Citations Report

Clinical Practice : Citations & Metrics Report

Articles published in Clinical Practice have been cited by esteemed scholars and scientists all around the world.

Clinical Practice has got h-index 29, which means every article in Clinical Practice has got 29 average citations.

Following are the list of articles that have cited the articles published in Clinical Practice.

  2021 2020 2019 2018 2017 2016

Year wise published articles

50 27 55 66 38 13

Year wise citations received

494 462 352 277 260 226
Journal total citations count 3847
Journal impact factor 12.24
Journal 5 years impact factor 8.50
Journal cite score 10.62
Journal h-index 29
Journal h-index since 2018 21
Journal Impact Factor 2020 formula
IF= Citations(y)/{Publications(y-1)+ Publications(y-2)} Y= Year
Journal 5-year Impact Factor 2020 formula
Citations(2016 + 2017 + 2018 + 2019 + 2020)/
{Published articles(2016 + 2017 + 2018 + 2019 + 2020)}
Journal citescore
Citescorey = Citationsy + Citationsy-1 + Citationsy-2 + Citations y-3 / Published articlesy + Published articlesy-1 + Published articlesy-2 + Published articles y-3
  • Willger SD, Grim SL, Dolben EL, Shipunova A, Hampton TH, et al. 2014. Characterization and quantification of the fungal microbiome in serial samples from individuals with cystic fibrosis. Microbiome, 2(1), p.40.

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  • Rabin HR and Surette MG, 2012. The cystic fibrosis airway microbiome. Current opinion in pulmonary medicine, 18(6), pp.622-627.

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  • Zemanick ET, Wagner BD, Robertson CE, Stevens MJ, Szefler SJ, et al. 2015. Assessment of airway microbiota and inflammation in cystic fibrosis using multiple sampling methods. Annals of the American Thoracic Society, 12(2), pp.221-229.

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  • Sibley CD, Church DL, Surette MG, Dowd SE and Parkins MD, 2012. Pyrosequencing reveals the complex polymicrobial nature of invasive pyogenic infections: microbial constituents of empyema, liver abscess, and intracerebral abscess. European journal of clinical microbiology & infectious diseases, 31(10), pp.2679-2691.

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  • Olson AB, Sibley CD, Schmidt L, Wilcox MA, Surette MG, et al. 2010. Development of real-time PCR assays for detection of the Streptococcus milleri group from cystic fibrosis clinical specimens by targeting the cpn60 and 16S rRNA genes. Journal of clinical microbiology, 48(4), pp.1150-1160.

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  • Mossialos D and Amoutzias GD, 2009. Role of siderophores in cystic fibrosis pathogenesis: Foes or friends?. International Journal of Medical Microbiology, 299(2), pp.87-98.

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  • Kuznetsov V, Lee HK, Maurer-Stroh S, Molnár MJ, Pongor S, et al. 2013. How bioinformatics influences health informatics: usage of biomolecular sequences, expression profiles and automated microscopic image analyses for clinical needs and public health. Health Information Science and Systems, 1(1), p.2.

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  • Hélène M, Estelle JB and Anne-Laure M, 2012. Atypical bacteria in the CF airways: diversity, clinical consequences, emergence and adaptation. INTECH Open Access Publisher.

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  • Baldan R, Cigana C, Testa F, Bianconi I, De Simone M, et al. 2014. Adaptation of Pseudomonas aeruginosa in cystic fibrosis airways influences virulence of Staphylococcus aureus in vitro and murine models of co-infection. PLoS One, 9(3), p.e89614.

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  • Flume PA, 2011. Pneumothorax in cystic fibrosis. Current opinion in pulmonary medicine, 17(4), pp.220-225.

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  • Lopes SP, Azevedo NF and Pereira MO, 2015. Microbiome in cystic fibrosis: shaping polymicrobial interactions for advances in antibiotic therapy. Critical reviews in microbiology, 41(3), pp.353-365.

