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Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neurons.
Kozlova A, Zhang S, Kotlar AV, Jamison B, Zhang H, Shi S, Forrest MP, McDaid J, Cutler DJ, Epstein MP, Zwick ME, Pang ZP, Sanders AR, Warren ST, Gejman PV, Mulle JG, Duan J. Kozlova A, et al. Among authors: warren st. Am J Hum Genet. 2022 Aug 4;109(8):1500-1519. doi: 10.1016/j.ajhg.2022.07.001. Am J Hum Genet. 2022. PMID: 35931052 Free PMC article.
The pathophysiology of fragile x syndrome.
Penagarikano O, Mulle JG, Warren ST. Penagarikano O, et al. Among authors: warren st. Annu Rev Genomics Hum Genet. 2007;8:109-29. doi: 10.1146/annurev.genom.8.080706.092249. Annu Rev Genomics Hum Genet. 2007. PMID: 17477822 Review.
Replication stress induces tumor-like microdeletions in FHIT/FRA3B.
Durkin SG, Ragland RL, Arlt MF, Mulle JG, Warren ST, Glover TW. Durkin SG, et al. Among authors: warren st. Proc Natl Acad Sci U S A. 2008 Jan 8;105(1):246-51. doi: 10.1073/pnas.0708097105. Epub 2007 Dec 27. Proc Natl Acad Sci U S A. 2008. PMID: 18162546 Free PMC article.
Microarray-based mutation detection in the dystrophin gene.
Hegde MR, Chin EL, Mulle JG, Okou DT, Warren ST, Zwick ME. Hegde MR, et al. Among authors: warren st. Hum Mutat. 2008 Sep;29(9):1091-9. doi: 10.1002/humu.20831. Hum Mutat. 2008. PMID: 18663755 Free PMC article.
Microdeletions of 3q29 confer high risk for schizophrenia.
Mulle JG, Dodd AF, McGrath JA, Wolyniec PS, Mitchell AA, Shetty AC, Sobreira NL, Valle D, Rudd MK, Satten G, Cutler DJ, Pulver AE, Warren ST. Mulle JG, et al. Among authors: warren st. Am J Hum Genet. 2010 Aug 13;87(2):229-36. doi: 10.1016/j.ajhg.2010.07.013. Am J Hum Genet. 2010. PMID: 20691406 Free PMC article.
215 results