Evidence map›Paper›PMID 30444213›Full record

ArticleJournal of clinical research in pediatric endocrinology2019

Novel Compound Heterozygous Variants in the

Mei Yan, Julaiti Dilihuma, Yanfei Luo, Baoerhan Reyilanmu, Yiping Shen, Maimaiti Mireguli

Open access · goldAbstract readCase Reports
In one paragraph

Article in Journal of clinical research in pediatric endocrinology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

3 citing papers in PubMed, 34 citations in OpenAlex.

  1. Genetic variants (LhcgrBiology of sex differences · 2025
    Article
  2. Article
  3. Review
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.

Mei YanFirst Affiliated Hospital of Xinjiang Medical University, Department of Pediatrics, Xinjiang Uygur Autonomous Region, ChinaORCID 0000-0002-6559-3770
Julaiti DilihumaFirst Affiliated Hospital of Xinjiang Medical University, Department of Pediatrics, Xinjiang Uygur Autonomous Region, ChinaORCID 0000-0001-5522-0535
Yanfei LuoFirst Affiliated Hospital of Xinjiang Medical University, Department of Pediatrics, Xinjiang Uygur Autonomous Region, ChinaORCID 0000-0002-8739-3876
Baoerhan ReyilanmuFirst Affiliated Hospital of Xinjiang Medical University, Department of Pediatrics, Xinjiang Uygur Autonomous Region, ChinaORCID 0000-0002-1664-9918
Yiping ShenBoston Children’s Hospital Harvard Medical School, Department of Genetics and Genomics, Massachusetts, United StatesORCID 0000-0001-5820-0839
Maimaiti MireguliFirst Affiliated Hospital of Xinjiang Medical University, Department of Pediatrics, Xinjiang Uygur Autonomous Region, ChinaORCID 0000-0003-4800-2462
Xinjiang Medical University · CNBoston Children's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The

Indexed as

MutationChild, PreschoolDisorder of Sex Development, 46,XYFemaleGenitalia, FemaleHumansMalePenisPrognosisReceptors, LHTestisLHCGR protein, humanReceptors, LHDisorder of sexual differentiationLeydig cell hypoplasiaLHCGR genenovel variants

Identifiers

PMID30444213
PMCPMC6571543
OpenAlexW2900846896

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.