Projects per year
Personal profile
Expertise
- molecular genetics with a special focus on cardiogenetics
Expertise
Cardiogenetics research: multi-omics, oligogenic to polygenic inheritance
Innovative technologies in clinical laboratory genetics
Education/Academic qualification
Medical Genetics, Interuniversity Certificate in Human Genetics, Vrije Universiteit Brussel
Award Date: 23 Jun 2009
Virology, PhD, Utrecht University
Award Date: 27 Oct 2005
External positions
Steering Committee Member, Interuniversity Institute of Bioinformatics in Brussels
Sep 2013 → …Coordinator, Vrije Universiteit Brussel (VUB)-Université Libre de Bruxelles (ULB), UZ Brussel,Brussels Interuniversity Genomics High Throughput Core (BRIGHTcore)
Jan 2013 → …Lab coordinator, Universitair Ziekenhuis Brussel
Apr 2011 → …Genetic Lab supervisor, Universitair Ziekenhuis Brussel
1 Jan 2008 → …Fingerprint
Dive into the research topics where Sonia Van Dooren is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 1 Similar Profiles
Network
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
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OZR3913: Cofinancing OZR FWO Hercules MZW - High-parametric single-cell protein profiling in intact tissues
Movahedi, K., van Grunsven, L., Rooman, I., Van Ginderachter, J., Smolders, I., Neyns, B., Vanhaecke, T., Laoui, D., Breckpot, K., De Veirman, K., Stijlemans, B., Van Schependom, J., Magez, S., Goyvaerts, C., De Kock, J., De Leu, N., Massie, A., Hellemans, K., Spits, C., De Bundel, D., De Trez, C., Hernot, S., Van Dooren, S., Aerts, J., Staels, W. & Tuyaerts, S.
25/02/22 → 25/02/26
Project: Fundamental
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EUAR56: Horizon 2020: HosmartAI: Hospital Smart development based on AI.
Vranken, W., Schoors, D., De Canck, H., Vandemeulebroucke, J., Duerinck, J., Olsen, C., Van Dooren, S. & Quinn, P.
1/01/21 → 31/05/24
Project: Fundamental
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OZR3733: Bilateral cooperation within the framework of a joint doctoral project: benchfee for joint PhD VUB - ULB, BUTTIN Julia
1/10/20 → 30/09/24
Project: Fundamental
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OZR3588: Financiering FWO hercules: ERA platform: Extended RNA Analysis platform - version 2.0
Rooman, I., Bouwens, L., Heimberg, H., Neyns, B., Vranken, W., Vanhaecke, T., Massie, A., van Grunsven, L., De Bruyne, E., De Bundel, D., Forsyth, R., Breckpot, K., Van Dooren, S., De Kock, J., Njemini, R. & Laoui, D.
1/05/20 → 30/04/24
Project: Fundamental
Research output
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Heart rate variability and microvolt T wave alternans changes during ajmaline test may predict prognosis in Brugada syndrome
Călburean, P-A., Pannone, L., Sorgente, A., Gauthey, A., Monaco, C., Strazdas, A., Almorad, A., Bisignani, A., Bala, G., Ramak, R., Overeinder, I., Ströker, E., Pappaert, G., Van Dooren, S., de Ravel, T., La Meir, M., Brugada, P., Sieira, J., Chierchia, G-B. & de Asmundis, C., Feb 2023, In: Clinical autonomic research : official journal of the Clinical Autonomic Research Society. 33, 1, p. 51-62 12 p.Research output: Contribution to journal › Article › peer-review
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Results From A Large Prospective Genetic Study In Children With Brugada Syndrome
Osei, R., Pannone, L., Bisignani, A., Gauthey, A., Sorgente, A., Vergara, P., Monaco, C., Rocca, D. G. D., Del Monte, A., Strazdas, A., Mojica, J., Al Housari, M., Miraglia, V., Mouram, S., Paparella, G., Ramak, R., Overeinder, I., Bala, G., Almorad, A., Ströker, E. & 8 others, , 17 Mar 2023.Research output: Unpublished contribution to conference › Poster
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A FAIR Brugada Syndrome data repository to facilitate cardiogenetic research
Ruiz, M. M. T., Daneels, D., Pappaert, G., Cannaerts, E., de Ravel, T., de Asmundis, C., Sieira, J., Nowe, A., Brugrada, P., Olsen, C., Lenaerts, T. & Van Dooren, S., Apr 2022, In: European Journal of Human Genetics. 30, SUPPL 1, p. 185-185Research output: Contribution to journal › Meeting abstract (Journal)
