Corinne Bareil
Institut de Génétique Moléculaire de Montpellier(FR)
Publications by Year
Research Areas
Cystic Fibrosis Research Advances, Retinal Development and Disorders, Tracheal and airway disorders, Neonatal Respiratory Health Research, Genomics and Rare Diseases
Most-Cited Works
- → Mutations in RPE65 cause Leber's congenital amaurosis(1997)608 cited
- → Recommendations for the classification of diseases as CFTR-related disorders(2011)417 cited
- → Gene Expression Signature in Advanced Colorectal Cancer Patients Select Drugs and Response for the Use of Leucovorin, Fluorouracil, and Irinotecan(2007)208 cited
- → Impact of RNA degradation on gene expression profiles: Assessment of different methods to reliably determine RNA quality(2006)182 cited
- → Segregation of a mutation in CNGB1 encoding the β-subunit of the rod cGMP-gated channel in a family with autosomal recessive retinitis pigmentosa(2001)121 cited
- → CFTR-France, a national relational patient database for sharing genetic and phenotypic data associated with rareCFTRvariants(2017)89 cited
- → Mapping of a New Locus for Autosomal Recessive Demyelinating Charcot-Marie-Tooth Disease to 19q13.1-13.3 in a Large Consanguineous Lebanese Family: Exclusion of MAG as a Candidate Gene(2000)87 cited
- → CFTR gene variants, epidemiology and molecular pathology(2020)75 cited
- → Autosomal recessive retinal dystrophy associated with two novel mutations in the RPE65 gene(1998)62 cited
- → A new autosomal recessive non-progressive congenital cerebellar ataxia associated with mental retardation, optic atrophy, and skin abnormalities (CAMOS) maps to chromosome 15q24-q26 in a large consanguineous Lebanese Druze family(2002)37 cited