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  • Dennersten U, Lannefors L, Höglund P, Hellberg K, Johansson H, et al. 2009. Lung function in the aging Swedish cystic fibrosis population. Respiratory medicine, 103(7), pp.1076-1082.

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  • Dickson RP, Erb-Downward JR and Huffnagle GB, 2015. Homeostasis and its disruption in the lung microbiome. American Journal of Physiology-Lung Cellular and Molecular Physiology, 309(10), pp.L1047-L1055.

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  • Payne MS, Goss KC, Connett GJ, Legg JP, Bruce KD, et al. 2012. A quantitative analysis of Ureaplasma urealyticum and Ureaplasma parvum compared with host immune response in preterm neonates at risk of developing bronchopulmonary dysplasia. Journal of clinical microbiology, 50(3), pp.909-914.

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  • Michon AL, Jumas-Bilak E, Chiron R, Lamy B and Marchandin H, 2014. Advances toward the elucidation of hypertonic saline effects on Pseudomonas aeruginosa from cystic fibrosis patients. PloS one, 9(2), p.e90164.

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  • Sato Y, Civiello M, Bell SC, Willis BL and Bourne DG, 2016. Integrated approach to understanding the onset and pathogenesis of black band disease in corals. Environmental microbiology.

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  • Dalhoff A, 2014. Pharmacokinetics and pharmacodynamics of aerosolized antibacterial agents in chronically infected cystic fibrosis patients. Clinical microbiology reviews, 27(4), pp.753-782.

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  • Rejzek M, Kannathasan VS, Wing C, Preston A, Westman EL, et al. 2009. Chemical synthesis of UDP-Glc-2, 3-diNAcA, a key intermediate in cell surface polysaccharide biosynthesis in the human respiratory pathogens B. pertussis and P. aeruginosa. Organic & biomolecular chemistry, 7(6), pp.1203-1210.

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  • Magalhães AP, Azevedo NF, Pereira MO and Lopes SP, 2016. The cystic fibrosis microbiome in an ecological perspective and its impact in antibiotic therapy. Applied microbiology and biotechnology, 100(3), pp.1163-1181.

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  • McNeely D, Moore JE, Elborn JS, Millar BC, Rendall J, et al. 2009. Isolation of Burkholderia cenocepacia and Burkholderia vietnamiensis from human sewage. International journal of environmental health research, 19(2), pp.157-162.

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  • Sibley CD, Grinwis ME, Rabin HR and Surette MG, 2010. Azithromycin paradox in the treatment of cystic fibrosis airway disease. Future microbiology, 5(9), pp.1315-1319.

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  • Kaur J, Pethani BP, Kumar S, Kim M, Sunna A, et al. 2015. Pseudomonas aeruginosa inhibits the growth of Scedosporium aurantiacum, an opportunistic fungal pathogen isolated from the lungs of cystic fibrosis patients.

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  • Goldberg JB, 2010. Emergence of Pseudomonas aeruginosa in cystic fibrosis lung infections. In Pseudomonas (pp. 141-175). Springer Netherlands.

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  • Lopes SP, Carvalho DT, Pereira MO and Azevedo NF, 2017. Discriminating between typical and atypical cystic fibrosis-related bacterial species by multiplex PNA-FISH. Biotechnology and Bioengineering, 114(2), pp.355-376.

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  • Cribbs SK and Beck JM, 2017. Microbiome in the pathogenesis of cystic fibrosis and lung transplant-related disease. Translational Research, 179, pp.84-96.

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  • Johnson EJ, Zemanick ET, Accurso FJ, Wagner BD, Robertson CE, et al. 2016. Molecular Identification of Staphylococcus aureus in Airway Samples from Children with Cystic Fibrosis. PloS one, 11(1), p.e0147643.

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  • Dharmaprakash A, Thandavarayan R, Joseph I and Thomas S, 2015. Development of broad-spectrum antibiofilm drugs: strategies and challenges. Future microbiology, 10(6), pp.1035-1048.

