Full list of publications in peer reviewed scientific journals
My current H-factor is 64, with an average of 75 citations for my 221 peer-reviewed publications, 131 of which have been cited at least 25 times each.
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2022
M. Fenckova, V. Muha , D. Mariappa, M. Catinozzi, I. Czajewski, L.E.R. Blok, A.T. Ferenbach, E. Storkebaum, A. Schenck and D.M.F. van Aalten, “Intellectual disability-associated disruption of O-GlcNAc cycling impairs habituation learning in Drosophila“, PLOS Genet. (2022), 18, e1010159.
K. Yan, M. Stanley, B. Kowalski, O.G. Raimi, A.T. Ferenbach, P. Wei, W. Fang and D.M.F. van Aalten, “Genetic validation of Aspergillus fumigatus phosphoglucomutase as a viable therapeutic target in invasive aspergillosis”, J.Biol.Chem. (2022), 298, 102003.
C.W. Mitchell, I. Czajewski, and D.M.F. van Aalten, “Bioinformatic prediction of putative conveyers of O-GlcNAc Transferase intellectual disability”, J.Biol.Chem. (2022), 298(9) 102276.
Y. Zhou, K. Yan, Q. Qin, O.G. Raimi, C. Du, B. Wang, C.S. Ahamefule, B. Kowalski, C. Jin, D.M.F. van Aalten* and W. Fang, “Phosphoglucose isomerase is important for Aspergillus fumigatus cell wall biogenesis”, mBio (2022), 13(4):e0142622.
L.R. Soria, G. Makris, A.M. D'Alessio, A. De Angelis, I. Boffa, V.M. Pravata, V. Rüfenacht, S. Attanasio, E. Nusco, P. Arena, A.T. Ferenbach, D. Paris, P. Cuomo, A. Motta, M. Nitzahn, G.S. Lipshutz, A. Martínez-Pizarro, E. Richard, L.R. Desviat, J. Häberle, D.M.F van Aalten, and N. Brunetti-Pierri, "O-GlcNAcylation enhances CPS1 catalytic efficiency for ammonia and promotes ureagenesis", Nature Comms. (2022), 13:5212.
2023
I. Czajewski and D.M.F. van Aalten, “The role of O-GlcNAcylation in development”, Development (2023), 150 (6):dev201370.
Y. Zhang, H. Yu, D. Wang, X. Lei, Y. Meng, N. Zhang, F. Chen, L. Lv, Q. Pan, H. Qin, Z. Zhang, D.M.F. van Aalten and Kai Yuan, “Protein O-GlcNAcylation homeostasis regulates facultative heterochromatin to fine-tune sog-Dpp signaling during Drosophila early embryogenesis”, J.Genet.Genomics (2023), 50(12):948-959
M. Omelková, M. Murray, C.D. Fenger, T.B. Hammer, V.M. Pravata, S.G. Bartual, I. Czajewski, A. Bayat, A.T. Ferenbach, M.P. Stavridis and D.M.F. van Aalten, “An O-GlcNAc transferase pathogenic variant that affects pluripotent stem cell self-renewal”, Dis.Model.Mech. (2023), 16 (6):dmm049132.
S. Arnaouteli, N.C. Bamford, G.B. Brandani, R.J. Morris, M. Schor, J.T. Carrington, L. Hobley, D.M.F. van Aalten*, N.R. Stanley-Wall* and Cait E MacPhee*, “Lateral interactions govern self-assembly of the bacterial biofilm matrix protein BslA”, PNAS (2023), 120(45):e2312022120. (* co-corresponding authors)
2024
C.W. Mitchell, S.G. Bartual, A.T. Ferenbach, C. Scavenius and D.M.F. van Aalten, “Exploiting O-GlcNAc transferase promiscuity to dissect site-specific O-GlcNAcylation”, Glycobiology (2024), 33, 12, 1172–1181.
H. Yu, D. Liu, Y. Zhang, R. Tang, X. Fan, S. Mao, L. Lv, F. Chen, H. Qin, Z. Zhang, D.M.F. van Aalten, B. Yang and K. Yuan, “Tissue-specific O-GlcNAcylation profiling identifies substrates in translational machinery in Drosophila mushroom body contributing to olfactory learning”, eLife (2024), 13:e91269.
F. Authier, N. Ondruskova, A.T. Ferenbach, A.D. McNeilly and D.M.F. van Aalten, “Neurodevelopmental defects in a mouse model of O-GlcNAc transferase intellectual disability”, Dis.Model.Mech. (2024), 17, dmm050671.
