Research output

Research output per year 1993 2009 2010 2011 2012 2013 2014 2015 2016 2017 2018 2019 2020 2021 2022 2023

• 17017 Citations
• 60 h-index
• 450 Article
• 15 Meeting abstract (Journal)
• 14 Meeting abstract (Book)
• 12 Editorial
• 28 More
  • 10 Scientific review
  • 6 Conference paper
  • 6 Letter
  • 4 Comment/debate
  • 1 Book
  • 1 Poster

Research output per year

Research output per year

Search results

• 2016

  A comprehensive cardiomyopathy gene panel

  Peeters, U., Daneels, D., Biervliet, M., Caljon, B., Pappaert, G., Brugada, P., Bonduelle, M-L. & Van Dooren, S., 4 Feb 2016, BeSHG & NVHG First Joint Meeting "Genetics & Society". Leuven: Belgian Society of Human Genetics, p. 181-181 1 p. P111

  Research output: Chapter in Book/Report/Conference proceeding › Meeting abstract (Book) › Research

  Open Access

  File

  • Cardiomyopathies 100%
  • Genes 41%
  • Cardiac Arrhythmias 34%
  • HapMap Project 29%
  • Arrhythmogenic Right Ventricular Dysplasia 19%
  245 Downloads (Pure)

• Whole exome sequencing as a tool to identify novel causal variants and genes for Brugada syndrome

  Daneels, D., Bonduelle, M-L., Peeters, U., Brugada, P., Pappaert, G. & Van Dooren, S., 21 May 2016, The EUROPEAN HUMAN GENETICS CONFERENCE 2016.

  Research output: Chapter in Book/Report/Conference proceeding › Meeting abstract (Book) › Research

  • Brugada Syndrome 100%
  • Whole Exome Sequencing 86%
  • Genes 29%
  • Cardiac Arrhythmias 23%
  • Channelopathies 12%
• 2015

  Functional Effects of a 2 Base Pair Deletion in β1b in a Brugada Syndrome Patient

  Peeters, U., Scornik, F., Riuro, H., Pérez, G., Brugada, P., Bonduelle, M., Brugada, R. & Van Dooren, S., 2015, Abstract book PhD Day 2015. Vrije Universiteit Brussel, p. 34-34 1 p. 22

  Research output: Chapter in Book/Report/Conference proceeding › Meeting abstract (Book) › Research

  • Brugada Syndrome 100%
  • Base Pairing 74%
  • Genes 29%
  • Mutation 18%
  • Ion Channels 15%

• Prolonged Right Ventricular Ejection Delay in Brugada Syndrome depends on the type of SCN5a mutation. A bridge between Tissue Velocity Imaging and Genetics

  Van Malderen, S., Daneels, D., Van Dooren, S., Kerkhove, D., Peeters, U., Theuns, D., Meuwissen, M., Biervliet, M., Droogmans, S., Van Camp, G., Weytjens, C., Bonduelle, M-L. & Brugada, P., 8 Oct 2015, Arrhythmias for every Cardiologist. p. 619-620 2 p.

  Research output: Chapter in Book/Report/Conference proceeding › Meeting abstract (Book) › Research

  • Brugada Syndrome 100%
  • Mutation 40%
  • Syncope 13%
  • Cardiac Arrhythmias 10%
  • Genotype 8%
• 2014

  Mutation Analysis of the SCN5A Gene in 122 Brugada Syndrome Probands

  Daneels, D., Peeters, U., Brugada, P., Bonduelle, M-L., Gazzo, A., Raimondi, D., Peirsman, L., Timmermans, I., Pappaert, G., Van Malderen, S., Biervliet, M., Verdonck, D. & Van Dooren, S., 2014, Third PhD Day at the Medical Campus VUB, Brussels, Belgium. p. 7-7 1 p.

  Research output: Chapter in Book/Report/Conference proceeding › Meeting abstract (Book) › Research

  • Brugada Syndrome 100%
  • Mutation 40%
  • Electrocardiography 33%
  • Channelopathies 29%
  • Genes 29%

• Mutation analysis of the SCN5A gene in 147 Brugada syndrome probands

  Daneels, D., Peeters, U., Brugada, P., Bonduelle, M-L., Raimondi, D., Tanyalcin, I., Peirsman, L., Timmermans, I., Pappaert, G., Van Malderen, S., Biervliet, M., Verdonck, D. & Van Dooren, S., 7 Feb 2014, Abstract book of the 14th Annual Meeting of the Belgian Society of Human Genetics. p. 78-78 1 p.

  Research output: Chapter in Book/Report/Conference proceeding › Meeting abstract (Book) › Research

  • Brugada Syndrome 100%
  • Electrocardiography 53%
  • Mutation 40%
  • Ajmaline 32%
  • Genes 29%
• 2013

  Genotype-phenotype discrepancies in Brugada syndrome

  Van Dooren, S., Brugada, P., Daneels, D., Peeters, U., Peirsman, L., Timmermans, I., Pappaert, G. & Bonduelle, M-L., 15 Mar 2013, Abstract book of the 13th Annual Meeting of the Belgian Society of Human Genetics. p. 140-140 1 p.

