Researcher
K. Keymolen
- Keywords:Medicine
- Disciplines:Pediatrics, Anthropological genetics, Molecular and cell biology not elsewhere classified
- Users of research expertise:
Klinische Genetica
Kindergeneeskunde
Dysmorpholgie
Neurogenetica
Genodermatose
Affiliations
- Clinical sciences (Department)
Member
From1 Feb 2020 → Today - Clinical sciences (Department)
Member
From1 Oct 2019 → 30 Sep 2021 - Faculty of Medicine and Pharmacy (Faculty)
Member
From28 Sep 2015 → 7 Jun 2016 - Reproduction and Genetics (Research group)
Member
From21 Jun 2010 → 31 Oct 2011 - Department of Embryology and Genetics (Department)
Member
From1 Nov 2009 → 31 Oct 2011 - Medical Genetics (Department)
Member
From1 Jan 2008 → Today - Clinical sciences (Department)
Member
From1 Sep 1999 → 30 Nov 2018
Publications
1 - 10 of 57
- Analysis of parental contribution for aneuploidy detection (APCAD)(2022)
Authors: Pieter Verdyck, Veerle Berckmoes, Sven Van Laere, K Keymolen, Catharina Olsen, M De Rycke
Pages: 459-468Number of pages: 10 - Implementation of fetal clinical exome sequencing(2022)
Authors: Martina Marangoni, Guillaume Smits, Gilles Ceysens, Elena Costa, Robert Coulon, Caroline Daelemans, Caroline De Coninck, Sara Derisbourg, Kalina Gajewska, Giulia Garofalo, et al.
Pages: 344-363Number of pages: 20 - A prenatal case of lissencephaly with cerebellar hypoplasia: New mutation in RELN gene(2021)
Authors: Claire Balza, Giulia Garofalo, Teresa Cos, Julie Desir, Xin Kang, Kathelijn Keymolen, Julie Soblet, Kim van Berkel, Catheline Vilain, Wafa Ben Abbou, et al.
Number of pages: 5 - Parameters of poor prognosis in preimplantation genetic testing for monogenic disorders(2021)
Authors: A Van Der Kelen, S Santos-Ribeiro, Anick De Vos, Pieter Verdyck, M. De Rycke, V Berckmoes, H Tournaye, C Blockeel, Michel De Vos, Frederik J. Hes, et al.
Pages: 2558–2566Number of pages: 9 - Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly(2021)
Authors: Sarah Duerinckx, Julie Désir, Camille Perazzolo, Cindy Badoer, Valérie Jacquemin, Julie Soblet, Isabelle Maystadt, Yusuf Tunca, Bettina Blaumeiser, Berten Ceulemans, et al.
Number of pages: 19 - Novel Variant in COL4A1 Causes Extensive Prenatal Intracranial Hemorrhage and Porencephaly(2021)
Authors: Stefanie Brock, Alex Michotte, Elisa Done, Astrid Leus, Mieke M Cannie, Kari De Pierre, Ramses G Forsyth, Katrien Stouffs, Kathelijn Keymolen, Boyan I Dimitrov, et al.
Pages: 807-810Number of pages: 4 - Defining the phenotypical spectrum associated with variants in TUBB2A(2021)
Authors: Stefanie Brock, Tim Vanderhasselt, Sietske Vermaning, Kathelijn Keymolen, Luc Regal, Romina Romaniello, Dagmar Wieczorek, Tim Matthias Storm, Karin Schaeferhoff, Ute Hehr, et al.
Pages: 1-8Number of pages: 8 - Clinical experience of preimplantation genetic testing(2020)
Authors: M. De Rycke, V Berckmoes, Anick De Vos, Stefanie Van De Voorde, Pieter Verdyck, W Verpoest, K Keymolen
Pages: A45-A58Number of pages: 14 - Multiple vitrification-warming and biopsy procedures on human embryos(2020)
Authors: Anick De Vos, Lisbet Van Landuyt, M De Rycke, Pieter Verdyck, Greta Verheyen, Andrea Buysse, F Belva, Kathelijn Keymolen, H Tournaye, W Verpoest
Pages: 2488-2496Number of pages: 9 - Prenatally detected copy number variants in a national cohort a postnatal follow-up study(2020)
Authors: Joke Muys, Yves Jacquemyn, Bettina Blaumeiser, Laura Bourlard, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Anne De Leener, Marjan De Rademaeker, Julie Désir, et al.
Pages: 1272-1283Number of pages: 12