Common and rare variant genetic contributions in African Americans with autism.

Cirnigliaro M., Lowe JK., Flynn-Carroll AO., Kumagai ME., Gibson DS., Fu JM., Dong S., Hou K., Pillalamarri V., Abbacchi AM., Gulsrud AC., Miller J., Zhang Y., Graham ET., Akinyemi EO., Adams MF., Clay AN., Arteaga SA., Choi H., Kochis RM., Peña-Velasco JE., Hoekstra JN., Besterman AD., Mehta S., Hadzic T., Wilson RB., Brown TR., Hernandez LM., Marrus N., Molholm S., Klaiman C., Cantor RM., Talkowski ME., Sanders SJ., Arking DE., Pasaniuc B., Klin A., Constantino JN., Genetics of Neurodevelopment in African Americans (GENAA) Consortium ., Geschwind DH.

DOI

10.1101/2025.11.18.25340532

Type

Preprint

Publication Date

2025-11-19T00:00:00+00:00

Keywords

African, European, GWAS, PGS, autism spectrum disorder, de novo PTVs and missense variants, developmental disorder, gene discovery, genetically inferred ancestry, genotyping, local ancestry, neurodevelopmental disorder, pTDT, rare CNVs, whole-exome sequencing

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