Evidence map›Paper›PMID 19629752›Full record

ArticleFamilial cancer2009

Identification of a de novo BRCA1 mutation in a woman with early onset bilateral breast cancer.

Emma Edwards, Catharina Yearwood, Julie Sillibourne, Diana Baralle, Diana Eccles

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in Familial cancer, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 16% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Novel De NovoInternational journal of molecular sciences · 2025
    Article
  3. Article
  4. A New de novoThe application of clinical genetics · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. The importance of BRCA1 and BRCA2 genes mutations in breast cancer development.Medical journal of the Islamic Republic of Iran · 2016
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 2 countries.

Emma EdwardsWessex Clinical Genetics Service, Princess Anne Hospital, Level G, Southampton, Hampshire SO16 5YA, UK. Emma.Edwards@suht.swest.nhs.uk
Catharina Yearwood
Julie Sillibourne
Diana Baralle
Diana Eccles
Princess Anne Hospital · GBSalisbury University · USSt George's Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

De novo mutations are rarely reported in BRCA1 and BRCA2. We report a proven BRCA1 de novo mutation in a woman diagnosed with young onset bilateral breast cancer with a limited family history.

Indexed as

Genes, BRCA1AdultAge of OnsetBRCA1 ProteinBreast NeoplasmsCarcinoma, Ductal, BreastFemaleHumansMutationPedigreeBRCA1 Protein

Identifiers

PMID19629752
OpenAlexW2054954150

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.