CrushSCI.com
Journal Selection & Manuscript Polishing Services
Journal of Cystic Fibrosis journal cover Medicine
Back to journal directory

Review Cycle Records

Journal of Cystic Fibrosis

Elsevier SCIE Non-OA
2026 Emerging Zone 32025 CAS Zone 22025 JCR Q1
130.2Average days
117Median days
40Fastest days
225Longest days
1,7082025 publications

Paper Review Records

All Paper Review Records

10 valid samples · Newest publication first
Review days = acceptance date − received date. PDF, DOI, and publisher-page sources are retained.

161 days

Lung mucus burden and treatment response assessed by MRI in the post-modulator era

AuthorsAlexander M Matheson; Evan Prather; Matthew M Willmering; Jaime Mata; Giles Santyr; Felix A Ratjen; Elizabeth L Kramer; Zackary I Cleveland; Jason C Woods

AffiliationsCenter for Pulmonary Imaging Research, Cincinnati Children's Hospital, Cincinnati, OH, United States; Pulmonary Medicine, Cincinnati Children's Hospital, Cincinnati, OH, United States; Department of Pediatrics, The University of Cincinnati, Cincinnati, OH, United States; College of Medicine, The University of Cincinnati, Cincinnati, OH, United States; University of Virginia, Virginia, VA, United States; Department of Radiology, The Hospital for Sick Children, Toronto, ON, Canada; Translational Medicine Program, The Hospital for Sick Children, Toronto, ON, Canada

Source PDF DOI Publisher page
124 days

Expiratory lung MRI: a simple, sensitive method to quantify and visualise regional gas trapping in cystic fibrosis

AuthorsAmy V Simmons; Laurie J Smith; Zoe Somerville; Hannah Faulke; William Clark; David Hughes; Ina Aldag; Noreen West; Alberto M Biancardi; Jim M Wild; Neil J Stewart

AffiliationsPOLARIS, Division of Clinical Medicine, Faculty of Health, The University of Sheffield, United Kingdom; INSIGNEO Institute for in silico Medicine, The University of Sheffield, Sheffield, United Kingdom; Sheffield Children’s Hospital NHS Foundation Trust, Sheffield, United Kingdom

Source PDF DOI Publisher page
92 days

International Delphi consensus recommendations for the follow-up of children born to people with CF and exposed to CFTR modulators in utero or through breastfeeding; endorsed by the European Cystic Fibrosis Society

AuthorsIdan Bokobza; Traci M. Kazmerski; Louise Thomson; Rebecca V. Scott; Amy Downes; Claire L. Hogg; Siân Bentley; Elaine Bowman; Lynn Sinitsky; Olivia Beaumont; Ladina Weitnauer; Quitterie Reynaud; Philippe Reix; Imogen Felton; Jane C. Davies

AffiliationsImperial College London, Imperial Biomedical Research Centre, National Heart & Lung Institute, London, United Kingdom; Royal Brompton & Harefield Hospitals, part of Guys and St Thomas' Hospital NHS Foundation Trust, Department of Paediatric Respiratory Medicine, London, United Kingdom; University of Pittsburgh School of Medicine, Department of Pediatrics, Pittsburgh, United States; Royal Hospital for Children Glasgow, Department of Paediatric Respiratory Medicine, Glasgow, United Kingdom; Chelsea & Westminster Hospital, Department of Diabetes & Endocrinology, London, United Kingdom; Royal Brompton & Harefield Hospitals, part of Guys and St Thomas' Hospital NHS Foundation Trust, Adult Cystic Fibrosis Centre, London, United Kingdom; Imperial College London, Department of Metabolism, Digestion and Reproduction, London, United Kingdom; Royal Brompton & Harefield Hospitals, part of Guys and St Thomas' Hospital NHS Foundation Trust, Pharmacy Department, London, United Kingdom; West Hertfordshire Teaching Hospitals NHS Trust, Watford, United Kingdom; King's College Hospital, London, United Kingdom; Centre Hospitalier Universitaire Vaudois, Adult CF centre, Lausanne, Switzerland; Hospices Civils de Lyon – Hôpital Lyon Sud, Adult Cystic Fibrosis Center, Internal Medicine and Vascular Pathology Department, Lyon, France; University Claude Bernard Lyon 1, Research on Healthcare Performance (RESHAPE), INSERM U1290, Lyon, France; Hospices civils de Lyon - Hôpital Femme Mère Enfant, Centre de ressources et de compétences pour la mucoviscidose, Lyon, France

