Endocrine manifestations in adults with 22q11.2 deletion syndrome: a retrospective single-center cohort study von Soubry, E., David, K., Swillen, A., Vergaelen, E., Docx Op de Beeck, M., Hulsmans, M., Charleer, S., Decallonne, B.

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Efficacy of inflammation-based stratification for add-on celecoxib or minocycline in major depressive disorder: Protocol of the INSTA-MD double-blind placebo-controlled randomised... von Wessa, C., Janssens, J., Coppens, V., El Abdellati, K., Vergaelen, E., van den Ameele, S., Baeken, C., Zeeuws, D., Milaneschi, Y., Lamers, F., Penninx, B., Claes, S., Morrens, M., De Picker, L.

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P.6.f.005 Prevalence of substance use and the relation with psychosis and catechol-O-methyltransferase in patients with chromosome 22q11 deletion syndrome von Vingerhoets, W.A.M, Van Oudenaren, M.J.F, Van Duin, E.D.A, Bloemen, O.J.N, Booij, J, Evers, L.J.M, Boot, E, Vergaelen, E, Vogels, A, Swillen, A, Van Amelsvoort, T.A.M.J

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Endocrine manifestations in adults with 22q11.2 deletion syndrome: a retrospective single-center cohort study von Soubry, E, David, K, Swillen, A, Vergaelen, E, Op de Beeck, M. Docx, Hulsmans, M, Charleer, S, Decallonne, B

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Bridging brain and body in 22q11. Broadening the psychiatric profile in adults with 22q11.2 deletion syndrome and exploring a possible role for the immune system von Vergaelen, E

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The 22q11.2 deletion syndrome as a model to investigate the role of T-cells in psychosis? von Vergaelen, E., Schiweck, C., Swillen, A., Drexhage, H., Claes, S.

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Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2 von Boot, E, Butcher, NJ, Udow, S, Marras, C, Mok, KY, Kaneko, S, Barrett, MJ, Prontera, P, Berman, BD, Masellis, M, Dufournet, B, Nguyen, K, Charles, P, Mutez, E, Danaila, T, Jacquette, A, Colin, O, Drapier, S, Borg, M, Fiksinski, AM, Vergaelen, E, Swillen, A, Vogels, A, Plate, A, Perandones, C, Gasser, T, Clerinx, K, Bourdain, F, Mills, K, Williams, NM, Wood, NW, Booij, J, Lang, AE, Bassett, AS, International Research Group on 22q11.2DS-associated Parkinson's

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Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome von Davies, Robert W., Fiksinski, Ania M., Breetvelt, Elemi J., Williams, Nigel M., Hooper, Stephen R., Monfeuga, Thomas, Bassett, Anne S., Owen, Michael J., Gur, Raquel E., Morrow, Bernice E., McDonald-McGinn, Donna M., Swillen, Ann, Chow, Eva W. C., van den Bree, Marianne, Emanuel, Beverly S., Vermeesch, Joris R., van Amelsvoort, Therese, Arango, Celso, Armando, Marco, Campbell, Linda E., Cubells, Joseph F., Eliez, Stephan, Garcia-Minaur, Sixto, Gothelf, Doron, Kates, Wendy R., Murphy, Kieran C., Murphy, Clodagh M., Murphy, Declan G., Philip, Nicole, Repetto, Gabriela M., Shashi, Vandana, Simon, Tony J., Suñer, Damiàn Heine, Vicari, Stefano, Scherer, Stephen W., Bearden, Carrie E., Vorstman, Jacob A. S.

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Cognitive Decline Preceding the Onset of Psychosis in Patients With 22q11.2 Deletion Syndrome von Vorstman, Jacob A. S, Breetvelt, Elemi J, Duijff, Sasja N, Eliez, Stephan, Schneider, Maude, Jalbrzikowski, Maria, Armando, Marco, Vicari, Stefano, Shashi, Vandana, Hooper, Stephen R, Chow, Eva W. C, Fung, Wai Lun Alan, Butcher, Nancy J, Young, Donald A, McDonald-McGinn, Donna M, Vogels, Annick, van Amelsvoort, Therese, Gothelf, Doron, Weinberger, Ronnie, Weizman, Abraham, Klaassen, Petra W. J, Koops, Sanne, Kates, Wendy R, Antshel, Kevin M, Simon, Tony J, Ousley, Opal Y, Swillen, Ann, Gur, Raquel E, Bearden, Carrie E, Kahn, René S, Bassett, Anne S

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Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology von Morrison, Sinead, Chawner, Samuel J. R. A., van Amelsvoort, Therese A. M. J., Swillen, Ann, Vingerhoets, Claudia, Vergaelen, Elfi, Linden, David E. J., Linden, Stefanie, Owen, Michael J., van den Bree, Marianne B. M.

