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Olivia Boyer

Affiliation : Hôpital Necker-Enfants Malades · Inserm · Université Paris Cité · Institut Necker Enfants Malades · Assistance Publique – Hôpitaux de Paris · Institut des Maladies Génétiques Imagine

• 8Publications (affiliation in France)
• 395Total publications
• 7968Citations
• 49h-index

ORCIDOpenAlex

Research profile

Olivia Boyer has 8 indexed publications (2010–2021). Their work appears mainly in “Scientific Reports”, “Journal of the American Society of Nephrology” and “Nature Genetics”. Their most cited article, “Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly” (2017), has been cited 220 times. 2 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers, including institutions in Spain, Canada.

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Research areas

• Renal Diseases and Glomerulopathies
• Vasculitis and related conditions
• Chronic Kidney Disease and Diabetes
• Renal Transplantation Outcomes and Treatments
• Complement system in diseases

Publications (8)

• Early childhood height-adjusted total kidney volume as a risk marker of kidney survival in ARPKD
  2021 · Scientific Reports · cited 26 times
• Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD)
  2020 · Scientific Reports · cited 28 times
• Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
  2017 · Nature Genetics · cited 220 times
• Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome
  2017 · Pediatric Nephrology · cited 41 times
• Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease
  2015 · Journal of the American Society of Nephrology · cited 89 times
• A Homozygous Missense Mutation in the Ciliary Gene TTC21B Causes Familial FSGS
  2014 · Journal of the American Society of Nephrology · cited 119 times
• NPHS2Mutations in Steroid-Resistant Nephrotic Syndrome: A Mutation Update and the Associated Phenotypic Spectrum
  2013 · Human Mutation · cited 94 times
• Mutational analysis of the PLCE1 gene in steroid resistant nephrotic syndrome
  2010 · Journal of Medical Genetics · cited 92 times

Publication venues

• Scientific Reports × 2
• Journal of the American Society of Nephrology × 2
• Nature Genetics × 1
• Pediatric Nephrology × 1
• Human Mutation × 1
• Journal of Medical Genetics × 1

Publications per year

• 20211
• 20201
• 20172
• 20151
• 20141
• 20131
• 20101

Collaborations

Partner institutions : Sorbonne Paris Cité · Université Paris Descartes · Hôpital Robert-Debré · Centre National de la Recherche Scientifique · Centre Hospitalier Universitaire de Bordeaux

Co-authors’ countries : Spain · Canada

Co-authors

• Olivier Gribouval
• Corinne Antignac
• Géraldine Mollet
• Georges Deschênes
• Véronique Baudouin
• Sylvie Cloarec
• Marie-Claire Gübler
• Michel Fischbach
• Bruno Ranchin
• Claire Dossier
• Fabien Névo
• Rémi Salomon

Bibliographic data from OpenAlex (open database).