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    • Holling, T., Bhavani, G. S., Elsner, . von ., Shah, H., Kausthubham, N., Bhattacharyya, S. S., Shukla, A., Mortier, G. R., Schinke, T., Danyukova, T., Pohl, S., Kutsche, K., & Girisha, K. M. (2022). A homozygous hypomorphic BNIP1 variant causes an increase in autophagosomes and reduced autophagic flux and results in a spondylo-epiphyseal dysplasia. Human Mutation, 43(5), 625–642. https://doi.org/10.1002/HUMU.2...;

    • Hojland, A. T., Tavernier, L. J. M., Schrauwen, I., Sommen, M., Topsakal, V., Schatteman, I., Dhooge, I., Huber, A., Zanetti, D., Kunst, H. P. M., Hoischen, A., Petersen, M. B., Van Camp, G., & Fransen, E. (2022). A wide range of protective and predisposing variants in aggrecan influence the susceptibility for otosclerosis. Human Genetics, 141(3-4), 951–963. https://doi.org/10.1007/S00439...;

    • Gommeren, H., Bosmans, J., Moyaert, J., Mertens, G., Cras, P., Engelborghs, S., Van Ombergen, A., Gilles, A., Fransen, E., Berg, . van . de ., Janssens de Varebeke, S., & Van Rompaey, V. (2022). Accelerated cognitive decline associated with hearing loss and bilateral vestibulopathy : insights from a prospective cross-sectional study using the repeatable battery for the assessment of neuropsychological status adjusted for the hearing impaired in the DFNA9 population. Ear and Hearing, 1–13. https://doi.org/10.1097/AUD.00...;

    • Boeren, M., Van Breedam, E., Buyle-Huybrecht, T., Lebrun, M., Meysman, P., Sadzot-Delvaux, C., van Tendeloo, V. F., Mortier, G., Laukens, K., Ogunjimi, B., Ponsaerts, P., & Delputte, P. (2022). Activation of interferon-stimulated genes following varicella-zoster virus infection in a human iPSC-derived neuronal in vitro model depends on exogenous interferon-α. Viruses, 14(11), 1–24. https://doi.org/10.3390/V14112...;

    • Basmanav, F. B., Cesarato, N., Kumar, S., Borisov, O., Kokordelis, P., Ralser, D. J., Wehner, M., Axt, D., Xiong, X., Thiele, H., Dolgin, V., Gossmann, Y., Fricker, N., Dewenter, M. K., Weller, K., Suri, M., Reichenbach, H., Oji, V., Addor, M.-C., … Betz, R. C. (2022). Assessment of the genetic spectrum of uncombable hair syndrome in a cohort of 107 individuals. JAMA Dermatology, 158(11), 1245–1253. https://doi.org/10.1001/JAMADE...;

    • Ha, M. K., Bartholomeus, E., Van Os, L., Dandelooy, J., Leysen, J., Aerts, O., Siozopoulou, V., Smet, D., Gielen, J., Guerti, K., Maeseneer, D., Herregods, N., Lechkar, B., Wittoek, R., Geens, E., Claes, L., Zaqout, M., Dewals, W., Lemay, A., … Ogunjimi, B. (2022). Blood transcriptomics to facilitate diagnosis and stratification in pediatric rheumatic diseases : a proof of concept study. Pediatric Rheumatology, 20(1), 1–10. https://doi.org/10.1186/S12969...;

    • Lauffer, P., Boudin, E., Kaay, . van . der ., Koene, S., Haeringen, . van ., Tellingen, . van ., Van Hul, W., Prickett, T. C. R., Mortier, G., Espiner, E. A., & Duyvenvoorde, . van . (2022). Broadening the spectrum of loss-of-function variants in NPR-C-related extreme tall stature. Journal of the Endocrine Society, 6(4). https://doi.org/10.1210/JENDSO...;

    • Das, L., Dhiman, V., Dutta, P., Sood, A., Prakash, M., Kaur, S., Steenackers, E., Hendrickx, G., Dayal, D., Van Hul, W., & Bhadada, S. K. (2022). Camurati-Engelmann disease complicated by hypopituitarism : management challenges and literature review of outcomes with bisphosphonates. 8(2), 58–64. https://doi.org/10.1016/J.AACE...;

    • Katta Mohan Kumar, G., & Mortier, G. (2022). Clinical and genomic elucidation of skeletal dysplasias. University of Antwerp, Faculty of Medicine & Health Sciences, Department of Medical Genetics.

