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
31 - 40 of 44
- Gastric emptying and gastro-oesophageal reflux in children with cystic fibrosis(2016)
Authors: Bruno Hauser, Jean De Schepper, Anne Malfroot, Elke De Wachter, Iris De Schutter, K. Keymolen, Yvan Vandenplas
Pages: 540-547 - GTF2E2 Mutations Destabilize the General Transcription Factor Complex TFIIE in Individuals with DNA Repair-Proficient Trichothiodystrophy(2016)
Authors: Christiane Kuschal, Elena Botta, Donata Orioli, John J Digiovanna, Sara Seneca, K. Keymolen, Deborah Tamura, Elizabeth Heller, Sikandar G Khan, Giuseppina Caligiuri, et al.
Pages: 627-642 - SCN4A variants and Brugada syndrome(2016)
Authors: Véronique Bissay, Sophie Van Malderen, K. Keymolen, Willy Lissens, Uschi Peeters, Dorien Daneels, Anna C Jansen, Gudrun Pappaert, Pedro Brugada, Jacques De Keyser, et al.
Pages: 400-407 - A prospective study of the clinical utility of prenatal chromosomal microarray analysis in fetuses with ultrasound abnormalities and an exploration of a framework for reporting unclassified variants and risk factors.(2014)
Authors: PD Brady, Barbara Delle Chiaie, G Christenhusz, K. Dierickx,, Kris Van den Bogaert, Björn Menten, S. Janssens, P. Defoort, E. Roets, Elke Sleurs, et al.
Pages: 469-476 - Thin genu of the corpus callosum points to mutation in FOXG1 in a child with acquired microcephaly, trigonocephaly, and intellectual developmental disorder: A case report and review of literature(2014)
Authors: Caroline De Bruyn, Tim Vanderhasselt, Ibrahim Tanyalcin, K. Keymolen, Katrijn Van Rompaey, Linda De Meirleir, Anna C Jansen
Pages: 420-426 - Thin genu of the corpus callosum points to mutation in FOXG1 in a child with acquiredmicrocephaly, trigonocephaly, and intellectual developmental disorder: A case report and review of literature(2014)
Authors: Caroline De Bruyn, Tim Vanderhasselt, Ibrahim Tanyalcin, K. Keymolen, Katrijn Van Rompaey, Liesbeth De Meirleir, Anna C Jansen, L. Lagae
Pages: 420-426 - Facilitating the Fragile X post- and prenatal genetic diagnostic testing workflow by use of the Abbott FMR1 TP-PCR and FMR1 sizing PCR products.(2011)
Authors: Sonia Van Dooren, Sara Seneca, Kristof Endels, K. Keymolen, Marjan De Rademaeker, Van Berkel Kim, Willy Lissens, Maryse Bonduelle
Pages: 178-178 - Pregnancy outcome in carriers of Robertsonian translocations.(2011)
Authors: K. Keymolen, K; Van Berkel, Anniek Vorsselmans, C. Staessen, Ingeborg Liebaers
Pages: 2381-2385 - Specific Congenital Malformations after Exposure to Cyclophosphamide, Epirubicin and 5-Fluorouracil during the First Trimester of Pregnancy(2011)
Authors: M. Leyder, Monica Laubach, Maria Breugelmans, K. Keymolen, Jacques De Grève, Walter Foulon
Pages: 141-144 - Pregnancy outcome in carriers of Robertsonian translocations(2011)
Authors: K. Keymolen, Kim Van Berkel, Anniek Vorsselmans, Catherine Staessen
Pages: 2381-5