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Are Disease-Specific Patient-Reported Outcomes Measures (PROMs) Used in Cardio Genetics? A Review
Van Pottelberghe, S., Kupper, N., Scheirlynck, E., Callus, E., Amin, A. S., Wilde, A. A. M., Biller, R., Nekkebroeck, J., Van Dooren, S., Hes, F. J. & van der Crabben, S. N., 30 Oct 2022, In: Circulation. 146, Suppl_1, p. 1-1 1 p., 11823.Research output: Contribution to journal › Meeting abstract (Journal)
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Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
KORA-Study Group, 26 Apr 2022, In: Nature Genetics. 54, 5, 8 p., 735.Research output: Contribution to journal › Article › peer-review
Datasets
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Additional file 11: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families
Van Dooren, S. (Creator), Teugels, E. (Creator), Bonduelle, M. (Creator), Shahi, R. B. (Creator), De Brakeleer, S. (Creator), Vanhoeij, M. (Creator), De Grève, J. (Creator), Caljon, B. (Creator) & Pauwels, I. (Creator), figshare.ars, 2019
DOI: 10.6084/m9.figshare.7956680, http://10.1186/s12885-019-5494-7
Dataset
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Additional file 8: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families
Van Dooren, S. (Creator), Teugels, E. (Creator), Bonduelle, M. (Creator), Shahi, R. B. (Creator), De Brakeleer, S. (Creator), Caljon, B. (Creator) & De Grève, J. (Creator), figshare.ars, 2019
DOI: 10.6084/m9.figshare.7956728, http://10.1186/s12885-019-5494-7
Dataset
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Additional file 1: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families
Van Dooren, S. (Creator), Teugels, E. (Creator), Bonduelle, M. (Creator), Shahi, R. B. (Creator), De Brakeleer, S. (Creator), Caljon, B. (Creator) & De Grève, J. (Creator), figshare.ars, 5 Apr 2019
DOI: 10.6084/m9.figshare.7956686, http://10.1186/s12885-019-5494-7
Dataset
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Additional file 6: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families
Van Dooren, S. (Creator), Teugels, E. (Creator), Bonduelle, M. (Creator), Shahi, R. B. (Creator), De Brakeleer, S. (Creator), Vanhoeij, M. (Creator), Joris, S. (Creator), Fontaine, C. (Creator), Pauwels, I. (Creator), Caljon, B. (Creator) & De Grève, J. (Creator), Springer, 2019
DOI: 10.6084/m9.figshare.7956710, http://10.1186/s12885-019-5494-7
Dataset
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Additional file 5: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families
Van Dooren, S. (Creator), Teugels, E. (Creator), Bonduelle, M. (Creator), Shahi, R. B. (Creator) & De Brakeleer, S. (Creator), figshare.ars, 2019
DOI: 10.6084/m9.figshare.7956704, http://10.1186/s12885-019-5494-7
Dataset
Activities
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40 years of Medical Genetics at UZ Brussel
Thomy de Ravel (Participant), Kim Van Berkel (Participant), Laura Polsler (Participant), Mary-Louise Bonduelle (Participant), Sonia Van Dooren (Participant), Toon Janssen (Participant), Elia Fernandez Gallardo (Participant) & Veerle Berckmoes (Participant)
1 Oct 2022Activity: Participating in or organising an event › Participation in conference
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22nd annual joint meeting BeSHG & NVHG
Frederik Jan Hes (Participant), Ingeborg Liebaers (Participant), Mary-Louise Bonduelle (Participant), Dirk De Smedt (Participant), Sophie Uyttebroeck (Participant), Stefanie Rosa Van de Voorde (Participant), Ileen Slegers (Participant), Annelore Van Der Kelen (Participant), Thomy de Ravel (Participant), Veronik Hutse (Participant), Julie Nekkebroeck (Participant), Aranza Cortés Jáuregui (Participant), Pascale De Becker (Participant), Freya Vaeyens (Participant), Bart Dequeker (Participant), Sara Seneca (Participant), Ann Van Den Bogaert (Participant), Eva Sammels (Participant), Annelies Fieuw (Participant), Alexander Gheldof (Participant), Catharina Olsen (Participant), Sonia Van Dooren (Participant), Kim Van Berkel (Participant), Boyan Dimitrov (Participant), Rani Cooreman (Participant), Saar Van Pottelberghe (Participant), Jelle Vlaeminck (Participant), Randy Osei (Participant) & Christiane Winter (Participant)