    • Weyns, A.-S., Verlaet, A. A. J., Breynaert, A., Naessens, T., Fransen, E., Verhelst, H., Van West, D., Ingelghem, V., Jonckheere, A. I., Beysen, D., Kenis, S., Moens, E., Roest, . van ., Savelkoul, H. F. J., de Bruyne, T., Pieters, L., Ceulemans, B., & Hermans, N. (2022). Clinical investigation of French maritime pine bark extract on attention-deficit hyperactivity disorder as compared to methylphenidate and placebo : part 1: efficacy in a randomised trial. Journal of Functional Foods, 97, 1–7. https://doi.org/10.1016/J.JFF....;

    • Weyns, A.-S., Verlaet, A. A. J., Van Herreweghe, M., Breynaert, A., Fransen, E., De Meester, I., Logie, E., Vanden Berghe, W., Verhelst, H., Van West, D., Ingelghem, V., Jonckheere, A. I., Beysen, D., Kenis, S., Moens, E., Roest, . van ., Savelkoul, H. F. J., de Bruyne, T., Pieters, L., … Hermans, N. (2022). Clinical investigation of French maritime pine bark extract on attention-deficit hyperactivity disorder as compared to methylphenidate and placebo : part 2: oxidative stress and immunological modulation. Journal of Functional Foods, 97, 1–12. https://doi.org/10.1016/J.JFF....;

    • Rumman, R. K., Slorach, C., Hui, W., Lopez, C., Larios, G., Fan, S., Franco-Cereceda, A., Loeys, B., Mohamed, S. A., Dietz, H., Mital, S., Andelfinger, G., Mertens, L., & Grattan, M. (2022). Clinical research regional vascular changes and aortic dilatation in pediatric patients with bicuspid aortic valve. Canadian Journal of Cardiology, 38(5), 688–694. https://doi.org/10.1016/J.CJCA...;

    • Persu, A., Dobrowolski, P., Gornik, H. L., Olin, J. W., Adlam, D., Azizi, M., Boutouyrie, P., Bruno, R. M., Boulanger, M., Demoulin, J.-B., Ganesh, S. K., Guzik, T. J., Januszewicz, M., Kovacic, J. C., Kruk, M., Leeuw, . de ., Loeys, B. L., Pappaccogli, M., Perik, M. H. A. M., … Januszewicz, A. (2022). Current progress in clinical, molecular, and genetic aspects of adult fibromuscular dysplasia. Cardiovascular Research, 118(1), 65–83. https://doi.org/10.1093/CVR/CV...;

    • Schalk, A., Cousin, M. A., Challman, T. D., Wain, K. E., Powis, Z., Minks, K., Trimouille, A., Lasseaux, E., Lacombre, D., Angelini, C., Michaud, V., Van-Gils, J., Spataro, N., Ruiz, A., Gabau, E., Stolerman, E., Washington, C., Louie, R. J., Lanpher, B. C., … Gerard, B. (2022). De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability. Journal of Medical Genetics, 59, 965–975. https://doi.org/10.1136/JMEDGE...;

    • Mohiuddin, M., Kooy, R. F., & Pearson, C. E. (2022). De novo mutations, genetic mosaicism and human disease. Frontiers in Genetics, 13, 1–20. https://doi.org/10.3389/FGENE....;

    • Boen, H. M., Loeys, B. L., Alaerts, M., Saenen, J. B., Goovaerts, I., Van Laer, L., Vorlat, A., Vermeulen, T., Franssen, C., Pauwels, P., Rodrigus, I., Heidbuchel, H., & van Craenenbroeck, E. M. (2022). Diagnostic yield of genetic testing in heart transplant recipients with prior cardiomyopathy. Journal of Heart and Lung Transplantation, 41(9), 1218–1227. https://doi.org/10.1016/J.HEAL...;

    • De Kinderen, P., Meester, J., Loeys, B., Peeters, S., Gouze, E., Woods, S., Mortier, G., & Verstraeten, A. (2022). Differentiation of induced pluripotent stem cells into chondrocytes : methods and applications for disease modelling and drug discovery. Journal of Bone and Mineral Research, 37(3), 397–410. https://doi.org/10.1002/JBMR.4...;

    • Vries, . de ., Van Hul, W., & Eekhoff, E. M. (2022). Editorial : innovative models in bone biology: what can be learned from rare bone diseases?. Frontiers in Endocrinology, 13, 1–3. https://doi.org/10.3389/FENDO....;

