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Isabelle Sermet-Gaudelus

Isabelle Sermet-Gaudelus

D-Index & Metrics

Molecular Biology

D-Index
59
Citations
15904
World Ranking
2006
National Ranking
70

Overview

Isabelle Sermet-Gaudelus is affiliated with Necker-Enfants Malades Hospital in France and has contributed extensively to the field of medicine, focusing primarily on pulmonary and respiratory medicine. Their research spans multiple subfields including molecular biology, infectious diseases, epidemiology, and genetics, with a particular emphasis on cystic fibrosis and respiratory disorders in pediatric populations.

The scientist's publication record includes over 335 works in medicine, with significant contributions to journals such as the Journal of Cystic Fibrosis, where they have published 81 papers, bioRxiv (Cold Spring Harbor Laboratory) with 12 publications, and the European Respiratory Journal featuring 7 articles. Other frequent venues include The Lancet Respiratory Medicine and the International Journal of Molecular Sciences.

Research topics most commonly addressed by Isabelle Sermet-Gaudelus include:

  • Cystic Fibrosis Research Advances
  • Neonatal Respiratory Health Research
  • Tracheal and airway disorders
  • Pediatric health and respiratory diseases
  • Asthma and respiratory diseases
  • Respiratory viral infections research
  • Inhalation and Respiratory Drug Delivery

Frequent co-authors in their work include Philippe Reix, Iwona Pranke, Alexandre Hinzpeter, Aurélie Hatton, and Pierre-Régis Burgel. These collaborations have contributed to an extensive body of work advancing the understanding and treatment of respiratory and genetic disorders related to cystic fibrosis.

Some recent publications by Isabelle Sermet-Gaudelus include:

  • "Neuroimaging manifestations in children with SARS-CoV-2 infection: a multinational, multicentre collaborative study," 2020, The Lancet Child & Adolescent Health
  • "Impact of COVID-19 on people with cystic fibrosis," 2020, The Lancet Respiratory Medicine
  • "A multinational report to characterise SARS-CoV-2 infection in people with cystic fibrosis," 2020, Journal of Cystic Fibrosis
  • "Updated guidance on the management of children with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome/cystic fibrosis screen positive, inconclusive diagnosis (CRMS/CFSPID)," 2020, Journal of Cystic Fibrosis
  • "Airway Surface Liquid pH Regulation in Airway Epithelium Current Understandings and Gaps in Knowledge," 2021, International Journal of Molecular Sciences

Best Publications

  • A CFTR potentiator in patients with cystic fibrosis and the G551D mutation

    Bonnie W. Ramsey;Jane Davies;N. Gerard McElvaney;Elizabeth Tullis

  • Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation

    Philip M. Farrell;Terry B. White;Clement L. Ren;Sarah E. Hempstead

  • SLC34A3 Mutations in Patients with Hereditary Hypophosphatemic Rickets with Hypercalciuria Predict a Key Role for the Sodium-Phosphate Cotransporter NaPi-IIc in Maintaining Phosphate Homeostasis

    Clemens Bergwitz;Nicole M. Roslin;Martin Tieder;J.C. Loredo-Osti

  • US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosis

    R. Andres Floto;R. Andres Floto;Kenneth N. Olivier;Lisa Saiman;Charles L. Daley

  • Recommendations for the classification of diseases as CFTR-related disorders

    Cristina Bombieri;M Claustres;K De Boeck;N Derichs

  • Ataluren for the treatment of nonsense-mutation cystic fibrosis: a randomised, double-blind, placebo-controlled phase 3 trial

    Eitan Kerem;Michael W Konstan;Kris De Boeck;Frank J Accurso

  • European best practice guidelines for cystic fibrosis neonatal screening

    Carlo Castellani;Kevin W. Southern;Keith Brownlee;Jeannette Dankert Roelse

  • Ataluren (PTC124) Induces Cystic Fibrosis Transmembrane Conductance Regulator Protein Expression and Activity in Children with Nonsense Mutation Cystic Fibrosis

    Unknown

  • Long-term safety and efficacy of ivacaftor in patients with cystic fibrosis who have the Gly551Asp-CFTR mutation: a phase 3, open-label extension study (PERSIST)

    Edward F McKone;Drucy Borowitz;Pavel Drevinek;Matthias Griese;Matthias Griese

  • European cystic fibrosis bone mineralisation guidelines.

    Isabelle Sermet-Gaudelus;Maria Luisa Bianchi;Michèle Garabédian;Robert M. Aris

  • In vitro prediction of stop-codon suppression by intravenous gentamicin in patients with cystic fibrosis: a pilot study

    Isabelle Sermet-Gaudelus;Isabelle Sermet-Gaudelus;Michel Renouil;Anne Fajac;Laure Bidou;Laure Bidou

  • Age-Related Prevalence and Distribution of Nontuberculous Mycobacterial Species among Patients with Cystic Fibrosis

    Catherine Pierre-Audigier;Agnès Ferroni;Isabelle Sermet-Gaudelus;Muriel Le Bourgeois

  • Mycobacterium abscessus and children with cystic fibrosis.

    Isabelle Sermet-Gaudelus;Muriel Le Bourgeois;Catherine Pierre-Audigier;Catherine Offredo

  • Association between Staphylococcus aureus alone or combined with Pseudomonas aeruginosa and the clinical condition of patients with cystic fibrosis.

    Unknown

  • Pseudomonas aeruginosa eradicates Staphylococcus aureus by manipulating the host immunity

    Erwan Pernet;Erwan Pernet;Erwan Pernet;Laurent Guillemot;Laurent Guillemot;Pierre-Régis Burgel;Clémence Martin

  • Impact of COVID-19 on people with cystic fibrosis.

    Unknown

  • New clinical diagnostic procedures for cystic fibrosis in Europe

    K. De Boeck;N. Derichs;I. Fajac;H.R. de Jonge

  • Correction of CFTR function in nasal epithelial cells from cystic fibrosis patients predicts improvement of respiratory function by CFTR modulators

    Iwona M. Pranke;Aurélie Hatton;Juliette Simonin;Jean Philippe Jais

  • Real-Life Safety and Effectiveness of Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis

    Unknown

  • The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screening

    Thauvin-Robinet C;Munck A;Huet F;Génin E

Frequent Co-Authors

Aleksander Edelman
Aleksander Edelman Université Paris Cité
Patrick Berche
Patrick Berche Université Paris Cité
Jean-Louis Gaillard
Jean-Louis Gaillard Hôpital Ambroise-Paré
Steven M. Rowe
Steven M. Rowe University of Alabama at Birmingham
J. Stuart Elborn
J. Stuart Elborn Queen's University Belfast
Claire E. Wainwright
Claire E. Wainwright University of Queensland
Michael W. Konstan
Michael W. Konstan Case Western Reserve University
Felix Ratjen
Felix Ratjen University of Toronto
Xavier Nassif
Xavier Nassif Université Paris Cité

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