Jan Hellemans
Jan Hellemans
Biogazelle
Verified email at biogazelle.com
Title
Cited by
Cited by
Year
The MIQE Guidelines: Minimum Information for Publication of Quantitative Real-Time PCR Experiments
SA Bustin, V Benes, JA Garson, J Hellemans, J Huggett, M Kubista, ...
Clinical chemistry 55 (4), 611-622, 2009
100102009
qBase relative quantification framework and software for management and automated analysis of real-time quantitative PCR data
J Hellemans, G Mortier, A De Paepe, F Speleman, J Vandesompele
Genome biology 8 (2), 1-14, 2007
31592007
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2
BL Loeys, J Chen, ER Neptune, DP Judge, M Podowski, T Holm, ...
Nature genetics 37 (3), 275-281, 2005
14742005
How to do successful gene expression analysis using real-time PCR
S Derveaux, J Vandesompele, J Hellemans
Methods 50 (4), 227-230, 2010
6132010
A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium
Z Su, PP Łabaj, S Li, J Thierry-Mieg, D Thierry-Mieg, W Shi, C Wang, ...
Nature biotechnology 32 (9), 903-914, 2014
5302014
The Digital MIQE Guidelines: Minimum Information for Publication of Quantitative Digital PCR Experiments
JF Huggett, CA Foy, V Benes, K Emslie, JA Garson, R Haynes, ...
Clinical chemistry 59 (6), 892-902, 2013
4832013
Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis
J Hellemans, O Preobrazhenska, A Willaert, P Debeer, PCM Verdonk, ...
Nature genetics 36 (11), 1213-1218, 2004
4292004
Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin
EA Otto, B Loeys, H Khanna, J Hellemans, R Sudbrak, S Fan, U Muerb, ...
Nature genetics 37 (3), 282-288, 2005
3802005
Accurate and objective copy number profiling using real-time quantitative PCR
B D’haene, J Vandesompele, J Hellemans
Methods 50 (4), 262-270, 2010
2952010
The need for transparency and good practices in the qPCR literature
SA Bustin, V Benes, J Garson, J Hellemans, J Huggett, M Kubista, ...
Nature methods 10 (11), 1063-1067, 2013
2142013
Evaluation of qPCR curve analysis methods for reliable biomarker discovery: bias, resolution, precision, and implications
JM Ruijter, MW Pfaffl, S Zhao, AN Spiess, G Boggy, J Blom, RG Rutledge, ...
Methods 59 (1), 32-46, 2013
1942013
Predicting outcomes for children with neuroblastoma using a multigene-expression signature: a retrospective SIOPEN/COG/GPOH study
J Vermeulen, K De Preter, A Naranjo, L Vercruysse, N Van Roy, ...
The lancet oncology 10 (7), 663-671, 2009
1712009
Measurable impact of RNA quality on gene expression results from quantitative PCR
J Vermeulen, K De Preter, S Lefever, J Nuytens, F De Vloed, S Derveaux, ...
Nucleic acids research 39 (9), e63-e63, 2011
1652011
RDML: structured language and reporting guidelines for real-time quantitative PCR data
S Lefever, J Hellemans, F Pattyn, DR Przybylski, C Taylor, R Geurts, ...
Nucleic acids research 37 (7), 2065-2069, 2009
1512009
Homozygous mutations in IHH cause acrocapitofemoral dysplasia, an autosomal recessive disorder with cone-shaped epiphyses in hands and hips
J Hellemans, PJ Coucke, A Giedion, A De Paepe, P Kramer, F Beemer, ...
The American Journal of Human Genetics 72 (4), 1040-1046, 2003
1372003
miRNA expression profiling: from reference genes to global mean normalization
B D’haene, P Mestdagh, J Hellemans, J Vandesompele
Next-Generation MicroRNA Expression Profiling Technology, 261-272, 2012
1292012
Recurrent mutation in the first zinc finger of the orphan nuclear receptor NR2E3 causes autosomal dominant retinitis pigmentosa
F Coppieters, BP Leroy, D Beysen, J Hellemans, K De Bosscher, ...
The American Journal of Human Genetics 81 (1), 147-157, 2007
1002007
Single-nucleotide polymorphisms and other mismatches reduce performance of quantitative PCR assays
S Lefever, F Pattyn, J Hellemans, J Vandesompele
Clinical chemistry 59 (10), 1470-1480, 2013
912013
Osteopoikilosis, short stature and mental retardation as key features of a new microdeletion syndrome on 12q14
B Menten, K Buysse, F Zahir, J Hellemans, SJ Hamilton, T Costa, ...
Journal of medical genetics 44 (4), 264-268, 2007
832007
Germline LEMD3 mutations are rare in sporadic patients with isolated melorheostosis
J Hellemans, P Debeer, M Wright, A Janecke, KW Kjaer, PCM Verdonk, ...
Human mutation 27 (3), 290-290, 2006
812006
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