Evidence map›Paper›PMID 38952179›Full record

ArticleJournal of clinical research in pediatric endocrinology2026

Hereditary Severe Insulin-resistance Syndrome and Acanthosis Nigricans Caused by Novel Mutations in the

Chen Chongyang, Zhao Yangting, Li Kai, Lv Xiaoyu, Wang Yawen, Zhen Donghu, Fu Songbo, Ma Lihua, Zhou Liyuan, Liu Jingfang

Abstract read
In one paragraph

Article in Journal of clinical research in pediatric endocrinology, 2026. 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

10 authors.

Chen ChongyangLanzhou University The First Clinical Medical College, Lanzhou, Gansu, ChinaORCID 0000-0002-3370-5408
Zhao YangtingLanzhou University The First Clinical Medical College, Lanzhou, Gansu, ChinaORCID 0009-0004-8267-5999
Li KaiLanzhou University The First Clinical Medical College, Lanzhou, Gansu, ChinaORCID 0009-0004-1744-676X
Lv XiaoyuLanzhou University The First Clinical Medical College, Lanzhou, Gansu, ChinaORCID 0000-0003-1491-6506
Wang YawenLanzhou University The First Clinical Medical College, Lanzhou, Gansu, ChinaORCID 0009-0007-2667-0941
Zhen DonghuLanzhou University The First Clinical Medical College, Lanzhou, Gansu, ChinaORCID 0000-0001-7535-0695
Fu SongboLanzhou University The First Clinical Medical College, Lanzhou, Gansu, ChinaORCID 0000-0003-0611-6015
Ma LihuaThe First Hospital of Lanzhou University, Department of Endocrinology, Lanzhou, Gansu, ChinaORCID 0000-0002-1735-6631
Zhou LiyuanThe First Hospital of Lanzhou University, Department of Endocrinology, Lanzhou, Gansu, ChinaORCID 0009-0002-6387-1308
Liu JingfangLanzhou University The First Clinical Medical College, Lanzhou, Gansu, ChinaORCID 0000-0003-1908-4454

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Most cases of hereditary severe insulin-resistance syndrome (H-SIRS) are linked to mutations in the insulin receptor (

Indexed as

Acanthosis NigricansAntigens, CDInsulin ResistanceMutationReceptor, InsulinChildFemaleHumansHyperinsulinismAntigens, CDINSR protein, humanReceptor, Insulinacanthosis nigrihyperandrogenismhyperinsulinemiaimpaired glucose regulationInsulin receptorinsulin resistance

Identifiers

PMID38952179
PMCPMC13325959

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.