Guillaume Canaud

Hôpital Necker-Enfants Malades — France

Medicine · Health Sciences

34h-index5.7kcitations119works3.22yr avg
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Research Topics

Renal Diseases and Glomerulopathies(48), Renal Transplantation Outcomes and Treatments(17), Vascular Malformations and Hemangiomas(16), Systemic Lupus Erythematosus Research(14), Vasculitis and related conditions(11)

Publications119 total

Development of 2023 ACR/EULAR Antiphospholipid Syndrome Classification Criteria, Phase III-A/B Report: Defining and Structuring the Clinical and Laboratory Domains
Current Rheumatology Reports·2025
#2710 Podocyte-specific YAP activation triggers crescentic glomerulonephritis through a crosstalk with parietal epithelial cells
Nephrology Dialysis Transplantation·2025Open Access
Prevalence of kidney complications in a large cohort of patients with recessive dystrophic epidermolysis bullosa
British Journal of Dermatology·2025
Podocyte-specific YAP activation triggers crescentic glomerulonephritis through cross-talk with parietal epithelial cells
Science Translational Medicine·2025· 7 cited
Hyperglycemic hyperosmolar coma induced by alpelisib in PIK3CA-related overgrowth spectrum (PROS)
Annales de Dermatologie et de Vénéréologie·2025
118: Randomized, Double-Blind, Phase 2 Study of Alpelisib in Pediatric and Adult Patients With PIK3CA-Related Overgrowth Spectrum (PROS)
Journal of Investigative Dermatology·2025Open Access
A phase II double-blind multicentre, placebo-controlled trial to assess the efficacy and safety of alpelisib (BYL719) in paediatric and adult patients with Megalencephaly-CApillary malformation Polymicrogyria syndrome (MCAP): the SESAM study protocol
BMJ Open·2024· 4 citedOpen Access
SA53 Epidemiology and Hospital Management of Patients With PROS in France
Value in Health·2024
Identifying News Genes Involved in Unexplained Erythrocytosis Throught a Clinical Database
Blood·2024
Epik-P2: A Phase 2 Study of Alpelisib (ALP) in Pediatric and Adult Patients (pts) with <i>PIK3CA</i>-Related Overgrowth Spectrum (PROS)
Blood·2024· 3 cited
Unique presentation of a novel gain-of-function mutation in MTOR
Genes & Diseases·2024Open Access
Des membres inférieurs asymétriques
La Revue de Médecine Interne·2024
Sotorasib for Vascular Malformations Associated with <i>KRAS</i> G12C Mutation
New England Journal of Medicine·2024· 25 cited
Paediatric strategy forum for medicinal product development of PI3-K, mTOR, AKT and GSK3β inhibitors in children and adolescents with cancer
European Journal of Cancer·2024· 9 citedOpen Access
Réintroduction de l’ALPELISIB en cas d’hypersensibilité chez deux patients atteints du syndrome de CLOVES
Revue française d'allergologie·2024
A cystic and bullous lung disease associated with a PIK3CA-related overgrowth syndrome
ERJ Open Research·2024Open Access
Thérapie ciblée pour les syndromes de surcroissance et anomalies vasculaires secondaires à une mutation PIK3CA
JMV-Journal de Médecine Vasculaire·2024
PIK3CA-Related Disorders: From Disease Mechanism to Evidence-Based Treatments
Annual Review of Genomics and Human Genetics·2024· 13 citedOpen Access
A Phase II double-blind multi-center, placebocontrolled trial, to assess the efficacy and safety of alpelisib (BYL719) in pediatric and adult patients with Megalencephaly-CApillary malformation Polymicrogyria syndrome (MCAP): the SESAM trial
SPIRE - Sciences Po Institutional REpository·2024
IL-22 is secreted by proximal tubule cells and regulates DNA damage response and cell death in acute kidney injury
Kidney International·2023· 24 citedOpen Access
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Frequent Co-authors

Christophe Legendre(24), Fabiola Terzi(13), Laure‐Hélène Noël(9), Dany Anglicheau(9), Frank Martinez(8), Frank Bienaimé(7), Julien Zuber(7), Quitterie Venot(5), Clément Hoguin(5), Laurent Guibaud(5), Éric Thervet(5), Marion Rabant(5), Sophia Ladraa(4), Jean–Paul Duong Van Huyen(4), Christine Broissand(4), Renaud Snanoudj(4), Gérard Friedlander(4), Marie-Claire Gübler(4), F. Martinez(4), Antoine Fraissenon(4)