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Medicine

D-Index
82
Citations
23550
World Ranking
16172
National Ranking
529

Overview

Chantal Loirat is affiliated with Grenoble Alpes University in France. Their research primarily spans the fields of Medicine and Biochemistry, Genetics and Molecular Biology, with specific focus areas including Immunology, Nephrology, Genetics, Pediatrics, Perinatology and Child Health, and History.

The main topics of their work cover Complement system in diseases, Renal Diseases and Glomerulopathies, Adenosine and Purinergic Signaling, Pregnancy and preeclampsia studies, Neurological Complications and Syndromes, Genetic and Kidney Cyst Diseases, and Renal and related cancers.

Their frequent co-authors include Fádi Fakhouri, Marc Fila, Olivia Boyer, François Provôt, and Yahsou Delmas. Over time, they have published in several notable scientific venues. These venues include Blood, Kidney International, Perfectionnement en Pédiatrie, UNC Libraries, and médecine/sciences.

Notable papers associated with Chantal Loirat include:

  • Eculizumab discontinuation in children and adults with atypical hemolytic-uremic syndrome: a prospective multicenter study, 2020, Blood
  • Management of thrombotic microangiopathy in pregnancy and postpartum: report from an international working group, 2020, Blood
  • The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies, 2023, Kidney International
  • Histoire de la dialyse en pédiatrie, 2021, Perfectionnement en Pédiatrie
  • Schimke immunoosseous dysplasia: defining skeletal features, 2020, UNC Libraries

Best Publications

  • Terminal Complement Inhibitor Eculizumab in Atypical Hemolytic–Uremic Syndrome

    C.M. Legendre;C. Licht;P. Muus;L.A. Greenbaum

  • Genetics and Outcome of Atypical Hemolytic Uremic Syndrome: A Nationwide French Series Comparing Children and Adults

    Véronique Fremeaux-Bacchi;Fadi Fakhouri;Arnaud Garnier;Frank Bienaimé

  • Atypical hemolytic uremic syndrome

    Chantal Loirat;Véronique Frémeaux-Bacchi

  • Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference

    Timothy H.J. Goodship;H. Terence Cook;Fadi Fakhouri;Fernando C. Fervenza

  • An international consensus approach to the management of atypical hemolytic uremic syndrome in children.

    Chantal Loirat;Fadi Fakhouri;Gema Ariceta;Nesrin Besbas

  • Haemolytic uraemic syndrome.

    Fadi Fakhouri;Julien Zuber;Véronique Frémeaux-Bacchi;Chantal Loirat

  • Anti–Factor H Autoantibodies Associated with Atypical Hemolytic Uremic Syndrome

    Marie-Agnès Dragon-Durey;Chantal Loirat;Sylvie Cloarec;Marie-Alice Macher

  • Differential Impact of Complement Mutations on Clinical Characteristics in Atypical Hemolytic Uremic Syndrome

    Anne-Laure Sellier-Leclerc;Veronique Fremeaux-Bacchi;Marie-Agnès Dragon-Durey;Marie-Alice Macher

  • Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome

    Mathieu Lemaire;Véronique Frémeaux-Bacchi;Franz Schaefer;Murim Choi

  • Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies

    Julien Zuber;Fadi Fakhouri;Lubka T. Roumenina;Chantal Loirat

  • Heterozygous and Homozygous Factor H Deficiencies Associated with Hemolytic Uremic Syndrome or Membranoproliferative Glomerulonephritis: Report and Genetic Analysis of 16 Cases

    Marie-Agnès Dragon-Durey;Véronique Frémeaux-Bacchi;Chantal Loirat;Jacques Blouin

  • Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome

    V Fremeaux-Bacchi;MA Dragon-Durey;J Blouin;C Vigneau

  • Efficacy and safety of eculizumab in atypical hemolytic uremic syndrome from 2-year extensions of phase 2 studies

    Christoph Licht;Larry A. Greenbaum;Petra Muus;Sunil Babu

  • Clinical Features of Anti-Factor H Autoantibody–Associated Hemolytic Uremic Syndrome

    Marie-Agnès Dragon-Durey;Sidharth Kumar Sethi;Arvind Bagga;Caroline Blanc

  • Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia.

    Cornelius F. Boerkoel;Hiroshi Takashima;Joy John;Jiong Yan

  • A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disorders.

    N. Besbas;D. Karpman;D. Landau;C. Loirat

  • Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database

    C. Jeanpierre;E. Denamur;I. Henry;M.-O. Cabanis

  • Eculizumab for Atypical Hemolytic Uremic Syndrome Recurrence in Renal Transplantation

    J. Zuber;M. Le Quintrec;S. Krid;C. Bertoye

  • Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndrome.

    M. Le Quintrec;J. Zuber;B. Moulin;N. Kamar

  • Initial presentation of childhood-onset systemic lupus erythematosus: a French multicenter study.

    B Bader-Meunier;J B Armengaud;E Haddad;R Salomon

Frequent Co-Authors

Marie-Agnès Dragon-Durey
Marie-Agnès Dragon-Durey Université Paris Cité
Patrick Niaudet
Patrick Niaudet Necker-Enfants Malades Hospital
Christophe Legendre
Christophe Legendre Necker-Enfants Malades Hospital
Timothy H.J. Goodship
Timothy H.J. Goodship Newcastle University
Wolf H. Fridman
Wolf H. Fridman Université Paris Cité
Catherine Sautès-Fridman
Catherine Sautès-Fridman Université Paris Cité
Richard R. Furman
Richard R. Furman NewYork–Presbyterian Hospital
Pierre Cochat
Pierre Cochat Claude Bernard University Lyon 1

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