Evidence map›Paper›PMID 33437386›Full record

ArticleAmerican journal of translational research2020

Analysis of mutations in six Chinese families with autosomal dominant polycystic kidney disease.

Hanlu Wang, Sen Dai, Jianhui Zhang, Yi Li, Yumian Gan, Tao Lu, Yaobin Zhu, Jiabin Wu, Ning Lin, Faqiang Tang and 1 more

Abstract read
In one paragraph

Article in American journal of translational research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Hanlu WangShengli Clinical Medical College of Fujian Medical University Fuzhou 350001, China.
Sen DaiShengli Clinical Medical College of Fujian Medical University Fuzhou 350001, China.
Jianhui ZhangShengli Clinical Medical College of Fujian Medical University Fuzhou 350001, China.
Yi LiDepartment of Pharmaceutics, School of Pharmacy, China Pharmaceutical University Nanjing 210009, China.
Yumian GanShengli Clinical Medical College of Fujian Medical University Fuzhou 350001, China.
Tao LuShengli Clinical Medical College of Fujian Medical University Fuzhou 350001, China.
Yaobin ZhuDepartment of Traditional Chinese Medicine, The First Affiliated Hospital, Fujian Medical University Fuzhou 350001, China.
Jiabin WuShengli Clinical Medical College of Fujian Medical University Fuzhou 350001, China.
Ning LinShengli Clinical Medical College of Fujian Medical University Fuzhou 350001, China.
Faqiang TangShengli Clinical Medical College of Fujian Medical University Fuzhou 350001, China.
Jiewei LuoShengli Clinical Medical College of Fujian Medical University Fuzhou 350001, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autosomal dominant polycystic kidney disease (ADPKD) is the common hereditary kidney disease, resulting from mutations in polycystic kidney disease 1 (

Indexed as

Autosomal dominant polycystic kidney diseasefamily researchgene mutationpolycystic kidney disease 1polycystic kidney disease 2

Identifiers

PMID33437386
PMCPMC7791523

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.