Fabien Lesne
Université d'Orléans(FR)Sorbonne Université(FR)Assistance Publique – Hôpitaux de Paris(FR)Pitié-Salpêtrière Hospital(FR)Centre hospitalier universitaire d'Orléans(FR)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, SARS-CoV-2 detection and testing, Mitochondrial Function and Pathology, Retinal Development and Disorders, Fetal and Pediatric Neurological Disorders
Most-Cited Works
- → Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance(2017)96 cited
- → Delayed‐onset Friedreich's ataxia revisited(2015)68 cited
- → Effect of Tenofovir Disoproxil Fumarate and Emtricitabine on nasopharyngeal SARS-CoV-2 viral load burden amongst outpatients with COVID-19: A pilot, randomized, open-label phase 2 trial(2021)64 cited
- → ARID1Bmutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability(2016)36 cited
- → Copy Number Variations Found in Patients with a Corpus Callosum Abnormality and Intellectual Disability(2017)36 cited
- → Diagnostic accuracy of a rapid antigen triple test (SARS-CoV-2, respiratory syncytial virus, and influenza) using anterior nasal swabs versus multiplex RT-PCR in children in an emergency department(2023)28 cited