Get started
Work

A functional assay–based procedure to classify mismatch repair gene variants in Lynch syndrome

Year: 2018
Type: article
DOI: 10.1038/s41436-018-0372-2
Authors: Mark Drost, Yvonne Tiersma, Bryony A. Thompson, Jane H. Frederiksen, Guido Keijzers, Dylan Glubb, Scott Kathe, Jan Osinga, Helga Westers, Lisa Pappas, Kenneth M. Boucher, Siska Molenkamp, José B. Zonneveld, Christi J. van Asperen, David E. Goldgar, Susan S. Wallace, Rolf H. Sijmons, Amanda B. Spurdle, Lene J. Rasmussen, Marc S. Greenblatt, Niels de Wind, Sean V. Tavtigian
Institutions: Leiden University Medical Center, The University of Melbourne, University of Utah, Huntsman Cancer Institute, University of Copenhagen, QIMR Berghofer Medical Research Institute, University of Vermont, University Medical Center Groningen, University of Groningen, Leiden University
Language: English
Field: Medicine
Open Access status: bronze
Funders: Harboefonden, Olav Thon Stiftelsen, National Institutes of Health, Medical Research Council, National Health and Medical Research Council, National Cancer Institute
Awards: G1385029473, G174519574, G19326933, G4474127375, Common and rare sequence variants in breast cancer risk, G6717222331, G858682239, Research Fellowship – Genetic Epidemiology studies of hormonal cancers to inform improved healthcare, G9000100043, G9000153296
OpenAlex ID: W2902849227
FWCI: 4.019
Cites: 32
Cited by: 56
Related to: 10