Jan Hellemans


Ontology type: schema:Person     


Person Info

NAME

Jan

SURNAME

Hellemans

Publications in SciGraph latest 50 shown

  • 2017-12 Benchmarking of RNA-sequencing analysis workflows using whole-transcriptome RT-qPCR expression data in SCIENTIFIC REPORTS
  • 2017-12 High-throughput PCR assay design for targeted resequencing using primerXL in BMC BIOINFORMATICS
  • 2016-07-05 Long non-coding RNA expression profiling in the NCI60 cancer cell line panel using high-throughput RT-qPCR in SCIENTIFIC DATA
  • 2015-12 RDML-Ninja and RDMLdb for standardized exchange of qPCR data in BMC BIOINFORMATICS
  • 2014-12 Target enrichment using parallel nanoliter quantitative PCR amplification in BMC GENOMICS
  • 2014 Selection of Reliable Reference Genes for RT-qPCR Analysis in QUANTITATIVE REAL-TIME PCR
  • 2012-12 Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform in BMC MEDICAL GENOMICS
  • 2012-06 In This Issue in GENETICS IN MEDICINE
  • 2012-06 Massively parallel sequencing for early molecular diagnosis in Leber congenital amaurosis in GENETICS IN MEDICINE
  • 2012 miRNA Expression Profiling: From Reference Genes to Global Mean Normalization in NEXT-GENERATION MICRORNA EXPRESSION PROFILING TECHNOLOGY
  • 2010-12 Analysing 454 amplicon resequencing experiments using the modular and database oriented Variant Identification Pipeline in BMC BIOINFORMATICS
  • 2010-07 The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2) in HUMAN GENETICS
  • 2009-12 ZnT3 mRNA levels are reduced in Alzheimer's disease post-mortem brain in MOLECULAR NEURODEGENERATION
  • 2009-12 The Heterozygous Lemd3+/GT Mouse Is Not a Murine Model for Osteopoikilosis in Humans in CALCIFIED TISSUE INTERNATIONAL
  • 2007-02 qBase relative quantification framework and software for management and automated analysis of real-time quantitative PCR data in GENOME BIOLOGY
  • 2005-03 A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2 in NATURE GENETICS
  • 2004-11 Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis in NATURE GENETICS
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