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Paul J. van Diest

Researcher at Utrecht University

Publications -  514
Citations -  22750

Paul J. van Diest is an academic researcher from Utrecht University. The author has contributed to research in topics: Breast cancer & Cancer. The author has an hindex of 70, co-authored 459 publications receiving 18892 citations. Previous affiliations of Paul J. van Diest include University Medical Center Utrecht & VU University Medical Center.

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Loss of expression of FANCD2 protein in sporadic and hereditary breast cancer.

TL;DR: FANCD2 expression is absent in 10–20% of sporadic and BRCA1-related breast cancers, indicating that somatic inactivating (epi)genetic events in FAN CD2 may be important in both sporadic and hereditary breast carcinogenesis.
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Validation of tissue microarray technology in squamous cell carcinoma of the esophagus

TL;DR: TMA technology appears to be a valid method for immunohistochemical analysis of molecular markers in ESCC provided that the staining pattern in the tumor is homogeneous.
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Epidermal Growth Factor Receptor Expression in High-Grade Osteosarcomas Is Associated with a Good Clinical Outcome

TL;DR: Expression and amplification of EGFR are frequently observed in high-grade osteosarcomas and are associated with improved prognosis in a dose-responsive way, implying that low EGFR expression possibly predicts lack of response to conventional treatment inhigh-grade fractures and may warrant a more intensive therapeutic approach, although not based on EGFR targeting.
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St Gallen 2015 subtyping of luminal breast cancers : impact of different Ki67-based proliferation assessment methods

TL;DR: The proportion of BCs classified as luminal A-like is highly influenced by the Ki67-LI assessment method, which may have a direct effect on the proportion of patients considered having low-risk disease and thus influence therapeutic decision making.
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Simultaneous detection of TOP2A and HER2 gene amplification by multiplex ligation-dependent probe amplification in breast cancer

TL;DR: A new polymerase chain reaction-based test, called multiplex ligation-dependent probe amplification (MLPA), is validated as a simple and quick method to simultaneously assess HER-2/neu and TopoIIα gene amplification status in paraffin-embedded breast cancer samples and thus an attractive supplement or alternative to CISH.