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Tag: copy number variation
All (107)
News (63)
Projects (39)
Events (5)
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
March 15, 2022
Copy number variation and pathogenic variant analyses of SPARK exomes
January 28, 2022
Simons Searchlight: December 2021 data release
December 20, 2021
Simons Searchlight to host conference on
CSNK2A1, HIVEP2, MED13L
and
SETBP1
genes
December 13, 2021
New iPSC lines from Simons Searchlight participants are now available
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