The Ehlers-Danlos syndrome, a disorder with many faces von De Paepe, A, Malfait, F

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Acceptability and feasibility of the mHealth intervention ‘MyDayPlan’ to increase physical activity in a general adult population von Degroote, L, Van Dyck, D, De Bourdeaudhuij, I, De Paepe, A, Crombez, G

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Effectiveness of the mHealth intervention ‘MyDayPlan’ to increase physical activity: an aggregated single case approach von Degroote, L, De Paepe, A, De Bourdeaudhuij, I, Van Dyck, D, Crombez, G

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Zebrafish Collagen Type I: Molecular and Biochemical Characterization of the Major Structural Protein in Bone and Skin von Gistelinck, C., Gioia, R., Gagliardi, A., Tonelli, F., Marchese, L., Bianchi, L., Landi, C., Bini, L., Huysseune, A., Witten, P. E., Staes, A., Gevaert, K., De Rocker, N., Menten, B., Malfait, F., Leikin, S., Carra, S., Tenni, R., Rossi, A., De Paepe, A., Coucke, P., Willaert, A., Forlino, A.

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The molecular genetics of Marfan syndrome and related disorders von Robinson, P N, Arteaga-Solis, E, Baldock, C, Collod-Béroud, G, Booms, P, De Paepe, A, Dietz, H C, Guo, G, Handford, P A, Judge, D P, Kielty, C M, Loeys, B, Milewicz, D M, Ney, A, Ramirez, F, Reinhardt, D P, Tiedemann, K, Whiteman, P, Godfrey, M

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The genetic basis of the joint hypermobility syndromes von Malfait, F., Hakim, A. J., De Paepe, A., Grahame, R.

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Identification of a novel recurrent 1q42.2-1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas von Fieuw, Annelies, Kumps, Candy, Schramm, Alexander, Pattyn, Filip, Menten, Björn, Antonacci, Francesca, Sudmant, Peter, Schulte, Johannes H., Van Roy, N, Vergult, Sarah, Buckley, Patrick G., De Paepe, A, Noguera, Rosa, Versteeg, Rogier, Stallings, Raymond, Eggert, Angelika, Vandesompele, Jo, De Preter, K, Speleman, Frank

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Clinical and genetic aspects of Ehlers-Danlos syndrome, classic type von Malfait, Fransiska, Wenstrup, Richard J., De Paepe, Anne

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Total absence of the alpha2(I) chain of collagen type I causes a rare form of Ehlers-Danlos syndrome with hypermobility and propensity to cardiac valvular problems von Malfait, F, Symoens, S, Coucke, P, Nunes, L, De Almeida, S, De Paepe, A

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Two Cases of Post-Traumatic Mucormycosis due to Mucor circinelloides: Salvage Therapy with a Combination of Adjunctive Therapies von De Paepe, A., Dams, K., Robert, D., Jacobs, R., Ten Kate, G. L., Van Ierssel, S., Jansens, H., Lammens, M., Van Beeck, A., Jorens, P. G.

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Active enhancer and chromatin accessibility landscapes chart the regulatory network of primary multiple myeloma von Jin, Yi, Chen, Kenian, De Paepe, Ayla, Hellqvist, Eva, Krstic, Aleksandra D., Metang, Lauren, Gustafsson, Charlotte, Davis, Richard E., Levy, Yair M., Surapaneni, Rakesh, Wallblom, Ann, Nahi, Hareth, Mansson, Robert, Lin, Yin C.

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High-throughput ChIPmentation: freely scalable, single day ChIPseq data generation from very low cell-numbers von Gustafsson, Charlotte, De Paepe, Ayla, Schmidl, Christian, Månsson, Robert

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Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome von Beysen, D., Raes, J., Leroy, B.P., Lucassen, A., Yates, J.R.W., Clayton-Smith, J., Ilyina, H., Brooks, S. Sklower, Christin-Maitre, S., Fellous, M., Fryns, J.P., Kim, J.R., Lapunzina, P., Lemyre, E., Meire, F., Messiaen, L.M., Oley, C., Splitt, M., Thomson, J., Peer, Y. Van de, Veitia, R.A., De Paepe, A., De Baere, E.

