Projecten per jaar
Persoonlijk profiel
Expertise
- molecular genetics with a special focus on cardiogenetics
Expertise
Onderozek in de cardiogenetica: mulit-omics, oligogenic tot polygenic overerving
Innovatieve technolgieënin klinische laboratorium genetica
Opleiding / Academische kwalificatie
Medische Genetica, Interuniversity Certificate in Human Genetics, Vrije Universiteit Brussel
Datum van toekenning: 23 jun 2009
Virologie, PhD, Utrecht University
Datum van toekenning: 27 okt 2005
Externe posities
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, UZ Brussel
apr 2011 → …
Genetic Lab supervisor, UZ Brussel
1 jan 2008 → …
Vingerafdruk
Verdiep u in de onderzoeksgebieden waarop Sonia Van Dooren actief is. Deze onderwerplabels komen uit het werk van deze persoon. Samen vormen ze een unieke vingerafdruk.
- 1 Soortgelijke profielen
Samenwerkingen en hoofdonderzoeksgebieden uit de afgelopen vijf jaar
Recente externe samenwerking op landen-/regioniveau. Duik in de details door op de stippen te klikken of
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IRP27: TumorScope: Digitaal gezondheidsonderzoek rond data, AI en wettelijke uitdagingen aan de VUB en het UZB
Vranken, W., Vandemeulebroucke, J., Cornu, P., Quinn, P., Van Dooren, S., Duerinck, J., Olsen, C. & Forsyth, R.
1/11/24 → 30/04/27
Project: Fundamenteel
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OZR4159: Bilateral cooperation within the framework of a joint doctoral project: benchfee for joint PhD VUB - ULB, OSEI Randy
1/10/22 → 30/09/26
Project: Fundamenteel
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IRP20: TumorScope: VUB en UZ Brussel expertise als hefboom naar een onderzoeksplatform voor digitale gezondheid.
Vranken, W., Vandemeulebroucke, J., Cornu, P., Forsyth, R., Quinn, P., Van Dooren, S. & Duerinck, J.
1/11/19 → 30/09/25
Project: Fundamenteel
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EUAR56: Horizon 2020: HosmartAI: Ziekenhuis Slimme ontwikkeling op basis van 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: Fundamenteel
Onderzoeksoutput
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A milder form of NSRP1-associated neurodevelopmental disorder, caused by a missense variant in the nuclear localization signal
Neuens, S., Kausar, M., Kang, S-K., Soblet, J., Van Dooren, S., Olsen, C., Janssen, T., Caljon, B., Jun, C-D., Smits, G., Coppens, S. & Vilain, C., okt 2024, In: American Journal of Medical Genetics. Part A. 194, 10, 5 blz., e63727.Onderzoeksoutput: Article › peer review
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Are disease-specific patient-reported outcomes measures (PROMs) used in cardiogenetics? A systematic review
van Pottelberghe, S., Kupper, N., Scheirlynck, E., Amin, A. S., Wilde, A. A. M., Hofman, N., Callus, E., Biller, R., Nekkebroeck, J., Van Dooren, S., Hes, F. J. & van der Crabben, S. N., jun 2024, In: European Journal of Human Genetics. 32, 6, blz. 607-618 12 blz.Onderzoeksoutput: Article › peer review
Open AccessBestand5 Citaten (Scopus)9 Downloads (Pure) -
Correlations of ventricular fibrillation and monomorphic ventricular tachycardia with SCN5A mutations and other clinical variables in Brugada syndrome
Pannone, L., Bisignani, A., Osei, R., Gauthey, A., Sorgente, A., Monaco, C., Della Rocca, D. G., Del Monte, A., Strazdas, A., Mojica, J., Al Housari, M., Miraglia, V., Mouram, S., Vetta, G., Paparella, G., Doundoulakis, I., Overeinder, I., Bala, G., Almorad, A., Ströker, E. & 9 anderen, , 17 aug 2024, In: Heart Rhythm. 1 blz.Onderzoeksoutput: Article › peer review
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Genetic Testing in Brugada Syndrome: A 30-Year Experience
Pannone, L., Bisignani, A., Osei, R., Gauthey, A., Sorgente, A., Monaco, C., Della Rocca, D. G., Del Monte, A., Strazdas, A., Mojica, J., Al Housari, M., Miraglia, V., Mouram, S., Vetta, G., Paparella, G., Ramak, R., Overeinder, I., Bala, G., Almorad, A., Ströker, E. & 9 anderen, , 1 apr 2024, In: Circulation: Arrhythmia and Electrophysiology. 17, 4, 8 blz., e012374.Onderzoeksoutput: Article › peer review
Open AccessBestand9 Citaten (Scopus)2 Downloads (Pure) -
In Vivo Mapping of Human Ventricular Fibrillation in Brugada Syndrome: The Role of Repolarization Heterogeneity
Pannone, L., Della Rocca, D. G., Vergara, P., Sorgente, A., Del Monte, A., Vetta, G., Cespon Fernandez, M., Talevi, G., Eltsov, I., Calburean, P-A., Overeinder, I., Bala, G., Almorad, A., Ströker, E., Pappaert, G., Sieira, J., de Ravel, T., Van Dooren, S., Gharaviri, A., La Meir, M. & 4 anderen, , dec 2024, In: Circulation: Arrhythmia and Electrophysiology. 17, 12, blz. e013290 9 blz., e013290.Onderzoeksoutput: Article › peer review
Datasets
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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 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 4: 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.7956698, http://10.1186/s12885-019-5494-7
Dataset
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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 9: 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.7956737, http://10.1186/s12885-019-5494-7
Dataset
Activiteiten
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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 okt 2022Activiteit: 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 2022Activiteit: 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 mei 2021Activiteit: 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 2021Activiteit: 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 mrt 2020Activiteit: Participation in conference
Knipsels
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Evolutie DNA-technieken levert nieuwe profielen op in zaak Bende van Nijvel
8/01/20 → 3/03/20
2 Mediabijdrages
Pers / media: !!Expert Comment
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Geen geheimen in de genen: van kankerbehandeling tot preventieve geneeskunde
6/09/19
1 Mediabijdrage
Pers / media: !!Expert Comment
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Willen we al onze afwijkingen wel kennen?
5/09/19 → 6/09/19
2 Mediabijdrages
Pers / media: !!Expert Comment
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BRIGHTcore, nog doeltreffendere moleculaire diagnostiek voor genetische aandoeningen
11/12/15 → 15/01/16
2 items van Media-aandacht
Pers / media: !!Research
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Een moleculair geneticus op bezoek in De Schuur!
15/04/15
1 Mediabijdrage
Pers / media: !!Expert Comment
Scriptie
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Non-invasive prenatal testing for fetal aneuploidy by genome-wide massively parallel sequencing, a clinical outcome study
Auteur: Adam, S., Van Dooren, S., Bonduelle, M. & Kim, V. B., 19 jun 2017Scriptie/Masterproef: Master's Thesis