Michael R. Knowles

Active 1981–2025

Also published as
Michael R Knowles
156
Papers
27,591
Citations
93
h-index
150
i10-index

Citations

Citations per year for Michael R. Knowles1983: 2 citations1984: 1 citations1985: 4 citations1986: 6 citations1987: 7 citations1988: 16 citations1989: 31 citations1990: 27 citations1991: 42 citations1992: 63 citations1993: 57 citations1994: 54 citations1995: 83 citations1996: 80 citations1997: 90 citations1998: 81 citations1999: 147 citations2000: 118 citations2001: 93 citations2002: 185 citations2003: 153 citations2004: 179 citations2005: 152 citations2006: 166 citations2007: 232 citations2008: 205 citations2009: 204 citations2010: 168 citations2011: 165 citations2012: 176 citations2013: 240 citations2014: 265 citations2015: 266 citations2016: 245 citations2017: 182 citations2018: 216 citations2019: 729 citations2020: 697 citations2021: 698 citations2022: 495 citations2023: 304 citations2024: 583 citations2025: 197 citations

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,344 citing papers, 31.8% of this breakdownUnited Kingdom: 677 citing papers, 9.2% of this breakdownGermany: 462 citing papers, 6.3% of this breakdownCanada: 421 citing papers, 5.7% of this breakdownFrance: 370 citing papers, 5% of this breakdownItaly: 304 citing papers, 4.1% of this breakdownChina: 271 citing papers, 3.7% of this breakdownAustralia: 236 citing papers, 3.2% of this breakdownNetherlands: 198 citing papers, 2.7% of this breakdownSwitzerland: 176 citing papers, 2.4% of this breakdownSpain: 155 citing papers, 2.1% of this breakdownBelgium: 142 citing papers, 1.9% of this breakdown
0%31.8%Other 21.9%

Fields

  • Medicine62.1%
  • Biochemistry, Genetics and Molecular Biology29.6%
  • Neuroscience2.2%
  • Immunology and Microbiology1.7%
  • Pharmacology, Toxicology and Pharmaceutics0.8%
  • Engineering0.6%
  • Other3%

Topics

  • Cystic Fibrosis Research Advances15.3%
  • Neonatal Respiratory Health Research8%
  • Genetic and Kidney Cyst Diseases4.1%
  • Tracheal and airway disorders3.8%
  • Asthma and respiratory diseases2.2%
  • Ion Transport and Channel Regulation1.5%
  • Other65.1%

Coauthors

All papers

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  1. Adult Patients With Bronchiectasis

    Authors: , , , , , , , , , , , , , , , , - CHEST Journal 2016 cited by 430

  2. Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice Guideline

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , - American Journal of Respiratory and Critical Care Medicine 2018 cited by 488

  3. Mucus clearance as a primary innate defense mechanism for mammalian airways

    Authors: , - Journal of Clinical Investigation 2002 cited by 1,088

  4. Airway Mucus Hyperconcentration in Non–Cystic Fibrosis Bronchiectasis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , - American Journal of Respiratory and Critical Care Medicine 2019 cited by 132

  5. Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review

    Authors: , , , , , , , , , , , , , - Pediatric Pulmonology 2015 cited by 447

  6. De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , - The American Journal of Human Genetics 2019 cited by 213

  7. Primary Ciliary Dyskinesia: Longitudinal Study of Lung Disease by Ultrastructure Defect and Genotype

    Authors: , , , , , , , , , , , , , , - American Journal of Respiratory and Critical Care Medicine 2018 cited by 183

  8. Clinical Features of Childhood Primary Ciliary Dyskinesia By Genotype and Ultrastructural Phenotype

    Authors: , , , , , , , , , , , , , , , - American Journal of Respiratory and Critical Care Medicine 2014 cited by 274

  9. Clinical Features and Associated Likelihood of Primary Ciliary Dyskinesia in Children and Adolescents

    Authors: , , , , , , , , , , , , , , , , - Annals of the American Thoracic Society 2016 cited by 216

