Olivia BOYER | Institut Imagine

Présentation

Olivia BOYER

Laboratoire des Maladies Rénales Héréditaires

Contact :

olivia.boyer@institutimagine.org

À propos

Publications scientifiques

Publications

2025

Artificial intelligence and perspective for rare genetic kidney diseases., Kidney Int
2024

Steroid-Resistant Nephrotic Syndrome due to Variants Is Not Associated With ..., Kidney Int Rep
2023

The genetic landscape and clinical spectrum of nephronophthisis and related c..., Kidney Int
2023

The Smart Data Extractor, a Clinician Friendly Solution to Accelerate and Imp..., Stud Health Technol Inform
2023

Overcoming the challenges associated with identification of deep intronic var..., Clin Genet
2022

Human kidney-derived hematopoietic stem cells can support long-term multiline..., Kidney Int
2020

Donor-targeted serotherapy as a rescue therapy for steroid-resistant acute GV..., Am J Transplant
2019

Human C-terminal CUBN variants associate with chronic proteinuria and normal ..., J Clin Invest
2019

Defects in tA tRNA modification due to GON7 and YRDC mutations lead to Gallow..., Nat Commun
2019

TBC1D8B Loss-of-Function Mutations Lead to X-Linked Nephrotic Syndrome via De..., Am J Hum Genet
2017

Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microc..., Nat Genet
2017

Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis an..., J Clin Invest