Genetics Reproduction and Development

Onderzoeksoutput

Onderzoeksoutput per jaar 1970 2010 2011 2012 2013 2014 2015 2016 2017 2018 2019 2020 2021 2022 2023 2024 2030

• 82372 Citaties
• 135 h-index
• 1560 Article
• 280 Meeting abstract (Journal)
• 257 Poster
• 190 Meeting abstract (Book)
• 399 Meer
  • 79 Conference paper
  • 78 Chapter
  • 52 Other scientific journal contribution
  • 39 Editorial
  • 34 Unpublished abstract
  • 33 PhD Thesis
  • 31 Scientific review
  • 14 Letter
  • 13 Comment/debate
  • 7 Patent
  • 6 Book
  • 3 Other contribution
  • 3 Voordruk
  • 2 Foreword/postscript
  • 2 Other
  • 1 Other report
  • 1 Book/Film/Article review
  • 1 Special issue

Onderzoeksoutput per jaar

Onderzoeksoutput per jaar

Zoekresultaten

• 2023

  Clinical utility of FMR1 screening: risk factor or monogenic cause for POI

  Okutman, Ö., Van Der Kelen, A., Viville, S. & Verpoest, W., jun. 2023, ESHRE 2023 Abstract book. Issue Supplement-1 redactie Human reproduction, Vol. 38. blz. 714-714 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

  Open Access

• Mosaic Angelman Syndrome: expanded phenotype spectrum of Angelman syndrome caused by mosaic imprinting defect

  Bansagi, B. K., 2023, Eurodysmorpho abstract book. ERN ITHACA, blz. 55-55 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

• Two unrelated patients with Nail-Patella syndrome and unusual additional features

  Vanden Eynde, N. E. M., de Ravel, T., Poelsler, L., Gheldof, A., Seneca, S., Janssens, P., Bissay, V., Keymolen, K., Hes, F. J. & Dimitrov, B., sep. 2023, Eurodysmorpho abstract book. blz. 22 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

  • Nail-Patella Syndrome 100%
  • Horns 23%
  • Patella 23%
  • Nails 19%
  • Elbow 19%
• 2021

  Focal facial dermal dysplasia type IV

  Van de Voorde, S. R., Verpoest, W., Buysse, A., Keymolen, K., Hes, F. J. & Dimitrov, B., sep. 2021, EuroDysmorpho: 31st European Meeting on Dysmorphology. ERN ITHACA, blz. 13-13

  Onderzoeksoutput: Meeting abstract (Book)
• 2019

  Abstracts of the 35th Annual Meeting of the ESHRE, Vienna, Austria 24 to 26 June 2019

  Racca, A., Santos-Ribeiro, S., De Coppel, J., Tournaye, H. & Blockeel, C., 1 jul. 2019, impact of elevated progesterone on cumulative live birth rates: an analysis of 956 freeze only cycles.. blz. I417 P-601

  Onderzoeksoutput: Meeting abstract (Book)

• Contrast Media Iodine Concentration inthe Left Ventricle Affects the Level of Radiation-Induced DNA Damage during CCTA

  Van Cauteren, T., Tanaka, K., Belsack, D., Van Gompel, G., Kersemans, V., Jochmans, K., De Mey, J. & Buls, N., 5 dec. 2019, Contrast Media Iodine Concentration inthe Left Ventricle Affects the Level of Radiation-Induced DNA Damage during CCTA.

