Evidence map›Paper›PMID 33776926›Full record

ReviewFrontiers in endocrinology2021

Molecular Genetic and Genomic Alterations in Cushing's Syndrome and Primary Aldosteronism.

Crystal D C Kamilaris, Constantine A Stratakis, Fady Hannah-Shmouni

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

14 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Review
  3. Unrecognized primary aldosteronism may confound outcomes in adrenal Cushing's syndrome.Therapeutic advances in endocrinology and metabolism · 2026
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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

3 authors at 2 institutions in 1 country.

Crystal D C KamilarisSection on Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD), National Institutes of Health (NIH), Bethesda, MD, United States.
Constantine A StratakisSection on Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD), National Institutes of Health (NIH), Bethesda, MD, United States.
Fady Hannah-ShmouniSection on Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD), National Institutes of Health (NIH), Bethesda, MD, United States.
National Institutes of Health · USEunice Kennedy Shriver National Institute of Child Health and Human Development · US

Funding

Molecular Genetics of Endocrine Tumors and Related DisordersZIAHD008920 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI STRATAKIS, CONSTANTINE A. · 2012 to 2021
$25.8M
Endocrine-immune reproductive system interactionsZ01HD008720 · NICHD · CHILD HEALTH AND HUMAN DEVELOPMENT · PI CHROUSOS, GEORGE P · 2000 to 2000
–
Intramural NIH HHS Z01 HD008720
6 · The paper itself

Abstract

The genetic alterations that cause the development of glucocorticoid and/or mineralocorticoid producing benign adrenocortical tumors and hyperplasias have largely been elucidated over the past two decades through advances in genomics. In benign aldosterone-producing adrenocortical tumors and hyperplasias, alteration of intracellular calcium signaling has been found to be significant in aldosterone hypersecretion, with causative defects including those in

Indexed as

Adrenal Cortex NeoplasmsAdrenocortical AdenomaCalcium Channels, L-TypeCushing SyndromeCyclic AMP-Dependent Protein Kinase Catalytic SubunitsG Protein-Coupled Inwardly-Rectifying Potassium ChannelsHumansHyperaldosteronismSodium-Potassium-Exchanging ATPaseATP1A1 protein, humanCACNA1D protein, humanCalcium Channels, L-TypeCyclic AMP-Dependent Protein Kinase Catalytic SubunitsG Protein-Coupled Inwardly-Rectifying Potassium ChannelsKCNJ5 protein, humanPRKACA protein, humanPRKACB protein, humanSodium-Potassium-Exchanging ATPaseadrenocortical adenomaadrenocortical hyperplasiaCushing’s syndromegeneticsprimary aldosteronism

Identifiers

PMID33776926
PMCPMC7994620
OpenAlexW3139517745

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.