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Showing results 4 to 6 of 6

4
Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome

Roosing, Susanne; Hofree, Matan; Kim, Sehyun; Scott, Eric; Copeland, Brett; Romani, Marta; Silhavy, Jennifer L; et al, ELIFE, v.4, 2015-05

5
Non-coding de novo mutations in chromatin interactions are implicated in autism spectrum disorder

Kim, Il Bin; Lee, Taeyeop; Lee, Junehawk; Kim, Jonghun; Lee, Suho; Koh, In Gyeong; Kim, Jae Hyun; et al, MOLECULAR PSYCHIATRY, v.27, no.11, pp.4680 - 4694, 2022-07

6
Virmid: accurate detection of somatic mutations with sample impurity inference

Kim, Sangwoo; Jeong, Kyowon; Bhutani, Kunal; Lee, Jeong Ho; Patel, Anand; Scott, Eric; Nam, Hojung; et al, GENOME BIOLOGY, v.14, no.8, 2013

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