Tag: copy number variation

March 06, 2023

A new approach to analyzing genomic association data finds convergence of both rare and common genetic influences on autism at chromosome 16p By Azra Jaferi

August 18, 2022

Clinical trial of arbaclofen for 16p11.2 deletion has launched By Rachel Jurd

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January 28, 2022

Simons Searchlight: December 2021 data release

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December 20, 2021

Simons Searchlight to host conference on CSNK2A1, HIVEP2, MED13L and SETBP1 genes

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December 13, 2021

New iPSC lines from Simons Searchlight participants are now available

December 10, 2021

A Conversation with SFARI scientists Alan Packer, Pamela Feliciano and Misia Kowanda about SFARI gene lists By Christopher Feldsine

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