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An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Kaminsky EB, Kaul V, Paschall J, Church DM, Bunke B, Kunig D, Moreno-De-Luca D, Moreno-De-Luca A, Mulle JG, Warren ST, Richard G, Compton JG, Fuller AE, Gliem TJ, Huang S, Collinson MN, Beal SJ, Ackley T, Pickering DL, Golden DM, Aston E, Whitby H, Shetty S, Rossi MR, Rudd MK, South ST, Brothman AR, Sanger WG, Iyer RK, Crolla JA, Thorland EC, Aradhya S, Ledbetter DH, Martin CL. Kaminsky EB, et al. Among authors: warren st. Genet Med. 2011 Sep;13(9):777-84. doi: 10.1097/GIM.0b013e31822c79f9. Genet Med. 2011. PMID: 21844811 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