Evidence map›Paper›PMID 33477375›Full record

ArticleInternational journal of molecular sciences2021

A Case Report of Germline Compound Heterozygous Mutations in the

Ava Kwong, Cecilia Y S Ho, Vivian Y Shin, Chun Hang Au, Tsun Leung Chan, Edmond S K Ma

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Biallelic GermlineInternational journal of molecular sciences · 2024
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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

6 authors at 2 institutions in 2 countries.

Ava KwongDepartment of Surgery, The University of Hong Kong and University of Hong Kong-Shenzhen Hospital, Hong Kong, China.
Cecilia Y S HoDepartment of Molecular Pathology, Hong Kong Sanatorium & Hospital, Hong Kong, China.
Vivian Y ShinDepartment of Surgery, The University of Hong Kong and University of Hong Kong-Shenzhen Hospital, Hong Kong, China.
Chun Hang AuDepartment of Molecular Pathology, Hong Kong Sanatorium & Hospital, Hong Kong, China.ORCID 0000-0002-1707-0991
Tsun Leung ChanHong Kong Hereditary Breast Cancer Family Registry, Hong Kong, China.
Edmond S K MaHong Kong Hereditary Breast Cancer Family Registry, Hong Kong, China.ORCID 0000-0002-1259-2205
Hong Kong Sanatorium and Hospital · HKUniversity of Hong Kong - Shenzhen Hospital · CN

Funding

Asian Fund for Cancer Research NilDr. Ellen Li Charitable Foundation NilHealth and Medical Research Fund 03143406Hong Kong Hereditary Breast Cancer Family Registry NilKerry Kuok Foundation Nil
6 · The paper itself

Abstract

The germline carrier of the

Indexed as

BRCA1 ProteinBreast NeoplasmsFanconi AnemiaFemaleGenes, BRCA1Genetic Predisposition to DiseaseGerm CellsGerm-Line MutationHeterozygoteHumansMiddle AgedOvarian NeoplasmsPedigreeBRCA1 ProteinBRCA1 protein, humanChinesecompound heterozygous mutationsFanconi anemiahereditary breast cancer

Identifiers

PMID33477375
PMCPMC7830606
OpenAlexW3123760077

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.