  Onderzoeksoutput: Meeting abstract (Book)

• Cumulative live birth rates in women with poor ovarian response (POR) meeting the Bologna criteria: the . importance of the phenotype

  Romito, A., Blockeel, C., Errazuriz Valenzuela, J., De Vos, M., Santos-Ribeiro, S., Van Der Kelen, A., Mackens, S., Racca, A., Benedetti Panici, P., Tournaye, H. & Drakopoulos, P., 1 jul. 2019, Abstracts of the 35th Annual Meeting of the ESHRE, Vienna, Austria 24 to 26 June 2019. www.humrep.oxofordjournals.org, Vol. 35. blz. i115 o-256

  Onderzoeksoutput: Meeting abstract (Book)

  • Birth Rate 100%
  • Live Birth 89%
  • Phenotype 51%
  • Ovarian Reserve 35%
  • Ovulation Induction 20%
• 2018

  Premature ovarian Insufficiency: a case report of a particular syndromic association

  Sassi, A., Pintiaux, A., Desir, J., Bourlard, L., Daneels, D., Van Dooren, S., Bonduelle, M-L. & Delbaere, A., 2018, Premature ovarian Insufficiency: a case report of a particular syndromic association.

  Onderzoeksoutput: Meeting abstract (Book)
• 2017

  Endometriumenigma: waarom planten humane embryo's vaker niet in dan wel?

  Santos-Ribeiro S, Mackens, S., Blockeel, C., Tournaye, H. & Van De Velde, H., 2017, Endometriumenigma: waarom planten humane embryo's vaker niet in dan wel.

  Onderzoeksoutput: Meeting abstract (Book)

• Genodermatoses can be bitter things: they can be like splits in the skin that won't heal (adapted from F. Scott Fitzgerald)

  Keymolen, K., De Raeve, L., De Rademaeker, M., Stouffs, K. & Leemans, G., 2017, http://eurodysmorpho.org/wp-content/uploads/2018/02/EuroDysmorpho-Abstract-book-2017.pdf. ERN ITHACA, blz. 16-16 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

• Incidence of uncommon fetal aneuploidies detected by non-invasive prenatal testing

  Leila, D., Brison, N., Van den Bogaert, K., Dehaspe, L., Janssens, K., Blaumeiser, B., Van Dooren, S., Van Den Bogaert, A., Keymolen, K., Désir, J., Bonduelle, M-L., Peeters, H., Van Esch, H., de Ravel, T., Legius, E., De Vriendt, K. & Vermeesch, J. R., 17 feb. 2017, 17th Annual Meeting of the Belgian Society of Human Genetics: Human Genetics goes Somatic. Belgian Society of Human Genetics, blz. 100-100 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

  Open Access

  Bestand

  • Intrauterine 100%
  • Aneuploidy 66%
  • Sampling 51%
  • Trisomy Chromosome 16 51%
  • Trisomy 38%
  770 Downloads (Pure)

• Trisomy 21/mosaic Turner detected in fetus by non-invasive prenatal testing

  Fieremans, N., Fieuw, A., Janssen, T., Staessen, C., Caljon, B., Croes, D., Daneels, D., Keymolen, K., Van Berkel, K., Bonduelle, M-L., Van Den Bogaert, A. & Van Dooren, S., 17 feb. 2017, Trisomy 21/mosaic Turner detected in fetus by non-invasive prenatal testing: Human Genetics Goes Somatic. Belgian Society of Human Genetics, blz. 118-118 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

  • Uniparental disomy of Chromosome 21 100%
  • Aneuploidy 57%
  • Fetus 42%
  • Mosaicism 26%
  • Down Syndrome 22%

• Two cases of a "skeletal" syndrome: the illustration of a variable, broad clinical spectrum

  De Rademaeker, M., Dimitrov, B., Laumen, A. & Keymolen, K., 2017, Two cases of a "skeletal" syndrome: the illustration of a variable, broad clinical spectrum. ERN ITHACA, blz. 42-42 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)
• 2016

  A BCOR VARIANT IN A MALE

  De Rademaeker, M., De Meirleir, L., Houtman, A. C., Stouffs, K., Van Dooren, S., Croes, D. & Keymolen, K., 7 sep. 2016, 27th European Dysmorphology Meeting. blz. 33-33 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

  Open Access

  Bestand

  • Microphthalmos 100%
  • Syndromic 1 Microphthalmia 84%
  • Radioulnar Synostosis 75%
  • Co-Repressor Proteins 36%
  • Genes 28%
  98 Downloads (Pure)

