Dissecting the contribution of common variants to risk of rare neurodevelopmental conditions

Huang QQ., Wigdor EM., Campbell P., Malawsky DS., Samocha KE., Chundru VK., Danecek P., Lindsay S., Marchant T., Musa MK., Amanat S., Bonifanti D., Sheridan E., Radford EJ., Barrett JC., Wright CF., Firth HV., Warrier V., Young AS., Hurles M., Martin HC.

DOI

10.1101/2024.03.05.24303772

Type

Publication Date

06/03/2024

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