Researcher
K. Keymolen
- Research Expertise:
Klinische Genetica
Kindergeneeskunde
Dysmorpholgie
Neurogenetica
Genodermatose
- Keywords:Medicine
- Disciplines:Genetics, Paediatrics, Anthropological genetics
- Users of research expertise:
Klinische Genetica
Kindergeneeskunde
Dysmorpholgie
Neurogenetica
Genodermatose
Affiliations
- Medical Genetics (Department)
Member
From1 Jan 2008 → Today - Clinical sciences (Department)
Member
From1 Feb 2020 → 20 Oct 2022 - Clinical sciences (Department)
Member
From1 Oct 2019 → 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 - Clinical sciences (Department)
Member
From1 Sep 1999 → 30 Nov 2018
Publications
1 - 10 of 44
- Cleavage-stage or blastocyst-stage embryo biopsy has no impact on growth and health in children up to 2 years of age(2023)
Authors: Florence Belva, Fiskani Kondowe, Anick De Vos, K. Keymolen, Andrea Buysse, Frederik Hes, Veerle Berckmoes, Pieter Verdyck, W Verpoest, Martine De Rijcke
- Congenital hydrocephalus(2023)
Authors: Valerie Jacquemin, Nassim Versbraegen, Sarah Duerinckx, Annick Massart, Julie Soblet, Camille Perazzolo, Nicolas Deconinck, Elise Brischoux-Boucher, Anne De Leener, Nicole Revencu, et al.
- Impact of embryo vitrification on children's health, including growth up to two years of age, in comparison with results following a fresh embryo transfer(2023)
Authors: Florence Belva, Christophe Blockeel, Kathelijn Keymolen, Andrea Buysse, Maryse Bonduelle, G Verheyen, Mathieu Roelants, Herman Tournaye, Frederik Hes, Lisbet Van Landuyt
Pages: 932-941 - Predictive heatmap in Preimplantation Genetic Testing for Monogenic disorders (PGT-M) and Structural Rearrangements (PGT-SR)(2023)Edition: Supp 1 2023Volume: 38
Authors: Annelore Van Der Kelen, Veerle Berckmoes, K. Keymolen, L Poelsler, Wilfried Cools, Anick De Vos, Michel De Vos, C. Blockeel, Elia Fernandez Gallardo, Martine De Rijcke, et al.
Pages: 709-709Number of pages: 1 - Overlapping cortical malformations in patients with pathogenic variants in GRIN1 and GRIN2B(2023)
Authors: Stefanie Brock, Annie Laquerriere, Florent Marguet, Scott J Myers, Yuan Hongjie, Diana Baralle, Tim Vanderhasselt, Katrien Stouffs, K. Keymolen, Sukhan Kim, et al.
Pages: 183-192 - Analysis of parental contribution for aneuploidy detection (APCAD)(2022)
Authors: Pieter Verdyck, Veerle Berckmoes, Sven Van Laere, K. Keymolen, Catharina Olsen, Martine De Rijcke
Pages: 459-468 - 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 Geymonat, et al.
Pages: 344-363 - 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.
- Parameters of poor prognosis in preimplantation genetic testing for monogenic disorders(2021)
Authors: Annelore Van Der Kelen, S. Santos-Ribeiro, Anick De Vos, Pieter Verdyck, Martine De Rijcke, Veerle Berckmoes, H Tournaye, C. Blockeel, Michel De Vos, Frederik Hes, et al.
Pages:  2558–2566 - Novel Variant in COL4A1 Causes Extensive Prenatal Intracranial Hemorrhage and Porencephaly(2021)
Authors: Stefanie Brock, Alex Michotte, Elisa Done, Astrid Leus, Mieke Cannie, Kari De Pierre, Ramses Forsyth, Katrien Stouffs, K. Keymolen, Boyan Dimitrov, et al.
Pages: 807-810