Researcher
Jan Hellemans
- Disciplines:Paediatrics and neonatology, Molecular and cell biology, Systems biology, Nursing, Genetics
Affiliations
- Department of Molecular biotechnology (Department)
Member
From1 Oct 2010 → 31 Dec 2010 - Department of Pediatrics and medical genetics (Department)
Member
From1 Apr 2001 → 31 Dec 2011
Projects
1 - 3 of 3
- Deciphering the molecular pathogenesis of neuroblastoma through next generation genome analysisFrom1 Oct 2010 → 30 Sep 2012Funding: FWO fellowships, BOF - Other initiatives
- Elucidation of the genetic defect in sporadic melorheostosis and study of the precise role of LEMD3 in bone homeostasisFrom1 Jan 2009 → 31 Dec 2012Funding: BOF - Doctoral projects
- Anlaysis of the genetic defect in melorheostosis and the study of the molecular and biological effects of LEMD3 haploinsufficiencyFrom1 Oct 2007 → 30 Sep 2010Funding: BOF - Other initiatives, FWO fellowships
Publications
1 - 10 of 33
- A unified censored normal regression model for qPCR differential gene expression analysis(2017)
Authors: Peter Pipelers, Lieven Clement, Matthijs Vynck, Jan Hellemans, Jo Vandesompele, Olivier Thas
- Benchmarking of RNA-sequencing analysis workflows using whole-transcriptome RT-qPCR expression data(2016)
Authors: Ariane De Ganck, Jan Hellemans, Pieter Mestdagh
Number of pages: 1 - Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform(2012)
Authors: Sarah De Keulenaer, Jan Hellemans, Jean-Pierre Renard, Joachim De Schrijver, Hendrik Van de Voorde, Mohammad Amin Tabatabaiefar, Filip Van Nieuwerburgh, Filip Pattyn, Bieke Scharlaken, Dieter Deforce, et al.
- Practical tools to implement massive parallel pyrosequencing of PCR products in next generation molecular diagnostics(2011)
Authors: Joachim De Schrijver, Lieven Clement, Machteld Baetens, Sarah De Keulenaer, Dieter Deforce, Filip Van Nieuwerburgh, Sofie Bekaert, Filip Pattyn, Jan Hellemans
- Improved Molecular Diagnostics of Idiopathic Short Stature and Allied Disorders: Quantitative Polymerase Chain Reaction-Based Copy Number Profiling of SHOX and Pseudoautosomal Region 1(2010)
Authors: B D'haene, Jan Hellemans, Margarita Craen, Jean De Schepper, K Devriendt, JP Fryns, K Keymolen, Eveline Debals, A de Klein, EM de Jong, et al.
Pages: 3010 - 3018 - Meeting report from the second 'Minimum Information for Biological and Biomedical Investigations' (MIBBI) workshop(2010)
Authors: Carsten Kettner, Dawn Field, Susanna-Assunta Sansone, Chris Taylor, Jan Aerts, Nigel Binns, Andrew Blake, Cedrik M Britten, Ario de Marco, Jennifer Fostel, et al.
- The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2)(2010)
Authors: Fransiska Malfait, Lut Van Laer, Jan Hellemans, T Hermanns-Le, A Benmansour, A Verloes
Pages: 79 - 88 - Analysing 454 amplicon resequencing experiments using the modular and database oriented Variant Identification Pipeline(2010)
Authors: Joachim De Schrijver, Nick Sabbe, Filip Pattyn, Filip Van Nieuwerburgh, Dieter Deforce, Sofie Bekaert, Jan Hellemans
- Next generation sequencing: (r)evolutie in DNA sequenering en haar rol in de moderne geneeskunde(2010)
Authors: Jan Hellemans, Sofie Bekaert
Pages: 357 - 361 - ZnT3 mRNA levels are reduced in Alzheimer's disease post-mortem brain(2009)
Authors: N Beyer, DTR Coulson, S Heggarty, R Ravid, GB Irvine, Jan Hellemans, JA Johnston