    • Eekhoff, E. M. W., Vries, . de ., Sakkers, R. J. B., & Van Hul, W. (2022). Editorial: innovative therapies in bone biology : what can be learned from rare bone diseases?. Frontiers in Endocrinology, 13, 1–3. https://doi.org/10.3389/FENDO....;

    • Bersselaar, . van . den ., Verhagen, J. M. A., Bekkers, J. A., Kempers, M., Houweling, A. C., Baars, M., Overwater, E., Hilhorst-Hofstee, Y., Barge-Schaapveld, D. Q. C. M., Rompen, E., Krapels, I. P. C., Dulfer, E., Wessels, M. W., Loeys, B. L., Verhagen, H. J. M., Maugeri, A., Roos-Hesselink, J. W., Bruggenwirth, H. T., & laar, V. D. (2022). Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohort. Genetics in Medicine, 24(10), 2112–2122. https://doi.org/10.1016/J.GIM....;

    • D'haenens, E., Vergult, S., Menten, B., Dheedene, A., Kooy, R. F., & Callewaert, B. (2022). Expanding the phenotype of B3GALNT2-related disorders. Genes, 13(4), 1–9. https://doi.org/10.3390/GENES1...;

    • Peeters, S., De Kinderen, P., Meester, J. A. N., Verstraeten, A., & Loeys, B. L. (2022). The fibrillinopathies : new insights with focus on the paradigm of opposing phenotypes for both FBN1 and FBN2. Human Mutation, 43(7), 815–831. https://doi.org/10.1002/HUMU.2...;

    • Velchev, J. D., Verstraeten, A., Meester, J., Ponsaerts, P., Richer, J., Alaerts, M., & Loeys, B. (2022). Generation and validation of an iPSC line (BBANTWi008-A) from a Loeys-Dietz Syndrome type 3 patient. Stem Cell Research, 64, 1–4. https://doi.org/10.1016/J.SCR....;

    • Perik, M., Verstraeten, A., Nijak-Paeske, A., Rabaut, L., Van Laer, L., & Loeys, B. (2022). Generation of a human TGFB3-hIPSC line, BBANTWi010-A, from a Loeys-Dietz syndrome type V patient. Stem Cell Research, 65, 1–4. https://doi.org/10.1016/J.SCR....;

    • Simons, E., Nijak, A., Loeys, B., & Alaerts, M. (2022). Generation of two induced pluripotent stem cell (iPSC) lines (BBANTWi006-A, BBANTWi007-A) from Brugada syndrome patients carrying an SCN5A mutation. Stem Cell Research, 60, 1–4. https://doi.org/10.1016/J.SCR....;

    • Tavernier, L. J. M., Fransen, E., Valgaeren, H., & Van Camp, G. (2022). Genetics of otosclerosis : finally catching up with other complex traits?. Human Genetics, 141, 939–950. https://doi.org/10.1007/S00439...;

    • Barc, J., Tadros, R., Glinge, C., Chiang, D. Y., Jouni, M., Simonet, F., Jurgens, S. J., Baudic, M., Nicastro, M., Potet, F., Offerhaus, J. A., Walsh, R., Choi, S. H., Verkerk, A. O., Mizusawa, Y., Anys, S., Minois, D., Arnaud, M., Duchateau, J., … Bezzina, C. R. (2022). Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nature Genetics, 54(3), 232–239. https://doi.org/10.1038/S41588...;

    • Ibrahim, J., op de Beeck, K., Fransen, E., Peeters, M., & Van Camp, G. (2022). Genome-wide DNA methylation profiling and identification of potential pan-cancer and tumor-specific biomarkers. Molecular Oncology, 16(12), 2432–2447. https://doi.org/10.1002/1878-0...;

    • Nijak-Paeske, A., Loeys, B. L., Alaerts, M., & Labro, A. J. (2022). Genomics and innovative induced pluripotent stem cell (iPSC) modeling to improve understanding of pathomechanisms underlying Brugada syndrome (BrS). University of Antwerp, Faculty of Medicine and Health Sciences, Department of Medical Genetics.

