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  • Linkedin: www.linkedin.com/in/catherine-roullier-b0610659
Number of documents

26

CV Catherine Roullier


Journal articles22 documents

  • Allegra Aron, Emily Gentry, Kerry Mcphail, Louis-Félix Nothias, Mélissa Nothias-Esposito, et al.. Reproducible molecular networking of untargeted mass spectrometry data using GNPS. Nature Protocols, Nature Publishing Group, 2020, 15 (6), pp.1954-1991. ⟨10.1038/s41596-020-0317-5⟩. ⟨hal-03015872⟩
  • Divya Arora, Prasoon Gupta, Sundeep Jaglan, Catherine Roullier, Olivier Grovel, et al.. Expanding the chemical diversity through microorganisms co-culture: Current status and outlook. Biotechnology Advances, Elsevier, 2020, 40, pp.107521. ⟨10.1016/j.biotechadv.2020.107521⟩. ⟨hal-03015863⟩
  • Francesco Pisapia, Manoëlla Sibat, Ryuichi Watanabe, Catherine Roullier, Toshiyuki Suzuki, et al.. Characterization of maitotoxin‐4 (MTX4) using electrospray positive mode ionization high‐resolution mass spectrometry and UV spectroscopy. Rapid Communications in Mass Spectrometry, Wiley, 2020, 34 (19), ⟨10.1002/rcm.8859⟩. ⟨hal-03015946⟩
  • Lucie Ory, Emmanuel Gentil, Decha Kumla, Anake Kijjoa, El‐hassane Nazih, et al.. Detection of ergosterol using liquid chromatography/electrospray ionization mass spectrometry: Investigation of unusual in‐source reactions. Rapid Communications in Mass Spectrometry, Wiley, 2020, 34 (12), ⟨10.1002/rcm.8780⟩. ⟨hal-03015867⟩
  • Lucie Ory, El-Hassane Nazih, Sahar Daoud, Julia Mocquard, Mélanie Bourjot, et al.. Targeting bioactive compounds in natural extracts - Development of a comprehensive workflow combining chemical and biological data. Analytica Chimica Acta, Elsevier Masson, 2019, 1070, pp.29-42. ⟨10.1016/j.aca.2019.04.038⟩. ⟨hal-02273499⟩
  • Thi Phuong Thuy Hoang, Catherine Roullier, Grégory Genta-Jouve, Marie-Claude Boumard, Thibaut Robiou Du Pont, et al.. C25 steroids from the marine mussel-derived fungus Penicillium ubiquetum MMS330. Phytochemistry Letters, Elsevier, 2019, 34, pp.18-24. ⟨10.1016/j.phytol.2019.09.002⟩. ⟨hal-03015939⟩
  • Thi Phuong Thuy Hoang, Catherine Roullier, Marie-Claude Boumard, Thibaut Robiou Du Pont, Hassan Nazih, et al.. Metabolomics-Driven Discovery of Meroterpenoids from a Mussel-Derived Penicillium ubiquetum. Journal of Natural Products, American Chemical Society, 2018, 81 (11), pp.2501-2511. ⟨10.1021/acs.jnatprod.8b00569⟩. ⟨hal-03015858⟩
  • Gabriel Castro-Falcón, Natalie Millán-Aguiñaga, Catherine Roullier, Paul Jensen, Chambers Hughes. Nitrosopyridine Probe To Detect Polyketide Natural Products with Conjugated Alkenes: Discovery of Novodaryamide and Nocarditriene. ACS Chemical Biology, American Chemical Society, 2018, 13 (11), pp.3097-3106. ⟨10.1021/acschembio.8b00598⟩. ⟨hal-03015853⟩
  • Maherizo Gedice Fernand, Catherine Roullier, Yann Guitton, Julie Lalande, Sandrine Lacoste, et al.. Fungi isolated from Madagascar shrimps - investigation of the Aspergillus niger metabolism by combined LC-MS and NMR metabolomics studies. Aquaculture, Elsevier, 2017, 479, pp.750-758. ⟨10.1016/j.aquaculture.2017.07.015⟩. ⟨hal-03015843⟩
  • David Overy, Hebelin Correa, Catherine Roullier, Wei-Chiung Chi, Ka-Lai Pang, et al.. Does Osmotic Stress Affect Natural Product Expression in Fungi?. Marine drugs, MDPI, 2017, 15 (8), pp.254. ⟨10.3390/md15080254⟩. ⟨hal-03015848⟩
  • Samuel Bertrand, Yann Guitton, Catherine Roullier. Successes and pitfalls in automated dereplication strategy using liquid chromatography coupled to mass spectrometry data: A CASMI 2016 experience. Phytochemistry Letters, Elsevier, 2017, 21, pp.297-305. ⟨10.1016/j.phytol.2016.12.025⟩. ⟨hal-03015840⟩
  • Cindy Staerck, Anne Landreau, Gaëtan Herbette, Catherine Roullier, Samuel Bertrand, et al.. The secreted polyketide boydone A is responsible for the anti-Staphylococcus aureus activity of Scedosporium boydii. FEMS Microbiology Letters, Wiley-Blackwell, 2017, 364 (22), ⟨10.1093/femsle/fnx223⟩. ⟨hal-02407052⟩
  • Francesco Pisapia, Manoëlla Sibat, Christine Herrenknecht, Korian Lhaute, Greta Gaiani, et al.. Maitotoxin-4, a Novel MTX Analog Produced by Gambierdiscus excentricus. Marine drugs, MDPI, 2017, 15 (7), pp.1-31. ⟨10.3390/md15070220⟩. ⟨anses-01570046⟩
  • Catherine Roullier, Yann Guitton, Marine Valéry, Séverine Amand, Soizic Prado, et al.. Automated Detection of Natural Halogenated Compounds from LC-MS Profiles–Application to the Isolation of Bioactive Chlorinated Compounds from Marine-Derived Fungi. Analytical Chemistry, American Chemical Society, 2016, 88 (18), pp.9143-9150. ⟨10.1021/acs.analchem.6b02128⟩. ⟨hal-03015826⟩
  • Catherine Roullier, Samuel Bertrand, Élodie Blanchet, Mathilde Peigné, Thibaut Robiou Du Pont, et al.. Time Dependency of Chemodiversity and Biosynthetic Pathways: An LC-MS Metabolomic Study of Marine-Sourced Penicillium. Marine drugs, MDPI, 2016, 14 (5), pp.103. ⟨10.3390/md14050103⟩. ⟨hal-03015824⟩
  • Yousef Dashti, Marie-Laure Vial, Stephen Wood, George Mellick, Catherine Roullier, et al.. Kororamide B, a brominated alkaloid from the bryozoan Amathia tortuosa and its effects on Parkinson's disease cells. Tetrahedron, Elsevier, 2015, 71 (41), pp.7879-7884. ⟨10.1016/j.tet.2015.08.017⟩. ⟨hal-03015823⟩
  • Hoan Vu, Catherine Roullier, Marc Campitelli, Katharine Trenholme, Donald Gardiner, et al.. Plasmodium Gametocyte Inhibition Identified from a Natural-Product-Based Fragment Library. ACS Chemical Biology, American Chemical Society, 2013, 8 (12), pp.2654-2659. ⟨10.1021/cb400582b⟩. ⟨hal-03015819⟩
  • Angélique Carroux, Anne-Isaline van Bohemen, Catherine Roullier, Thibaut Robiou Du Pont, Marieke Vansteelandt, et al.. Unprecedented 17-residue peptaibiotics produced by marine-derived Trichoderma atroviride.. Chemistry and Biodiversity, Wiley, 2013, 10 (5), pp.772-86. ⟨10.1002/cbdv.201200398⟩. ⟨hal-00862780⟩
  • Catherine Roullier, Marylene Chollet-Krugler, Eva-Maria Pferschy-Wenzig, Anne Maillard, Gerald N Rechberger, et al.. Characterization and identification of mycosporines-like compounds in cyanolichens. Isolation of mycosporine hydroxyglutamicol from Nephroma laevigatum Ach.. Phytochemistry, Elsevier, 2011, 72 (11-12), pp.1348-57. ⟨10.1016/j.phytochem.2011.04.002⟩. ⟨hal-00843484⟩
  • Catherine Roullier, Marylene Chollet-Krugler, Pierre van de Weghe, Françoise Lohézic-Le Dévéhat, Joël Boustie. A novel aryl-hydrazide from the marine lichen Lichina pygmaea: isolation, synthesis of derivatives, and cytotoxicity assays.. Bioorganic and Medicinal Chemistry Letters, Elsevier, 2010, 20 (15), pp.4582-6. ⟨10.1016/j.bmcl.2010.06.013⟩. ⟨hal-00844454⟩
  • Catherine Roullier, Marylene Chollet-Krugler, Aurélie Bernard, Joël Boustie. Multiple dual-mode centrifugal partition chromatography as an efficient method for the purification of a mycosporine from a crude methanolic extract of Lichina pygmaea. Journal of Chromatography B Biomedical Sciences and Applications, Elsevier, 2009, 877 (22), pp.2067-2073. ⟨10.1016/j.jchromb.2009.05.040⟩. ⟨hal-03015797⟩
  • Jérôme Quintin, Catherine Roullier, Sylviane Thoret, Guy Lewin. Synthesis and anti-tubulin evaluation of chromone-based analogues of combretastatins. Tetrahedron, Elsevier, 2006, 62 (17), pp.4038-4051. ⟨10.1016/j.tet.2006.02.024⟩. ⟨hal-03015791⟩

