Ganapathi, Mythily

Comparative analysis of chromatin landscape in regulatory regions of human housekeeping and tissue specific genes

Ganapathi, M., Srivastava, P., Sutar, S. K. D., Kumar, K., Dasgupta, D., Pal Singh, G., Brahmachari, V., & Brahmachari, S. K. (2005) · BMC Bioinformatics

Genomics and Chromatin DynamicsChromosomal and Genetic Variations

Cited by 66

Spliceosome Malfunction Causes Neurodevelopmental Disorders with Overlapping Features

Li, D., Wang, Q., Bayat, A., Battig, M. R., Zhou, Y., Bosch, D. G. M., van Haaften, G., Granger, L., Petersen, A. K., Pérez-Jurado, L. A., et al. (2024) · Journal of Clinical Investigation

Genetics and Neurodevelopmental DisordersRNA Research and Splicing

Cited by 46

A homozygous splice variant in ATP5PO , disrupts mitochondrial complex V function and causes Leigh syndrome in two unrelated families

Ganapathi, M., Friocourt, G., Gueguen, N., Friederich, M. W., Le Gac, G., Okur, V., Loaëc, N., Ludwig, T., Ka, C., Tanji, K., et al. (2022) · Journal of Inherited Metabolic Disease

Mitochondrial Function and PathologyMetabolism and Genetic Disorders

Cited by 18

Pathogenetic mechanisms of muscle-specific ribosomes in dilated cardiomyopathy

Murphy, M. R., Ganapathi, M., Lee, T. M., Fisher, J. M., Patel, M. V., Jayakar, P., Buchanan, A., Rippert, A. L., Ahrens-Nicklas, R. C., Nair, D., et al. (2025) · Nature Cardiovascular Research

Cardiomyopathy and Myosin StudiesRNA and protein synthesis mechanisms

Cited by 4