Journal of Cystic Fibrosis
Published by Elsevier
ISSN : 1569-1993 eISSN : 1873-5010
Abbreviation : J. Cyst. Fibros.
Aims & Scope
The Journal of Cystic Fibrosis is the official journal of the European Cystic Fibrosis Society.
The journal is devoted to promoting the research and treatment of cystic fibrosis.
To this end the journal publishes original scientific articles, editorials, case reports, short communications and other information relevant to cystic fibrosis.
The journal also publishes news and articles concerning the activities and policies of the ECFS as well as those of other societies related the ECFS.
View Aims & ScopeMetrics & Ranking
Impact Factor
Year | Value |
---|---|
2025 | 6 |
2024 | 5.40 |
Journal Rank
Year | Value |
---|---|
2024 | 1778 |
Journal Citation Indicator
Year | Value |
---|---|
2024 | 2708 |
SJR (SCImago Journal Rank)
Year | Value |
---|---|
2024 | 1.772 |
Quartile
Year | Value |
---|---|
2024 | Q1 |
h-index
Year | Value |
---|---|
2024 | 98 |
Impact Factor Trend
Abstracting & Indexing
Journal is indexed in leading academic databases, ensuring global visibility and accessibility of our peer-reviewed research.
Subjects & Keywords
Journal’s research areas, covering key disciplines and specialized sub-topics in Medicine, designed to support cutting-edge academic discovery.
Most Cited Articles
The Most Cited Articles section features the journal's most impactful research, based on citation counts. These articles have been referenced frequently by other researchers, indicating their significant contribution to their respective fields.
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ECFS best practice guidelines: the 2018 revision
Citation: 621
Authors: Carlo, Alistair J.A., Scott C., Harry G.M., Anne, Felix, Isabelle, Kevin W., Jurg, Patrick A., Pavla, Nataliya, Maya N., Sue, Helen, Barry, Sarah Jane, Alan R., Giovanni, Thomas O.F., Susan P., Pavel
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Evaluation of a new definition for chronic Pseudomonas aeruginosa infection in cystic fibrosis patients
Citation: 599
Authors: Tim W.R., Keith G., Steven P., Miles, James M.
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Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice
Citation: 463
Authors: C., H., M., J.J., E., P., E., B.M., C., A., T., M., G.R., E., J., I., P., C., E., M., B., M., A., P.F., D., P., M., M., M., J., J.S.
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European Cystic Fibrosis Society Standards of Care: Best Practice guidelines
Citation: 441
Authors: Alan R., Scott C., Snezana, Mandy, Alistair, Patrick, Nataliya, Anne, Felix, Sarah Jane, Isabelle, Kevin W., Giovanni, Gerald, Sue
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Inflammation in cystic fibrosis lung disease: Pathogenesis and therapy
Citation: 412
Authors: André M., Dominik, Michael W., James F.
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Treatment of lung infection in patients with cystic fibrosis: Current and future strategies
Citation: 411
Authors: Gerd, Patrick, Harry, J. Stuart
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High treatment burden in adults with cystic fibrosis: Challenges to disease self-management
Citation: 401
Authors: Gregory S., Deborah E., Walter M.
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Ivacaftor potentiation of multiple CFTR channels with gating mutations
Citation: 369
Authors: Haihui, Bill, Chien-Jung, Jennings, Dong, James P., Art, John, Sheila, Katherine, Beth J., Fredrick
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Chronic Mycobacterium abscessus infection and lung function decline in cystic fibrosis
Citation: 355
Authors: Charles R., Denise A., Peter, Alan, Peadar G.
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Recommendations for the classification of diseases as CFTR-related disorders
Citation: 345
Authors: C., M., K., N., J., E., I., M., M., M., C., D., C., H., G.R., P., P., J.S., K., B., E., M., M., A., D., M., D.N., K.W., M., E., J., P.F., C.