Book sections4 documents

  • Vanessa Rédou, Marine Vallet, Laurence Meslet-Cladière, Abhishek Kumar, Ka-Lai Pang, et al.. Marine Fungi. The Marine Microbiome, Springer International Publishing, pp.99-153, 2016, ⟨10.1007/978-3-319-33000-6_4⟩. ⟨hal-03015911⟩
  • Marieke Vansteelandt, Catherine Roullier, Elodie Blanchet, Yann Guitton, Yves-François Pouchus, et al.. Impact of Marine-Derived Penicillium Species in the Discovery of New Potential Antitumor Drugs. Outstanding Marine Molecules, Wiley-VCH Verlag GmbH & Co. KGaA, pp.45-84, 2014, ⟨10.1002/9783527681501.ch03⟩. ⟨hal-03015903⟩
  • Stéphane La Barre, Catherine Roullier, Joël Boustie. Mycosporine-Like Amino Acids (MAAs) in Biological Photosystems. Stéphane La Barre, Jean-Michel Kornprobst (eds.). Outstanding Marine Molecules: Chemistry, Biology, Analysis, Wiley-VCH Verlag GmbH, pp.333-360, 2014, ⟨10.1002/9783527681501.ch15⟩. ⟨hal-01116105⟩
  • N. Ruiz, Catherine Roullier, K. Petit, C. Sallenave-Namont, O. Grovel, et al.. Marine-derived Trichoderma: a source of new bioactive metabolites.. Trichoderma: biology and applications, CABI, pp.247-279, 2013, ⟨10.1079/9781780642475.0247⟩. ⟨hal-03015897⟩