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Cited by 73Cystic Fibrosis Research AdvancesObesity, Physical Activity, DietGenetic and Kidney Cyst Diseases

The DOI matches its Crossref record; 13 of the 13 references it cites were found in a registry or an index.

Overweight and Obesity in ΔF508 Homozygous Cystic Fibrosis

Kastner-Cole, Dagmar, Palmer, Colin N.A., Ogston, Simon A., Mehta, Anil, Mukhopadhyay, Somnath·2005·The Journal of Pediatrics

Abstract

Overweight (9%) and obesity (1%) in patients with cystic fibrosis homozygous for the deltaF508 mutation (CFdeltaF508) were non-trivial. Children with CFdeltaF508, in contrast to the general population, showed a positive association between body mass index and lung function for all body mass index z-scores.

Overview

Integrity signals

Registry

Crossref · 10.1016/j.jpeds.2005.06.003

Cites

13 of 13 references verified0 citation errors · 0 not checkable

Statistics

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Verification

Claims the paper makes

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Claims other papers make about this one

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Citations

Cites

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Cited by

Metadata

Authors
Kastner-Cole, D., Palmer, C. N. A., Ogston, S. A., Mehta, A., & Mukhopadhyay, S.
Affiliations
  • Ninewells Hospital (GB)
  • University of Dundee (GB)
Corresponding author
Mukhopadhyay, Somnath
Venue
The Journal of Pediatrics
Publisher
Elsevier BV
Published
2005-09
Volume
147
Issue
3
Pages
402-404
ISSN
0022-3476 (ISSN-L)
OpenAlex
W2076512750
Cited by
73
References
13
Citations by year
2026: 5 · 2025: 1 · 2024: 6 · 2023: 3 · 2022: 4 · 2021: 8 · 2020: 4 · 2019: 4 · 2017: 3 · 2016: 2 · 2015: 7 · 2014: 7 · 2013: 6 · 2012: 5
FWCI
0.79
Type
journal article
Language
en
Open access
closed
Licence
www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations
  • The Journal of Pediatrics (publishedVersion)
  • PubMed (publishedVersion)
  • Discovery Research Portal (University of Dundee) (publishedVersion)
Topics
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Cystic Fibrosis Research Advances
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Obesity, Physical Activity, Diet
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and Kidney Cyst Diseases
Keywords
cystic fibrosis, F508del mutation, obesity, overweight, body mass index, lung function, children
MeSH terms
Adolescent, Adult, Child, Child, Preschool, Cystic Fibrosis, Female, Forced Expiratory Volume, Homozygote, Humans, Infant, Lung, Male, Middle Aged, Nutritional Status, Obesity, Body Mass Index, Cystic Fibrosis Transmembrane Conductance Regulator

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

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Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.