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Paper · 36537518

ISPAD Clinical Practice Consensus Guidelines 2022: The diagnosis and management of monogenic diabetes in children and adolescents.

Greeley SAW and 10 others. Pediatr Diabetes, 2022. Cited by 135 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. ISPAD Clinical Practice Consensus Guidelines 2022: The diagnosis and management of monogenic diabetes in children and adolescents. Papers, record 36537518. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/36537518

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
ISPAD Clinical Practice Consensus Guidelines 2022: The diagnosis and management of monogenic diabetes in children and adolescents.
PubMed
Journal
Pediatr Diabetes
PubMed
Year
2022
PubMed
Publication types
Journal Article
PubMed
Citations, by iCite
135
iCite
Relative citation ratio, by iCite
11.9
iCite
Revised in PubMed
2024-03-05
PubMed

Authors11

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Greeley SAWSiri Atma W
2Polak MMichel
3Njølstad PRPål R
4Barbetti FFabriziohttps://orcid.org/0000-0003-4687-980X
5Williams RRachel
6Castano LLuis
7Raile KKlemens
8Chi DVDung Vu
9Habeb AAbdelhadi
10Hattersley ATAndrew T

1 to 10 of 11Source PubMed

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Topics6

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
Diabetes Mellitus, Type 2Major topic
Child
Adolescent
Humans
Mutation
Consensus

Source PubMed

Grants1

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

Grant, as the record writes itAgencyCountryNIH projectStated by
R01 DK104942NIDDK NIH HHSUnited StatesR01DK104942PubMed

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References287

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
115,028,826Acquired and inherited lipodystrophies.N Engl J Med2004https://conductscience.org/library/papers/15028826PubMed
217,668,386Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effects.Am J Hum Genet2007https://conductscience.org/library/papers/17668386PubMed
312,471,198Transient neonatal diabetes, a disorder of imprinting.J Med Genet2002https://conductscience.org/library/papers/12471198PubMed
426,587,058A new compound heterozygosis for inactivating mutations in the glucokinase gene as cause of permanent neonatal diabetes mellitus (PNDM) in double-first cousins.Diabetol Metab Syndr2015https://conductscience.org/library/papers/26587058PubMed
529,233,499The role of the carboxyl ester lipase (CEL) gene in pancreatic disease.Pancreatology2018https://conductscience.org/library/papers/29233499PubMed
615,115,830Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes.N Engl J Med2004https://conductscience.org/library/papers/15115830PubMed
717,446,535Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood.Diabetes2007https://conductscience.org/library/papers/17446535PubMed
82,102,678A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.Nature1990https://conductscience.org/library/papers/2102678PubMed
920,160,352Wolfram syndrome 1 gene negatively regulates ER stress signaling in rodent and human cells.J Clin Invest2010https://conductscience.org/library/papers/20160352PubMed
1033,029,656Type 1 diabetes can present before the age of 6 months and is characterised by autoimmunity and rapid loss of beta cells.Diabetologia2020https://conductscience.org/library/papers/33029656PubMed

Cited by108

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 135 citations.

PMIDTitleJournalYearIn PapersSource
42,953,899Increasing Awareness and Identification of Maturity-Onset Diabetes of the Young in a Pediatric Diabetes Program.Pediatr Qual Saf2026https://conductscience.org/library/papers/42953899PubMed
42,806,279Genotype-Dependent Functional and Pharmacological Profiling of Rare GCK Variants Reveals Implications for Precision Management of Monogenic Diabetes.Diabetes Obes Metab2026https://conductscience.org/library/papers/42806279PubMed
42,784,019Brachydactyly Type A1 Caused by an IHH Variant in a Patient with Disproportionate Short Stature: A Case Report.Reports (MDPI)2026https://conductscience.org/library/papers/42784019PubMed
42,747,450The management of type 1 diabetes in adults. The updated 2026 consensus report by the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD).Diabetologia2026https://conductscience.org/library/papers/42747450PubMed
42,629,605TBC1D4-Related Monogenic Diabetes: Molecular Mechanisms, Clinical Recognition, and Therapeutic Implications.J Diabetes2026https://conductscience.org/library/papers/42629605PubMed
42,620,571HLA class II alleles and haplotypes associated with susceptibility to type 1 diabetes and to type 1 diabetes with concomitant autoimmune diseases: a cross-sectional study from Eastern Croatia.Front Endocrinol (Lausanne)2026https://conductscience.org/library/papers/42620571PubMed
42,559,753Glycemic and Renal Effects of SGLT2 Inhibitors in Monogenic Diabetes: A Real-World National Study.Diabetes Obes Metab2026https://conductscience.org/library/papers/42559753PubMed
42,472,134HNF1A-Maturity-Onset Diabetes of the Young (MODY) in a Family With a Rare Silent Variant: Clinical Challenges and Variable Expressivity.Cureus2026https://conductscience.org/library/papers/42472134PubMed
42,470,517
Genetic spectrum and treatment implications of maturity-onset diabetes of the young in the eastern Black Sea region of Türkiye: a combined adult and pediatric cohort of 296 patients with identification of rare and novel variants.
Mol Biol Rep2026https://conductscience.org/library/papers/42470517PubMed
42,353,846DNAJC3-Related Syndromic Monogenic Diabetes Without Clinically Evident Neurological Manifestations in an Adult: Expanding the Phenotypic Spectrum.Genes (Basel)2026https://conductscience.org/library/papers/42353846PubMed

1 to 10 of 108

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Genes52

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

Sources 11

  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • HGNCCC0
  • iCiteCC BY 4.0
  • NCBI GenePublic domain (US government)
  • NIH RePORTER's grant and paper linksPublic domain
  • Open TargetsCC0 1.0
  • PMC's ID filePublic domain (US government)
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • HGNCCC0: https://www.genenames.org/about/license/
  • iCiteCC BY 4.0
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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