Vincent A. Funari, Ph.D. - Publications

Affiliations: 
2002 Boston University, Boston, MA, United States 
Area:
Molecular Biology

22 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
2016 Wheeler ML, Limon JJ, Bar AS, Leal CA, Gargus M, Tang J, Brown J, Funari VA, Wang HL, Crother TR, Arditi M, Underhill DM, Iliev ID. Immunological Consequences of Intestinal Fungal Dysbiosis. Cell Host & Microbe. PMID 27237365 DOI: 10.1016/j.chom.2016.05.003  0.72
2015 Xu N, Geller DH, Jones MR, Funari VA, Azziz R, Goodarzi MO. Comprehensive assessment of expression of insulin signaling pathway components in subcutaneous adipose tissue of women with and without polycystic ovary syndrome. Journal of Clinical & Translational Endocrinology. 2: 99-104. PMID 26236647 DOI: 10.1016/j.jcte.2015.06.002  0.72
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  0.72
2015 Frykman PK, Nordenskjöld A, Kawaguchi A, Hui TT, Granström AL, Cheng Z, Tang J, Underhill DM, Iliev I, Funari VA, Wester T. Characterization of Bacterial and Fungal Microbiome in Children with Hirschsprung Disease with and without a History of Enterocolitis: A Multicenter Study. Plos One. 10: e0124172. PMID 25909773 DOI: 10.1371/journal.pone.0124172  0.72
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  0.72
2015 Giamarellos-Bourboulis E, Tang J, Pyleris E, Pistiki A, Barbatzas C, Brown J, Lee CC, Harkins TT, Kim G, Weitsman S, Barlow GM, Funari VA, Pimentel M. Molecular assessment of differences in the duodenal microbiome in subjects with irritable bowel syndrome. Scandinavian Journal of Gastroenterology. 50: 1076-87. PMID 25865706 DOI: 10.3109/00365521.2015.1027261  0.72
2015 Seksenyan A, Kadavallore A, Walts AE, de la Torre B, Berel D, Strom SP, Aliahmad P, Funari VA, Kaye J. TOX3 is expressed in mammary ER(+) epithelial cells and regulates ER target genes in luminal breast cancer. Bmc Cancer. 15: 22. PMID 25632947 DOI: 10.1186/s12885-015-1018-2  0.72
2014 Sareen D, Saghizadeh M, Ornelas L, Winkler MA, Narwani K, Sahabian A, Funari VA, Tang J, Spurka L, Punj V, Maguen E, Rabinowitz YS, Svendsen CN, Ljubimov AV. Differentiation of human limbal-derived induced pluripotent stem cells into limbal-like epithelium. Stem Cells Translational Medicine. 3: 1002-12. PMID 25069777 DOI: 10.5966/sctm.2014-0076  0.72
2013 Funari VA, Winkler M, Brown J, Dimitrijevich SD, Ljubimov AV, Saghizadeh M. Differentially expressed wound healing-related microRNAs in the human diabetic cornea. Plos One. 8: e84425. PMID 24376808 DOI: 10.1371/journal.pone.0084425  0.72
2012 Iliev ID, Funari VA, Taylor KD, Nguyen Q, Reyes CN, Strom SP, Brown J, Becker CA, Fleshner PR, Dubinsky M, Rotter JI, Wang HL, McGovern DP, Brown GD, Underhill DM. Interactions between commensal fungi and the C-type lectin receptor Dectin-1 influence colitis. Science (New York, N.Y.). 336: 1314-7. PMID 22674328 DOI: 10.1126/science.1221789  0.72
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  0.72
2012 Nemec SF, Cohn DH, Krakow D, Funari VA, Rimoin DL, Lachman RS. The importance of conventional radiography in the mutational analysis of skeletal dysplasias (the TRPV4 mutational family). Pediatric Radiology. 42: 15-23. PMID 21863289 DOI: 10.1007/s00247-011-2229-6  0.72
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  0.72
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  0.72
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  0.72
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  0.72
2009 Merrill AE, Merriman B, Farrington-Rock C, Camacho N, Sebald ET, Funari VA, Schibler MJ, Firestein MH, Cohn ZA, Priore MA, Thompson AK, Rimoin DL, Nelson SF, Cohn DH, Krakow D. Ciliary abnormalities due to defects in the retrograde transport protein DYNC2H1 in short-rib polydactyly syndrome. American Journal of Human Genetics. 84: 542-9. PMID 19361615 DOI: 10.1016/j.ajhg.2009.03.015  0.72
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  0.72
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  0.72
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  0.72
2007 Funari VA, Crandall JE, Tolan DR. Fructose metabolism in the cerebellum. Cerebellum (London, England). 6: 130-40. PMID 17510913 DOI: 10.1080/14734220601064759  0.72
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  0.72
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