Evidence map›Paper›PMID 32884827›Full record

ArticleHuman genome variation2020

Early-onset breast cancer in a woman with a germline mobile element insertion resulting in

Natalie Deuitch, Shao-Tzu Li, Eliza Courtney, Tarryn Shaw, Rebecca Dent, Veronique Tan, Lauren Yackowski, Rebecca Torene, Windy Berkofsky-Fessler, Joanne Ngeow

Open access · goldAbstract read
In one paragraph

Article in Human genome variation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. A NovelHuman mutation · 2023
    Article
  4. Mechanisms of disease-associated SINE-VNTR-Alus.Experimental biology and medicine (Maywood, N.J.) · 2022
    Review
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

10 authors at 3 institutions in 2 countries.

Natalie DeuitchCancer Genetics Service, Division of Medical Oncology, National Cancer Centre, Singapore, Singapore.ORCID 0000-0002-0146-1162
Shao-Tzu LiCancer Genetics Service, Division of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Eliza CourtneyCancer Genetics Service, Division of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Tarryn ShawCancer Genetics Service, Division of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Rebecca DentDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Veronique TanDivision of Breast Surgical Oncology, National Cancer Centre, Singapore, Singapore.
Lauren YackowskiHereditary Cancer Program, GeneDx, Gaithersburg, MD USA.
Rebecca ToreneHereditary Cancer Program, GeneDx, Gaithersburg, MD USA.
Windy Berkofsky-FesslerHereditary Cancer Program, GeneDx, Gaithersburg, MD USA.
Joanne NgeowCancer Genetics Service, Division of Medical Oncology, National Cancer Centre, Singapore, Singapore.
National Cancer Centre Singapore · SGHereditary Disease Foundation · USNanyang Technological University · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mobile element insertions (MEIs) contribute to genomic diversity, but they can be responsible for human disease in some cases. Initial clinical testing (

Indexed as

Cancer genomicsNext-generation sequencing

Identifiers

PMID32884827
PMCPMC7447638
OpenAlexW3081077495

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.