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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.
Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma.
Narooie-Nejad M, Paylakhi SH, Shojaee S, Fazlali Z, Rezaei Kanavi M, Nilforushan N, Yazdani S, Babrzadeh F, Suri F, Ronaghi M, Elahi E, Paisán-Ruiz C. Narooie-Nejad M, et al. Among authors: ronaghi m. Hum Mol Genet. 2009 Oct 15;18(20):3969-77. doi: 10.1093/hmg/ddp338. Epub 2009 Aug 4. Hum Mol Genet. 2009. PMID: 19656777
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
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.
Pyrosequencing: a tool for DNA sequencing analysis.
Elahi E, Ronaghi M. Elahi E, et al. Among authors: ronaghi m. Methods Mol Biol. 2004;255:211-9. doi: 10.1385/1-59259-752-1:211. Methods Mol Biol. 2004. PMID: 15020827 No abstract available.
113 results