Researcher
Björn Menten
- Keywords:prenatal genetic testing, genomics, whole genome sequencing, long read sequencing, preimplantation genetic testing
- Disciplines:Epigenetics, Analysis of next-generation sequence data, Bioinformatics of disease, Bioinformatics data integration and network biology, Data visualisation and high-throughput image analysis, Ontologies, data curation and text mining, Development of bioinformatics software, tools and databases, Immunogenetics, Clinical genetics and molecular diagnostics, Medical epigenomics, Medical metagenomics, Medical genomics, Single-cell data analysis, Genetics, Structural bioinformatics and computational proteomics, Bioinformatics and computational biology not elsewhere classified
Affiliations
- Department of Biomolecular Medicine (Department)
Member
From1 Oct 2018 → Today - Dean's Office of the Faculty of Medicine and Health Sciences (Administrative office)
Member
From1 Oct 2003 → 30 Sep 2005 - Department of Pediatrics and medical genetics (Department)
Member
From1 Feb 2003 → 30 Sep 2018
Projects
11 - 20 of 25
- Immunomonitoring of patients with non-small cell lung carcinoma treated with a tumor mutanome-targeted dendritic cell vaccineFrom1 Jan 2018 → 31 Dec 2021Funding: BOF - Doctoral projects
- Fetal cell isolation and characterization for cell-based non-invasive prenatal genetic diagnosisFrom1 Oct 2017 → 30 Sep 2021Funding: BOF - Doctoral projects
- Sequencing Expertise Centre (Life Sciences)From1 Feb 2017 → 30 Nov 2022Funding: BOF - Doctoral projects
- Improving outcome of immune checkpoint blockade in lung cancer by combination with a tumor mutanome-targeted dendritic cell vaccineFrom1 Jan 2017 → 31 Dec 2021Funding: Nonprofit institution or equivalents
- Improving outcome of immune checkpoint blockade in lung cancer by combination with a tumor mutanome-targeted dendritic cell vaccineFrom1 Jan 2017 → 31 Dec 2021Funding: Nonprofit institution or equivalents
- Improving outcome of immune checkpoint blockade in lung cancer by combination with a tumor mutanome-targeted dendritic cell vaccineFrom1 Jan 2017 → 31 Dec 2021Funding: Nonprofit institution or equivalents
- IViMOVA: In Vitro Maturation and vitrification of oocytes collected during OVarian cortex cryopreservation: a realistic fertility preservation therapy for trans menFrom1 Oct 2016 → 30 Sep 2021Funding: FWO Applied Biomedical Research (TBM)
- Elucidating the dark matter of the genome in central nervous system disorders.From1 Jan 2016 → 31 Dec 2017Funding: Foundations, funds and other with scientific goal
- Lab equipment necessary for the generation, manipulation and genome editing of pluripotent stem cellsFrom1 Jun 2015 → 31 May 2018Funding: BOF - Other initiatives
- IsoFlux System: Isolation of rare cells from biological samplesFrom1 Jun 2015 → 31 May 2017Funding: BOF - Other initiatives
Publications
1 - 10 of 47
- Implicit bias in diagnosing mosaicism amongst preimplantation genetic testing providers : results from a multicenter study of 36 395 blastocysts(2024)
Authors: Mina Popovic, Lorena Borot, Aline R. Lorenzon, Ana Luiza Rossi de Castro Lopes, Denny Sakkas, Belen Lledo, Ruth Morales, Jose Antonio Ortiz, Nikolaos Polyzos, Monica Parriego, et al.
Pages: 258 - 274 - Single-cell profiling identifies a novel human polyclonal unconventional T cell lineage(2023)
Authors: Lore Billiet, Laurenz De Cock, Guillem Sanchez Sanchez, Rupert Mayer, Glenn Goetgeluk, Stijn De Munter, Melissa Pille, Joline Ingels, Hanne Jansen, Karin Weening, et al.
- Retained chromosomal integrity following CRISPR-Cas9-based mutational correction in human embryos(2023)
Authors: Bieke Bekaert, Annekatrien Boel, Lisa De Witte, Winter Vandenberghe, Mina Popovic, Panagiotis Stamatiadis, Gwenny Cosemans, Athina-Maria De Loore, Susana Marina Chuva de Sousa Lopes, Petra De Sutter, et al.
Pages: 2326 - 2341 - Structural variants disrupt a critical regulatory region downstream of FOXG1(2023)Volume: 31
Authors: Eva D'haene, Lies Vantomme, Björn Menten, Bert Callewaert, Elfride De Baere, Sarah Vergult
Pages: 28 - 28 - Spindle transfer rescues poor embryo development of in vitro matured ovarian tissue oocytes from transgender men(2022)Volume: 37
Authors: Antonia Christodoulaki, H. He, M. Zhou, Arantxa Cardona Barberán, Chloë De Roo, S. M. Chuva De Sousa Lopes, Björn Menten, Ann Van Soom, Petra De Sutter, Annekatrien Boel, et al.
Number of pages: 1 - Application of an ultrasensitive NGS-based blood test for the diagnosis of early-stage lung cancer : sensitivity, a hurdle still difficult to overcome(2022)
Authors: Malaïka Van der Linden, Bram Van Gaever, Lennart Raman, Karim Vermaelen, Ingel Demedts, Veerle Surmont, Ulrike Himpe, Yolande Lievens, Liesbeth Ferdinande, Franceska Dedeurwaerdere, et al.
- Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models(2022)
Authors: Kiana Mohajeri, Rachita Yadav, Eva D'haene, Philip M. Boone, Serkan Erdin, Dadi Gao, Mariana Moyses-Oliveira, Riya Bhavsar, Benjamin B. Currall, Kathryn O'Keefe, et al.
Pages: 2049 - 2067 - A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene(2022)
Authors: Maria del Rocio Pérez Baca, Eva Jacobs, Lies Vantomme, Pontus LeBlanc, Elke Bogaert, Annelies Dheedene, Laurenz De Cock, Bart Dermaut, Aidin Foroutan, Jennifer Kerkhof, et al.
Number of pages: 1 - Benchmarking of long-read structural variant callers on a recently released truth set using Oxford Nanopore data(2021)
Authors: Griet De Clercq, Bram Van Gaever, Lies Vantomme, Annelies Dheedene, Björn Menten
Number of pages: 1 - Recurrent chromosomal imbalances provide selective advantage to human embryonic stem cells under enhanced replicative stress conditions(2021)
Authors: Liselot Mus, Stéphane Van Haver, Mina Popovic, Wim Trypsteen, Steve Lefever, Nadja Zeltner, Yudelca Ogando, Eva Jacobs, Geertrui Denecker, Ellen Sanders, et al.
Pages: 272 - 281