  10. Primary Ciliary Dyskinesia

    Authors: , , , , , , , - American Journal of Respiratory and Critical Care Medicine 2003 cited by 851

  11. DNAH5 Mutations are a Common Cause of Primary Ciliary Dyskinesia with Outer Dynein Arm Defects

    Authors: , , , , , , , , , , , , , , , , , , , - American Journal of Respiratory and Critical Care Medicine 2006 cited by 355

  12. Primary Ciliary Dyskinesia. Recent Advances in Diagnostics, Genetics, and Characterization of Clinical Disease

    Authors: , , , , - American Journal of Respiratory and Critical Care Medicine 2013 cited by 507

  13. Mucus Clearance and Lung Function in Cystic Fibrosis with Hypertonic Saline

    Authors: , , , , , - New England Journal of Medicine 2006 cited by 689

  14. Recommendations for the classification of diseases as CFTR-related disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Julian Zielenski, П. Ф. Пигнатти, Claude Férec - Journal of Cystic Fibrosis 2011 cited by 421

  15. Mislocalization of DNAH5 and DNAH9 in Respiratory Cells from Patients with Primary Ciliary Dyskinesia

    Authors: , , , , , , , - American Journal of Respiratory and Critical Care Medicine 2005 cited by 316

  16. Cryo-electron tomography reveals ciliary defects underlying human RSPH1 primary ciliary dyskinesia

    Authors: , , , , , , , , - Nature Communications 2014 cited by 167

  17. Pulmonary Nontuberculous Mycobacterial Infection. A Multisystem, Multigenic Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , - American Journal of Respiratory and Critical Care Medicine 2015 cited by 161

  18. Congenital Heart Disease and Other Heterotaxic Defects in a Large Cohort of Patients With Primary Ciliary Dyskinesia

    Authors: , , , , , , , , , , , , , , , - Circulation 2007 cited by 451

  19. Primary Ciliary Dyskinesia

    Authors: , , - Clinics in Chest Medicine 2016 cited by 273

  20. Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure

    Authors: , , , , , , , , , , , , , , , , , , , , - Thorax 2011 cited by 231

  21. A human ciliopathy reveals essential functions for NEK10 in airway mucociliary clearance

    Authors: , , , , , , , , , , , , , , , , , , , , - Nature Medicine 2020 cited by 73

  22. Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Philippe Gautier, Finn R. Reinholt, Robert A. Hirst, Chris O’Callaghan, Ketil Heimdal, Mathieu Bottier, Estelle Escudier, Suzanne Crowley, Maria Descartes, Ethylin Wang Jabs, Priti Kenia, Jeanne Amiel, Giacomo Maria Bacci, Claudia Calogero, Viviana Palazzo, Lucia Tiberi, Ulrike Blümlein, Andrew Rogers, Jennifer Wambach, Daniel J. Wegner, Anne B. Fulton, Margaret A. Kenna, Margaret Rosenfeld, Ingrid A. Holm, Alan J. Quigley, Emma A. Hall, Laura C. Murphy, Diane Cassidy, Alex von Kriegsheim, Diane M. Cassidy, Alex von Kriegsheim, Jean‐François Papon, Laurent Pasquier, Marlène Murris, James D. Chalmers, Claire Hogg, Kenneth Macleod, Don S. Urquhart, Stefan Unger, Timothy J. Aitman, Serge Amselem, Margaret W. Leigh, Michael R. Knowles, Heymut Omran, Hannah M. Mitchison, Alan Brown, Joseph A. Marsh, Julie P. I. Welburn, Shih-Chieh Ti, Amjad Horani, Jean‐Michel Rozet, Isabelle Perrault, Pleasantine Mill, Isabelle Perrault, Pleasantine Mill - Science 2024 cited by 45

  23. Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole-Genome Analysis of 7,840 Patients

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , - American Journal of Respiratory and Critical Care Medicine 2023 cited by 38

  24. Small-molecule eRF3a degraders rescue CFTR nonsense mutations by promoting premature termination codon readthrough

    Authors: , , , , , , , , , , , , , , , - Journal of Clinical Investigation 2022 cited by 35