M. Murray, L. Davidson, A.T. Ferenbach, D. Lefeber and D.M.F. van Aalten, “Neuroectoderm phenotypes in a human stem cell model of O-GlcNAc transferase-associated intellectual disability”, Mol.Genet.Metab. (2024), 142, 108492.
J.M. Mayfield, N.L. Hitefield, I.Czajewski, L. Vanhye, L. Holden, E. Morava, D.M.F. van Aalten* and L. Wells*, “O-GlcNAc transferase congenital disorder of glycosylation (OGT-CDG): Potential mechanistic targets revealed by evaluating the OGT interactome”, J.Biol.Chem. (2024), 300, 107599. (* co-corresponding authors)
I. Czajewski, B. Swain, J. Xu, L. McDowall, A.T. Ferenbach and D.M.F. van Aalten, “Rescuable sleep and synaptogenesis phenotypes in a Drosophila model of O-GlcNAc transferase intellectual disability”, eLife (2024), 13:e90376.
2025
H. Yuan, C.W. Mitchell, A.T. Ferenbach, M.T. Bonati, A. Feresin, P.J. Benke, Q.K.G. Tan and D.M.F. van Aalten, “Exploiting O-GlcNAc dyshomeostasis to screen O-GlcNAc transferase intellectual disability variants”, Stem Cell Rep. (2025), 20, 102380.
C.W. Mitchell, H. Yuan, A.T. Ferenbach, M. Sønderstrup-Jensen and D.M.F. van Aalten, “O-GlcNAcylation of the intellectual disability protein DDX3X exerts proteostatic cell cycle control”, Open Biol. (2025), 15, 250064.
S.B. Hansen, S.G. Bartual, H. Yuan, O.G. Raimi, A. Gorelik, A.T. Ferenbach, K. Lytje, J.S. Pedersen, T. Drace, T. Boesen and D.M.F. van Aalten, “Multi-domain O-GlcNAcase structures reveal allosteric regulatory mechanisms”, Nature Comms. (2025), 16, 8828.
A.M. D'Alessio, H. Yuan, L.R. Soria, S.B. Hansen, I. Boffa, P. Arena, B. Attianese, M. O'Sullivan, N. Cullinan, L. Pang, D.M.F. van Aalten, N. Brunetti-Pierri and S.A. Lynch, “An OGT missense variant with impaired enzyme activity in a child with severe developmental delay and hepatoblastoma”, Am.J.Med.Genet. A (2025), 0:e64275.
V.M. Pravata, H. Jiang, A.T. Ferenbach, A. Lamond and D.M.F. van Aalten, “Zscan4 as a candidate conveyor of early developmental defects in O-GlcNAc transferase intellectual disability”, Mol.Cell.Prot. (2025), 24, 101077.
2026
K. Yan, M. Stanley, O. Raimi, A.T. Ferenbach, H.C. Dorfmueller and D.M.F. van Aalten, “Cell wall target fragment discovery using a low-cost minimal fragment library”, FEBS Lett. (2026), in press.
F. Authier, I. Faress, C.S. Skoven, I. Esperón-Abril, S.T. Balasubramaniam, K.-S. Coquelin, A. Jan, J.R. Nyengaard, C. Scavenius, B. Attianese, O.G. Sevillano-Quispe, S.F. Eskildsen, J.S. Thomsen, B. Hansen and D.M.F. van Aalten, “Pathogenic O-GlcNAc dyshomeostasis leads to cortical dysplasia and behavioural deficits”, eLife (2026), accepted with revisions.
F. Authier, I. Esperon-Abril, K.S. Coquelin, C.S. Skoven, S.F. Eskildsen, N. Ondruskova, A.T. Ferenbach, J.S. Thomsen, B. Hansen and D.M.F. van Aalten, “Genetic rescue of pathogenic O-GlcNAc dyshomeostasis associated with microcephaly and motor deficits”, eNeuro (2026), in press.
F. Authier, B. Attianese, O.G. Sevillano-Quispe, K.S. Coquelin, S.G. Bartual, H. Yuan, M.P. Vazquez, I. Esperon-Abril, A.T. Ferenbach, C. Scavenius, D. Doummar, P. Charles, C. Mignot, B. Keren, M. Krygier, M. Mazurkiewicz-Bełdzińska, P.D. Rohde, P. Qvist and D.M.F. van Aalten, “O-GlcNAcase dosage variants are associated with neuronal deficits and intellectual disability”, J.Clin.Invest. (2026), accepted with revisions.