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A new recurrent inversion, inv(7)(p15q34), leads to transcriptional activation of HOXA10 and HOXA11 in a subset of T-cell acute lymphoblastic leukemias von SPELEMAN, F, CAUWELIER, B, BOOGAERTS, M, DE MOERLOOSE, B, BENOIT, Y, SELLESLAG, D, BILLIET, J, ROBERT, A, HUGUET, F, VANDENBERGHE, P, DE PAEPE, A, MARYNEN, P, DASTUGUE, N, HAGEMEIJER, A, COOLS, J, VERHASSELT, B, POPPE, B, VAN ROY, N, VANDESOMPELE, J, GRAUX, C, UYTTEBROECK, A

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Ehlers-Danlos arthrochalasia type (VIIA-B) - expanding the phenotype: from prenatal life through adulthood von Klaassens, M, Reinstein, E, Hilhorst-Hofstee, Y, Schrander, JJP, Malfait, F, Staal, H, ten Have, LC, Blaauw, J, Roggeveen, HCJ, Krakow, D, De Paepe, A, van Steensel, MAM, Pals, G, Graham, JM, Schrander-Stumpel, CTRM

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BRCA1 and BRCA2 germline mutation spectrum and frequencies in Belgian breast/ovarian cancer families von Claes, K, Poppe, B, Coene, I, Paepe, A De, Messiaen, L

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COVID-19 in three waves in a tertiary referral hospital in Belgium: a comparison of patient characteristics, management, and outcome von De Paepe, Andreas, Vlieghe, Erika, Brusselaers, Nele, Soentjens, Patrick, Theunissen, Caroline, Brosius, Isabel, Grouwels, Jeroen, Van Petersen, Lida, van Tiggelen, Hanne, Verbrugghe, Walter, Jorens, Philippe G, Lapperre, Thérèse, Peeters, Karen, Vermeulen, Griet, van Ierssel, Sabrina H

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Comprehensive mapping of the effects of azacitidine on DNA methylation, repressive/permissive histone marks and gene expression in primary cells from patients with MDS and MDS-rela... von Tobiasson, Magnus, Abdulkadir, Hani, Lennartsson, Andreas, Katayama, Shintaro, Marabita, Francesco, De Paepe, Ayla, Karimi, Mohsen, Krjutskov, Kaarel, Einarsdottir, Elisabet, Grövdal, Michael, Jansson, Monika, Ben Azenkoud, Asmaa, Corddedu, Lina, Lehmann, Sören, Ekwall, Karl, Kere, Juha, Hellström-Lindberg, Eva, Ungerstedt, Johanna

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Effect of Mutation Type and Location on Clinical Outcome in 1,013 Probands with Marfan Syndrome or Related Phenotypes and FBN1 Mutations: An International Study von Faivre, L., Collod-Beroud, G., Loeys, B.L., Child, A., Binquet, C., Gautier, E., Callewaert, B., Arbustini, E., Mayer, K., Arslan-Kirchner, M., Kiotsekoglou, A., Comeglio, P., Marziliano, N., Dietz, H.C., Halliday, D., Beroud, C., Bonithon-Kopp, C., Claustres, M., Muti, C., Plauchu, H., Robinson, P.N., Adès, L.C., Biggin, A., Benetts, B., Brett, M., Holman, K.J., De Backer, J., Coucke, P., Francke, U., De Paepe, A., Jondeau, G., Boileau, C.

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Molecular cytogenetic study of 126 unselected T-ALL cases reveals high incidence of TCRβ locus rearrangements and putative new T-cell oncogenes von CAUWELIER, B, DASTUGUE, N, COOLS, J, POPPE, B, HERENS, C, DE PAEPE, A, HAGEMEIJER, A, SPELEMAN, F

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