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
21 - 30 of 44
- Factors influencing the clinical outcome of preimplantation genetic testing for polycystic kidney disease(2019)
Authors: Veerle Berckmoes, Pieter Verdyck, Pascale De Becker, Alexis De Vos, G Verheyen, Patricia Vanderniepen, W Verpoest, Ingeborg Liebaers, Maryse Bonduelle, K. Keymolen, et al.
Pages: 949-958 - Fetal and neonatal neurogenetics(2019)
Authors: Anna C Jansen, K. Keymolen
Pages: 105-132 - The Belgian MicroArray Prenatal (BEMAPRE) database(2018)
Authors: Joke Muys, Bettina Blaumeiser, Yves Jacquemyn, Claude Bandelier, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Winnie Courtens, Anne De Leener, Marjan De Rademaeker, et al.
Pages: 1120-1128 - Expanding the clinical spectrum of biallelic ZNF335 variants(2018)
Authors: Katrien Stouffs, A B Stergachis, Tim Vanderhasselt, A Dica, Sabine Janssens, Laura Vandervore, Alexander Gheldof, Olaf Bodamer, Kathelijn Keymolen, Sara Seneca, et al.
Pages: 246-251 - Tubulinopathies continued(2018)
Authors: Stefanie Brock, Katrien Stouffs, Emmanuel Scalais, Marc D'Hooghe, K. Keymolen, Renzo Guerrini, William B Dobyns, Nataliya Di Donato, Anna C Jansen
Pages: 1132-1142 - Can clinical characteristics be criteria to perform chromosomal microarray-analysis in children and adolescents with autism spectrum disorders?(2018)
Authors: Melissa Sys, Ann Van Den Bogaert, Bram Roosens, Annik Lampo, Anna C Jansen, Sara Wouters, K. Keymolen
Pages: 225-232 - Central nervous system gadolinium accumulation in patients undergoing periodical contrast MRI screening for hereditary tumor syndromes.(2018)
Authors: Eveline Vergauwen, A Vanbinst, Carola Brussaard, Paul Janssens, Clerck D De, Lint M Van, Anne Cees Houtman, O Michel, K. Keymolen, Bieke Lefevere, et al.
- Pancreas and gallbladder agenesis in a newborn with semilobar holoprosencephaly, a case report(2017)
Authors: Robert Hilbrands, K. Keymolen, Alex Michotte, Miriam Marichal, Filip Cools, Annieta Goossens, Pieter in 't Veld, Jean De Schepper, Andrew Hattersley, Henry Heimberg
Pages: 57 - CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy(2017)
Authors: Lise Barbé, Stella Lanni, Arturo Lopez-Castel, Silvie Franck, Claudia Spits, K. Keymolen, Sara Seneca, Stephanie Tomé, Ioana Miron, Julie Letourneau, et al.
Pages: 488-505 - Loss of SYNJ1 dual phosphatase activity leads to early onset refractory seizures and progressive neurological decline(2016)
Authors: Katia Hardies, Yiying Cai, Claude Jardel, Anna C Jansen, Mian Cao, Patrick May, Tania Djemie, Caroline Hachon Le Camus, K. Keymolen, Tine Deconinck, et al.
Pages: 2420-2430