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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 1
2004 2
2005 2
2008 1
2010 1
2011 1
2012 1
2013 5
2014 2
2015 3
2016 3
2019 2
2022 1
2024 0

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22 results

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Page 1
The GeneCards Suite: From Gene Data Mining to Disease Genome Sequence Analyses.
Stelzer G, Rosen N, Plaschkes I, Zimmerman S, Twik M, Fishilevich S, Stein TI, Nudel R, Lieder I, Mazor Y, Kaplan S, Dahary D, Warshawsky D, Guan-Golan Y, Kohn A, Rappaport N, Safran M, Lancet D. Stelzer G, et al. Among authors: dahary d. Curr Protoc Bioinformatics. 2016 Jun 20;54:1.30.1-1.30.33. doi: 10.1002/cpbi.5. Curr Protoc Bioinformatics. 2016. PMID: 27322403
In search of antisense.
Lavorgna G, Dahary D, Lehner B, Sorek R, Sanderson CM, Casari G. Lavorgna G, et al. Among authors: dahary d. Trends Biochem Sci. 2004 Feb;29(2):88-94. doi: 10.1016/j.tibs.2003.12.002. Trends Biochem Sci. 2004. PMID: 15102435 Review.
Genome analysis and knowledge-driven variant interpretation with TGex.
Dahary D, Golan Y, Mazor Y, Zelig O, Barshir R, Twik M, Iny Stein T, Rosner G, Kariv R, Chen F, Zhang Q, Shen Y, Safran M, Lancet D, Fishilevich S. Dahary D, et al. BMC Med Genomics. 2019 Dec 30;12(1):200. doi: 10.1186/s12920-019-0647-8. BMC Med Genomics. 2019. PMID: 31888639 Free PMC article.
Is there any sense in antisense editing?
Neeman Y, Dahary D, Levanon EY, Sorek R, Eisenberg E. Neeman Y, et al. Among authors: dahary d. Trends Genet. 2005 Oct;21(10):544-7. doi: 10.1016/j.tig.2005.08.005. Trends Genet. 2005. PMID: 16099531
VarElect: the phenotype-based variation prioritizer of the GeneCards Suite.
Stelzer G, Plaschkes I, Oz-Levi D, Alkelai A, Olender T, Zimmerman S, Twik M, Belinky F, Fishilevich S, Nudel R, Guan-Golan Y, Warshawsky D, Dahary D, Kohn A, Mazor Y, Kaplan S, Iny Stein T, Baris HN, Rappaport N, Safran M, Lancet D. Stelzer G, et al. Among authors: dahary d. BMC Genomics. 2016 Jun 23;17 Suppl 2(Suppl 2):444. doi: 10.1186/s12864-016-2722-2. BMC Genomics. 2016. PMID: 27357693 Free PMC article.
Microcephaly thin corpus callosum intellectual disability syndrome caused by mutated TAF2.
Hellman-Aharony S, Smirin-Yosef P, Halevy A, Pasmanik-Chor M, Yeheskel A, Har-Zahav A, Maya I, Straussberg R, Dahary D, Haviv A, Shohat M, Basel-Vanagaite L. Hellman-Aharony S, et al. Among authors: dahary d. Pediatr Neurol. 2013 Dec;49(6):411-416.e1. doi: 10.1016/j.pediatrneurol.2013.07.017. Epub 2013 Sep 29. Pediatr Neurol. 2013. PMID: 24084144
22 results