Examining the role of common variants in rare neurodevelopmental conditions.
Huang QQ, Wigdor EM, Malawsky DS, Campbell P, Samocha KE, Chundru VK, Danecek P, Lindsay S, Marchant T, Koko M, Amanat S, Bonfanti D, Sheridan E, Radford EJ, Barrett JC, Wright CF, Firth HV, Warrier V, Strudwick Young A, Hurles ME, Martin HC.
Huang QQ, et al. Among authors: barrett jc.
Nature. 2024 Nov 20. doi: 10.1038/s41586-024-08217-y. Online ahead of print.
Nature. 2024.
PMID: 39567701