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In Situ Cross-Linked Nanofibers by Aqueous Electrospinning of Selenol-Functionalized Poly(2-oxazoline)s von Li, Yin, Vergaelen, Maarten, Pan, Xiangqiang, Du Prez, Filip E, Hoogenboom, Richard, De Clerck, Karen

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22q11.2 Deletion and Duplication Syndromes and COVID-19 von Crowley, T. Blaine, McGinn, Donna McDonald, Sullivan, Kathleen E.

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Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects von Zhao, Yingjie, Diacou, Alexander, Johnston, H. Richard, Musfee, Fadi I., McDonald-McGinn, Donna M., McGinn, Daniel, Crowley, T. Blaine, Repetto, Gabriela M., Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris R., Kates, Wendy R., Digilio, M. Cristina, Unolt, Marta, Marino, Bruno, Pontillo, Maria, Armando, Marco, Di Fabio, Fabio, Vicari, Stefano, van den Bree, Marianne, Moss, Hayley, Owen, Michael J., Murphy, Kieran C., Murphy, Clodagh M., Murphy, Declan, Schoch, Kelly, Shashi, Vandana, Tassone, Flora, Simon, Tony J., Shprintzen, Robert J., Campbell, Linda, Philip, Nicole, Heine-Suñer, Damian, García-Miñaúr, Sixto, Fernández, Luis, Antonarakis, Stylianos E., Biondi, Massimo, Boot, Erik, Breetvelt, Elemi, Busa, Tiffany, Butcher, Nancy, Buzzanca, Antonino, Carmel, Miri, Cleynen, Isabelle, Cutler, David, Dallapiccola, Bruno, de la Fuente Sanches, María Angeles, Epstein, Michael P., Evers, Rens, Fernandez, Luis, Fritsch, Rosemarie, Algas, Fernando García, Guo, Tingwei, Gur, Raquel, Hestand, Matthew S., Heung, Tracy, Hooper, Stephen, Jin, Andrea, Kushan-Wells, Leila, Laorden-Nieto, Alejandra Teresa, Lattanzi, Guido, Marshall, Christian, McCabe, Kathryn, Michaelovsky, Elena, Ornstein, Claudia, Silversides, Candice, Tran, Oanh, van Duin, Esther D.A., Vergaelen, Elfi, Warren, Steve T., Weinberger, Ronnie, Weizman, Abraham, Zhang, Zhengdong, Zwick, Michael, Bearden, Carrie E., Vingerhoets, Claudia, van Amelsvoort, Therese, Eliez, Stephan, Schneider, Maude, Vorstman, Jacob A.S., Gothelf, Doron, Zackai, Elaine, Agopian, A.J., Gur, Raquel E., Bassett, Anne S., Emanuel, Beverly S., Goldmuntz, Elizabeth, Mitchell, Laura E., Wang, Tao, Morrow, Bernice E.

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Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome von Bassett, Anne S, Lowther, Chelsea, Merico, Daniele, Costain, Gregory, Chow, Eva W. C, van Amelsvoort, Therese, McDonald-McGinn, Donna, Gur, Raquel E, Swillen, Ann, Van den Bree, Marianne, Murphy, Clodagh, Murphy, Kieran, Gothelf, Doron, Bearden, Carrie E, Eliez, Stephan, Kates, Wendy, Philip, Nicole, Sashi, Vandana, Campbell, Linda, Vorstman, Jacob, Cubells, Joseph, Repetto, Gabriela M, Simon, Tony, Boot, Erik, Heung, Tracy, Evers, Rens, Vingerhoets, Claudia, van Duin, Esther, Zackai, Elaine, Vergaelen, Elfi, Devriendt, Koen, Vermeesch, Joris R, Owen, Michael, Michaelovosky, Elena, Kushan, Leila, Schneider, Maude, Fremont, Wanda, Busa, Tiffany, Hooper, Stephen, McCabe, Kathryn, Duijff, Sasja, Isaev, Karin, Pellecchia, Giovanna, Wei, John, Gazzellone, Matthew J, Scherer, Stephen W, Emanuel, Beverly S, Guo, Tingwei, Morrow, Bernice E, Marshall, Christian R