Source PDF DOI Publisher page
110 days

Dupilumab in the treatment of severe chronic rhinosinusitis with nasal polyps (CRSwNP) in cystic fibrosis patients

AuthorsAttilio Di Girolamo; Mattia Cristallo; Michelina Francesca Daddato; Federico Spataro; Giuseppina Leonetti; Pamela Vitullo; Eustachio Nettis

AffiliationsDepartment of Precision and Regenerative Medicine and Ionian Area, Regional Reference Center for Allergic and Immunological Diseases, Bari, Italy; Department of Precision and Regenerative Medicine and Ionian Area - DiMePRe-J, Post Graduate School of Allergy and Clinical Immunology, Guido Baccelli Unit of Internal Medicine, University of Bari Aldo Moro, 70124 Bari, Italy; Department of Precision and Regenerative Medicine and Ionian Area - DiMePRe-J, Section of Pharmacology, University of Bari Aldo Moro, 70124 Bari, Italy; Pediatric Cystic Fibrosis Centre, Azienda Universitaria Ospedaliera Consorziale Policlinico, Bari, Italy; Cystic Fibrosis Support Center, Ospedale G. Tatarella di Cerignola, Cerignola, Italy

Source PDF DOI Publisher page
151 days

Investigation of HE4 expression concerning epithelial-mesenchymal transition (EMT) in cystic fibrosis epithelial cells

AuthorsMarianna Pócsi; György Jázon Balla; Ferenc Fenyvesi; Ágnes Rusznyák; Zsolt Fejes; István Balogh; Milan Macek; Margarida D. Amaral; Béla Nagy

AffiliationsDepartment of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary; Department of Molecular and Nanopharmaceutics, Faculty of Pharmacy, University of Debrecen, Debrecen, Hungary; Division of Clinical Genetics, Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary; Department of Biology and Medical Genetics, 2nd Faculty of Medicine and Motol University Hospital, Charles University, Prague, Czech Republic; BioISI- Biosystems & Integrative Sciences Institute, Faculty of Sciences, University of Lisboa, Lisboa, Portugal

Source PDF DOI Publisher page
203 days

Altered responsiveness to photic stimuli contribute to circadian disruption in cystic fibrosis

AuthorsDanica F. Patton-Parfyonov; Eden N. Kenner; Deborah A. Corey; Thomas J. Kelley; Rebecca Darrah

AffiliationsDepartment of Genetics and Genome Sciences, School of Medicine, Case Western Reserve University, Cleveland, OH 44106

Source PDF DOI Publisher page
105 days

Effects of Elexacaftor/Tezacaftor/Ivacaftor on cough frequency, physical activity patterns, and sleep quality in adolescents and adults with cystic fibrosis

AuthorsEva Van Braeckel; Andrew T. Braun; Nicholas J. Simmonds; Peter J. Barry; Jane C. Davies; Marie E. Egan; Allen Lapey; Marcus A. Mall; Edward F. McKone; Daniel Peckham; Marijke Proesmans; Bonnie Ramsey; Saioa Vicente Santamaria; Daniel Smith; Jennifer L. Taylor-Cousar; Elizabeth Tullis; Elke De Wachter; Nick Withers; Neil Ahluwalia; Sarah Conner; Mark Jennings; Yiyue Lou; Tanya G. Weinstock; Dominic Keating

