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Identification of PSMB5 as a genetic modifier of fragile X-associated tremor/ataxia syndrome.
Kong HE, Lim J, Linsalata A, Kang Y, Malik I, Allen EG, Cao Y, Shubeck L, Johnston R, Huang Y, Gu Y, Guo X, Zwick ME, Qin Z, Wingo TS, Juncos J, Nelson DL, Epstein MP, Cutler DJ, Todd PK, Sherman SL, Warren ST, Jin P. Kong HE, et al. Among authors: zwick me. Proc Natl Acad Sci U S A. 2022 May 31;119(22):e2118124119. doi: 10.1073/pnas.2118124119. Epub 2022 May 26. Proc Natl Acad Sci U S A. 2022. PMID: 35617426 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: zwick me. Hum Mutat. 2008 Sep;29(9):1091-9. doi: 10.1002/humu.20831. Hum Mutat. 2008. PMID: 18663755 Free PMC article.
Microarray oligonucleotide probe designer (MOPeD): A web service.
Patel VC, Mondal K, Shetty AC, Horner VL, Bedoyan JK, Martin D, Caspary T, Cutler DJ, Zwick ME. Patel VC, et al. Among authors: zwick me. Open Access Bioinformatics. 2010 Nov 1;2(2010):145-155. doi: 10.2147/OAB.S13741. Open Access Bioinformatics. 2010. PMID: 21379402 Free PMC article.
Targeted sequencing of the human X chromosome exome.
Mondal K, Shetty AC, Patel V, Cutler DJ, Zwick ME. Mondal K, et al. Among authors: zwick me. Genomics. 2011 Oct;98(4):260-5. doi: 10.1016/j.ygeno.2011.04.004. Epub 2011 Apr 16. Genomics. 2011. PMID: 21524701 Free PMC article.
88 results