    • Johannesen, K. M., Liu, Y., Koko, M., Gjerulfsen, C. E., Sonnenberg, L., Schubert, J., Fenger, C. D., Eltokhi, A., Rannap, M., Koch, N. A., Lauxmann, S., Krüger, J., Kegele, J., Canafoglia, L., Franceschetti, S., Mayer, T., Rebstock, J., Zacher, P., Ruf, S., … Møller, R. S. (2022). Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications. Brain, 145(9), 2991–3009. https://doi.org/10.1093/BRAIN/...;

    • Beyltjens, T., Boudin, E., Revencu, N., Boeckx, N., Bertrand, M., Schuetz, L., Haack, T. B., Weber, A., Biliouri, E., Vinksel, M., Zagozen, A., Peterlin, B., Pai, S., Telegrafi, A., Henderson, L. B., Ells, C., Turner, L., Wuyts, W., Van Hul, W., … Mortier, G. R. (2022). Heterozygous pathogenic variants involving CBFB cause a new skeletal disorder resembling cleidocranial dysplasia. Journal of Medical Genetics, 1–7. https://doi.org/10.1136/JMG-20...;

    • Meuwissen, M., Verstraeten, A., Ranza, E., Iwaszkiewicz, J., Bastiaansen, M., Mateiu, L., Nemegeer, M., Meester, J. A. N., Afenjar, A., Amaral, M., Ballhausen, D., Barnett, S., Barth, M., Asselbergh, B., Spaas, K., Heeman, B., Bassetti, J., Blackburn, P., Schaer, M., … Loeys, B. (2022). Heterozygous variants in CTR9, which encodes a major component of the PAF1 complex, are associated with a neurodevelopmental disorder. Genetics in Medicine, 24(7), 1583–1591. https://doi.org/10.1016/J.GIM....;

    • Huybrechts, Y., Boudin, E., Hendrickx, G., Steenackers, E., Hamdy, N., Mortier, G., Martinez Diaz-Guerra, G., Bracamonte, M. S., Appelman-Dijkstra, N. M., & Van Hul, W. (2022). Identification of compound heterozygous variants in LRP4 demonstrates that a pathogenic variant outside the third β-propeller domain can cause sclerosteosis. Genes, 13(1). https://doi.org/10.3390/GENES1...;

    • 's Jongers, B., Hotterbeekx, A., Bielen, K., Vervliet, P., Boddaert, J., Lammens, C., Fransen, E., Baggerman, G., Covaci, A., Goossens, H., Malhotra-Kumar, S., Jorens, P. G., & Kumar-Singh, S. (2022). Identification of potential urinary metabolite biomarkers of Pseudomonas aeruginosa ventilator-associated pneumonia. Biomarker Insights, 17, 1–11. https://doi.org/10.1177/117727...;

    • De Groef, A., Hallemans, A., Gebruers, N., Meirte, J., Saeys, W., Truijen, S., Haenen, V., Johnson, C., Meert, L., Peeters, L., Fransen, E., Meeus, M., & Durnez, L. (2022). The impact of COVID-19 lockdown on the general health status of people with chronic health conditions in Belgium : a cross-sectional survey study. Physiotherapy: Theory and Practice, 1–16. https://doi.org/10.1080/095939...;

    • Marangoni, M., Smits, G., Ceysens, G., Costa, E., Coulon, R., Daelemans, C., Coninck, D., Derisbourg, S., Gajewska, K., Garofalo, G., Gounongbe, C., Guizani, M., Holoye, A., Houba, C., Makhoul, J., Norgaard, C., Regnard, C., Romee, S., Soto, J., … Migeotte, I. (2022). Implementation of fetal clinical exome sequencing : comparing prospective and retrospective cohorts. Genetics in Medicine, 24(2), 344–363. https://doi.org/10.1016/J.GIM....;

    • Marangoni, M., Smits, G., Ceysens, G., Costa, E., Coulon, R., Daelemans, C., Coninck, D., Derisbourg, S., Gajewska, K., Garofalo, G., Gounongbe, C., Guizani, M., Holoye, A., Houba, C., Makhoul, J., Norgaard, C., Regnard, C., Romee, S., Soto, J., … Migeotte, I. (2022). Implementation of fetal clinical exome sequencing : comparing prospective and retrospective cohorts. Obstetrical and Gynecological Survey, 77(8), 465–467. https://doi.org/10.1097/01.OGX...;

    • Castelletti, S., Gray, B., Basso, C., Behr, E. R., Crotti, L., Elliott, P. M., Gonzalez Corcia, C. M., D'Ascenzi, F., Ingles, J., Loeys, B., Pantazis, A., Pieles, G. E., Saenen, J., Brugada, G. S., Garza, . de . la ., Sharma, S., Van Craenebroek, E. M., Wilde, A., & Papadakis, M. (2022). Indications and utility of cardiac genetic testing in athletes. European Journal of Preventive Cardiology, 29(12), 1582–1591. https://doi.org/10.1093/EURJPC...;

