D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Medicine D-index 143 Citations 68,189 528 World Ranking 839 National Ranking 502
Biology and Biochemistry D-index 148 Citations 70,794 526 World Ranking 132 National Ranking 101

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Internal medicine
  • Enzyme

His primary areas of investigation include Cystic fibrosis, Cell biology, Cystic fibrosis transmembrane conductance regulator, Pathology and Internal medicine. The study incorporates disciplines such as Immunology, Pathogenesis, Molecular biology, Respiratory system and Airway in addition to Cystic fibrosis. His Cell biology research includes elements of Biochemistry, Adenosine, Respiratory epithelium and Epithelial sodium channel.

His research in Cystic fibrosis transmembrane conductance regulator intersects with topics in Chloride channel, Genetic enhancement and Secretion. His Pathology research integrates issues from Respiratory disease and Gene targeting, Gene. His Internal medicine research is multidisciplinary, relying on both Endocrinology and Amiloride.

His most cited work include:

  • Evidence for Periciliary Liquid Layer Depletion, Not Abnormal Ion Composition, in the Pathogenesis of Cystic Fibrosis Airways Disease (991 citations)
  • Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients (960 citations)
  • CFTR as a cAMP-dependent regulator of sodium channels (948 citations)

What are the main themes of his work throughout his whole career to date?

His scientific interests lie mostly in Cystic fibrosis, Pathology, Internal medicine, Cell biology and Immunology. His studies examine the connections between Cystic fibrosis and genetics, as well as such issues in Molecular biology, with regards to Cell culture. The concepts of his Pathology study are interwoven with issues in In vivo and Respiratory system.

His Internal medicine study incorporates themes from Gastroenterology, Endocrinology and Amiloride. Richard C. Boucher works mostly in the field of Cell biology, limiting it down to topics relating to Apical membrane and, in certain cases, Epithelial polarity. His work carried out in the field of Immunology brings together such families of science as Bronchoalveolar lavage and Mucin.

He most often published in these fields:

  • Cystic fibrosis (38.15%)
  • Pathology (23.17%)
  • Internal medicine (22.13%)

What were the highlights of his more recent work (between 2012-2021)?

  • Cystic fibrosis (38.15%)
  • Immunology (16.90%)
  • Pathology (23.17%)

In recent papers he was focusing on the following fields of study:

Richard C. Boucher focuses on Cystic fibrosis, Immunology, Pathology, Airway and Internal medicine. His research in Cystic fibrosis is mostly focused on Cystic fibrosis transmembrane conductance regulator. His research integrates issues of Bronchoalveolar lavage, Lung and Mucin in his study of Immunology.

His Pathology study incorporates themes from Amiloride, Primary ciliary dyskinesia, In vivo and Lung disease. His work investigates the relationship between Airway and topics such as Pharmacology that intersect with problems in Long acting. His Internal medicine research is multidisciplinary, relying on both Gastroenterology, Endocrinology and Cardiology.

Between 2012 and 2021, his most popular works were:

  • Correction: Corrigendum: Non-invasive airway health assessment: Synchrotron imaging reveals effects of rehydrating treatments on mucociliary transit in-vivo (567 citations)
  • SARS-CoV-2 Reverse Genetics Reveals a Variable Infection Gradient in the Respiratory Tract. (420 citations)
  • Muc5b is required for airway defence (407 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Enzyme
  • Internal medicine

His primary scientific interests are in Cystic fibrosis, Immunology, Lung, Pathology and Mucin. Richard C. Boucher studies Cystic fibrosis transmembrane conductance regulator which is a part of Cystic fibrosis. He has researched Immunology in several fields, including Obstructive lung disease, Case-control study and Lung microbiome.

Richard C. Boucher combines subjects such as In vivo and Respiratory system with his study of Pathology. His work deals with themes such as Mucociliary clearance and Microbiology, which intersect with Mucin. His study in Airway is interdisciplinary in nature, drawing from both Hypertonic saline and Internal medicine.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients

Dieter Worlitzsch;Robert Tarran;Martina Ulrich;Ute Schwab.
Journal of Clinical Investigation (2002)

1464 Citations

Mucus clearance as a primary innate defense mechanism for mammalian airways

Michael R. Knowles;Richard C. Boucher.
Journal of Clinical Investigation (2002)

1430 Citations

Evidence for Periciliary Liquid Layer Depletion, Not Abnormal Ion Composition, in the Pathogenesis of Cystic Fibrosis Airways Disease

Hirotoshi Matsui;Barbara R Grubb;Robert Tarran;Scott H Randell.
Cell (1998)

1415 Citations

CFTR as a cAMP-dependent regulator of sodium channels.

MJ Stutts;CM Canessa;JC Olsen;M Hamrick.
Science (1995)

1300 Citations

Correction: Corrigendum: Non-invasive airway health assessment: Synchrotron imaging reveals effects of rehydrating treatments on mucociliary transit in-vivo

Martin Donnelley;Kaye S. Morgan;Karen K. W. Siu;Nigel R. Farrow.
Scientific Reports (2014)

1140 Citations

An Animal Model for Cystic Fibrosis Made by Gene Targeting

John N. Snouwaert;Kristen K. Brigman;Anne M. Latour;Nadia N. Malouf.
Science (1992)

1136 Citations

SARS-CoV-2 Reverse Genetics Reveals a Variable Infection Gradient in the Respiratory Tract.

Yixuan J. Hou;Kenichi Okuda;Caitlin E. Edwards;David R. Martinez.
Cell (2020)

1033 Citations

Early death due to defective neonatal lung liquid clearance in alpha-ENaC-deficient mice

Edith Hummler;Pierre Barker;John Gatzy;Friedrich Beermann.
Nature Genetics (1996)

1009 Citations

Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice.

Marcus Mall;Barbara R Grubb;Jack R Harkema;Wanda K O'Neal.
Nature Medicine (2004)

999 Citations

Mucus clearance and lung function in cystic fibrosis with hypertonic saline.

Scott H. Donaldson;William D. Bennett;Kirby L. Zeman;Michael R. Knowles.
The New England Journal of Medicine (2006)

790 Citations

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