Sebastien Lebon (Sébastien Lebon)

ORCID

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 6

Top Venues

American journal of medical genetics. Part A

Neurology

Genes

Cells

University Hospital of Lausanne

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University Hospital of Lausanne Nov 1o 2008

Switzerland

Médecin associé :: Woman Mother Child

Publications

Beryl Royer-Bertrand, Sebastien Lebon, Ailsa Craig, Johanna Maeder, Laureane Mittaz-Crettol, Heidi Fodstad, Andrea Superti-Furga, Jean-Marc Good
Developmental disorder and spastic paraparesis in two sisters with a TCF7L2 truncating variant inherited from a mosaic mother. American journal of medical genetics. Part A (2023)
Beryl Royer-Bertrand, Sebastien Lebon, Ailsa Craig, Johanna Maeder, Laureane Mittaz-Crettol, Heidi Fodstad, Andrea Superti-Furga, Jean-Marc Good
Developmental disorder and spastic paraparesis in two sisters with a TCF7L2 truncating variant inherited from a mosaic mother. American journal of medical genetics. Part A (2023)
Beryl Royer-Bertrand, Marine Jequier Gygax, Katarina Cisarova, Jill Anne Rosenfeld, Jennifer A Bassetti, Oana Moldovan, Emily O'Heir, Lindsay C Burrage, Jake Allen, Lisa T Emrick, Emma Eastman, Camille Kumps, Safdar Abbas, Geraldine Van Winckel, null null, Nadia Chabane, Elaine H Zackai, Sebastien Lebon, Beth Keena, Elizabeth Joyce Bhoj, Muhammad Umair, Dong Li, Kirsten Ann Donald, Andrea Superti-Furga
De novo variants in CACNA1E found in patients with intellectual disability, developmental regression and social cognition deficit but no seizures. Molecular autism 12 (1) (2021)
Sebastien Lebon, Mathieu Quinodoz, Virginie G Peter, Carole Gengler, Gaëlle Blanchard, Viviane Cina, Belinda Campos-Xavier, Carlo Rivolta, Andrea Superti-Furga
Agenesis of the Corpus Callosum with Facial Dysmorphism and Intellectual Disability in Sibs Associated with Compound Heterozygous KDM5B Variants. Genes 12 (9) (2021)
Gonzalo P Solis, Tatyana V Kozhanova, Alexey Koval, Svetlana S Zhilina, Tatyana I Mescheryakova, Aleksandr A Abramov, Evgeny V Ishmuratov, Ekaterina S Bolshakova, Karina V Osipova, Sergey O Ayvazyan, Sebastien Lebon, Ilya V Kanivets, Denis V Pyankov, Sabina Troccaz, Denis N Silachev, Nikolay N Zavadenko, Andrey G Prityko, Vladimir L Katanaev
Pediatric Encephalopathy: Clinical, Biochemical and Cellular Insights into the Role of Gln52 of GNAO1 and GNAI1 for the Dominant Disease. Cells 10 (10) (2021)
Alexandra Lipp, Cécile Adam, Jean-Philippe Brouland, Mahmoud Messerer, Jean-Baptiste Armengaud, Sandra Asner, Claudia Poloni, Maja Popovic-Beck, Eliane Roulet-Perez, Sebastien Lebon
Clinical Reasoning: Rapidly progressive gait disorder and cranial nerves involvement in a 9-year-old boy. Neurology 94 (3) (2020)

Sebastien Lebon.css-eqlu8i{font-size:small;padding-left:4px;} (Sébastien Lebon)

Publication Activity (10 Years)

Top Topics

Top Venues

Sebastien Lebon (Sébastien Lebon)