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GNAS, PDE4D, and PRKAR1A Mutations and GNAS Methylation Changes Are Not a Common Cause of Isolated Early-Onset Severe Obesity Among Finnish Children

Frontiers in Pediatrics(2020)10.3389/fped.2020.00145Source: DataRank Database

GNAS, PDE4D, and PRKAR1A Mutations and GNAS Methylation Changes Are Not a Common Cause of Isolated Early-Onset Severe Obesity Among Finnish Children is a research paper published in Frontiers in Pediatrics (2020). On theSindex it has a DataRank of 0. It has been cited 9 times.

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Open Access9 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (14 grants)Impact (FWCI 0.64)OA: goldTopics (23)IDs (PubMed, PMC, OpenAlex)Annotations (3)SDGs (3)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (7)

Minna Pekkinen ORCID,Monica Reyes,Taina Mustila,Heli Viljakainen ORCID,Harald Jüppner ORCID

Live enrichment

PubMed:32318528 PMC:PMC7155765 OpenAlex:https://openalex.org/W3015851931

NIDDK NIH HHS

Grant: R01 DK046718

Swedish Research Council

Grant: unidentified

unidentified

National Institutes of Health

Grant: 2R37DK046718-10

Molecular Definition of Pseudohypoparathyroidism

Päivikki ja Sakari Sohlbergin Säätiö

Stiftelsen Dorothea Olivia, Karl Walter och Jarl Walter Perkléns Minne

Academy of Finland

Sigrid Juséliuksen Säätiö

Vetenskapsrådet

Novo Nordisk Fonden

Lastentautien Tutkimussäätiö

Samfundet Folkhälsan

Helsingin Yliopisto

Helsingin ja Uudenmaan Sairaanhoitopiiri

National Institutes of Health

FWCI

0.64

Citation Percentile

0.7%

Citation Trend

2021

2022

2023

2024

2025

goldLicense: cc-by

journalhttps://doi.org/10.3389/fped.2020.00145

publisherhttps://doi.org/10.3389/fped.2020.00145

publisherhttps://www.frontiersin.org/article/10.3389/fped.2020.00145/full

repositoryhttps://pubmed.ncbi.nlm.nih.gov/32318528

repositoryhttps://doaj.org/article/abe3ed928a8744ada66ea43bbba7095f

Fields of Study

Genetic Syndromes and ImprintingCongenital heart defects researchGenomics and Rare Diseases0301 basic medicine03 medical and health sciences

Keywords

GNAS complex locusPseudohypoparathyroidismMultiplex ligation-dependent probe amplificationGeneticsEndocrinologyInternal medicineMedicineEpigeneticsExonBiologyGeneParathyroid hormoneGnasAcrodysostosisG Protein-camp-signalingChildhood-onset ObesityPediatricsRJ1-570

Sustainable Development Goals

SDG 2: 2. Zero hungerSDG 3: 3. Good healthSDG 0: Good health and well-being

GNAS, PDE4D, and PRKAR1A Mutations and GNAS Methylation Changes Are Not a Common Cause of Isolated Early-Onset Severe Obesity Among Finnish Children

FAIR Checklist

Authors (7)

Funding (14 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)