Virginie Scotet

Inserm — France

Medicine · Health Sciences

27h-index3.0kcitations101works0.02yr avg
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Research Topics

Cystic Fibrosis Research Advances(47), Neonatal Respiratory Health Research(23), Iron Metabolism and Disorders(21), Hemoglobinopathies and Related Disorders(17), Tracheal and airway disorders(10)

Publications101 total

P383 Incidence of cystic fibrosis in Brittany (western France): overview of 50 years of monitoring and 35 years of newborn screening
Journal of Cystic Fibrosis·2025
EPS2.02A new approach to project survival curves by birth cohort in people with cystic fibrosis, drawing on fifty years of experience in Brittany (Western France)
Journal of Cystic Fibrosis·2025
EPS6.02 Striking evolution of survival of cystic fibrosis patients in Brittany (western France): an analysis of the last 50 years by birth cohort
Journal of Cystic Fibrosis·2024
P102 Clear illustration of improved survival in cystic fibrosis using the Kaplan-Meier method: the 50-year experience of Brittany, France
Journal of Cystic Fibrosis·2023Open Access
WS03.04 Survival of people with cystic fibrosis: complete overview in France and first evaluation of the impact of modulators
Journal of Cystic Fibrosis·2023Open Access
The PRSS3P2 and TRY7 deletion copy number variant modifies risk for chronic pancreatitis
Pancreatology·2022· 6 citedOpen Access
Up‐to‐date incidence and initial characteristics of cystic fibrosis in Tunisia
Pediatric Pulmonology·2022· 2 cited
Prevalence of <i>HFE</i>‐related haemochromatosis and secondary causes of hyperferritinaemia and their association with iron overload in 1059 French patients treated by venesection
Alimentary Pharmacology & Therapeutics·2022· 10 cited
WS23.1 Time trends in the incidence of cystic fibrosis: review of the 40-year experience of Brittany (France) and comparison with other regions worldwide
Journal of Cystic Fibrosis·2020Open Access
P003 The diffusion processes of the CFTR mutations in Brittany (France)
Journal of Cystic Fibrosis·2020Open Access
WS09.5 Penetrance is a critical parameter for assessing the disease liability of CFTR variants
Journal of Cystic Fibrosis·2020Open Access
The Changing Epidemiology of Cystic Fibrosis: Incidence, Survival and Impact of the CFTR Gene Discovery
Genes·2020· 294 citedOpen Access
Penetrance is a critical parameter for assessing the disease liability of CFTR variants
Journal of Cystic Fibrosis·2020· 17 citedOpen Access
Newborn Screening for CF across the Globe—Where Is It Worthwhile?
International Journal of Neonatal Screening·2020· 113 citedOpen Access
Genetics of cystic fibrosis: Basics
Archives de Pédiatrie·2020· 23 cited
WS16-1 Analysis of time trends in incidence of cystic fibrosis in Brittany (western France) 30 years after implementation of newborn screening in that area
Journal of Cystic Fibrosis·2019Open Access
EPS5.02 Estimation of survival of cystic fibrosis patients in France by two different methods
Journal of Cystic Fibrosis·2018Open Access
Primary sclerosing cholangitis is associated with abnormalities in CFTR
Journal of Cystic Fibrosis·2018· 13 cited
Do pregnancies reduce iron overload in HFE hemochromatosis women? results from an observational prospective study
BMC Pregnancy and Childbirth·2018· 7 citedOpen Access
Effects of AMPD1 common mutation on the metabolic-chronotropic relationship: Insights from patients with myoadenylate deaminase deficiency
PLoS ONE·2017· 7 citedOpen Access
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Frequent Co-authors

Claude Férec(40), Marie‐Pierre Audrézet(15), Gérald Le Gac(10), I. Duguépéroux(10), Cédric Le Maréchal(8), G. Rault(8), Michel Roussey(7), Marc De Braekeleer(6), Philippe Parent(6), Martine Blayau(6), Jian‐Min Chen(5), I. Quéré(5), Anne‐Yvonne Mercier(5), C. L’Hostis(4), Emmanuelle Masson(4), Sandrine Jacolot(4), Catherine Mura(4), Hubert Journel(4), Karen Rouault(4), Philippe Saliou(4)