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Journal of Cystic Fibrosis : Impact Factor & More
eISSN: 1873-5010pISSN: 1569-1993
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Journal of Cystic Fibrosis Key Metrics
CiteScore 
8.2
Eigenfactor
0.005 - 0.01
H-Index
86
Impact Factor
5 - 10
Scite Index
0.88 5-Year SI
SJR
Q1Pulmonary and Respiratory Medicine
SNIP
1.6
Time to Publish
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Time to Publish
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% of papers by time taken from submission to publication
0 to 3 months22%
4 to 6 months55%
7 to 9 months20%
Above 9 months4%
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Topics Covered on Journal of Cystic Fibrosis
Cystic fibrosis
Clinical trial
Lung
Cystic fibrosis transmembrane conductance regulator
Pseudomonas aeruginosa
Adult patients
Insulin secretion
Aspergillus fumigatus
Overweight
Exercise
Ivacaftor
Glucose tolerance test
Inhalation
Azithromycin
Quality of life
Disease severity
Observational study
Lung function
Allele
Staphylococcus aureus
Journal of Cystic Fibrosis Journal Specifications
| Overview | |
| Publisher | ELSEVIER |
| Language | English |
| Frequency | Bi-monthly |
| General Details | |
| Language | English |
| Frequency | Bi-monthly |
| Publication Start Year | 2002 |
| Publisher URL | Visit website |
| Website URL | Visit website |
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Recently Published Papers in Journal of Cystic Fibrosis
A phase I study assessing the safety and tolerability of SPL84, an inhaled antisense oligonucleotide for treatment of cystic fibrosis patients with the 3849 +10kb C->T
- 1 Nov 2024
- Journal of Cystic Fibrosis
Using heart rate data from wrist worn activity trackers to define thresholds for moderate to vigorous physical activity in children and young people with cystic fibrosis
- 1 Nov 2024
- Journal of Cystic Fibrosis
Aging with CF: Characteristics of people with CF aged 40 and older in the United States
- 1 Nov 2024
- Journal of Cystic Fibrosis
News article
- 1 Nov 2024
- Journal of Cystic Fibrosis
Exogenous insulin does not reduce protein catabolism in pre-diabetic cystic fibrosis patients: A randomized clinical trial
- 1 Nov 2024
- Journal of Cystic Fibrosis
Pseudo-Bartter syndrome: A CFTR-related disorder?
- 31 Oct 2024
- Journal of Cystic Fibrosis
A phase I study assessing the safety and tolerability of SPL84, an inhaled antisense oligonucleotide for treatment of cystic fibrosis patients with the 3849 +10kb C->T
- 1 Nov 2024
- Journal of Cystic Fibrosis
Using heart rate data from wrist worn activity trackers to define thresholds for moderate to vigorous physical activity in children and young people with cystic fibrosis
- 1 Nov 2024
- Journal of Cystic Fibrosis
Aging with CF: Characteristics of people with CF aged 40 and older in the United States
- 1 Nov 2024
- Journal of Cystic Fibrosis
News article
- 1 Nov 2024
- Journal of Cystic Fibrosis
Exogenous insulin does not reduce protein catabolism in pre-diabetic cystic fibrosis patients: A randomized clinical trial
- 1 Nov 2024
- Journal of Cystic Fibrosis
Pseudo-Bartter syndrome: A CFTR-related disorder?
- 31 Oct 2024
- Journal of Cystic Fibrosis
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SJR Ranking, Topics covered, Indexing Database, Publication Review Time, Publication Type, Article Processing Charges & Recently Published papers
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FAQs on Journal of Cystic Fibrosis
How long has Journal of Cystic Fibrosis been actively publishing? 
Journal of Cystic Fibrosis has been in operation since 2002 till date.
What is the publishing frequency of Journal of Cystic Fibrosis?
Journal of Cystic Fibrosis published with a Bi-monthly frequency.
How many articles did Journal of Cystic Fibrosis publish last year?
In 2023, Journal of Cystic Fibrosis publsihed 1569 articles.
What is the eISSN & pISSN for Journal of Cystic Fibrosis?
For Journal of Cystic Fibrosis, eISSN is 1873-5010 and pISSN is 1569-1993.
What is Citescore for Journal of Cystic Fibrosis?
Citescore for Journal of Cystic Fibrosis is 8.2.
What is the H Index for Journal of Cystic Fibrosis ?
H Index for Journal of Cystic Fibrosis is 86.
What is SNIP score for Journal of Cystic Fibrosis?
SNIP score for Journal of Cystic Fibrosis is 1.6.
What is the SJR for Journal of Cystic Fibrosis?
SJR for Journal of Cystic Fibrosis is Q1.
Who is the publisher of Journal of Cystic Fibrosis?
ELSEVIER is the publisher of Journal of Cystic Fibrosis.