• 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, blz. 181-181 1 blz. P111

  Onderzoeksoutput: Meeting abstract (Book)

  Open Access

  Bestand

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

• Comprehensive method for the analysis of low-frequency mitochondrial SNVs and small and large deletions in DNA samples and single cells

  Zambelli, F., Vancampenhout, K., Daneels, D., Caljon, B., Van Dooren, S., Gianaroli, L., Sermon, K., Seneca, S. & Spits, C., 4 feb. 2016, BeSHG & NVHG First Joint Meeting "Genetics & Society". Belgian Society of Human Genetics, blz. 45-45 1 blz. O20

  Onderzoeksoutput: Meeting abstract (Book)

  • Mitochondrial DNA 100%
  • Nucleotides 86%
  • DNA 59%
  • Polymerase Chain Reaction 42%
  • Fibroblasts 26%

• Overgrowth and intellectual disability: two more patients with DNMT3A mutations

  Keymolen, K., De Meirleir, L., Daneels, D., Caljon, B., Van Dooren, S., Croes, D. & Legius, E., 7 sep. 2016, 27th European Dysmorphology Meeting. blz. 21-21 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

  Bestand

  • Intellectual Disability 100%
  • Mutation 59%
  • Viverridae 21%
  • Megalencephaly 21%
  • Pleural Cavity 19%
  163 Downloads (Pure)

• Quantification of low frequency variants of the mitochondrial DNA (mtDNA) in single cells by massive parallel sequencing (MPS)

  Zambelli, F., Daneels, D., Van Dooren, S., Caljon, B., Gianaroli, L., Van De Velde, H., Sermon, K., Seneca, S. & Spits, C., 3 jul. 2016, 32nd Annual Meeting in Helsinki; ESHRE 2016.

  Onderzoeksoutput: Meeting abstract (Book)

  • Mitochondrial DNA 100%
  • Oocytes 89%
  • Mutation 26%
  • Nucleotides 23%
  • Fibroblasts 14%

• 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 mei 2016, The EUROPEAN HUMAN GENETICS CONFERENCE 2016.

  Onderzoeksoutput: Meeting abstract (Book)

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

  DIDA: A first database of digenic diseases

  Gazzo, A., Daneels, D., Smits, G., Van Dooren, S., Cilia, E. & Lenaerts, T., 6 mrt. 2015, Abstract book of the 15th Annual Meeting of the Belgian Society of Human Genetics. Belgian Society of Human Genetics, blz. 37_37 126 blz. O14

  Onderzoeksoutput: Meeting abstract (Book)

  Open Access

  Bestand

  • Databases 100%
  • Genes 45%
  • Mutation 31%
  • Multifactorial Inheritance 19%
  • Names 15%
  774 Downloads (Pure)

• DIDA: a first database on digenic diseases

  Daneels, D., Gazzo, A., Bonduelle, M-L., Cilia, E., Lenaerts, T., Smits, G. & Van Dooren, S., 31 mrt. 2015, Abstract Book VUB DS-LSM PhD day Research Unlimited. blz. 18-18 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

  • Databases 100%
  • Genetic Databases 43%
  • Multifactorial Inheritance 41%
  • Penetrance 19%
  • Literature 17%

• DIDA - A first digenic diseases database

  Gazzo, A., Daneels, D., Smits, G., Van Dooren, S., Cilia, E. & Lenaerts, T., 6 jun. 2015, Abstract book of the Cold Spring Harbor Laboratory conference on Genome Informatics. blz. 84-84 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

  • Databases 100%
  • Genes 29%
  • Multifactorial Inheritance 25%
  • Genotype 14%
  • Bioinformatics 11%

• Exome based germline mutation detection in a panel of 372 cancer associated genes in BRCA1/2-negative familial breast cancer patients

