World's Best Scientists 2026 revealed!
Catherine Boileau

Catherine Boileau

D-Index & Metrics

Biology and Biochemistry

D-Index
92
Citations
40264
World Ranking
2172
National Ranking
45

Medicine

D-Index
95
Citations
41573
World Ranking
9934
National Ranking
304

Overview

Catherine Boileau is affiliated with Université Paris Cité in France and has contributed extensively to the fields of medicine and biochemistry, genetics, and molecular biology. Their research primarily focuses on pulmonary and respiratory medicine, genetics, cardiology and cardiovascular medicine, surgery, and infectious diseases.

The scientific work covers numerous topics including connective tissue disorders research, aortic disease and treatment approaches, lipoproteins and cardiovascular health, interstitial lung diseases and idiopathic pulmonary fibrosis, cardiac valve diseases and treatments, aortic aneurysm repair treatments, and SARS-CoV-2 and COVID-19 research.

Boileau's recent significant publications include:

  • "Marfan syndrome," 2021, Nature Reviews Disease Primers
  • "Methotrexate and rheumatoid arthritis associated interstitial lung disease," 2020, European Respiratory Journal
  • "APOE gene variants in primary dyslipidemia," 2021, Atherosclerosis
  • "Clinical relevance of genotype-phenotype correlations beyond vascular events in a cohort study of 1500 Marfan syndrome patients with FBN1 pathogenic variants," 2021, Genetics in Medicine
  • "Genetic and molecular architecture of familial hypercholesterolemia," 2022, Journal of Internal Medicine

Frequent co-authors collaborating with Boileau include:

  • Guillaume Jondeau
  • Pauline Arnaud
  • Nadine Hanna
  • Mathilde Varret
  • Caroline Kannengiesser

Boileau publishes often in several key journals, with a notable number of publications in:

  • Atherosclerosis
  • European Heart Journal
  • Revue du Rhumatisme
  • Journal of the American College of Cardiology
  • Journal of Medical Genetics

The body of work demonstrates a strong interdisciplinary approach, integrating genetics, cardiovascular studies, and pulmonary medicine, reflecting a comprehensive involvement in both clinical and molecular aspects of disease study and treatment research.

Best Publications

  • 2014 ESC Guidelines on the diagnosis and treatment of aortic diseases: Document covering acute and chronic aortic diseases of the thoracic and abdominal aorta of the adult. The Task Force for the Diagnosis and Treatment of Aortic Diseases of the European Society of Cardiology (ESC).

    Erbel R;Aboyans;Boileau C;Bossone E

  • Mutations in PCSK9 cause autosomal dominant hypercholesterolemia.

    Marianne Abifadel;Mathilde Varret;Jean-Pierre Rabès;Delphine Allard

  • Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: consensus statement of the European Atherosclerosis Society

    Borge G. Nordestgaard;M. John Chapman;Steve E. Humphries;Henry N. Ginsberg

  • Diagnosis and management of aortic dissection

    R. Erbel;F. Alfonso;C. Boileau;O. Dirsch

  • Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society

    Marina Cuchel;Eric Bruckert;Henry N. Ginsberg;Frederick J. Raal

  • Familial Hypercholesterolaemia in Children and Adolescents: Gaining Decades of Life by Optimizing Detection and Treatment

    Albert Wiegman;Samuel S. Gidding;Gerald F Watts;M John Chapman

  • NARC-1/PCSK9 and Its Natural Mutants ZYMOGEN CLEAVAGE AND EFFECTS ON THE LOW DENSITY LIPOPROTEIN (LDL) RECEPTOR AND LDL CHOLESTEROL

    Suzanne Benjannet;David Rhainds;Rachid Essalmani;Janice Mayne

  • Heterozygous TGFBR2 mutations in Marfan syndrome

    Takeshi Mizuguchi;Gwenaëlle Collod-Beroud;Takushi Akiyama;Marianne Abifadel

  • Homozigot ailevi hiperkolesterolemi: klinisyenlerin tanıyı ve klinik yönetimi geliştirmelerine yönelik yeni anlayışlar ve rehberlik. Avrupa Ateroskleroz Derneği’nin Ailevi Hiperkolesterolemi Üzerine Uzlaşı Paneli yazılı görüşü

    Marina Cuchel;Eric Bruckert;Henry N. Ginsberg;Frederick J. Raal

  • Effect of mutation type and location on clinical outcome in 1,013 probands with marfan syndrome or related phenotypes and FBN1 mutations : An international study

    L. Faivre;G. Collod-Beroud;G. Collod-Beroud;B.L. Loeys;A. Child

  • Mutations in STAT3 and IL12RB1 impair the development of human IL-17–producing T cells

    Ludovic de Beaucoudrey;Ludovic de Beaucoudrey;Anne Puel;Anne Puel;Orchidée Filipe-Santos;Orchidée Filipe-Santos;Aurélie Cobat;Aurélie Cobat

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

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

  • In Vivo Evidence That Furin from Hepatocytes Inactivates PCSK9

    Rachid Essalmani;Delia Susan-Resiga;Ann Chamberland;Marianne Abifadel

  • Update of the UMD-FBN1 mutation database and creation of an FBN1 polymorphism database.

    Gwenaëlle Collod-Béroud;Saga Le Bourdelles;Lesley Ades;Lesley Ades;Leena Ala-Kokko;Leena Ala-Kokko

  • TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome.

    Catherine Boileau;Dong Chuan Guo;Nadine Hanna;Ellen S. Regalado

  • Mutations and polymorphisms in the proprotein convertase subtilisin kexin 9 (PCSK9) gene in cholesterol metabolism and disease

    Marianne Abifadel;Jean-Pierre Rabès;Martine Devillers;Martine Devillers;Martine Devillers;Arnold Munnich;Arnold Munnich;Arnold Munnich

  • In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome

    L. Faivre;R. J. Gorlin;M. K. Wirtz;M. Godfrey

  • Comparison of Clinical Presentations and Outcomes Between Patients With TGFBR2 and FBN1 Mutations in Marfan Syndrome and Related Disorders

    David Attias;Chantal Stheneur;Carine Roy;Gwenaëlle Collod-Béroud

  • C57BL/6J and A/J mice fed a high-fat diet delineate components of metabolic syndrome.

    Catherine Gallou-Kabani;Alexandre Vigé;Marie-Sylvie Gross;Jean-Pierre Rabès

  • 2014 ESC Guidelines on the Diagnosis and Treatment of Aortic Diseases

    Raimund Erbel;Victor Aboyans;Catherine Boileau;Eduardo Bossone

Frequent Co-Authors

Guillaume Jondeau
Guillaume Jondeau Université Paris Cité
Yannick Allanore
Yannick Allanore Université Paris Cité
Christophe Béroud
Christophe Béroud Aix-Marseille University
Claudine Junien
Claudine Junien INRAE : Institut national de recherche pour l'agriculture, l'alimentation et l'environnement
Luc Mouthon
Luc Mouthon Université Paris Cité
Laurence Faivre
Laurence Faivre University of Burgundy
Jean Sibilia
Jean Sibilia University of Strasbourg
Eric Hachulla
Eric Hachulla University of Lille
Dianna M. Milewicz
Dianna M. Milewicz The University of Texas Health Science Center at Houston

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