Evidence map›Paper›PMID 31620170›Full record

ArticleFrontiers in genetics2019

Frequent Mutations of VHL Gene and the Clinical Phenotypes in the Largest Chinese Cohort With Von Hippel-Lindau Disease.

Baoan Hong, Kaifang Ma, Jingcheng Zhou, Jiufeng Zhang, Jiangyi Wang, Shengjie Liu, Zhongyuan Zhang, Lin Cai, Ning Zhang, Kan Gong

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 3 pooled it
2.1field-weighted citation impact, top 13% 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

29 citing papers in PubMed, 3 syntheses or guidelines pooled it, 46 citations in OpenAlex.

  1. Pooled it
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  4. Article
  5. Review
  6. Multiplatform curation in the development of ACMG/AMP specifications for Von Hippel-Lindau (VHL) disease.Genetics in medicine : official journal of the American College of Medical Genetics · 2026
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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

10 authors at 4 institutions in 1 country.

Baoan HongDepartment of Urology, Peking University First Hospital, Beijing, China.
Kaifang MaDepartment of Urology, Peking University First Hospital, Beijing, China.
Jingcheng ZhouDepartment of Urology, Peking University First Hospital, Beijing, China.
Jiufeng ZhangDepartment of Urology, Peking University First Hospital, Beijing, China.
Jiangyi WangDepartment of Urology, Peking University First Hospital, Beijing, China.
Shengjie LiuDepartment of Urology, Peking University First Hospital, Beijing, China.
Zhongyuan ZhangDepartment of Urology, Peking University First Hospital, Beijing, China.
Lin CaiDepartment of Urology, Peking University First Hospital, Beijing, China.
Ning ZhangDepartment of Urology, Beijing Cancer Hospital, Beijing, China.
Kan GongDepartment of Urology, Peking University First Hospital, Beijing, China.
Beijing Chest Hospital · CNPeking University First Hospital · CNPeking University · CNPeking University Cancer Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Von Hippel-Lindau (VHL) disease is a rare autosomal-dominant inherited tumor syndrome. We aimed to analyze the correlations between frequent

Indexed as

genotype–phenotype correlationonset agesurvivalVHL mutationvon Hippel–Lindau disease

Identifiers

PMID31620170
PMCPMC6759728
OpenAlexW2969675173

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.