Appraising Organised Screening Programmes for Testing for Genetic Susceptibility to Cancer

Overview

Journal BMJ

Specialty General Medicine

Date 2001 May 12

PMID 11348918

Citations 10

Authors

V Goel

Affiliations

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Citing Articles

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Neonatal and carrier screening for rare diseases: how innovation challenges screening criteria worldwide.

Cornel M, Rigter T, Jansen M, Henneman L J Community Genet. 2020; 12(2):257-265.

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Autonomy Challenges in Epigenetic Risk-Stratified Cancer Screening: How Can Patient Decision Aids Support Informed Consent?.

Alblas M, Schermer M, Vergouwe Y, Bolt I J Pers Med. 2019; 9(1).

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How is genetic testing evaluated? A systematic review of the literature.

Pitini E, De Vito C, Marzuillo C, DAndrea E, Rosso A, Federici A Eur J Hum Genet. 2018; 26(5):605-615.

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Population screening for BRCA1/BRCA2 mutations: lessons from qualitative analysis of the screening experience.

Lieberman S, Lahad A, Tomer A, Cohen C, Levy-Lahad E, Raz A Genet Med. 2016; 19(6):628-634.

PMID: 27906198 DOI: 10.1038/gim.2016.175.

References

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Burke W, Petersen G, Lynch P, Botkin J, Daly M, Garber J . Recommendations for follow-up care of individuals with an inherited predisposition to cancer. I. Hereditary nonpolyposis colon cancer. Cancer Genetics Studies Consortium. JAMA. 1997; 277(11):915-9. View