  Shahi, R. B., Caljon, B., De Brakeleer, S., Decoster, L., Fontaine, C., Vanacker, L., Vanhoeij, M., Ingrid, P., Bonduelle, M-L., Van Dooren, S., Croes, D., Teugels, E. & De Grève, J., 8 dec. 2015, Abstract book of the San Antonio Breast cancer Symposium: Cancer Res 2016;76(4 Suppl):Abstract nr PD7-04. Vol. 76. blz. 1271 1 blz. PD7-04

  Onderzoeksoutput: Meeting abstract (Book)

  • Familial Breast Cancer 100%
  • Exome 83%
  • Germ-Line Mutation 78%
  • Neoplasm Genes 75%
  • Single Nucleotide Polymorphism 38%

• 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, blz. 34-34 1 blz. 22

  Onderzoeksoutput: Meeting abstract (Book)

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

• GEVACT: Genomic Variant Classifier Tool

  Isel, G., Daneels, D., Van Dooren, S., Bonduelle, M-L., Farid, D. M., Croes, D., Nowe, A. & Sengupta, D., 7 dec. 2015, Abstract book of the 10th Benelux Bioinformatics Conference. blz. 65-65 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

  • Classifiers 100%
  • Genomics 45%
  • Screening 40%
  • Gene Frequency 37%
  • Cardiac Arrhythmias 32%

• Is skewed X chromosome inactivation in human embryonic stem cells driven by a culture advantage?

  Geens, M., Seriola Petit, A., Barbé, L., Santalo, J., Veiga, A., Spits, C. & Sermon, K., 17 jun. 2015, Human Reproduction. Oxford, Vol. 30. blz. 474 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

  • embryonic stem cells 100%
  • X chromosome 82%
  • inactivation 65%
  • methylation 16%
  • funding 14%

• Predicting oligogenic effects using digenic disease data: oral presentation

  Gazzo, A., Daneels, D., Bonduelle, M-L., Van Dooren, S., Smits, G. & Lenaerts, T., 7 dec. 2015, Abstract book of the 10th BeNeLux Bioinformatics Conference . blz. 22-22 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

  • Genes 100%
  • Multifactorial Inheritance 64%
  • Weights and Measures 33%

• 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 okt. 2015, Arrhythmias for every Cardiologist. blz. 619-620 2 blz.

  Onderzoeksoutput: Meeting abstract (Book)

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

• The broad clinical spectrum of amino acyl tRNA synthetase mutations.

  Seneca, S., D'hooghe, M., Van Der Knaap, M., Stouffs, K., Jonckheere, A., Vancoster, R., Vanlander, A., Smet, J. & De Meirleir, L., 6 mrt. 2015, BeSHG. Vol. 15.

  Onderzoeksoutput: Meeting abstract (Book)

  • Amino Acyl-tRNA Synthetases 100%
  • Mitochondrial Diseases 45%
  • Mutation 40%
  • Genes 29%
  • Mitochondrial Genome 22%
• 2014

  Analysis of the whole mitochondrial genome: translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench?

  Seneca, S., Vancampenhout, K., Vancoster, R., Lissens, W., Vanlander, A., Smet, J., De Paepe, B., Jonckheere, A., Stouffs, K., Daneels, D., Bonduelle, M-L. & De Meirleir, L., 15 jun. 2014, Euromit. blz. 396-396 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

  • Mitochondrial Genome 100%
  • Ions 65%
  • Nucleotides 64%
  • Genome 53%
  • Mitochondrial DNA 41%

• Convert your favorite protein modeling program into a mutation predictor: "MODICT"

  Tanyalcin, I., Coomans, D., Stouffs, K., Lissens, W. & Jansen, A., 7 feb. 2014, BeSHG.

  Onderzoeksoutput: Meeting abstract (Book)

  • mutation 100%
  • prediction 59%
  • proteins 49%
  • protein structure 30%
  • enzyme activity 19%

• Development of a pipeline for high throughput mitochondrial DNA (mtDNA) analysis.

