficit/hyperactivity disorder (ADHD). However, how common and rare genetic variants jointly contribute to individual liability requires further investigation in larger cohorts.

1,200 African American cases, 3,600 African American controls

Chapter III

Study Statistics

Key metrics and study information

4800
Total Participants
GWAS
Study Type
No
Replicated
African American or Afro-Caribbean
Ancestry
U.S.
Recruitment Country
Chapter IV

AI-Generated Summary

AI-generated by DNAGENICS

Independent AI summary of health and genetic findings from the published study

Important: This summary is AI-generated by DNAGENICS for informational purposes only. It was not created by, affiliated with, or endorsed by the researchers behind the original publication, and is based solely on that published research. It may contain errors or omissions. DNAGENICS disclaims all liability for any inaccuracies or consequences arising from use of this information. Verify all information against the original publication. This is not professional scientific review or medical advice.

AI Summary In Progress

Our AI-generated summary of this publication is being prepared. Please check back soon.