AffiliationsDepartment of Respiratory Medicine, Ghent University Hospital, Ghent, Belgium; Department of Internal Medicine and Paediatrics, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium; University of Wisconsin School of Medicine and Public Health, Madison, WI, USA; National Heart and Lung Institute, Imperial College London UK, Royal Brompton Hospital, part of Guy's and St Thomas' NHS Foundation Trust, London, UK; Manchester University NHS Foundation Trust, Manchester, UK; Division of Infection, Immunity and Respiratory Medicine, University of Manchester, Manchester, UK; Yale University, New Haven, CT, USA; Massachusetts General Hospital, Boston, MA, USA; Department of Pediatric Respiratory Medicine, Immunology and Critical Care Medicine, Charité - Universitätsmedizin Berlin, Berlin, Germany; German Center for Lung Research (DZL), associated partner site, Berlin, Germany; German Center for Child and Adolescent Health (DZKJ), partner site Berlin, Berlin, Germany; Cluster of Excellence ImmunoPreCept, Charité - Universitätsmedizin Berlin, Berlin, Germany; St Vincent’s University Hospital, Dublin, Ireland; St James’s University Hospital, Leeds, UK; University Hospital of Leuven, Leuven, Belgium; Seattle Children’s Hospital, Seattle, WA, USA; Hospital Ramón y Cajal, Madrid, Spain; The Prince Charles Hospital, Brisbane, Queensland, Australia; National Jewish Health, Denver, CO, USA; St Michael’s Hospital, Toronto, Ontario, Canada; Universitair Ziekenhuis Brussel, Vrije Universiteit Brussel, Brussels, Belgium; Royal Devon United Hospital NHS Foundation Trust, Exeter, UK; Vertex Pharmaceuticals Incorporated, Boston, MA, USA; Alfred Health, and Monash University, Melbourne, Victoria, Australia

Source PDF DOI Publisher page
91 days

Treatment with elexacaftor/tezacaftor/ivacaftor does not alter SpiroNose-derived electronic breath profiles in children with cystic fibrosis

AuthorsElias Seidl; Andrew Zikic; Srdjan Micic; Rianne de Vries; Julie Avolio; Alexander Moeller; Felix Ratjen; Hartmut Grasemann

AffiliationsDepartment of Respiratory Medicine, University Children's Hospital Zurich, Zurich, Switzerland; Division of Respiratory Medicine, Department of Pediatrics, The Hospital for Sick Children, Toronto, Canada; Breathomix BV, Bargelaan 200, Leiden, CW 2333, The Netherlands; Translational Medicine, Research Institute, Hospital for Sick Children, Toronto, ON M5G 1 × 8, Canada and University of Toronto, Toronto, Canada

Source PDF DOI Publisher page
225 days

Apical hyperosmotic challenge upregulates aquaporin-3 in human airway epithelia

AuthorsAlexander Sauter; Oliver H Wittekindt; Lara Gutjahr; Ronja Rössel; Manfred Frick; Sebastian FN Bode; Hanna Schmidt

AffiliationsInstitute of General Physiology, Ulm University; Albert-Einstein-Allee 11 89075, Ulm, Germany; Department of Pediatrics and Adolescent Medicine, Ulm University Medical Center; Eythstraße 24 89075, Ulm, Germany

Source PDF DOI Publisher page
40 days

Microbiological outcomes associated with Burkholderia species in people with cystic fibrosis receiving CFTR modulator therapy

AuthorsTimothy Riddles; Daniel Smith; David W Reid; Daniel Henderson; Arianne J Blanco; Vanessa Moore; Michelle Wood; Ieuan E S Evans

AffiliationsAdult Cystic Fibrosis Centre, The Prince Charles Hospital, Brisbane, QLD, Australia; Faculty of Medicine, University of Queensland, QLD, Brisbane, Australia; Lung Inflammation & Infection, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia; Department of Microbiology, Royal Brisbane Women’s Hospital, Brisbane, QLD, Australia

Source PDF DOI Publisher page

Expert Matching · Case Demo

Turn Your Submission Goalsinto a Verifiable Journal Plan

Share your field, deadline, and author profile. CrushSCI uses real review records to suggest a title direction, shortlist journals, and estimate timelines.

CrushSCI online

Client

I work in environmental engineering and need an SCI paper published within three months. I have no grant funding or prominent co-author. Which journals could I target?

CrushSCI

Yes. We will first screen for feasibility against the 90-day deadline, then identify comparable papers without grant support or prominent co-authors. The final shortlist will prioritize research quality and journal scope.

Suggested title
Machine Learning and Life-Cycle Assessment for Predicting and Optimizing Carbon Emissions in Urban Wastewater Treatment

SampleLatest 5 valid paper samples from 2026

Average review96.4 days

Median77 days

Contact CrushSCI

Contact CrushSCI

Leave your contact details so we can discuss your manuscript, editing needs, and submission plan.

Selected service: Paper Editing Service

Or leave your contact details

WhatsApp, Telegram, WeChat, and email are all optional, but at least one is required. Once received, we will contact you as soon as possible.