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Chris J.L.M. Meijer

Researcher at VU University Amsterdam

Publications -  745
Citations -  83366

Chris J.L.M. Meijer is an academic researcher from VU University Amsterdam. The author has contributed to research in topics: Cervical cancer & Cervical intraepithelial neoplasia. The author has an hindex of 128, co-authored 733 publications receiving 78705 citations. Previous affiliations of Chris J.L.M. Meijer include VU University Medical Center & Academic Center for Dentistry Amsterdam.

Papers
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Interleukin-12 Increases Proliferation and Interferon-γ Production but Not Cytolytic Activity of Human Antigen-Specific Effector Memory Cytotoxic T Lymphocytes: Power of the Effect Depends on the Functional Avidity of the T Cell and the Antigen Concentration

TL;DR: The data suggest that IL-12 is a good adjuvant for boosting CTL responses, in terms of proliferation and IFN-gamma production, the latter particularly for CTLs with low to intermediate avidity, such as tumor-associated self-antigen-specific CTLS.
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Human papillomavirus (HPV) prevalence and associated risk factors in women from Curaçao.

TL;DR: HPV-prevalence in the overall population is high and HPV16 was the most common genotype followed by 35 and 18 and HPV-type distribution found in Curaçao should be taken into account when considering the choice for prophylactic vaccination.
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Screening for cervical cancer.

TL;DR: The consent process for stored human biological samples has been extensively discussed in the literature as mentioned in this paper, generating debate about the appropriate consent process of storing these samples for research not specified at the time.
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Complementarity between miRNA expression analysis and DNA methylation analysis in hrHPV-positive cervical scrapes for the detection of cervical disease.

TL;DR: A panel of three miRNAs is discriminatory for CIN3 in hrHPV-positive scrapes and can complement DNA methylation analysis for the efficient detection of cervical disease.
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Differential diagnosis of cutaneous large cell lymphomas using monoclonal antibodies reactive in paraffin-embedded skin biopsy specimens.

TL;DR: The findings show that differentiation between clinically relevant subgroups can be obtained by a small panel of antibodies including L26, MB2, LNI, MTI, UCHLI, and Ber-H2.