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Global genetic analysis.
Elahi E, Kumm J, Ronaghi M. Elahi E, et al. Among authors: ronaghi m. J Biochem Mol Biol. 2004 Jan 31;37(1):11-27. doi: 10.5483/bmbrep.2004.37.1.011. J Biochem Mol Biol. 2004. PMID: 14761299 Review.
Mutation in ST6GALNAC5 identified in family with coronary artery disease.
InanlooRahatloo K, Parsa AF, Huse K, Rasooli P, Davaran S, Platzer M, Kramer M, Fan JB, Turk C, Amini S, Steemers F, Gunderson K, Ronaghi M, Elahi E. InanlooRahatloo K, et al. Among authors: ronaghi m. Sci Rep. 2014 Jan 8;4:3595. doi: 10.1038/srep03595. Sci Rep. 2014. PMID: 24399302 Free PMC article.
LTBP2 mutations cause Weill-Marchesani and Weill-Marchesani-like syndrome and affect disruptions in the extracellular matrix.
Haji-Seyed-Javadi R, Jelodari-Mamaghani S, Paylakhi SH, Yazdani S, Nilforushan N, Fan JB, Klotzle B, Mahmoudi MJ, Ebrahimian MJ, Chelich N, Taghiabadi E, Kamyab K, Boileau C, Paisan-Ruiz C, Ronaghi M, Elahi E. Haji-Seyed-Javadi R, et al. Among authors: ronaghi m. Hum Mutat. 2012 Aug;33(8):1182-7. doi: 10.1002/humu.22105. Epub 2012 May 29. Hum Mutat. 2012. PMID: 22539340
A haplotype framework for cystic fibrosis mutations in Iran.
Elahi E, Khodadad A, Kupershmidt I, Ghasemi F, Alinasab B, Naghizadeh R, Eason RG, Amini M, Esmaili M, Esmaeili Dooki MR, Sanati MH, Davis RW, Ronaghi M, Thorstenson YR. Elahi E, et al. Among authors: ronaghi m. J Mol Diagn. 2006 Feb;8(1):119-27. doi: 10.2353/jmoldx.2006.050063. J Mol Diagn. 2006. PMID: 16436643 Free PMC article.
112 results