Steven M. Rowe

Active 2000–2025

Also published as
Steven M Rowe
149
Papers
27,233
Citations
72
h-index
144
i10-index

Citations

Citations per year for Steven M. Rowe1992: 1 citations1998: 3 citations2000: 3 citations2001: 3 citations2002: 6 citations2003: 4 citations2004: 9 citations2005: 5 citations2006: 14 citations2007: 13 citations2008: 31 citations2009: 31 citations2010: 36 citations2011: 55 citations2012: 93 citations2013: 149 citations2014: 159 citations2015: 148 citations2016: 231 citations2017: 200 citations2018: 245 citations2019: 1,020 citations2020: 1,391 citations2021: 1,632 citations2022: 1,288 citations2023: 1,136 citations2024: 1,516 citations2025: 656 citations2026: 6 citations1993–1997: no citations, so these years are not shown1999: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,378 citing papers, 31.3% of this breakdownUnited Kingdom: 673 citing papers, 8.9% of this breakdownGermany: 492 citing papers, 6.5% of this breakdownItaly: 410 citing papers, 5.4% of this breakdownCanada: 403 citing papers, 5.3% of this breakdownChina: 378 citing papers, 5% of this breakdownFrance: 348 citing papers, 4.6% of this breakdownNetherlands: 272 citing papers, 3.6% of this breakdownAustralia: 266 citing papers, 3.5% of this breakdownBelgium: 164 citing papers, 2.2% of this breakdownSwitzerland: 137 citing papers, 1.8% of this breakdownSpain: 134 citing papers, 1.8% of this breakdown
0%31.3%Other 20.1%

Fields

  • Medicine70.7%
  • Biochemistry, Genetics and Molecular Biology19.2%
  • Immunology and Microbiology2.4%
  • Engineering1.6%
  • Neuroscience1.1%
  • Nursing0.9%
  • Other4.1%

Topics

  • Cystic Fibrosis Research Advances16.6%
  • Neonatal Respiratory Health Research9.1%
  • Tracheal and airway disorders3.3%
  • Asthma and respiratory diseases3.3%
  • Inhalation and Respiratory Drug Delivery2%
  • Chronic Obstructive Pulmonary Disease (COPD) Research1.7%
  • Other64%

Coauthors

All papers

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  1. Elexacaftor–Tezacaftor–Ivacaftor for Cystic Fibrosis with a Single Phe508del Allele

    Authors: , , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2019 cited by 2,116

  2. Efficacy and safety of the elexacaftor plus tezacaftor plus ivacaftor combination regimen in people with cystic fibrosis homozygous for the F508del mutation: a double-blind, randomised, phase 3 trial

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Bruce Barnett, Gary A. Mueller, Patrick A. Flume, F. R. Livingston, Nighat Mehdi, Charlotte C. Tenebäck, John Welter, Raksha Jain, Dana G. Kissner, K. Patel, Francisco J. Calimano, Jimmy Johannes, Cori Daines, Thomas G. Keens, Herschel Scher, Subramanyam Chittivelu, Sudhakar Reddivalam, Ross C. Klingsberg, Larry G. Johnson, Stijn Verhulst, Patricia Macedo, D.G. Downey, Gary Connett, E.F. Nash, Nicholas Withers, Timothy Lee, Marleen Bakker, Harry Heijerman, F. Vermeulen, Eva Van Braeckel, Christiane Knoop, Elke De Wachter, Renske van der Meer, Petrus Merkus, Christof J. Majoor - The Lancet 2019 cited by 1,367

  3. A revised airway epithelial hierarchy includes CFTR-expressing ionocytes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature, Nat. 2018 cited by 1,274

  4. The future of cystic fibrosis care: a global perspective

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ulrike Pypops, Karen S Raraigh, Steven M Rowe, Kevin W Southern, Sheila Sivam, Anne L Stephenson, Marco Zampoli, Felix Ratjen - The Lancet Respiratory Medicine 2019 cited by 961

