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
11 - 20 of 44
- Defining the phenotypical spectrum associated with variants in TUBB2A(2021)
Authors: Stefanie Brock, Tim Vanderhasselt, Sietske Vermaning, K. Keymolen, Luc Régal, Romina Romaniello, Dagmar Wieczorek, Tim Matthias Storm, Karin Schaeferhoff, Ute Hehr, et al.
Pages: 1-8 - Multiple vitrification-warming and biopsy procedures on human embryos(2020)
Authors: Anick De Vos, Lisbet Van Landuyt, Martine De Rijcke, Pieter Verdyck, G Verheyen, Andrea Buysse, Florence Belva, K. Keymolen, H Tournaye, Willem Verpoest
Pages: 2488-2496 - Clinical experience of preimplantation genetic testing(2020)
Authors: Martine De Rijcke, Veerle Berckmoes, Anick De Vos, Stefanie Rosa Van de Voorde, Pieter Verdyck, Willem Verpoest, K. Keymolen
Pages: A45-A58 - 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: 1272-1283 - Chromosomal abnormalities after ICSI in relation to semen parameters(2020)
Authors: Florence Belva, Maryse Bonduelle, andres buysse, Annaline Van den Bogaert, Frederik J Hes, M Roelants, G Verheyen, H Tournaye, K. Keymolen
Pages: 2149-2162 - An ACVRL1 gene mutation presenting as vein of Galen malformation at prenatal diagnosis(2020)
Authors: Caterina De Luca, Elisa Bevilacqua, Dominique A. Badr, Mieke Cannie, Teresa Cos Sanchez, Valerie Segers, K. Keymolen, Jacques Jani
Pages: 1255-1258 - ERCC2 mutations in two siblings with a severe trichothiodystrophy phenotype.(2020)
Authors: Leemans G, L. De Raeve, Kathelijn Keymolen
Pages: 876-879 - Preimplantation genetic testing with HLA matching(2020)
Authors: Martine De Rijcke, Anick De Vos, Florence Belva, Veerle Berckmoes, Maryse Bonduelle, Andrea Buysse, K. Keymolen, Ingeborg Liebaers, Julie Nekkebroeck, Peggy Verdyck, et al.
Pages: 445-454 - A clinical scoring system for congenital contractural arachnodactyly(2020)
Authors: Ilse Meerschaut, Shana De Coninck, Wouter Steyaert, Angela Barnicoat, Allan Bayat, Francesco Benedicenti, Siren Berland, Edward M. Blair, Jeroen Breckpot, Anna de Burca, et al.
Pages: 124-131 - A focused 35-minute whole body MRI screening protocol for patients with von Hippel-Lindau disease(2019)
Authors: A Vanbinst, Carola Brussaard, Evelynn Vergauwen, Vera Van Velthoven, Robert Kuijpers, Olaf Michel, Ina Foulon, Anna C Jansen, Bieke Lefevere, Susanne Bohler, et al.