Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.

By H. Hampel, W. Frankel, J. Panescu, Janet C Lockman, Kaisa Sotamaa, D. Fix, I. Comeras, Jennifer La Jeunesse, H. Nakagawa, J. Westman and 14 more. Cancer Research, 2006

609 citations recorded by the source corpus.

Subfields: Oncology, Pathology and Forensic Medicine

View Paper: https://www.semanticscholar.org/paper/6aa48a21be2f45dcb9364b5c64d02b76d5af2ab6

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

1. H. Hampel
2. W. Frankel
3. E. Martin
4. M. Arnold
5. J. Panescu
6. K. Khanduja
7. Kaisa Sotamaa
8. Janet C Lockman

Citations in the corpus

• Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts (2013, neutral): “%) comparable with CRC testing 39 40 (table 3).”
• Feasibility of screening for Lynch syndrome among patients with colorectal cancer. (2008, methodology): “Methods Sample processing, MSI testing, IHC staining methods, MLH1 promoter methylation testing, and mutation detection methods used in this study have been described in detail previously.(19,20)”