Evidence map›Paper›PMID 36157696›Full record

ArticleCase reports in oncology

Detection of BRCA1 Pathogenic Variant in a 24-Year-Old Endometrial Cancer Patient: Risks of Several Hereditary Tumor Syndromes Assessed Using Germline Multigene Panel Testing.

Xiaofei Wang, Keika Kaneko, Hiromi Arakawa, Eri Habano, Makiko Omi, Eri Nakashima, Hiroshi Kawachi, Akiko Tonooka, Kohei Omatsu, Hidetaka Nomura and 5 more

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Case reports in oncology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

15 authors.

Xiaofei WangDepartment of Medical Oncology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Keika KanekoDepartment of Clinical Genetics, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Hiromi ArakawaDepartment of Clinical Genetics, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Eri HabanoDepartment of Clinical Genetics, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Makiko OmiDepartment of Gynecology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Eri NakashimaDepartment of Breast Surgery, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Hiroshi KawachiDivision of Pathology, Cancer Institute, Japanese Foundation for Cancer Research, Tokyo, Japan.
Akiko TonookaDivision of Pathology, Cancer Institute, Japanese Foundation for Cancer Research, Tokyo, Japan.
Kohei OmatsuDepartment of Gynecology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Hidetaka NomuraDepartment of Gynecology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Mayu YunokawaDepartment of Gynecology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Hiroyuki KanaoDepartment of Gynecology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Shunji TakahashiDepartment of Medical Oncology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Takeshi NakajimaDepartment of Clinical Genetics, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Arisa UekiDepartment of Clinical Genetics, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A 24-year-old woman suspected of Lynch syndrome was found to carry a

Indexed as

BRCA1cancer syndromeEndometrial cancerHereditary breast and ovarianLynch syndromeMultigene panel testing

Identifiers

PMID36157696
PMCPMC9459637

What OpenQuestion holds

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Registered trials

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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.