    • Maes, R. R., Potters, G., Fransen, E., Van Schaeren, R., & Lenaerts, S. (2022). Influence of adding low concentration of oxygenates in mineral diesel oil and biodiesel on the concentration of NO, NO₂ and particulate matter in the exhaust gas of a one-cylinder diesel generator. International Journal of Environmental Research and Public Health, 19(13), 1–18. https://doi.org/10.3390/IJERPH...;

    • Savarirayan, R., Ireland, P., Irving, M., Thompson, D., Alves, I., Baratela, W. A. R., Betts, J., Bober, M. B., Boero, S., Briddell, J., Campbell, J., Campeau, P. M., Carl-Innig, P., Cheung, M. S., Cobourne, M., Cormier-Daire, V., Deladure-Molla, M., del Pino, M., Elphick, H., … Fredwall, S. O. (2022). International consensus statement on the diagnosis, multidisciplinary management and lifelong care of individuals with achondroplasia. Nature Reviews : Endocrinology, 18, 173–189. https://doi.org/10.1038/S41574...;

    • Arbustini, E., Behr, E. R., Carrier, L., Duijn, . van ., Evans, P., Favalli, V., Harst, . van . der ., Haugaa, K. H., Jondeau, G., Kaab, S., Kaski, J. P., Kavousi, M., Loeys, B., Pantazis, A., Pinto, Y., Schunkert, H., Toro, D., Thum, T., Urtis, M., … Elliott, P. (2022). Interpretation and actionability of genetic variants in cardiomyopathies : a position statement from the European Society of Cardiology Council on cardiovascular genomics. European Heart Journal, 43(20), 1901–1916. https://doi.org/10.1093/EURHEA...;

    • Rodrigues Bento, J., Krebsova, A., Van Gucht, I., Callejon, I. V., van Berendoncks, A., Votypka, P., Luyckx, I., Peldova, P., Laga, S., Havelka, M., Van Laer, L., Trunecka, P., Boeckx, N., Verstraeten, A., Macek, M., Meester, J. A. N., & Loeys, B. (2022). Isolated aneurysmal disease as an underestimated finding in individuals with JAG1 pathogenic variants. Human Mutation, 43(12), 1824–1828. https://doi.org/10.1002/HUMU.2...;

    • Verbrigghe, N., Meeran, K., Bahn, M., Canarini, A., Fransen, E., Fuchslueger, L., Ingrisch, J., Janssens, I. A., Richter, A., Sigurdsson, B. D., Soong, J. L., & Vicca, S. (2022). Long-term warming reduced microbial biomass but increased recent plant-derived C in microbes of a subarctic grassland. Soil Biology and Biochemistry, 167, 1–10. https://doi.org/10.1016/J.SOIL...;

    • Boons, G., Vandamme, T., Mariën, L., Lybaert, W., Roeyen, G., Rondou, T., Papadimitriou, K., Janssens, K., op de Beeck, B., Simoens, M., Demey, W., Dero, I., Van Camp, G., Peeters, M., & op de Beeck, K. (2022). Longitudinal copy-number alteration analysis in plasma cell-free DNA of neuroendocrine neoplasms is a novel specific biomarker for diagnosis, prognosis, and follow-up. Clinical Cancer Research, 28(2), 338–349. https://doi.org/10.1158/1078-0...;

    • Van Breedam, E., Nijak, A., Buyle-Huybrecht, T., Di Stefano, J., Boeren, M., Govaerts, J., Quarta, A., Swartenbroekx, T., Jacobs, E. Z., Menten, B., Gijsbers, R., Delputte, P., Alaerts, M., Hassannia, B., Loeys, B., Berneman, Z., Timmermans, J.-P., Jorens, P. G., Vanden Berghe, T., … Ponsaerts, P. (2022). Luminescent human iPSC-derived neurospheroids enable modeling of neurotoxicity after oxygen–glucose deprivation. Neurotherapeutics, 19, 550–569. https://doi.org/10.1007/S13311...;

    • Meester, J. A. N., Peeters, S., Van Den Heuvel, L., Vandeweyer, G., Fransen, E., Cappella, E., Dietz, H. C., Forbus, G., Gelb, B. D., Goldmuntz, E., Hoskoppal, A., Landstrom, A. P., Lee, T., Mital, S., Morris, S., Olson, A. K., Renard, M., Roden, D. M., Singh, M. N., … Loeys, B. L. (2022). Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort. Genetics in Medicine, 24(5), 1045–1053. https://doi.org/10.1016/J.GIM....;