  Vancampenhout, K., Croes, D., Daneels, D., Caljon, B., Lissens, W., Stouffs, K., De Meirleir, L., Jonckheere, A., Van Coster, R., Smet, J., De Paepe, B., Vanlander, A., Van Dooren, S., Bonduelle, M-L. & Seneca, S., 24 apr. 2014, BeMGI. 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

  • Mitochondrial DNA 100%
  • Mitochondrial Genome 59%
  • Mitochondrial Diseases 59%
  • Oxidative Phosphorylation 53%
  • Mutation 40%

• DIDA: A first database on digenic diseases

  Gazzo, A., Daneels, D., Smits, G., Van Dooren, S., Cilia, E. & Lenaerts, T., 8 dec. 2014, 9th Benelux Bioinformatics Conference Proceedings. blz. 19-19 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

  • Databases 100%
  • Genes 69%
  • Mutation 46%
  • Medical Genetics 27%
  • Genetics 27%

• Did lightning strike twice ?

  Seneca, S., Fosselle, E., Vancampenhout, K., Stouffs, K., Lissens, W., Jonckheere, A., Van Coster, R., Smet, J., De Paepe, B., Vanlander, A. & De Meirleir, L., 7 feb. 2014, BeSHG. blz. 52-52 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

  • Lightning 100%
  • Mitochondrial DNA 65%
  • Mitochondrial Genome 26%
  • Mutation 23%
  • Leucine 21%

• Did lightning strike twice ?

  Seneca, S., Fosselle, E., De Bleecker, J., Vancampenhout, K., Lissens, W., Stouffs, K., Jonckheere, A., Van Coster, R., Smet, J., De Paepe, B., Vanlander, A. & De Meirleir, L., 31 mei 2014, Abstractbook of European Society of Human Genetics. 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

  • Lightning 100%
  • Mitochondrial DNA 65%
  • Mutation 20%
  • Leucine 18%
  • Point Mutation 17%

• Differentiation capacity of chromosomally abnormal human embryonic stem cells

  Markouli, C., Geens, M., Nguyen Thi, H., Dziedzicka, D., Sermon, K. & Spits, C., 24 jun. 2014, 12th Annual Meeting of The International Society for Stem Cell Research (ISSCR).

  Onderzoeksoutput: Meeting abstract (Book)

  • embryonic stem cells 100%
  • mesoderm 38%
  • mutation 32%
  • cells 25%
  • protocols 22%

• Differentiation capacity of chromosomally abnormal human embryonic stem cells

  Markouli, C., Geens, M., Nguyen Thi, H., Dziedzicka, D., Sermon, K. & Spits, C., 12 sep. 2014, First meeting of the Belgian Society for Stem Cell Research (BeSSCR).

  Onderzoeksoutput: Meeting abstract (Book)

  • embryonic stem cells 100%
  • protocols 37%
  • mutation 36%
  • endoderm 33%
  • mesoderm 31%

• Gene expression during testicular development

  Van Saen, D., 2014, Belgian Society for Stem cell research.

  Onderzoeksoutput: Meeting abstract (Book)

  • testicular development 100%
  • stem cells 73%
  • germ cells 46%
  • gene expression 44%
  • Sertoli cells 42%

• Human embryonic stem cells show low-grade microsatellite instability

  Nguyen Thi, H., Markouli, C., Geens, M., Sermon, K. & Spits, C., 24 jun. 2014, ISSCR 12th annual meeting.

  Onderzoeksoutput: Meeting abstract (Book)

  • embryonic stem cells 100%
  • microsatellite repeats 58%
  • neoplasms 20%
  • cell lines 13%
  • mutation accumulation 12%

• Loss of heterozygosity study allows rapid diagnosis in unclear multisystemic neonatal disease

  Caberg, J-H., Dideberg, V., Viellevoye, R., Florkin, B., Kettelslegers, O., Boemer, F., Schoos, R., Lissens, W., Kalenga, M., Bours, V. & Debray, F-G., 7 feb. 2014, BeSHG.