21 Apr 2022 → 22 Apr 2022Activity: Participating in or organising an event › Participation in conference
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e-Seminar CRG 20/05/2021 - Spits Claudia
Andrea Buysse (Participant), Ben Caljon (Participant), Marleen Carlé (Participant), Dorien Daneels (Participant), Elke De Schutter (Participant), Simon Denil (Participant), Elia Fernandez Gallardo (Participant), Philippe Giron (Participant), Bruno Hinckel (Participant), Hideo Imamura (Participant), Boyan Dimitrov (Participant), Ken Maes (Participant), Freya Vaeyens (Participant), Kim Van Berkel (Participant), Sonia Van Dooren (Participant) & Elise Vantroys (Participant)
21 May 2021Activity: Participating in or organising an event › Participation in workshop, seminar
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Intervisiecoaching
Kathelijn Keymolen (Participant), Frederik Jan Hes (Participant), Ann Van Den Bogaert (Participant), Sara Seneca (Participant), Martine De Rycke (Participant), Dirk De Smedt (Participant) & Sonia Van Dooren (Participant)
20 Sep 2021 → 21 Sep 2021Activity: Participating in or organising an event › Participation in workshop, seminar
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20th Annual meeting of the Belgian Society of Human Genetics
Thomy De Ravel De L'Argentiere (Participant), Frederik Jan Hes (Participant), Veerle Berckmoes (Participant), Ben Caljon (Participant), Kim De Hauwere (Participant), Martine De Rycke (Participant), Annelies Fieuw (Participant), Alexander Gheldof (Participant), Lisa Kerkhove (Participant), Kathelijn Keymolen (Chair), Catharina Olsen (Participant), Sara Seneca (Participant), Ileen Slegers (Participant), Katrien Stouffs (Participant), Melissa Sys (Participant), Sophie Uyttebroeck (Participant), Kim Van Berkel (Participant), Sonia Van Dooren (Participant), Elise Vantroys (Participant), Pieter Verdyck (Participant), Hamide Yildirim (Participant), Boyan Dimitrov (Participant), Ann Van Den Bogaert (Participant), Dirk De Smedt (Participant), Dorien Daneels (Participant), Bruno Hinckel (Participant), Simon Denil (Participant), Kathelijn Keymolen (Member of programme committee) & Maria Filomena Cuevas Y Bretones (Participant)
6 Mar 2020Activity: Participating in or organising an event › Participation in conference
Press/Media
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Evolutie DNA-technieken levert nieuwe profielen op in zaak Bende van Nijvel
8/01/20 → 3/03/20
2 Media contributions
Press/Media: Expert Comment
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Willen we al onze afwijkingen wel kennen?
5/09/19 → 6/09/19
2 Media contributions
Press/Media: Expert Comment
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Geen geheimen in de genen: van kankerbehandeling tot preventieve geneeskunde
6/09/19
1 Media contribution
Press/Media: Expert Comment
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BRIGHTcore, nog doeltreffendere moleculaire diagnostiek voor genetische aandoeningen
11/12/15 → 15/01/16
2 items of Media coverage
Press/Media: Research
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Een moleculair geneticus op bezoek in De Schuur!
15/04/15
1 Media contribution
Press/Media: Expert Comment
Thesis
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Non-invasive prenatal testing for fetal aneuploidy by genome-wide massively parallel sequencing, a clinical outcome study
Author: Adam, S., Van Dooren, S., Bonduelle, M. & Kim, V. B., 19 Jun 2017Student thesis: Master's Thesis
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Omics approaches to unravel fermented food ecosystems
Author: Verce, M., Weckx, S., Angenon, G., Ruytinx, J., Van Dooren, S., Vandamme, P. & Ercolini, D., 13 Jul 2020Student thesis: Doctoral Thesis