    • Nijak, A., Simons, E., Vandendriessche, B., Van de Sande, D., Fransen, E., Sieliwonczyk, E., Van Gucht, I., van Craenenbroeck, E., Saenen, J., Heidbuchel, H., Ponsaerts, P., Labro, A. J., Snyders, D., De Vos, W., Schepers, D., Alaerts, M., & Loeys, B. L. (2022). Morpho-functional comparison of differentiation protocols to create iPSC-derived cardiomyocytes. Biology Open (bio), 11(2). https://doi.org/10.1242/BIO.05...;

    • Verkest, V., Pingnet, L., Fransen, E., & Declau, F. (2022). Multidimensionality of patient-reported outcome measures in rhinoplasty satisfaction. Facial Plastic Surgery, 38(5), 468–476. https://doi.org/10.1055/A-1760...;

    • Naesens, L., Nemegeer, J., Roelens, F., Vallaeys, L., Meuwissen, M., Janssens, K., Verloo, P., Ogunjimi, B., Hemelsoet, D., Hoste, L., Roels, L., Bruyne, D., Baere, D., Dorpe, V., Dendooven, A., Sieben, A., Rice, G. I., Kerre, T., Beyaert, R., … Haerynck, F. (2022). Mutations in RNU7-1 weaken secondary RNA structure, induce MCP-1 and CXCL10 in CSF, and result in Aicardi-Goutieres syndrome with severe end-organ involvement. Journal of Clinical Immunology, 42, 962–974. https://doi.org/10.1007/S10875...;

    • Schoenmaekers, C., De Laet, C., Kornilova, L., Glukhikh, D., Moore, S., MacDougall, H., Naumov, I., Fransen, E., Wille, L., Jillings, S., & Wuyts, F. L. (2022). Ocular counter-roll is less affected in experienced versus novice space crew after long-duration spaceflight. NPJ Microgravity, 8(1), 1–11. https://doi.org/10.1038/S41526...;

    • Huybrechts, Y., & Van Hul, W. (2022). Osteopetrosis associated with PLEKHM1 and SNX10 genes, both involved in osteoclast vesicular trafficking. Bone, 164, 1–5. https://doi.org/10.1016/J.BONE...;

    • Van Rompaey, V., Gommeren, H., Bosmans, J., Verdoodt, D., Janssens de Varebeke, S., Vrieze, . de ., Pennings, R., Berg, V. de ., Lammers, M., Vanderveken, O., Fransen, E., Van Camp, G., & Wijk, V. (2022). Pathogenic variants in the COCH gene that lead to hearing loss and vestibular deficit : update on DFNA9 and introducing DFNB110. B-ENT, 18(4), 273–283. https://doi.org/10.5152/B-ENT....;

    • Kempers, M. J. E., Wessels, M., van Berendoncks, A., Laar, . van . de ., Leeuw, . de ., & Loeys, B. (2022). Phenotype of COL3A1/COL5A2 deletion patients. European Journal of Medical Genetics, 65(10), 1–5. https://doi.org/10.1016/J.EJMG...;

    • Verkest, V., Pingnet, L., Fransen, E., & Declau, F. (2022). Piezo-assisted turbinoplasty versus partial turbinectomy in external septorhinoplasty : a prospective comparative study in 100 patients. Aesthetic Plastic Surgery, 46(3), 1323–1331. https://doi.org/10.1007/S00266...;

    • De Schutter, E., Ramon, J., Pfeuty, B., Tender, D., Stremersch, S., Raemdonck, K., op de Beeck, K., Declercq, W., Riquet, F. B., Braeckmans, K., & Vandenabeele, P. (2022). Plasma membrane perforation by GSDME during apoptosis-driven secondary necrosis. Cellular and Molecular Life Sciences, 79(1). https://doi.org/10.1007/S00018...;

    • Elias, G., Meysman, P., Bartholomeus, E., De Neuter, N., Keersmaekers, N., Suls, A., Jansens, H., Souquette, A., De Reu, H., Emonds, M.-P., Smits, E., Lion, E., Thomas, P. G., Mortier, G., Van Damme, P., Beutels, P., Laukens, K., Van Tendeloo, V., & Ogunjimi, B. (2022). Preexisting memory CD4 T cells in naïve individuals confer robust immunity upon hepatitis B vaccination. Elife, 11. https://doi.org/10.7554/ELIFE....;

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