  Onderzoeksoutput: Meeting abstract (Book)

  • loss of heterozygosity 100%
  • macrophage activation 25%
  • cholestasis 25%
  • cytolysis 24%
  • splenomegaly 24%

• Male fertility preservation. Where are we in 2014?

  Goossens, E., 6 jun. 2014, KLOTZ symposium.

  Onderzoeksoutput: Meeting abstract (Book)

  • male fertility 100%
  • cryopreservation 56%
  • preserves 53%
  • Sertoli cells 32%
  • spermatogenesis 28%
  12 Citaten (Scopus)

• 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. blz. 7-7 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

  • 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. blz. 78-78 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

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

• Optimization of embryoid body formation from single human embryonic stem cells cultured on laminin-521

  Dziedzicka, D., Markouli, C., Spits, C., Sermon, K. & Geens, M., 12 sep. 2014, First meeting of the Belgian Society for Stem Cell Research.

  Onderzoeksoutput: Meeting abstract (Book)

  • laminin 100%
  • embryonic stem cells 99%
  • protocols 24%
  • cells 19%
  • embryonic germ layers 11%

• Optimizing a massive parallel sequencing methodology for whole mitochondrial genome analysis at the diagnostic bench

  Vancampenhout, K., Caljon, B., De Meirleir, L., Vanlander, A., Smet, J., De Paepe, B., Debray, F-G., Lissens, W., Stouffs, K., Jonckheere, A., Vancoster, R. & Seneca, S., 1 apr. 2014, third edition on the medical campus. blz. 25-25 1 blz. (Research unlimited).

  Onderzoeksoutput: Meeting abstract (Book)

  • mitochondrial genome 100%
  • mitochondrial DNA 86%
  • methodology 27%
  • protocols 21%
  • ions 21%

• Optimizing a massive parallel sequencing methodology for whole mitochondrial genome analysis at the diagnostic bench

  Vancampenhout, K., Caljon, B., Spits, C., Jonckheere, A., Vancoster, R., Vanlander, A., Smet, J., De Paepe, B., Lissens, W., Stouffs, K., Bonduelle, M-L. & Seneca, S., 15 jun. 2014, Euromit. blz. 443-443 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

  • Mitochondrial Genome 100%
  • Ions 65%
  • Polymerase Chain Reaction 35%
  • Libraries 35%
  • DNA-Directed DNA Polymerase 22%

• Optimizing a massive parallel sequencing methodology for whole mitochondrial genome analysis at the diagnostic bench.

  Vancampenhout, K., Caljon, B., De Meirleir, L., Lissens, W., Stouffs, K., Jonckheere, A., Van Coster, R. & Seneca, S., 7 feb. 2014, BeSHG. blz. 36-36 1 blz.

  Onderzoeksoutput: Meeting abstract (Book)

  • mitochondrial genome 100%
  • ions 73%
  • mitochondrial DNA 69%
  • application coverage 52%
  • protocols 44%

• Spermatogoniale stamcellen en het banken van testiculair weefsel bij prepubertaire jongens

  Goossens, E., 20 nov. 2014, Klinisch Wetenschappelijke Vergadering - Afdeling Reproductieve Geneeskunde - UZ Gent.

  Onderzoeksoutput: Meeting abstract (Book)

• Spermatogonial stem cell based options to treat male infertility

  Goossens, E., 28 apr. 2014, ESHRE campus course.

  Onderzoeksoutput: Meeting abstract (Book)

  • male sterility 100%
  • stem cells 89%
  • cell transplantation 43%
  • mice 34%
  • cryopreservation 29%

• Stable non-random X chromosome inactivation in human embryonic stem cells: culture artefact rather than a parent-of-origin specific event

  Geens, M., Barbé, L., Dee, K., Spits, C. & Sermon, K., 2 jul. 2014, Annual Meeting of the European Society for Human Reproduction and Embryology (ESHRE).

  Onderzoeksoutput: Meeting abstract (Book)

  • embryonic stem cells 100%
  • X chromosome 82%
  • inactivation 65%
  • cell culture 63%
  • methylation 23%