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Vincent A. Funari, Ph.D. - Publications

Affiliations: 
2002 Boston University, Boston, MA, United States 
Area:
Molecular Biology
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29 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Paul M, Scarpa FJ, Wolfson WA, Weiss L, Funari VA, Blocker F. Role of epigenetic regulators in single-base substitution patterns in AML. Journal of Clinical Oncology. 38: e19500-e19500. DOI: 10.1200/Jco.2020.38.15_Suppl.E19500  0.309
2020 Scarpa FJ, Paul M, Wolfson WA, Weiss LM, Funari VA, Blocker F. STAG2-mutated AML patients: ASXL1 cohesin binding motif status and mutation landscape. Journal of Clinical Oncology. 38: 7538-7538. DOI: 10.1200/Jco.2020.38.15_Suppl.7538  0.304
2018 Wong C, Funari V, Albitar M. Immunophenotyping Using Targeted RNA NGS Recapitulates Traditional AML and CLL FLOW Fingerprints Blood. 132: 5256-5256. DOI: 10.1182/Blood-2018-99-119085  0.329
2017 Bankoti R, Ogawa C, Nguyen T, Emadi L, Couse M, Salehi S, Fan X, Dhall D, Wang Y, Brown J, Funari V, Tang J, Martins GA. Differential regulation of Effector and Regulatory T cell function by Blimp1. Scientific Reports. 7: 12078. PMID 28935958 DOI: 10.1038/S41598-017-12171-3  0.31
2017 Ready D, Yagiz K, Amin P, Yildiz Y, Funari V, Bozdag S, Cinar B. Mapping the STK4/Hippo signaling network in prostate cancer cell. Plos One. 12: e0184590. PMID 28880957 DOI: 10.1371/Journal.Pone.0184590  0.343
2017 Kanska J, Aspuria PP, Taylor-Harding B, Spurka L, Funari V, Orsulic S, Karlan BY, Wiedemeyer WR. Glucose deprivation elicits phenotypic plasticity via ZEB1-mediated expression of NNMT. Oncotarget. PMID 28412735 DOI: 10.18632/Oncotarget.15429  0.31
2017 Ma W, Dios ID, Funari V, Sudarsanam S, Jiang S, Agersborg S, Hummel J, Blocker F, Albitar M. IDH1 and IDH2 : Founding or Progressor Mutations in Myeloid Neoplasms Blood. 130: 405-405. DOI: 10.1182/Blood.V130.Suppl_1.405.405  0.31
2017 Ma W, Dios ID, Funari V, Sudarsanam S, Jiang S, Agersborg S, Hummel J, Blocker F, Albitar M. FLT3 Mutation in Acute Myeloid Leukemia: Primary or Secondary Mutation? Blood. 130: 2668-2668. DOI: 10.1182/Blood.V130.Suppl_1.2668.2668  0.306
2017 Albitar M, Sudarsanam S, Ma W, Jiang S, Chen W, Funari V, Brodie S, Agersborg S. Abstract 5618: Correlation between MET gene amplification and TP53 mutation in upregulating PD-L1 expression in EGFR wild-type lung cancer Cancer Research. 77: 5618-5618. DOI: 10.1158/1538-7445.Am2017-5618  0.306
2016 Xu Y, Mizuno T, Sridharan A, Du Y, Guo M, Tang J, Wikenheiser-Brokamp KA, Perl AT, Funari VA, Gokey JJ, Stripp BR, Whitsett JA. Single-cell RNA sequencing identifies diverse roles of epithelial cells in idiopathic pulmonary fibrosis. Jci Insight. 1: e90558. PMID 27942595 DOI: 10.1172/Jci.Insight.90558  0.313
2016 Ready D, Yildiz Y, Funari V, Bozdag S, Cinar B. Abstract 4401: Disclosing the Hippo signaling networks in castration-resistant prostate cancer Cancer Research. 76: 4401-4401. DOI: 10.1158/1538-7445.Am2016-4401  0.308
2015 Ignatius Irudayam J, Contreras D, Spurka L, Ren S, Kanagavel V, Ramaiah A, Annamalai A, French SW, Klein AS, Funari V, Arumugaswami V. Profile of Inflammation-associated genes during Hepatic Differentiation of Human Pluripotent Stem Cells. Data in Brief. 5: 871-8. PMID 26702414 DOI: 10.1016/J.Dib.2015.10.023  0.329
2015 Ignatius Irudayam J, Contreras D, Spurka L, Subramanian A, Allen J, Ren S, Kanagavel V, Nguyen Q, Ramaiah A, Ramamoorthy K, French SW, Klein AS, Funari V, Arumugaswami V. Characterization of type I interferon pathway during hepatic differentiation of human pluripotent stem cells and hepatitis C virus infection. Stem Cell Research. 15: 354-364. PMID 26313525 DOI: 10.1016/J.Scr.2015.08.003  0.303
2015 Hatada S, Subramanian A, Mandefro B, Ren S, Kim HW, Tang J, Funari V, Baloh RH, Sareen D, Arumugaswami V, Svendsen CN. Low-Dose Irradiation Enhances Gene Targeting in Human Pluripotent Stem Cells. Stem Cells Translational Medicine. PMID 26185257 DOI: 10.5966/Sctm.2015-0050  0.312
