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Page 1
smyRNA: a novel Ab initio ncRNA gene finder.
Salari R, Aksay C, Karakoc E, Unrau PJ, Hajirasouliha I, Sahinalp SC. Salari R, et al. Among authors: karakoc e. PLoS One. 2009;4(5):e5433. doi: 10.1371/journal.pone.0005433. Epub 2009 May 5. PLoS One. 2009. PMID: 19415115 Free PMC article.
taveRNA: a web suite for RNA algorithms and applications.
Aksay C, Salari R, Karakoc E, Alkan C, Sahinalp SC. Aksay C, et al. Among authors: karakoc e. Nucleic Acids Res. 2007 Jul;35(Web Server issue):W325-9. doi: 10.1093/nar/gkm303. Epub 2007 May 8. Nucleic Acids Res. 2007. PMID: 17488837 Free PMC article.
Transmission disequilibrium of small CNVs in simplex autism.
Krumm N, O'Roak BJ, Karakoc E, Mohajeri K, Nelson B, Vives L, Jacquemont S, Munson J, Bernier R, Eichler EE. Krumm N, et al. Among authors: karakoc e. Am J Hum Genet. 2013 Oct 3;93(4):595-606. doi: 10.1016/j.ajhg.2013.07.024. Epub 2013 Sep 12. Am J Hum Genet. 2013. PMID: 24035194 Free PMC article.
Altered splicing of ATP6AP2 causes X-linked parkinsonism with spasticity (XPDS).
Korvatska O, Strand NS, Berndt JD, Strovas T, Chen DH, Leverenz JB, Kiianitsa K, Mata IF, Karakoc E, Greenup JL, Bonkowski E, Chuang J, Moon RT, Eichler EE, Nickerson DA, Zabetian CP, Kraemer BC, Bird TD, Raskind WH. Korvatska O, et al. Among authors: karakoc e. Hum Mol Genet. 2013 Aug 15;22(16):3259-68. doi: 10.1093/hmg/ddt180. Epub 2013 Apr 16. Hum Mol Genet. 2013. PMID: 23595882 Free PMC article.
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
O'Roak BJ, Deriziotis P, Lee C, Vives L, Schwartz JJ, Girirajan S, Karakoc E, Mackenzie AP, Ng SB, Baker C, Rieder MJ, Nickerson DA, Bernier R, Fisher SE, Shendure J, Eichler EE. O'Roak BJ, et al. Among authors: karakoc e. Nat Genet. 2011 Jun;43(6):585-9. doi: 10.1038/ng.835. Epub 2011 May 15. Nat Genet. 2011. PMID: 21572417 Free PMC article.
90 results