D-Index & Metrics Best Publications
Véronique Frémeaux-Bacchi

Véronique Frémeaux-Bacchi

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
Immunology D-index 85 Citations 25,221 266 World Ranking 820 National Ranking 28
Medicine D-index 90 Citations 28,372 334 World Ranking 7684 National Ranking 220

Overview

What is she best known for?

The fields of study she is best known for:

  • Internal medicine
  • Gene
  • Disease

Her primary areas of investigation include Immunology, Atypical hemolytic uremic syndrome, Alternative complement pathway, Complement system and Factor H. Her Immunology research is multidisciplinary, incorporating perspectives in Thrombotic microangiopathy and Kidney disease. Her research in Atypical hemolytic uremic syndrome intersects with topics in Microangiopathic hemolytic anemia, Eculizumab, Preeclampsia and Internal medicine, Disease.

Her Complement system study which covers Complement that intersects with Haemolytic-uraemic syndrome, C3-convertase and End stage renal disease. Her study in Factor H is interdisciplinary in nature, drawing from both Membranoproliferative glomerulonephritis, Glomerulonephritis and Haplotype. Her biological study spans a wide range of topics, including Mutation and Complement factor B.

Her most cited work include:

  • Complement System Part I - Molecular Mechanisms of Activation and Regulation. (594 citations)
  • Complement-Binding Anti-HLA Antibodies and Kidney-Allograft Survival (566 citations)
  • Atypical hemolytic uremic syndrome (419 citations)

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

Véronique Frémeaux-Bacchi mostly deals with Immunology, Atypical hemolytic uremic syndrome, Complement system, Internal medicine and Alternative complement pathway. Many of her studies on Immunology involve topics that are commonly interrelated, such as Transplantation. The Atypical hemolytic uremic syndrome study combines topics in areas such as Thrombotic microangiopathy, Disease, Complement factor B, Eculizumab and Hemolytic anemia.

Her Complement system study combines topics from a wide range of disciplines, such as Molecular biology and Complement. Her Internal medicine research includes themes of Gastroenterology and Endocrinology. Her Alternative complement pathway study combines topics in areas such as Membranoproliferative glomerulonephritis, Glomerulonephritis and Glomerulopathy.

She most often published in these fields:

  • Immunology (52.32%)
  • Atypical hemolytic uremic syndrome (35.57%)
  • Complement system (28.61%)

What were the highlights of her more recent work (between 2016-2021)?

  • Immunology (52.32%)
  • Complement system (28.61%)
  • Atypical hemolytic uremic syndrome (35.57%)

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

Immunology, Complement system, Atypical hemolytic uremic syndrome, Internal medicine and Eculizumab are her primary areas of study. Within one scientific family, she focuses on topics pertaining to Glomerulopathy under Immunology, and may sometimes address concerns connected to Kidney disease and Nephrotic syndrome. Her primary area of study in Complement system is in the field of Alternative complement pathway.

Her Atypical hemolytic uremic syndrome study incorporates themes from Complement factor I, Discontinuation, Factor H, Hazard ratio and CD46. Her Internal medicine research is multidisciplinary, relying on both Gastroenterology, Endocrinology and Streptococcus pneumoniae. Véronique Frémeaux-Bacchi interconnects Thrombotic microangiopathy, Disease, Retrospective cohort study, Kidney transplantation and Dialysis in the investigation of issues within Eculizumab.

Between 2016 and 2021, her most popular works were:

  • Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference (254 citations)
  • Haemolytic uraemic syndrome. (181 citations)
  • Pathogenic Variants in Complement Genes and Risk of Atypical Hemolytic Uremic Syndrome Relapse after Eculizumab Discontinuation (91 citations)

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

Complement System Part I - Molecular Mechanisms of Activation and Regulation

Nicolas S. Merle;Nicolas S. Merle;Nicolas S. Merle;Sarah Elizabeth Church;Sarah Elizabeth Church;Sarah Elizabeth Church;Veronique Fremeaux-Bacchi;Lubka T. Roumenina;Lubka T. Roumenina;Lubka T. Roumenina.
Frontiers in Immunology (2015)

1157 Citations

Complement-Binding Anti-HLA Antibodies and Kidney-Allograft Survival

Alexandre Loupy;Carmen Lefaucheur;Dewi Vernerey;Christof Prugger.
The New England Journal of Medicine (2013)

801 Citations

Complement System Part II: Role in Immunity.

Nicolas S. Merle;Remi Noe;Lise Halbwachs-Mecarelli;Veronique Fremeaux-Bacchi.
Frontiers in Immunology (2015)

782 Citations

Atypical hemolytic uremic syndrome

Chantal Loirat;Véronique Frémeaux-Bacchi.
Orphanet Journal of Rare Diseases (2011)

697 Citations

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.
Clinical Journal of The American Society of Nephrology (2013)

666 Citations

C3 glomerulopathy: consensus report

Matthew C. Pickering;Vivette D. D'agati;Carla M. Nester;Richard J. Smith.
Kidney International (2013)

557 Citations

Anti–Factor H Autoantibodies Associated with Atypical Hemolytic Uremic Syndrome

Marie-Agnès Dragon-Durey;Chantal Loirat;Sylvie Cloarec;Marie-Alice Macher.
Journal of The American Society of Nephrology (2005)

539 Citations

Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies

Aude Servais;Aude Servais;Laure-Hélène Noël;Lubka T. Roumenina;Moglie Le Quintrec.
Kidney International (2012)

508 Citations

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

Chantal Loirat;Fadi Fakhouri;Gema Ariceta;Nesrin Besbas.
Pediatric Nephrology (2016)

506 Citations

Pregnancy-Associated Hemolytic Uremic Syndrome Revisited in the Era of Complement Gene Mutations

Fadi Fakhouri;Lubka Roumenina;François Provot;Marion Sallée.
Journal of The American Society of Nephrology (2010)

502 Citations

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