2015 Seehus CR, Aliahmad P, de la Torre B, Iliev ID, Spurka L, Funari VA, Kaye J. The development of innate lymphoid cells requires TOX-dependent generation of a common innate lymphoid cell progenitor. Nature Immunology. 16: 599-608. PMID 25915732 DOI: 10.1038/Ni.3168  0.331
2015 Tang J, Iliev ID, Brown J, Underhill DM, Funari VA. Mycobiome: Approaches to analysis of intestinal fungi. Journal of Immunological Methods. 421: 112-21. PMID 25891793 DOI: 10.1016/J.Jim.2015.04.004  0.306
2012 Lee JH, Huynh M, Silhavy JL, Kim S, Dixon-Salazar T, Heiberg A, Scott E, Bafna V, Hill KJ, Collazo A, Funari V, Russ C, Gabriel SB, Mathern GW, Gleeson JG. De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly. Nature Genetics. 44: 941-5. PMID 22729223 DOI: 10.1038/Ng.2329  0.33
2012 Tompson SW, Faqeih EA, Ala-Kokko L, Hecht JT, Miki R, Funari T, Funari VA, Nevarez L, Krakow D, Cohn DH. Dominant and recessive forms of fibrochondrogenesis resulting from mutations at a second locus, COL11A2. American Journal of Medical Genetics. Part A. 158: 309-14. PMID 22246659 DOI: 10.1002/Ajmg.A.34406  0.338
2012 Seksenyan A, Kadavallore A, Torre Bdl, Aliahmad P, Asirvatham A, Walts AE, Bose S, Berel D, Strom S, Funari V, Audeh W, Kaye J. Abstract 1311: Expression and activity of nuclear factor TOX3 in breast cancer Cancer Research. 72: 1311-1311. DOI: 10.1158/1538-7445.Am2012-1311  0.313
2010 Funari VA, Krakow D, Nevarez L, Chen Z, Funari TL, Vatanavicharn N, Wilcox WR, Rimoin DL, Nelson SF, Cohn DH. BMPER mutation in diaphanospondylodysostosis identified by ancestral autozygosity mapping and targeted high-throughput sequencing. American Journal of Human Genetics. 87: 532-7. PMID 20869035 DOI: 10.1016/J.Ajhg.2010.08.015  0.351
2010 Funari VA, Voevodski K, Leyfer D, Yerkes L, Cramer D, Tolan DR. Quantitative gene expression profiles in real time from expressed sequence tag databases. Gene Expression. 14: 321-36. PMID 20635574 DOI: 10.3727/105221610X12717040569820  0.56
2010 Smits P, Bolton AD, Funari V, Hong M, Boyden ED, Lu L, Manning DK, Dwyer ND, Moran JL, Prysak M, Merriman B, Nelson SF, Bonafé L, Superti-Furga A, Ikegawa S, et al. Lethal skeletal dysplasia in mice and humans lacking the golgin GMAP-210. The New England Journal of Medicine. 362: 206-16. PMID 20089971 DOI: 10.1056/Nejmoa0900158  0.322
2009 Day A, Dong J, Funari VA, Harry B, Strom SP, Cohn DH, Nelson SF. Disease gene characterization through large-scale co-expression analysis. Plos One. 4: e8491. PMID 20046828 DOI: 10.1371/Journal.Pone.0008491  0.351
2009 Lee H, O'Connor BD, Merriman B, Funari VA, Homer N, Chen Z, Cohn DH, Nelson SF. Improving the efficiency of genomic loci capture using oligonucleotide arrays for high throughput resequencing. Bmc Genomics. 10: 646. PMID 20043857 DOI: 10.1186/1471-2164-10-646  0.317
2009 Tompson SW, Merriman B, Funari VA, Fresquet M, Lachman RS, Rimoin DL, Nelson SF, Briggs MD, Cohn DH, Krakow D. A recessive skeletal dysplasia, SEMD aggrecan type, results from a missense mutation affecting the C-type lectin domain of aggrecan. American Journal of Human Genetics. 84: 72-9. PMID 19110214 DOI: 10.1016/J.Ajhg.2008.12.001  0.328
2008 Rock MJ, Prenen J, Funari VA, Funari TL, Merriman B, Nelson SF, Lachman RS, Wilcox WR, Reyno S, Quadrelli R, Vaglio A, Owsianik G, Janssens A, Voets T, Ikegawa S, et al. Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia. Nature Genetics. 40: 999-1003. PMID 18587396 DOI: 10.1038/Ng.166  0.313
2007 Funari VA, Day A, Krakow D, Cohn ZA, Chen Z, Nelson SF, Cohn DH. Cartilage-selective genes identified in genome-scale analysis of non-cartilage and cartilage gene expression. Bmc Genomics. 8: 165. PMID 17565682 DOI: 10.1186/1471-2164-8-165  0.323
2007 Funari VA, Crandall JE, Tolan DR. Fructose metabolism in the cerebellum. Cerebellum (London, England). 6: 130-40. PMID 17510913 DOI: 10.1080/14734220601064759  0.543
2005 Funari VA, Herrera VL, Freeman D, Tolan DR. Genes required for fructose metabolism are expressed in Purkinje cells in the cerebellum. Brain Research. Molecular Brain Research. 142: 115-22. PMID 16266770 DOI: 10.1016/J.Molbrainres.2005.09.019  0.566
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