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SUN-PO296: Paediatric Parenteral Nutrition Compliance: A Simulated Comparison Between the Old (2005) Versus the New (2018) ESPEN/ESPGHAN/ESPR/CSPEN Guidelines von Vercaigne, N., Meers, G., Collier, H., Hauser, B., Vergaelen, K., De Waele, E., Cortoos, P.-J., Steurbaut, S.

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Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2 von Boot, Erik, Butcher, Nancy J, Udow, Sean, Marras, Connie, Mok, Kin Y, Kaneko, Satoshi, Barrett, Matthew J, Prontera, Paolo, Berman, Brian D, Masellis, Mario, Dufournet, Boris, Nguyen, Karine, Charles, Perrine, Mutez, Eugénie, Danaila, Teodor, Jacquette, Aurélia, Colin, Olivier, Drapier, Sophie, Borg, Michel, Fiksinski, Ania M, Vergaelen, Elfi, Swillen, Ann, Vogels, Annick, Plate, Annika, Perandones, Claudia, Gasser, Thomas, Clerinx, Kristien, Bourdain, Frédéric, Mills, Kelly, Williams, Nigel M, Wood, Nicholas W, Booij, Jan, Lang, Anthony E, Bassett, Anne S

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Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements (Retraction of Vol 101, Pg 616, 2017) von Demaerel, Wolfram, Hestand, Matthew S, Vergaelen, Elfi, Swillen, Ann, Lopez-Sanchez, Marcos, Perez-Jurado, Luis A, McDonald-McGinn, Donna M, Zackai, Elaine, Emanuel, Beverly S, Morrow, Bernice E, Breckpot, Jeroen, Devriendt, Koenraad, Vermeesch, Joris R

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Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins von Vervoort, Lisanne, Demaerel, Wolfram, Rengifo, Laura Y, Odrzywolski, Adrian, Vergaelen, Elfi, Hestand, Matthew S, Breckpot, Jeroen, Devriendt, Koen, Swillen, Ann, McDonald-McGinn, Donna M, Fiksinski, Ania M, Zinkstok, Janneke R, Morrow, Bernice E, Heung, Tracy, Vorstman, Jacob A.S, Bassett, Anne S, Chow, Eva W.C, Shashi, Vandana, Vermeesch, Joris R

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Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins von Vervoort, Lisanne, Demaerel, Wolfram, Rengifo, Laura Y, Odrzywolski, Adrian, Vergaelen, Elfi, Hestand, Matthew S, Breckpot, Jeroen, Devriendt, Koen, Swillen, Ann, McDonald-McGinn, Donna M, Fiksinski, Ania M, Zinkstok, Janneke R, Morrow, Bernice E, Heung, Tracy, Vorstman, Jacob A S, Bassett, Anne S, Chow, Eva W C, Shashi, Vandana, Vermeesch, Joris R

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Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects von Zhao, Yingjie, Guo, Tingwei, Fiksinski, Ania, Breetvelt, Elemi, McDonald‐McGinn, Donna M., Crowley, Terrence B., Diacou, Alexander, Schneider, Maude, Eliez, Stephan, Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris, Chow, Eva W. C., Gothelf, Doron, Duijff, Sasja, Evers, Rens, Amelsvoort, Thérèse A., Bree, Marianne, Owen, Michael, Niarchou, Maria, Bearden, Carrie E., Ornstein, Claudia, Pontillo, Maria, Buzzanca, Antonino, Vicari, Stefano, Armando, Marco, Murphy, Kieran C., Murphy, Clodagh, Garcia‐Minaur, Sixto, Philip, Nicole, Campbell, Linda, Morey‐Cañellas, Jaume, Raventos, Jasna, Rosell, Jordi, Heine‐Suner, Damian, Shprintzen, Robert J., Gur, Raquel E., Zackai, Elaine, Emanuel, Beverly S., Wang, Tao, Kates, Wendy R., Bassett, Anne S., Vorstman, Jacob A. S., Morrow, Bernice E.

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