| Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13 in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome) G Matthijs, E Schollen, E Pardon, M Veiga-Da-Cunha, J Jaeken, ... Nature genetics 16 (1), 88-92, 1997 | 425 | 1997 |
| Short‐term control of glucokinase activity: role of a regulatory protein E Van Schaftingen, M Detheux, MV Da Cunha The FASEB journal 8 (6), 414-419, 1994 | 300 | 1994 |
| Sequence of a putative glucose 6‐phosphate translocase, mutated in glycogen storage disease type Ib1 I Gerin, M Veiga-da-Cunha, Y Achouri, JF Collet, E Van Schaftingen FEBS letters 419 (2-3), 235-238, 1997 | 269 | 1997 |
| Molecular identification of carnosine synthase as ATP-grasp domain-containing protein 1 (ATPGD1) J Drozak, M Veiga-da-Cunha, D Vertommen, V Stroobant, ... Journal of biological chemistry 285 (13), 9346-9356, 2010 | 245 | 2010 |
| A gene encoding a putative FAD-dependent L-2-hydroxyglutarate dehydrogenase is mutated in L-2-hydroxyglutaric aciduria R Rzem, M Veiga-da-Cunha, G Noël, S Goffette, MC Nassogne, B Tabarki, ... Proceedings of the National Academy of Sciences 101 (48), 16849-16854, 2004 | 226 | 2004 |
| l‐2‐Hydroxyglutaric aciduria, a defect of metabolite repair R Rzem, MF Vincent, E Van Schaftingen, M Veiga‐da‐Cunha Journal of Inherited Metabolic Disease: Official Journal of the Society for …, 2007 | 165 | 2007 |
| Identification of a dehydrogenase acting on D-2-hydroxyglutarate Y Achouri, G Noël, D Vertommen, MH Rider, M Veiga-Da-Cunha, ... Biochemical Journal 381 (1), 35-42, 2004 | 157 | 2004 |
| l-2-Hydroxyglutaric aciduria, a disorder of metabolite repair E Van Schaftingen, R Rzem, M Veiga-da-Cunha Journal of inherited metabolic disease 32, 135-142, 2009 | 148 | 2009 |
| Failure to eliminate a phosphorylated glucose analog leads to neutropenia in patients with G6PT and G6PC3 deficiency M Veiga-da-Cunha, N Chevalier, X Stephenne, JP Defour, N Paczia, ... Proceedings of the National Academy of Sciences 116 (4), 1241-1250, 2019 | 146 | 2019 |
| A gene on chromosome 11q23 coding for a putative glucose-6-phosphate translocase is mutated in glycogen-storage disease types Ib and Ic M Veiga-da-Cunha, I Gerin, YT Chen, T de Barsy, P de Lonlay, ... The American Journal of Human Genetics 63 (4), 976-983, 1998 | 137 | 1998 |
| Pathway and regulation of erythritol formation in Leuconostoc oenos M Veiga-da-Cunha, H Santos, E Van Schaftingen Journal of Bacteriology 175 (13), 3941-3948, 1993 | 137 | 1993 |
| Treating neutropenia and neutrophil dysfunction in glycogen storage disease type Ib with an SGLT2 inhibitor SB Wortmann, JLK Van Hove, TGJ Derks, N Chevalier, V Knight, A Koller, ... Blood, The Journal of the American Society of Hematology 136 (9), 1033-1043, 2020 | 134 | 2020 |
| Insights into the structure and regulation of glucokinase from a novel mutation (V62M), which causes maturity-onset diabetes of the young AL Gloyn, S Odili, D Zelent, C Buettger, HAJ Castleden, AM Steele, ... Journal of Biological Chemistry 280 (14), 14105-14113, 2005 | 128 | 2005 |
| The putative glucose 6-phosphate translocase gene is mutated in essentially all cases of glycogen storage disease type I non-a M Veiga-da-Cunha, I Gerin, YT Chen, PJ Lee, JV Leonard, I Maire, ... European Journal of Human Genetics 7 (6), 717-723, 1999 | 125 | 1999 |
| Glucokinase regulatory protein is essential for the proper subcellular localisation of liver glucokinase N De La Iglesia, M Veiga-da-Cunha, E Van Schaftingen, JJ Guinovart, ... FEBS letters 456 (2), 332-338, 1999 | 119 | 1999 |
| SETD3 protein is the actin-specific histidine N-methyltransferase S Kwiatkowski, AK Seliga, D Vertommen, M Terreri, T Ishikawa, ... Elife 7, e37921, 2018 | 106 | 2018 |
| Sugar-glycerol cofermentations in lactobacilli: the fate of lactate M Veiga da Cunha, MA Foster Journal of bacteriology 174 (3), 1013-1019, 1992 | 106 | 1992 |
| A conserved phosphatase destroys toxic glycolytic side products in mammals and yeast F Collard, F Baldin, I Gerin, J Bolsée, G Noël, J Graff, M Veiga-da-Cunha, ... Nature chemical biology 12 (8), 601-607, 2016 | 105 | 2016 |
| Enzymatic repair of Amadori products E Van Schaftingen, F Collard, E Wiame, M Veiga-da-Cunha Amino acids 42, 1143-1150, 2012 | 104 | 2012 |
| Carnosine and anserine homeostasis in skeletal muscle and heart is controlled by β‐alanine transamination L Blancquaert, SP Baba, S Kwiatkowski, J Stautemas, S Stegen, ... The Journal of physiology 594 (17), 4849-4863, 2016 | 103 | 2016 |
Emile Van Schaftingende Duve Institute, Université catholique de LouvainEmail yang diverifikasi di uclouvain.be