World's Best Scientists 2026 revealed!

D-Index & Metrics

Medicine

D-Index
76
Citations
16867
World Ranking
18929
National Ranking
632

Overview

Annick Clement is affiliated with Université Paris Cité in France and specializes in Medicine, with a focus on Pulmonary and Respiratory Medicine. Their research encompasses several subfields including Physiology, Genetics, Surgery, and Pathology and Forensic Medicine.

The scientist's main topics of work cover:

  • Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
  • Neonatal Respiratory Health Research
  • Medical Imaging and Pathology Studies
  • Sarcoidosis and Beryllium Toxicity Research
  • Genomics and Rare Diseases
  • Genetic factors in colorectal cancer
  • Occupational exposure and asthma

Annick Clement has coauthored frequently with several researchers, including:

  • Nadia Nathan
  • Hilario Nunès
  • Serge Amselem
  • Bruno Crestani
  • Céline Delestrain

The publication venues where Annick Clement has contributed multiple works include:

  • UNC Libraries
  • Orphanet Journal of Rare Diseases
  • ERJ Open Research
  • European Journal of Pediatrics
  • Thorax

Recent scholarly papers linked to this research activity are:

  • Interstitial lung diseases in children, 2020, La Presse Médicale
  • Functional assessment and phenotypic heterogeneity of SFTPA1 and SFTPA2 mutations in interstitial lung diseases and lung cancer, 2020, European Respiratory Journal
  • RaDiCo, the French national research program on rare disease cohorts, 2021, Orphanet Journal of Rare Diseases
  • Study design of a randomised, placebo-controlled trial of nintedanib in children and adolescents with fibrosing interstitial lung disease, 2021, ERJ Open Research
  • French practical guidelines for the diagnosis and management of idiopathic pulmonary fibrosis - 2021 update. Full-length version, 2022, Respiratory Medicine and Research

Best Publications

  • Bronchoalveolar lavage in children. ERS Task Force on bronchoalveolar lavage in children. European Respiratory Society.

    J de Blic;F Midulla;A Barbato;A Clement

  • Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia.

    Gaëlle Pennarun;Estelle Escudier;Catherine Chapelin;Anne-Marie Bridoux

  • MUC5B Promoter Variant and Rheumatoid Arthritis with Interstitial Lung Disease.

    Pierre-Antoine Juge;Joyce S Lee;Esther Ebstein;Hiroshi Furukawa

  • CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs

    Anne-Christine Merveille;Erica E Davis;Anita Becker-Heck;Anita Becker-Heck;Marie Legendre

  • Long term effects of azithromycin in patients with cystic fibrosis: a double blind, placebo controlled trial

    Clement A;Tamalet A;Leroux E;Ravilly S

  • RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa

    Anne Moore;Estelle Escudier;Gilles Roger;Aline Tamalet

  • Facial side effects during noninvasive positive pressure ventilation in children

    Brigitte Fauroux;Jean-François Lavis;Frédéric Nicot;Arnaud Picard

  • Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis

    Harriet Corvol;Harriet Corvol;Scott M Blackman;Pierre-Yves Boëlle;Paul J Gallins

  • Alveolar epithelial cells: master regulators of lung homeostasis.

    Loïc Guillot;Nadia Nathan;Olivier Tabary;Guillaume Thouvenin

  • European protocols for the diagnosis and initial treatment of interstitial lung disease in children

    Andrew Bush;Steve Cunningham;Jacques de Blic;Angelo Barbato

  • Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosis.

    Pierre-Antoine Juge;Raphaël Borie;Caroline Kannengiesser;Steven Gazal;Steven Gazal

  • Task force on chronic interstitial lung disease in immunocompetent children

    A Clement

  • Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis

    Lei Sun;Johanna M. Rommens;Harriet Corvol;Harriet Corvol;Weili Li

  • Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defects.

    Esther Kott;Marie Legendre;Bruno Copin;Jean-François Papon

  • Loss-of-Function Mutations in LRRC6, a Gene Essential for Proper Axonemal Assembly of Inner and Outer Dynein Arms, Cause Primary Ciliary Dyskinesia

    Esther Kott;Philippe Duquesnoy;Bruno Copin;Marie Legendre

  • Distinct sputum cytokine profiles in cystic fibrosis and other chronic inflammatory airway disease

    E Osika;JM Cavaillon;K Chadelat;M Boule

  • Noninvasive positive pressure ventilation in infants with upper airway obstruction: comparison of continuous and bilevel positive pressure.

    Sandrine Essouri;Frédéric Nicot;Annick Clément;Erea-Noel Garabedian

  • Cystic fibrosis‐related diabetes mellitus: clinical impact of prediabetes and effects of insulin therapy*

    M A Rolon;K Benali;A Munck;J Navarro

  • Physiologic Benefits of Mechanical Insufflation-Exsufflation in Children With Neuromuscular Diseases

    Brigitte Fauroux;Nathalie Guillemot;Guillaume Aubertin;Nadia Nathan

  • Loss-of-function mutations in the human ortholog of Chlamydomonas reinhardtii ODA7 disrupt dynein arm assembly and cause primary ciliary dyskinesia.

    Philippe Duquesnoy;Estelle Escudier;Laetitia Vincensini;Laetitia Vincensini;Judy Freshour

Frequent Co-Authors

Pierre-Yves Boëlle
Pierre-Yves Boëlle Sorbonne University
Dominique Valeyre
Dominique Valeyre Université Paris Cité
Vincent Cottin
Vincent Cottin Claude Bernard University Lyon 1
Andrew Bush
Andrew Bush Imperial College London
Felix Ratjen
Felix Ratjen University of Toronto
Michael I. Polkey
Michael I. Polkey National Institutes of Health
Catherine Boileau
Catherine Boileau Université Paris Cité
Philippe Froguel
Philippe Froguel Imperial College London

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