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Article

Whole exome sequencing in ADHD trios from single and multi-incident families implicates new candidate genes and highlights polygenic transmission.

European journal of human genetics : EJHG - 1 Aug 2020

Al-Mubarak Bashayer R, Omar Aisha, Baz Batoul, Al-Abdulaziz Basma, Magrashi Amna I, Al-Yemni Eman, Jabaan Amjad, Monies Dorota, Abouelhoda Mohamed, Abebe Dejene, Ghaziuddin Mohammad, Al-Tassan Nada A

Abstract excerpt

Several types of genetic alterations occurring at numerous loci have been described in attention deficit hyperactivity disorder (ADHD). However, the role of rare single nucleotide variants (SNVs) remains under investigated. Here, we sought to identify rare SNVs with predicted deleterious effect that may contribute to ADHD risk. We chose to study ADHD families (including multi-incident) from a population with a...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 32238911
DOI: 10.1038/s41431-020-0619-7
PMCID: PMC7382449

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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