Evidence map›Paper›PMID 38075079›Full record

ArticleFrontiers in endocrinology2023

Sunita M C De Sousa, Angeline Shen, Christopher J Yates, Roderick Clifton-Bligh, Stephen Santoreneos, James King, John Toubia, Giampaolo Trivellin, Andrea G Lania, Constantine A Stratakis and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2023. 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
2.4field-weighted citation impact, top 10% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Genetics of familial acromegaly and pituitary gigantism.The Journal of clinical endocrinology and metabolism · 2026
    Review
  3. Article
  4. Article
  5. 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

12 authors at 8 institutions in 4 countries.

Sunita M C De SousaEndocrine & Metabolic Unit, Royal Adelaide Hospital, Adelaide, SA, Australia.
Angeline ShenDepartment of Diabetes and Endocrinology, Royal Melbourne Hospital, Melbourne, VIC, Australia.
Christopher J YatesDepartment of Diabetes and Endocrinology, Royal Melbourne Hospital, Melbourne, VIC, Australia.
Roderick Clifton-BlighCancer Genetics Laboratory, Kolling Institute, Royal North Shore Hospital, Sydney, NSW, Australia.
Stephen SantoreneosDepartment of Neurosurgery, Royal Adelaide Hospital, Adelaide, SA, Australia.
James KingDepartment of Surgery, University of Melbourne, Melbourne, VIC, Australia.
John ToubiaACRF Cancer Genomics Facility, Centre for Cancer Biology, University of South Australia and SA Pathology, Adelaide, SA, Australia.
Giampaolo TrivellinDepartment of Biomedical Sciences, Humanitas University, Milan, Italy.
Andrea G LaniaDepartment of Biomedical Sciences, Humanitas University, Milan, Italy.
Constantine A StratakisSection on Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Bethesda, MD, United States.
David J TorpyEndocrine & Metabolic Unit, Royal Adelaide Hospital, Adelaide, SA, Australia.
Hamish S ScottAdelaide Medical School, University of Adelaide, Adelaide, SA, Australia.
Humanitas University · ITThe Royal Melbourne Hospital · AUThe University of Adelaide · AUUniversity of South Australia · AUNational Institutes of Health · USRoyal Adelaide Hospital · AURoyal North Shore Hospital · AUThe University of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Germline loss-of-function variants in Methods: We performed exome sequencing of germline and tumour DNA from 29 individuals with functioning pituitary adenomas (12 prolactinomas, 10 thyrotrophinomas, 7 cyclical Cushing's disease). An unfiltered analysis was undertaken of all Results: We identified five coding, non-synonymous Conclusion: This is the second study to demonstrate a high yield of suspected loss-of-function, predominantly germline,

Indexed as

ACTH-Secreting Pituitary AdenomaAdenomaPituitary ACTH HypersecretionPituitary NeoplasmsProlactinomaAmidine-LyasesHumansMixed Function OxygenasesMultienzyme ComplexesAmidine-LyasesMixed Function OxygenasesMultienzyme ComplexesPAM protein, humanpeptidylglycine monooxygenaseCushing’s diseasepeptidylglycine α-amidating monooxygenasepituitary adenomasprolactinomathyrotrophinomawhole exome sequencing

Identifiers

PMID38075079
PMCPMC10710132
OpenAlexW4388939884

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.