Lekbir Baala
Université d'Orléans(FR)Centre National de la Recherche Scientifique(FR)Immunologie et Neurogénétique Expérimentales et Moléculaires(FR)Centre hospitalier universitaire d'Orléans(FR)
Publications by Year
Research Areas
Genetic and Kidney Cyst Diseases, Wnt/β-catenin signaling in development and cancer, Genetic Syndromes and Imprinting, Respiratory viral infections research, dental development and anomalies
Most-Cited Works
- → The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome(2007)489 cited
- → Claudin-1 gene mutations in neonatal sclerosing cholangitis associated with ichthyosis: A tight junction disease(2004)412 cited
- → Pleiotropic Effects of CEP290 (NPHP6) Mutations Extend to Meckel Syndrome(2007)281 cited
- → The Meckel-Gruber Syndrome Gene, MKS3, Is Mutated in Joubert Syndrome(2006)236 cited
- → Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis(2007)200 cited
- → Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus(2007)103 cited