  Research output: Chapter in Book/Report/Conference proceeding › Meeting abstract (Book) › Research

  • Brugada Syndrome 100%
  • Ajmaline 59%
  • Genotype 51%
  • Electrocardiography 49%
  • Phenotype 43%

• Identification of Novel Variants in Brugada Syndrome SCN1B to SCN4B Candidate Genes

  Peeters, U., Bonduelle, M-L., Peirsman, L., Endels, K., Comurcu-Bayrak, E., Breckpot, K., Brugada, P. & Van Dooren, S., 2013, VUB PhD Research Day 2013, Etterbeek, Belgium.

  Research output: Chapter in Book/Report/Conference proceeding › Meeting abstract (Book) › Research

  • Brugada Syndrome 100%
  • Genes 29%
  • Genetic Promoter Regions 28%
  • Clone Cells 23%
  • Initiator Codon 17%

• Novel Variants in Brugada Syndrome SCN1B to SCN4B Candidate Genes

  Peeters, U., Bonduelle, M-L., Brugada, P., Comurcu-Bayrak, E., Peirsman, L., Breckpot, K., Pappaert, G., Endels, K. & Van Dooren, S., 15 Mar 2013, Abstract book of the 13th Annual Meeting of the Belgian Society of Human Genetics. p. 141-141 1 p. (13th Annual Meeting of the Belgian Society of Human Genetics).

  Research output: Chapter in Book/Report/Conference proceeding › Meeting abstract (Book) › Research

  • Brugada Syndrome 100%
  • Genetic Promoter Regions 35%
  • Sodium Channels 32%
  • Genes 29%
  • Clone Cells 28%

• Whole exome sequencing as a tool to identify new causal variants and genes for Brugada syndrome

  Daneels, D., Bonduelle, M-L., Peeters, U., Brugada, P., Pappaert, G. & Van Dooren, S., 15 Mar 2013, Abstract book of the 13th Annual Meeting of the Belgian Society of Human Genetics. p. 147-147 1 p.

  Research output: Chapter in Book/Report/Conference proceeding › Meeting abstract (Book) › Research

  • Brugada Syndrome 100%
  • Whole Exome Sequencing 86%
  • Genes 29%
  • Exome 19%
  • Genomics 16%
• 2012

  IDENTIFICATION OF NOVEL VARIANTS IN BRUGADA SYNDROME CANDIDATE GENES

  Peeters, U., Bonduelle, M-L., Peirsman, L., Endels, K., Comurcu-Bayrak, E., Brugada, P., Breckpot, K. & Van Dooren, S., 2012, Second PhD day of the Medical Campus VUB, Brussels Belgium.

  Research output: Chapter in Book/Report/Conference proceeding › Meeting abstract (Book) › Research

  • Brugada Syndrome 100%
  • Sodium Channels 42%
  • Genes 29%
  • Genetic Promoter Regions 23%
  • Mutation 20%
• 2011

  S-057 Brugada Sendromunda sodyum kanalı beta-alt birimlerinin genetik analizleri

  Komurcu-Bayrak, E., Endels, K., Lissens, W., Seneca, S., Bayrak, F., Sarkozy, A., Brugada, P., Bonduelle, M-L. & Van Dooren, S., 27 Oct 2011, XXVII. Ullusal Kardiyologji Kongresi : Supplementum. Turkey: Archives of the Turkish Society of Cardiology

  Research output: Chapter in Book/Report/Conference proceeding › Meeting abstract (Book) › Research

  • Brugada Syndrome 100%
  • Sodium Channels 85%
  • Genes 11%
  • Mutation 10%
  • Voltage-Gated Sodium Channel beta-1 Subunit 8%
• 2008

  Analysis of human micro-array data to probe for a pathophysiological patient categorization. A systems biology perspective applied to Atrial Fibrillation.

  Vanhoutte, K., De Asmundis, C., Francesconi, A., Figys, J., Steurs, G., Boussy, T., Roos, M., Mueller, A., Massimo, L., Paparella, G., Van Caelenberg, K., Chierchia, J-B., Sarkozy, A., Brugada, P. & Zizi, M., Jul 2008, Bioinformatics to Systems Biology conference.

  Research output: Chapter in Book/Report/Conference proceeding › Meeting abstract (Book) › Research

• How to turn genetic noise into music. Systems biology in atrial fibrillation.

  Vanhoutte, K., De Asmundis, C., Francesconi, A., Figys, J., Steurs, G., Boussy, T., Roos, M., Mueller, A., Massimo, L., Paparella, G., Van Caelenberg, K., Chierchia, J-B., Sarkozy, A., Brugada, P. & Zizi, M., May 2008, ESF-WORKSHOP "SYSTEMS BIOLOGY IN MEDICINE".

  Research output: Chapter in Book/Report/Conference proceeding › Meeting abstract (Book) › Research