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Publications

  1. Laboratory genetic testing in clinical practice. Cogulu O, Alanay Y, Toruner GA.Biomed Res Int. 2013;2013:532897. doi: 10.1155/2013/532897. Epub 2013 Jul 14. No abstract available. PMID:23936813
  2. A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds.Tang Z, Berlin DS, Toji L, Toruner GA, Beiswanger C, Kulkarni S, Martin CL, Emanuel BS, Christman M, Gerry NP.G3 (Bethesda). 2013 Jul 8;3(7):1143-9. doi: 10.1534/g3.113.006577. Erratum in: G3 (Bethesda). 2013 Sep;3(9):1617. PMID:23665875
  3. A lactotransferrin single nucleotide polymorphism demonstrates biological activity that can reduce susceptibility to caries.Fine DH, Toruner GA, Velliyagounder K, Sampathkumar V, Godboley D, Furgang D.Infect Immun. 2013 May;81(5):1596-605. doi: 10.1128/IAI.01063-12. Epub 2013 Mar 4.PMID:23460521
  4. Immunological characterization and transcription profiling of peripheral blood (PB) monocytes in children with autism spectrum disorders (ASD) and specific polysaccharide antibody deficiency (SPAD): case study.Jyonouchi H, Geng L, Streck DL, Toruner GA.J Neuroinflammation. 2012 Jan 7;9:4. doi: 10.1186/1742-2094-9-4.PMID:22226452
  5. Terminal 14q deletion with unbalanced t(Y;14)(q12;q32) translocation.Bağci G, Cetin GO, Semerci N, Toruner GA, Cinbiş M.Clin Dysmorphol. 2012 Jan;21(1):37-41. doi: 10.1097/MCD.0b013e32834d6ba3.PMID:22143350
  6. Children with autism spectrum disorders (ASD) who exhibit chronic gastrointestinal (GI) symptoms and marked fluctuation of behavioral symptoms exhibit distinct innate immune abnormalities and transcriptional profiles of peripheral blood (PB) monocytes.Jyonouchi H, Geng L, Streck DL, Toruner GA.J Neuroimmunol. 2011 Sep 15;238(1-2):73-80. doi: 10.1016/j.jneuroim.2011.07.001. Epub 2011 Jul 30.PMID:21803429
  7. Profiling and functional analyses of microRNAs and their target gene products in human uterine leiomyomas.Zavadil J, Ye H, Liu Z, Wu J, Lee P, Hernando E, Soteropoulos P, Toruner GA, Wei JJ.PLoS One. 2010 Aug 24;5(8):e12362. doi: 10.1371/journal.pone.0012362.PMID:20808773
  8. Array comparative genomic hybridization analysis of adult acute leukemia patients.Yasar D, Karadogan I, Alanoglu G, Akkaya B, Luleci G, Salim O, Timuragaoglu A, Toruner GA, Berker-Karauzum S.Cancer Genet Cytogenet. 2010 Mar;197(2):122-9. doi: 10.1016/j.cancergencyto.2009.11.018.PMID:20193845
  9. Copy number variations in three children with sudden infant death.Toruner GA, Kurvathi R, Sugalski R, Shulman L, Twersky S, Pearson PG, Tozzi R, Schwalb MN, Wallerstein R.Clin Genet. 2009 Jul;76(1):63-8. doi: 10.1111/j.1399-0004.2009.01161.x.PMID:19659761
  10. Molecular and immunohistochemical evidence for the origin of uterine leiomyosarcomas from associated leiomyoma and symplastic leiomyoma-like areas.Mittal KR, Chen F, Wei JJ, Rijhvani K, Kurvathi R, Streck D, Dermody J, Toruner GA.Mod Pathol. 2009 Oct;22(10):1303-11. doi: 10.1038/modpathol.2009.96. Epub 2009 Jul 24.PMID:19633649
  11. Genome profiling of chondrosarcoma using oligonucleotide array-based comparative genomic hybridization.Hameed M, Ulger C, Yasar D, Limaye N, Kurvathi R, Streck D, Benevenia J, Patterson F, Dermody JJ, Toruner GA.Cancer Genet Cytogenet. 2009 Jul 15;192(2):56-9. doi: 10.1016/j.cancergencyto.2009.03.009.PMID:19596254
  12. Exclusion of APC and VHL gene deletions by array-based comparative hybridization in two patients with microscopically visible chromosomal aberrations.Wallerstein RJ, Brooks SS, Streck DL, Kurvathi R, Toruner GA.Cancer Genet Cytogenet. 2007 Oct 15;178(2):151-4.PMID:17954272
  13. Molecular signatures of trauma-hemorrhagic shock-induced lung injury: hemorrhage- and injury-associated genes.Feinman R, Deitch EA, Aris V, Chu HB, Abungu B, Caputo FJ, Galante A, Xu D, Lu Q, Colorado I, Streck D, Dermody J, Soteropoulos P.Shock. 2007 Sep;28(3):360-8.PMID:17545943
