Showing 1 - 16 results of 16 for search 'Swagemakers, S', query time: 0.30s
Refine Results
-
1
Feasibility of group cognitive behavioural therapy for insomnia (CBT-I) in bipolar disorder by O. Swagemakers, A. Nugter, F. Engelsbel, P. Schulte
Published 2021-04-01
Article -
2
Becoming a Care-Tizen: Contributing to Democracy Through Forest Commoning by Marta Nieto-Romero, Gustavo García-López, Paul Swagemakers, Bettina Bock
Published 2023-08-01
Article -
3
-
4
Stochastic particle transport by deep-water irregular breaking waves by Eeltink, D, Calvert, R, Swagemakers, JE, Xiao, Q, van den Bremer, TS
Published 2023Journal article -
5
Usefulness of Selected Acute-Phase Proteins in the Postsurgical Monitoring of Arthroscopy and Splint Bone Removal in Horses by Maciej Przewoźny, Magdalena Senderska-Płonowska, Anna Rząsa, Heliodor Wierzbicki, Jacek Borkowski, Jan-Hein Swagemakers, Agnieszka Żak-Bochenek, Tadeusz Stefaniak
Published 2021-10-01
Article -
6
-
7
Identification of intragenic exon deletions and duplication of TCF12 by whole genome or targeted sequencing as a cause of TCF12-related craniosynostosis by Goos, J, Fenwick, A, Swagemakers, S, McGowan, S, Knight, S, Twigg, S, Hoogeboom, A, van Dooren, M, Magielsen, F, Wall, S, Mathijssen, I, Wilkie, A, van der Spek, P, van den Ouweland, A
Published 2016Journal article -
8
A de novo substitution in BCL11B leads to loss of interaction with transcriptional complexes and craniosynostosis by Goos, J, Vogel, W, Mlcochova, H, Millard, C, Esfandiari, E, Selman, S, Calpena Corpas, E, Koelling, N, Carpenter, E, Swagemakers, S, van der Spek, P, Filtz, T, Schwabe, J, Iwaniec, U, Mathijssen, I, Leid, M, Twigg, S
Published 2019Journal article -
9
Gain-of-function mutations in ZIC1 are associated with coronal craniosynostosis and learning disability by Twigg, S, Forecki, J, Goos, J, Richardson, I, Hoogeboom, A, van den Ouweland, A, Swagemakers, S, Lequin, M, Van Antwerp, D, McGowan, S, Westbury, I, Miller, K, Wall, S, van der Spek, P, Mathijssen, I, Pauws, E, Merzdorf, C, Wilkie, A
Published 2015Journal article -
10
Evaluation of Immunohistochemical Markers, CK17 and SOX2, as Adjuncts to p53 for the Diagnosis of Differentiated Vulvar Intraepithelial Neoplasia (dVIN) by Shatavisha Dasgupta, Senada Koljenović, Thierry P. P. van den Bosch, Sigrid M. A. Swagemakers, Nick M. A. van der Hoeven, Ronald van Marion, Peter J. van der Spek, Helena C. van Doorn, Folkert J. van Kemenade, Patricia C. Ewing-Graham
Published 2021-04-01
Article -
11
Identification of mutations in TXNL4A in Burn-McKeown Syndrome and isolated choanal atresia by Goos, J, Swagemakers, S, Twigg, S, van Dooren, M, Hoogeboom, A, Beetz, C, Günther, S, Magielsen, F, Ockeloen, C, Ramos-Arroyo, M, Pfundt, R, Yntema, H, van der Spek, P, Stanier, P, Wieczorek, D, Wilkie, A, van den Ouweland, A, Mathijssen, I, Hurst, J
Published 2017Journal article -
12
Exploring Differentially Methylated Genes in Vulvar Squamous Cell Carcinoma by Shatavisha Dasgupta, Patricia C. Ewing-Graham, Sigrid M. A. Swagemakers, Thierry P. P. van den Bosch, Peggy N. Atmodimedjo, Michael M. P. J. Verbiest, Marit de Haan, Helena C. van Doorn, Peter J. van der Spek, Senada Koljenović, Folkert J. van Kemenade
Published 2021-07-01
Article -
13
Pathogenic variants in the paired-related homeobox 1 gene (PRRX1) cause craniosynostosis with incomplete penetrance by Tooze, RS, Miller, KA, Swagemakers, SMA, Calpena, E, McGowan, SJ, Boute, O, Collet, C, Johnson, D, Laffargue, F, de Leeuw, N, Morton, JV, Noons, P, Ockeloen, CW, Phipps, JM, Tan, TY, Timberlake, AT, Vanlerberghe, C, Wall, SA, Weber, A, Wilson, LC, Zackai, EH, Mathijssen, IMJ, Twigg, SRF, Wilkie, AOM
Published 2023Journal article -
14
Diagnostic value of exome and whole genome sequencing in craniosynostosis by Miller, K, Twigg, S, McGowan, S, Phipps, J, Fenwick, A, Johnson, D, Wall, S, Noons, P, Rees, K, Tidey, E, Craft, J, Taylor, J, Taylor, J, Goos, J, Swagemakers, S, Mathijssen, I, van der Spek, P, Lord, H, Lester, T, Abid, N, Cilliers, D, Hurst, J, Morton, J, Sweeney, E, Weber, A, Wilson, L, Wilkie, A
Published 2016Journal article -
15
Whole exome sequencing of patients with varicella-zoster virus and herpes simplex virus induced acute retinal necrosis reveals rare disease-associated genetic variants by Johanna L. Heinz, Johanna L. Heinz, Sigrid M. A. Swagemakers, Joanna von Hofsten, Joanna von Hofsten, Marie Helleberg, Marie Helleberg, Michelle M. Thomsen, Michelle M. Thomsen, Kerstin De Keukeleere, Kerstin De Keukeleere, Joke H. de Boer, Tomas Ilginis, Georges M. G. M. Verjans, Peter M. van Hagen, Peter J. van der Spek, Trine H. Mogensen, Trine H. Mogensen
Published 2023-10-01
Article -
16
De novo missense substitutions in the gene encoding CDK8, a regulator of the Mediator complex, cause a syndromic developmental disorder by Calpena, E, Hervieu, A, Kaserer, T, Swagemakers, SMA, Goos, JAC, Popoola, O, Ruiz, MJ, Dieber, T, Bownass, L, Brilstra, EH, Brimble, E, Foulds, N, Grebe, TA, Harder, AVE, Lees, MM, Monaghan, KG, Newbury-Ecob, RA, Ong, K-R, Osio, D, Santos, FJ, Ruzhnikov, MRZ, Telegrafi, A, van Binsbergen, E, van Dooren, MF, Deciphering Developmental Disorders Study, van der Spek, PJ, Twigg, SRF, Mathijssen, IMJ, Clarke, PA, Wilkie, A
Published 2019Journal article