Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Overview of attention for article published in Nature Communications, July 2023

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Study 8/11: Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals. We genome-wide analyzed of copy number variations association with seizures. https://t.co/lNrlgW2v4R

Open Access UCL Research: Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals https://t.co/Kx1yKkj8rT

RT @LalDennis: Highly recommend to join Sunday @DLSneurocyclist at #IEC2023 to hear about our work on copy number variants associated with…

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