Evidence map›Paper›PMID 37780997›Full record

ArticleThe Yale journal of biology and medicine2023

A Recurrent Mutation in Growth Hormone Receptor (

Rana Muhammad Kamran Shabbir, Gökhan Nalbant, Qamar Zaman, Aslıhan Tolun, Sajid Malik, Sara Mumtaz

Open access · diamondAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in The Yale journal of biology and medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Review
  2. [Growth plate regulation and short stature: mechanistic insights and therapeutic advances].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
    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 4 institutions in 2 countries.

Rana Muhammad Kamran ShabbirDepartment of Zoology, Division of Science and Technology, University of Education, Lahore, Pakistan.
Gökhan NalbantDepartment of Molecular Biology and Genetics, MOBGAM, Istanbul Technical University, Istanbul, Türkiye.
Qamar ZamanHuman Genetics Program, Department of Zoology, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.
Aslıhan TolunDepartment of Molecular Biology and Genetics, MOBGAM, Istanbul Technical University, Istanbul, Türkiye.
Sajid MalikHuman Genetics Program, Department of Zoology, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.
Sara MumtazDepartment of Biological Sciences, National University of Medical Sciences, Rawalpindi, Pakistan.
Istanbul Technical University · TRQuaid-i-Azam University · PKNational University of Medical Sciences · PKUniversity of Okara · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Laron syndrome (LS) is a rare autosomal recessively segregating disorder of severe short stature. The condition is characterized by short limbs, delayed puberty, hypoglycemia in infancy, and obesity. Mutations in growth hormone receptor (

Indexed as

Laron SyndromePuberty, DelayedHumansMutationObesityPakistanReceptors, SomatotropinReceptors, Somatotropindelayed pubertyfacial dysmorphismgrowth hormone insensitivityshort staturetruncal obesitywidely-spaced breasts

Identifiers

PMID37780997
PMCPMC10524814
OpenAlexW4387241525

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.