  5. Clinical Effectiveness of Elexacaftor/Tezacaftor/Ivacaftor in People with Cystic Fibrosis: A Clinical Trial

    Authors: , , , , , , , , , , , , , , , , , , , , , , - American Journal of Respiratory and Critical Care Medicine 2021 cited by 380

  6. Human distal airways contain a multipotent secretory cell that can regenerate alveoli

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature 2022 cited by 319

  7. A CFTR Potentiator in Patients with Cystic Fibrosis and the G551D Mutation

    Authors: , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2011 cited by 2,174

  8. Lumacaftor–Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508delCFTR

    Authors: , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2015 cited by 1,621

  9. Pharmacologic improvement of CFTR function rapidly decreases sputum pathogen density, but lung infections generally persist

    Authors: , , , , , , , , , , , , , - Journal of Clinical Investigation 2023 cited by 202

  10. VX-445–Tezacaftor–Ivacaftor in Patients with Cystic Fibrosis and One or Two Phe508del Alleles

    Authors: , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2018 cited by 727

  11. Engineered tRNAs suppress nonsense mutations in cells and in vivo

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature 2023 cited by 132

  12. Inhaled mRNA therapy for treatment of cystic fibrosis: Interim results of a randomized, double‐blind, placebo‐controlled phase 1/2 clinical study

    Authors: , , , , , , , , , , , , , , , , , , , - Journal of Cystic Fibrosis 2023 cited by 135

  13. Triple Therapy for Cystic Fibrosis Phe508del –Gating and –Residual Function Genotypes

    Authors: , , , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2021 cited by 275

  14. A Phase 3 Open-Label Study of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 through 11 Years of Age with Cystic Fibrosis and at Least One F508del Allele

    Authors: , , , , , , , , , , , , , , , , , , , , , - American Journal of Respiratory and Critical Care Medicine 2021 cited by 288

  15. Dual SMAD Signaling Inhibition Enables Long-Term Expansion of Diverse Epithelial Basal Cells

    Authors: , , , , , , , , , , , , , , , , , , , , - Cell stem cell 2016 cited by 409

  16. Cystic Fibrosis: Emergence of Highly Effective Targeted Therapeutics and Potential Clinical Implications

    Authors: , , - American Journal of Respiratory and Critical Care Medicine 2019 cited by 222

  17. Elexacaftor/tezacaftor/ivacaftor and gastrointestinal outcomes in cystic fibrosis: Report of promise-GI

    Authors: , , , , , , , , , , , , , , , , , , , , - Journal of Cystic Fibrosis 2022 cited by 123

  18. Long-term safety and efficacy of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis and at least oneF508delallele: 144-week interim results from a 192-week open-label extension study

    Authors: , , , , , , , , , , , , , , , , , , , , , , - European Respiratory Journal 2023 cited by 88

  19. Cystic fibrosis

    Authors: , , , , , - Nature Reviews Disease Primers 2015 cited by 534

  20. A small molecule that induces translational readthrough of CFTR nonsense mutations by eRF1 depletion

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Communications 2021 cited by 125

  21. Tezacaftor–Ivacaftor in Residual-Function Heterozygotes with Cystic Fibrosis

    Authors: , , , , , , , , , , , , - New England Journal of Medicine 2017 cited by 511

  22. CFTR modulator theratyping: Current status, gaps and future directions

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , - Journal of Cystic Fibrosis 2018 cited by 291

  23. Transgenic ferret models define pulmonary ionocyte diversity and function

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kathleen Scott, D Bartels, David K. Meyerholz, Steven M. Rowe, Xiaoming Liu, Ziying Yan, Adam L. Haber, Xingshen Sun, John F. Engelhardt - Nature 2023 cited by 71

  24. Ataluren stimulates ribosomal selection of near-cognate tRNAs to promote nonsense suppression

    Authors: , , , , , , , , , , , , , , , - National Academy of Sciences, Proceedings of the National Academy of Sciences 2016 cited by 223