Evidence map›Paper›PMID 32082363›Full record

ArticleFrontiers in genetics2019

Insertion of LINE-1 Retrotransposon Inducing Exon Inversion Causes a Rotor Syndrome Phenotype.

Donghu Zhou, Saiping Qi, Wei Zhang, Lina Wu, Anjian Xu, Xiaojin Li, Bei Zhang, Yanmeng Li, Siyu Jia, Hejing Wang and 4 more

Abstract 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. [Expert consensus on the diagnosis and therapy of inherited hyperbilirubinemia (version 2025)].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2025
    Article
  4. Article
  5. RecurrentFrontiers in medicine · 2025
    Article
  6. 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

14 authors.

Donghu ZhouExperimental Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Saiping QiExperimental Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Wei ZhangClinical Research Center for Rare Liver Diseases, Capital Medical University, Beijing, China.
Lina WuClinical Research Center for Rare Liver Diseases, Capital Medical University, Beijing, China.
Anjian XuExperimental Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Xiaojin LiExperimental Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Bei ZhangExperimental Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Yanmeng LiExperimental Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Siyu JiaExperimental Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Hejing WangExperimental Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Jidong JiaClinical Research Center for Rare Liver Diseases, Capital Medical University, Beijing, China.
Xiaojuan OuClinical Research Center for Rare Liver Diseases, Capital Medical University, Beijing, China.
Jian HuangExperimental Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Hong YouExperimental Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rotor syndrome, a rare autosomal-recessive genetic disorder characterized by conjugated hyperbilirubinemia, is caused by biallelic pathogenic variants in both

Indexed as

LINE-1 retrotransposonmutationRotor syndromeSLCO1B1SLCO1B3

Identifiers

PMID32082363
PMCPMC7005217

What OpenQuestion holds

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LicenceCC BY
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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.