Featured
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Viewpoint |
Should testing for mosaic genome-wide paternal uniparental disomy in Beckwith-Wiedemann spectrum (BWSp) be implemented in diagnostic testing?
- Saskia M. Maas
- , Izabela M. Krzyzewska
- & Jet Bliek
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Article |
Patient-reported anticipated barriers and benefits to sharing cancer genetic risk information with family members
- Kelsey Stuttgen Finn
- , Joel Pacyna
- & Richard Sharp
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Article
| Open AccessGuidelines for the Li–Fraumeni and heritable TP53-related cancer syndromes
- Thierry Frebourg
- , Svetlana Bajalica Lagercrantz
- & Marja Hietala
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Viewpoint
| Open Access
“Patient Journeys”: improving care by patient involvement
- Matt Bolz-Johnson
- , Jelena Meek
- & Nicoline Hoogerbrugge
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Article |
Differences in attitudes toward genetic testing among the public, patients, and health-care professionals in Korea
- Heesang Eum
- , Mangyeong Lee
- & Yoon Jung Chang
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Brief Communication |
Risk of multiple pancreatic cancers in CDKN2A-p16-Leiden mutation carriers
- Isaura Ibrahim
- , Babs G. Sibinga Mulder
- & Hans F. A. Vasen
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Correspondence |
Revisiting Wilms tumour surveillance in Beckwith–Wiedemann syndrome with IC2 methylation loss, reply
- Frédéric Brioude
- , Raoul Hennekam
- & Irene Netchine
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Article |
Comparison of the efficiency of colorectal cancer screening programs based on age and genetic risk for reduction of colorectal cancer mortality
- Oliver Stanesby
- & Mark Jenkins
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Review
| Open Access
Finding all BRCA pathogenic mutation carriers: best practice models
- Nicoline Hoogerbrugge
- & Marjolijn CJ Jongmans
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Review
| Open Access
New challenges for BRCA testing: a view from the diagnostic laboratory
- Andrew J Wallace
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Article |
APC gene hypermethylation and prostate cancer: a systematic review and meta-analysis
- Yang Chen
- , Jie Li
- & Yanling Hu
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Article |
MLH1 promoter hypermethylation in the analytical algorithm of Lynch syndrome: a cost-effectiveness study
- Mireia Gausachs
- , Pilar Mur
- & Gabriel Capellá
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Article |
Breast and ovarian cancer screening of non-carriers from BRCA1/2 mutation-positive families: 2-year follow-up of cohorts from France and Quebec
- Michel Dorval
- , Catherine Noguès
- & Claire Julian-Reynier
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Short Report |
Cervix smear abnormalities: linking pathology data in female twins, their mothers and sisters
- Jacqueline M Vink
- , Folkert J van Kemenade
- & Dorret I Boomsma
Identification of people with Lynch syndrome from those presenting with colorectal cancer in England: baseline analysis of the diagnostic pathway