Céline Becker

Mutations of NPHP2 and NPHP3 in infantile nephronophthisis.

K. Tory, C. Guyot, R. Salomon, 2009, Kidney international.

An intragenic FAT1 regulatory element deleted in muscular dystrophy patients drives muscle and mesenchyme expression during development

F. Helmbacher, Tarana Nigam, Angela K. Zimmermann, 2022, bioRxiv.

Longitudinal assessment of anti-SARS-CoV-2 antibody dynamics and clinical features following convalescence from a COVID-19 infection

V. Haselmann, M. Neumaier, Volker Ast, 2021, International Journal of Infectious Diseases.

Exploiting the CRISPR/Cas9 system to study alternative splicing in vivo: application to titin.

Isabelle Richard, S. Henriques, I. Richard, 2016, Human molecular genetics.