Lessons learned from genetic testing.

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

Who cites it

6 citing papers in PubMed.

1. Cost effectiveness of the cancer prevention program for carriers of the BRCA1/2 mutation.Revista de saude publica · 2018
   Article
2. Pre-test genetic counseling services for hereditary breast and ovarian cancer delivered by non-genetics professionals in the state of Florida.Clinical genetics · 2015
   Article
3. A statewide survey of practitioners to assess knowledge and clinical practices regarding hereditary breast and ovarian cancer.Genetic testing and molecular biomarkers · 2013
   Article
4. Genetic risk assessments in individuals at high risk for inherited breast cancer in the breast oncology care setting.Cancer control : journal of the Moffitt Cancer Center · 2012
   Review
5. How the electronic health record will change the future of health care.The Yale journal of biology and medicine · 2012
   Article
6. Genetics, genomics, and cancer risk assessment: State of the Art and Future Directions in the Era of Personalized Medicine.CA: a cancer journal for clinicians
   Review

Corrections and comments

• Comment on
  Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality.2010

Authors and funding

2 authors.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

Indexed as