| Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism D Coelho, JC Kim, IR Miousse, S Fung, M du Moulin, I Buers, T Suormala, ... Nature genetics 44 (10), 1152-1155, 2012 | 253 | 2012 |
| Gene identification for the cblD defect of vitamin B12 metabolism D Coelho, T Suormala, M Stucki, JP Lerner-Ellis, DS Rosenblatt, ... New England Journal of Medicine 358 (14), 1454-1464, 2008 | 212 | 2008 |
| Spectrum of mutations in MMACHC, allelic expression, and evidence for genotype–phenotype correlations JP Lerner‐Ellis, N Anastasio, J Liu, D Coelho, T Suormala, M Stucki, ... Human mutation 30 (7), 1072-1081, 2009 | 207 | 2009 |
| Flavanols and procyanidins of cocoa and chocolate inhibit growth and polyamine biosynthesis of human colonic cancer cells S Carnésecchi, Y Schneider, SA Lazarus, D Coehlo, F Gossé, F Raul Cancer letters 175 (2), 147-155, 2002 | 180 | 2002 |
| The cblD defect causes either isolated or combined deficiency of methylcobalamin and adenosylcobalamin synthesis T Suormala, MR Baumgartner, D Coelho, P Zavadakova, V Kozich, ... Journal of Biological Chemistry 279 (41), 42742-42749, 2004 | 155 | 2004 |
| Resveratrol analog (Z)‐3, 5, 4′‐trimethoxystilbene is a potent anti‐mitotic drug inhibiting tubulin polymerization Y Schneider, P Chabert, J Stutzmann, D Coelho, A Fougerousse, F Gossé, ... International journal of cancer 107 (2), 189-196, 2003 | 144 | 2003 |
| Mutation update and review of severe methylenetetrahydrofolate reductase deficiency DS Froese, M Huemer, T Suormala, P Burda, D Coelho, JL Guéant, ... Human mutation 37 (5), 427-438, 2016 | 117 | 2016 |
| APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients JL Guéant, C Chéry, A Oussalah, J Nadaf, D Coelho, T Josse, J Flayac, ... Nature Communications 9 (67), doi:10.1038/s41467-017-02306-5, 2018 | 83 | 2018 |
| Perturbation by geraniol of cell membrane permeability and signal transduction pathways in human colon cancer cells S Carnesecchi, A Bradaia, B Fischer, D Coelho, M Schöller-Guinard, ... Journal of Pharmacology and Experimental Therapeutics 303 (2), 711-715, 2002 | 79 | 2002 |
| 3‐Methylcrotonyl‐CoA carboxylase deficiency: mutation analysis in 28 probands, 9 symptomatic and 19 detected by newborn screening MF Dantas, T Suormala, A Randolph, D Coelho, B Fowler, D Valle, ... Human mutation 26 (2), 164-164, 2005 | 67 | 2005 |
| Caspase-3-like activity determines the type of cell death following ionizing radiation in MOLT-4 human leukaemia cells D Coelho, V Holl, D Weltin, T Lacornerie, P Magnenet, P Dufour, ... British journal of cancer 83 (5), 642-649, 2000 | 65 | 2000 |
| Molecular mechanisms leading to three different phenotypes in the cblD defect of intracellular cobalamin metabolism M Stucki, D Coelho, T Suormala, P Burda, B Fowler, MR Baumgartner Human molecular genetics 21 (6), 1410-1418, 2012 | 64 | 2012 |
| Nutritional models of foetal programming and nutrigenomic and epigenomic dysregulations of fatty acid metabolism in the liver and heart JL Guéant, R Elakoum, O Ziegler, D Coelho, E Feigerlova, JL Daval, ... Pflügers Archiv-European Journal of Physiology 466 (5), 833-850, 2014 | 63 | 2014 |
| Clinical and molecular heterogeneity in patients with the cblD inborn error of cobalamin metabolism IR Miousse, D Watkins, D Coelho, T Rupar, EA Crombez, E Vilain, ... The Journal of pediatrics 154 (4), 551-556, 2009 | 58 | 2009 |
| Caspase 8-mediated cleavage of the pro-apoptotic BCL-2 family member BID in p53-dependent apoptosis B Fischer, D Coelho, P Dufour, JP Bergerat, JM Denis, J Gueulette, ... Biochemical and biophysical research communications 306 (2), 516-522, 2003 | 54 | 2003 |
| Methionine synthase and methionine synthase reductase interact with MMACHC and with MMADHC C Bassila, R Ghemrawi, J Flayac, DS Froese, MR Baumgartner, ... Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1863 (1), 103-112, 2017 | 45 | 2017 |
| Apoptosis at the interface of immunosuppressive and anticancer activities the examples of two classes of chemical inducers, oxysterols and alkylating agents PL Bischoff, V Holl, D Coelho, P Dufour, B Luu, D Weltin Current medicinal chemistry 7 (7), 693-713, 2000 | 45 | 2000 |
| Interaction between methionine synthase isoforms and MMACHC: characterization in cblG-variant, cblG and cblC inherited causes of megaloblastic anemia. MB Fofou-Caillierez, NT Mrabet, C Chéry, N Dreumont, J Flayac, ... Human molecular genetics, 2013 | 39 | 2013 |
| Clinical or ATPase domain mutations in ABCD4 disrupt the interaction between the vitamin B12-trafficking proteins ABCD4 and LMBD1 V Fettelschoss, P Burda, C Sagné, D Coelho, C De Laet, S Lutz, ... Journal of Biological Chemistry 292 (28), 11980-11991, 2017 | 38 | 2017 |
| Sirt1-PPARS cross-talk in complex metabolic diseases and inherited disorders of the one carbon metabolism VJ Kosgei, D Coelho, RM Guéant-Rodriguez, JL Guéant Cells 9 (8), 1882, 2020 | 37 | 2020 |
