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15 result(s) for 'author#Roel Janssen' within BMC
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Citation: BMC Proceedings 2018 12(Suppl 1):3
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The 5th International Conference on Molecular Neurodegeneration: Overlapping Pathologies and Common Mechanisms
Citation: Molecular Neurodegeneration 2019 14(Suppl 1):30 -
5th International Symposium on Focused Ultrasound
Citation: Journal of Therapeutic Ultrasound 2016 4(Suppl 1):31 -
Reviewer acknowledgement 2015
The editors of BMC Public Health would like to thank all our reviewers who have contributed to the journal in Volume 15 (2015).
Citation: BMC Public Health 2016 16:189 -
A multidisciplinary approach unravels early and persistent effects of X-ray exposure at the onset of prenatal neurogenesis
In humans, in utero exposure to ionising radiation results in an increased prevalence of neurological aberrations, such as small head size, mental retardation and decreased IQ levels. Yet, the association between...
Citation: Journal of Neurodevelopmental Disorders 2015 7:3 -
Detection of SARS-CoV-2 infection in the general population by three prevailing rapid antigen tests: cross-sectional diagnostic accuracy study
Rapid antigen diagnostic tests (Ag-RDTs) are the most widely used point-of-care tests for detecting SARS-CoV-2 infection. Since the accuracy may have altered by changes in SARS-CoV-2 epidemiology, indications ...
Citation: BMC Medicine 2022 20:97 -
Head-to-head comparison of the accuracy of saliva and nasal rapid antigen SARS-CoV-2 self-testing: cross-sectional study
The diagnostic accuracy of unsupervised self-testing with rapid antigen diagnostic tests (Ag-RDTs) is mostly unknown. We studied the diagnostic accuracy of a self-performed SARS-CoV-2 saliva and nasal Ag-RDT i...
Citation: BMC Medicine 2022 20:406 -
Optimizing Nanopore sequencing-based detection of structural variants enables individualized circulating tumor DNA-based disease monitoring in cancer patients
Here, we describe a novel approach for rapid discovery of a set of tumor-specific genomic structural variants (SVs), based on a combination of low coverage cancer genome sequencing using Oxford Nanopore with a...
Citation: Genome Medicine 2021 13:86 -
GRIDSS2: comprehensive characterisation of somatic structural variation using single breakend variants and structural variant phasing
GRIDSS2 is the first structural variant caller to explicitly report single breakends—breakpoints in which only one side can be unambiguously determined. By treating single breakends as a fundamental genomic re...
Citation: Genome Biology 2021 22:202 -
MutationalPatterns: comprehensive genome-wide analysis of mutational processes
Base substitution catalogues represent historical records of mutational processes that have been active in a cell. Such processes can be distinguished by various characteristics, like mutation type, sequence c...
Citation: Genome Medicine 2018 10:33 -
MutationalPatterns: the one stop shop for the analysis of mutational processes
The collective of somatic mutations in a genome represents a record of mutational processes that have been operative in a cell. These processes can be investigated by extracting relevant mutational patterns fr...
Citation: BMC Genomics 2022 23:134 -
Association between convalescent plasma treatment and mortality in COVID-19: a collaborative systematic review and meta-analysis of randomized clinical trials
Convalescent plasma has been widely used to treat COVID-19 and is under investigation in numerous randomized clinical trials, but results are publicly available only for a small number of trials. The objective...
Citation: BMC Infectious Diseases 2021 21:1170 -
Blood-derived dendritic cell vaccinations induce immune responses that correlate with clinical outcome in patients with chemo-naive castration-resistant prostate cancer
Clinical benefit of cellular immunotherapy has been shown in patients with castration-resistant prostate cancer (CRPC). We investigated the immunological response and clinical outcome of vaccination with blood-de...
Citation: Journal for ImmunoTherapy of Cancer 2019 7:302 -
Prioritization of genes driving congenital phenotypes of patients with de novo genomic structural variants
Genomic structural variants (SVs) can affect many genes and regulatory elements. Therefore, the molecular mechanisms driving the phenotypes of patients carrying de novo SVs are frequently unknown.
Citation: Genome Medicine 2019 11:79 -
Modelling the risk of transfusion transmission from travelling donors
The EUFRAT (European Up-Front Risk Assessment Tool) was developed as an online risk assessment tool (http://eufrattool.ecdc.europa.eu) to help decision...
Citation: BMC Infectious Diseases 2016 16:143