Birling, Marie-Christine
Centre National de la Recherche Scientifique · Inserm · Institut de génétique et de biologie moléculaire et cellulaire · Phénotypage et ingénierie précliniques des systèmes d’organismes modèles · CELPHEDIA · Université de Strasbourg
4 papers on CoChatORCID 0000-0002-3372-8108
Most cited papers
- Verified
Prevalence of sexual dimorphism in mammalian phenotypic traits
Karp, N. A., Mason, J., Beaudet, A. L., Benjamini, Y., Bower, L., Braun, R. E., Brown, S. D. M., Chesler, E. J., Dickinson, M. E., Flenniken, A. M., et al. (2017) · Nature Communications
Sex and Gender in HealthcareGenetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Cited by 257
- Verified
Reciprocal effects on neurocognitive and metabolic phenotypes in mouse models of 16p11.2 deletion and duplication syndromes
Arbogast, T., Ouagazzal, A.-M., Chevalier, C., Kopanitsa, M., Afinowi, N., Migliavacca, E., Cowling, B. S., Birling, M.-C., Champy, M.-F., Reymond, A., et al. (2016) · PLOS Genetics
Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders
Cited by 151
- Verified
Site-Specific Recombinases for Manipulation of the Mouse Genome
Birling, M.-C., Gofflot, F., & Warot, X. (2009) · Methods in Molecular Biology
CRISPR and Genetic EngineeringAnimal Genetics and Reproduction
Cited by 106
- Verified
Ts66Yah, a mouse model of down syndrome with improved construct and face validity
Duchon, A., del Mar Muñiz Moreno, M., Chevalier, C., Nalesso, V., Andre, P., Fructuoso-Castellar, M., Mondino, M., Po, C., Noblet, V., Birling, M.-C., et al. (2022) · Disease Models & Mechanisms
Down syndrome and intellectual disability researchGenetics and Neurodevelopmental Disorders
Cited by 58
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