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  • Thornton CS, Brown EL, Alcantara J, Rabin HR and Parkins MD, 2015. Prevalence and impact of S treptococcus pneumoniae in adult cystic fibrosis patients: a retrospective chart review and capsular serotyping study. BMC pulmonary medicine, 15(1), p.49.

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  • Winward C, Sackley C, Metha Z, Rothwell PM (2009) A population-based study of the prevalence of fatigue after transient ischemic attack and minor stroke. Stroke 40: 757-761.

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  • Ormstad H, Aass HC, Amthor KF, Lund-Sørensen N, Sandvik L (2011) Serum cytokine and glucose levels as predictors of poststroke fatigue in acute ischemic stroke patients. Journal of neurology 258: 670-676.

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  • Chestnut TJ (2011) Fatigue in stroke rehabilitation patients: a pilot study. Physiotherapy Research International 16: 151-158.

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  • Liu CH, Tsai CH, Li TC, Yang YW, Huang WS, et al. (2016) Effects of the traditional Chinese herb Astragalus membranaceus in patients with poststroke fatigue: A double-blind, randomized, controlled preliminary study. Journal of Ethnopharmacology 194:954-962.

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  • Vinicuk C, Pintosh E (2016) Early rehabilitation after acute ischemic disorders of cerebral circulation. International neurological journal 8: 86.

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  • Vinychuk SM, Fartushna OY (2016) Early Rehabilitation after Acute Ischemic Cerebrovascular Events. INTERNATIONAL NEUROLOGICAL JOURNAL 8: 34-39.

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  • Thornton CS, Brown EL, Alcantara J, Rabin HR and Parkins MD, 2015. Prevalence and impact of S treptococcus pneumoniae in adult cystic fibrosis patients: a retrospective chart review and capsular serotyping study. BMC pulmonary medicine, 15(1), p.49.

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  • Vinychuk SM Fartushny OE (2016) Early rehabilitation after acute ischemic cerebrovascular events. International Neurology Journal 8: 34-39.

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  • Lo JB, Appel LE, Herbig SM, McCray SB, Thombre AG (2009) Formulation design and pharmaceutical development of a novel controlled release form of azithromycin for single-dose therapy. Drug development and industrial pharmacy 35: 1522-1529.

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  • Keravec M, Mounier J, Prestat E, Vallet S, Jansson JK, et al. 2015. Insights into the respiratory tract microbiota of patients with cystic fibrosis during early Pseudomonas aeruginosa colonization. SpringerPlus, 4(1), p.405.

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  • Blondeau JM (2006) Update on the use of the macrolides for community-acquired respiratory tract infections.

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  • Heirali A, McKeon S, Purighalla S, Storey DG, Rossi L, et al. 2016. Assessment of the microbial constituents of the home environment of individuals with cystic fibrosis (CF) and their association with lower airways infections. PloS one, 11(2), p.e0148534.

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  • Ormerod KL, George NM, Fraser JA, Wainwright C and Hugenholtz P, 2015. Comparative genomics of non-pseudomonal bacterial species colonising paediatric cystic fibrosis patients. PeerJ, 3, p.e1223.

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  • Jankovic J, Stacy M (2007) Medical management of levodopa-associated motor complications in patients with Parkinson’s disease. CNS drugs 21: 677-692.

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  • Thornton CS, Grinwis ME, Sibley CD, Parkins MD, Rabin HR, et al. 2015. Antibiotic susceptibility and molecular mechanisms of macrolide resistance in streptococci isolated from adult cystic fibrosis patients. Journal of Medical Microbiology, 64(11), pp.1375-1386.

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Journal Metrics:

Impact Factor: 12.24
Journal Citescore: 10.62
h-index: 29
PubMed NLM ID:  101579384
Journal Acceptance Rate: 40%
Article processing time : 30-45 Days

Google Scholar citation report
Citations : 3847

Clinical Practice received 3847 citations as per Google Scholar report


Clinical Practice peer review process verified at publons

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