Evidence map›Paper›PMID 24566764›Full record

ArticleFamilial cancer2014

Large genomic rearrangement of BRCA1 and BRCA2 genes in familial breast cancer patients in Korea.

Ja Young Cho, Dae-Yeon Cho, Sei Hyun Ahn, Su-Youn Choi, Inkyung Shin, Hyun Gyu Park, Jong Won Lee, Hee Jeong Kim, Jong Han Yu, Beom Seok Ko and 2 more

Abstract read
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In one paragraph

Article in Familial cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Journal of gynecologic oncology · 2018
    Article
  4. Article
  5. 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

12 authors at 4 institutions in 1 country.

Ja Young ChoDivision of Breast and Endocrine Surgery, Department of Surgery College of Medicine, University of Ulsan, Asan Medical Center, 388-1 Pungnap-dong, Songpa-gu, Seoul, 138-736, Korea.
Dae-Yeon Cho
Sei Hyun Ahn
Su-Youn Choi
Inkyung Shin
Hyun Gyu Park
Jong Won Lee
Hee Jeong Kim
Jong Han Yu
Beom Seok Ko
Bo Kyung Ku
Byung Ho Son
University of Ulsan · KRAsan Medical Center · KRCrystalGenomics (South Korea) · KRKorea Advanced Institute of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We screened large genomic rearrangements of the BRCA1 and BRCA2 genes in Korean, familial breast cancer patients. Multiplex ligation-dependent probe amplification assay was used to identify BRCA1 and BRCA2 genomic rearrangements in 226 Korean familial breast cancer patients with risk factors for BRCA1 and BRCA2 mutations, who previously tested negative for point mutations in the two genes. We identified only one large deletion (c.4186-1593_4676-1465del) in BRCA1. No large rearrangements were found in BRCA2. Our result indicates that large genomic rearrangement in the BRCA1 and BRCA2 genes does not seem like a major determinant of breast cancer susceptibility in the Korean population. A large-scale study needs to validate our result in Korea.

Indexed as

Gene RearrangementGenes, BRCA1Genes, BRCA2Sequence DeletionAsian PeopleBase SequenceBreast NeoplasmsExonsFemaleGenetic Predisposition to DiseaseHumansMultiplex Polymerase Chain ReactionOvarian NeoplasmsRepublic of KoreaRetrospective Studies

Identifiers

PMID24566764
OpenAlexW2051422299

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.