Lalande, Marc

Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization

Cavaillé, J., Buiting, K., Kiefmann, M., Lalande, M., Brannan, C. I., Horsthemke, B., Bachellerie, J.-P., Brosius, J., & Hüttenhofer, A. (2000) · Proceedings of the National Academy of Sciences

Genetic Syndromes and ImprintingRNA modifications and cancer

Cited by 601

The Angelman syndrome candidate gene, UBE3AIE6-AP, is imprinted in brain

Rougeulle, C., Glatt, H., & Lalande, M. (1997) · Nature Genetics

Genetic Syndromes and ImprintingGenetics and Neurodevelopmental Disorders

Cited by 416

Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes

Chamberlain, S. J., Chen, P.-F., Ng, K. Y., Bourgois-Rocha, F., Lemtiri-Chlieh, F., Levine, E. S., & Lalande, M. (2010) · Proceedings of the National Academy of Sciences

Genetic Syndromes and ImprintingPluripotent Stem Cells Research

Cited by 312

Analysis of the set of GABAA receptor genes in the human genome

Simon, J., Wakimoto, H., Fujita, N., Lalande, M., & Barnard, E. A. (2004) · Journal of Biological Chemistry

Neuroscience and Neuropharmacology ResearchReceptor Mechanisms and Signaling

Cited by 253

Recurrent copy number variations in human induced pluripotent stem cells

Martins-Taylor, K., Nisler, B. S., Taapken, S. M., Compton, T., Crandall, L., Montgomery, K. D., Lalande, M., & Xu, R.-H. (2011) · Nature Biotechnology

Pluripotent Stem Cells ResearchGenomic variations and chromosomal abnormalities

Cited by 213

Imprinted expression of UBE3A in non-neuronal cells from a Prader–Willi syndrome patient with an atypical deletion

Martins-Taylor, K., Hsiao, J. S., Chen, P.-F., Glatt-Deeley, H., De Smith, A. J., Blakemore, A. I. F., Lalande, M., & Chamberlain, S. J. (2014) · Human Molecular Genetics

Genetic Syndromes and ImprintingGenomics and Chromatin Dynamics

Cited by 66