115
Views
5
CrossRef citations to date
0
Altmetric
Review

Is there evidence that we should screen the general population for Lynch syndrome with genetic testing? A systematic review

, , , , , , , , & show all
Pages 49-60 | Published online: 20 Feb 2017

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (1)

John M. Conley, Anya E.R Prince, Arlene M. Davis, Jean Cadigan & Gabriel Lazaro-Munoz. (2020) Is Real-Time ELSI Realistic?. AJOB Empirical Bioethics 11:2, pages 134-144.
Read now

Articles from other publishers (4)

Abdul Rahman Ramdzan, Mohd Rizal Abdul Manaf, Azimatun Noor Aizuddin, Zarina A. Latiff, Keng Wee Teik, Gaik-Siew Ch'ng, Kurubaran Ganasegeran & Syed Mohamed Aljunid. (2021) Cost-Effectiveness of Colorectal Cancer Genetic Testing. International Journal of Environmental Research and Public Health 18:16, pages 8330.
Crossref
Kurt D. Christensen, Megan Bell, Carrie L. B. Zawatsky, Lauren N. Galbraith, Robert C. Green, Allison M. Hutchinson, Leila Jamal, Jessica L. LeBlanc, Jennifer R. Leonhard, Michelle Moore, Lisa Mullineaux, Natasha Petry, Dylan M. Platt, Sherin Shaaban, April Schultz, Bethany D. Tucker, Joel Van Heukelom, Elizabeth Wheeler, Emilie S. Zoltick & Catherine Hajek. (2021) Precision Population Medicine in Primary Care: The Sanford Chip Experience. Frontiers in Genetics 12.
Crossref
Erin Turbitt, Megan C. Roberts, Jennifer M. Taber, Erika A. Waters, Timothy S. McNeel, Barbara B. Biesecker & William M.P. Klein. (2019) Genetic counseling, genetic testing, and risk perceptions for breast and colorectal cancer: Results from the 2015 National Health Interview Survey. Preventive Medicine 123, pages 12-19.
Crossref
Laura V. Milko, Christine Rini, Megan A. Lewis, Rita M. Butterfield, Feng-Chang Lin, Ryan S. Paquin, Bradford C. Powell, Myra I. Roche, Katherine J. Souris, Donald B. BaileyJrJr, Jonathan S. Berg & Cynthia M. Powell. (2018) Evaluating parents’ decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized controlled trial protocol. Trials 19:1.
Crossref