  14. Further delineation of interstitial chromosome 6 deletion syndrome and review of the literature.Zherebtsov MM, Klein RT, Aviv H, Toruner GA, Hanna NN, Brooks SS.Clin Dysmorphol. 2007 Jul;16(3):135-40. Review.PMID:17551325
  15. Monozygous twins with a microdeletion syndrome involving BTK, DDP1, and two other genes; evidence of intact dendritic cell development and TLR responses.Jyonouchi H, Geng L, Törüner GA, Vinekar K, Feng D, Fitzgerald-Bocarsly P.Eur J Pediatr. 2008 Mar;167(3):317-21. Epub 2007 May 23.PMID:17520285
  16. An oligonucleotide based array-CGH system for detection of genome wide copy number changes including subtelomeric regions for genetic evaluation of mental retardation.Toruner GA, Streck DL, Schwalb MN, Dermody JJ.Am J Med Genet A. 2007 Apr 15;143A(8):824-9.PMID:17366576
  17. Arvanil and anandamide up-regulate CD36 expression in human peripheral blood mononuclear cells.Malfitano AM, Toruner GA, Gazzerro P, Laezza C, Husain S, Eletto D, Orlando P, De Petrocellis L, Terskiy A, Schwalb M, Vitale E, Bifulco M. Immunol Lett. 2007 Apr 15;109(2):145-54. Epub 2007 Mar 5.PMID:17360047
  18. Microtransponder-based multiplex assay for genotyping cystic fibrosis.Lin X, Flint JA, Azaro M, Coradetti T, Kopacka WM, Streck DL, Wang Z, Dermody J, Mandecki W.Clin Chem. 2007 Jul;53(7):1372-6. Epub 2007 May 17.PMID:17510306
  19. MDM2 T309G polymorphism is associated with bladder cancer. Onat OE, Tez M, Ozçelik T, Törüner GA.Anticancer Res. 2006 Sep-Oct;26(5A):3473-5.PMID:17094469
  20. Using the common sense model to understand perceived cancer risk in individuals testing for BRCA1/2 mutations.Kelly K, Leventhal H, Andrykowski M, Toppmeyer D, Much J, Dermody J, Marvin M, Baran J, Schwalb M.Psychooncology. 2005 Jan;14(1):34-48.PMID:15386791
  21. Dopamine receptor 4 (DRD4) 7-repeat allele predicts methylphenidate dose response in children with attention deficit hyperactivity disorder: a pharmacogenetic study.Hamarman S, Fossella J, Ulger C, Brimacombe M, Dermody J.J Child Adolesc Psychopharmacol. 2004 Winter;14(4):564-74.PMID:15662148
  22. Noise filtering and nonparametric analysis of microarray data underscores discriminating markers of oral, prostate, lung, ovarian and breast cancer.Aris VM, Cody MJ, Cheng J, Dermody JJ, Soteropoulos P, Recce M, Tolias PP.BMC Bioinformatics. 2004 Nov 29;5:185.
  23. Association between gene expression profile and tumor invasion in oral squamous cell carcinoma.Toruner GA, Ulger C, Alkan M, Galante AT, Rinaggio J, Wilk R, Tian B, Soteropoulos P, Hameed MR, Schwalb MN, Dermody JJ.Cancer Genet Cytogenet. 2004 Oct 1;154(1):27-35. PMID:15381369
  24. Gene expression after crush injury of human saphenous vein: using microarrays to define the transcriptional profile.Price RM, Tulsyan N, Dermody JJ, Schwalb M, Soteropoulos P, Castronuovo JJ Jr.J Am Coll Surg. 2004 Sep;199(3):411-8.PMID:15325611
  25. The decision to test in women receiving genetic counseling for BRCA1 and BRCA2 mutations.Kelly K, Leventhal H, Andrykowski M, Toppmeyer D, Much J, Dermody J, Marvin M, Baran J, Schwalb M.J Genet Couns. 2004 Jun;13(3):237-57.PMID:15604634
  26. Subjective and objective risk of breast cancer in Ashkenazi Jewish individuals at risk for BRCA1/2 mutations.Kelly K, Leventhal H, Marvin M, Toppmeyer D, Much J, Dermody J, Baran J, Schwalb M.Genet Test. 2004 Summer;8(2):139-47.PMID:15345111
  27. Comprehensive genome-wide comparison of DNA and RNA level scan using microarray technology for identification of candidate cancer-related genes in the HL-60 cell line.  Ulger C, Toruner GA, Alkan M, Mohammed M, Damani S, Kang J, Galante A, Aviv H, Soteropoulos P, Tolias PP, Schwalb MN, Dermody JJ.Cancer Genet Cytogenet. 2003 Nov;147(1):28-35.PMID:14580768
  28. High incidence of two methylenetetrahydrofolate reductase mutations (C677T and A1298C) in Hispanics.Chowdary D, Streck D, Schwalb MN, Dermody JJ.Genet Test. 2003 Fall;7(3):255-7.PMID:14642003