Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 396

The DOI matches its Crossref record; 44 of the 44 references it cites were found in a registry or an index.

Rapid targeted mutational analysis of human tumours: a clinical platform to guide personalized cancer medicine

Open access
Dias‐Santagata, Dora, Akhavanfard, Sara, David, Serena S., Vernovsky, Kathy, Kuhlmann, Georgiana, Boisvert, Susan L., Stubbs, Hannah, McDermott, Ultan, Settleman, Jeffrey, Kwak, Eunice L., Clark, Jeffrey W., Isakoff, Steven J., Sequist, Lecia V., Engelman, Jeffrey A., Lynch, Thomas J., Haber, Daniel A., Louis, David N., Ellisen, Leif W., Borger, Darrell R., Iafrate, A. John·2010·EMBO Molecular Medicine

Abstract

Targeted cancer therapy requires the rapid and accurate identification of genetic abnormalities predictive of therapeutic response. We sought to develop a high‐throughput genotyping platform that would allow prospective patient selection to the best available therapies, and that could readily and inexpensively be adopted by most clinical laboratories. We developed a highly sensitive multiplexed clinical assay that performs very well with nucleic acid derived from formalin fixation and paraffin embedding (FFPE) tissue, and tests for 120 previously described mutations in 13 cancer genes. Genetic profiling of 250 primary tumours was consistent with the documented oncogene mutational spectrum and identified rare events in some cancer types. The assay is currently being used for clinical testing of tumour samples and contributing to cancer patient management. This work therefore establishes a platform for real‐time targeted genotyping that can be widely adopted. We expect that efforts like this one will play an increasingly important role in cancer management. See accompanying article: 10.1002/emmm.201000071

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1002/emmm.201000070

Cites

44 of 44 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 44 references

Cited by

See all 396

Metadata

Authors
Dias‐Santagata, D., Akhavanfard, S., David, S. S., Vernovsky, K., Kuhlmann, G., Boisvert, S. L., Stubbs, H., McDermott, U., Settleman, J., Kwak, E. L., Clark, J. W., Isakoff, S. J., Sequist, L. V., Engelman, J. A., Lynch, T. J., Haber, D. A., Louis, D. N., Ellisen, L. W., Borger, D. R., & Iafrate, A. J.
Venue
EMBO Molecular Medicine
Published
2010-05
Volume
2
Issue
5
Pages
146-158
ISSN
  • 1757-4676 (ISSN-L)
  • 1757-4684
OpenAlex
W2104374250
Cited by
396
References
44
FWCI
12.46
Type
journal article
Language
en
Open access
gold

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Rapid targeted mutational analysis of human tumours: a clinical platform to guide personalized cancer medicine. https://app.cochat.ai/papers/10.1002/emmm.201000070
The paper
Dias‐Santagata, D., Akhavanfard, S., David, S. S., Vernovsky, K., Kuhlmann, G., Boisvert, S. L., Stubbs, H., McDermott, U., Settleman, J., Kwak, E. L., Clark, J. W., Isakoff, S. J., Sequist, L. V., Engelman, J. A., Lynch, T. J., Haber, D. A., Louis, D. N., Ellisen, L. W., Borger, D. R., & Iafrate, A. J. (2010). Rapid targeted mutational analysis of human tumours: a clinical platform to guide personalized cancer medicine. EMBO Molecular Medicine. https://doi.org/10.1002/emmm.201000070

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.