Shomron N - Search Results

1

Assessing the involvement of the placental microbiome and virome in preeclampsia using non coding RNA sequencing.

Yoffe L, Kuperman AA, Isakov O, Haguel D, Polsky AL, Farberov L, Pillar N, Gurevich V, Haviv I, Shomron N. Yoffe L, et al. Among authors: shomron n. J Perinat Med. 2021 Jun 11;49(9):1071-1083. doi: 10.1515/jpm-2021-0006. Print 2021 Nov 25. J Perinat Med. 2021. PMID: 34114389

2

Pathogen detection using short-RNA deep sequencing subtraction and assembly.

Isakov O, Modai S, Shomron N. Isakov O, et al. Among authors: shomron n. Bioinformatics. 2011 Aug 1;27(15):2027-30. doi: 10.1093/bioinformatics/btr349. Epub 2011 Jun 11. Bioinformatics. 2011. PMID: 21666269 Free PMC article.

3

miRviewer: a multispecies microRNA homologous viewer.

Kiezun A, Artzi S, Modai S, Volk N, Isakov O, Shomron N. Kiezun A, et al. Among authors: shomron n. BMC Res Notes. 2012 Feb 13;5:92. doi: 10.1186/1756-0500-5-92. BMC Res Notes. 2012. PMID: 22330228 Free PMC article.

4

Novel insight into the non-coding repertoire through deep sequencing analysis.

Isakov O, Ronen R, Kovarsky J, Gabay A, Gan I, Modai S, Shomron N. Isakov O, et al. Among authors: shomron n. Nucleic Acids Res. 2012 Jun;40(11):e86. doi: 10.1093/nar/gks228. Epub 2012 Mar 9. Nucleic Acids Res. 2012. PMID: 22406831 Free PMC article.

5

Familial pityriasis rubra pilaris is caused by mutations in CARD14.

Fuchs-Telem D, Sarig O, van Steensel MA, Isakov O, Israeli S, Nousbeck J, Richard K, Winnepenninckx V, Vernooij M, Shomron N, Uitto J, Fleckman P, Richard G, Sprecher E. Fuchs-Telem D, et al. Among authors: shomron n. Am J Hum Genet. 2012 Jul 13;91(1):163-70. doi: 10.1016/j.ajhg.2012.05.010. Epub 2012 Jun 14. Am J Hum Genet. 2012. PMID: 22703878 Free PMC article.

6

Analysis of insertion-deletion from deep-sequencing data: software evaluation for optimal detection.

Neuman JA, Isakov O, Shomron N. Neuman JA, et al. Among authors: shomron n. Brief Bioinform. 2013 Jan;14(1):46-55. doi: 10.1093/bib/bbs013. Epub 2012 Mar 24. Brief Bioinform. 2013. PMID: 22707752

7

The microRNA Transcriptome of Human Cytomegalovirus (HCMV).

Meshesha MK, Veksler-Lublinsky I, Isakov O, Reichenstein I, Shomron N, Kedem K, Ziv-Ukelson M, Bentwich Z, Avni YS. Meshesha MK, et al. Among authors: shomron n. Open Virol J. 2012;6:38-48. doi: 10.2174/1874357901206010038. Epub 2012 Apr 11. Open Virol J. 2012. PMID: 22715351 Free PMC article.

8

Exome sequencing analysis: a guide to disease variant detection.

Isakov O, Perrone M, Shomron N. Isakov O, et al. Among authors: shomron n. Methods Mol Biol. 2013;1038:137-58. doi: 10.1007/978-1-62703-514-9_8. Methods Mol Biol. 2013. PMID: 23872973

9

Meeting summary: Ethical aspects of whole exome and whole genome sequencing studies (WES/WGS) in rare diseases, Tel Aviv, Israel, January 2013.

Farberov L, Gilam A, Isakov O, Shomron N. Farberov L, et al. Among authors: shomron n. Genet Res (Camb). 2013 Jun;95(2-3):53-6. doi: 10.1017/S0016672313000104. Genet Res (Camb). 2013. PMID: 23938110

10

Missense mutation in the MEN1 gene discovered through whole exome sequencing co-segregates with familial hyperparathyroidism.

Isakov O, Rinella ES, Olchovsky D, Shimon I, Ostrer H, Shomron N, Friedman E. Isakov O, et al. Among authors: shomron n. Genet Res (Camb). 2013 Aug;95(4):114-20. doi: 10.1017/S0016672313000141. Genet Res (Camb). 2013. PMID: 24074368

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