Tzur, Shay

Gain-of-function mutation of microRNA-140 in human skeletal dysplasia

Grigelioniene, G., Suzuki, H. I., Taylan, F., Mirzamohammadi, F., Borochowitz, Z. U., Ayturk, U. M., Tzur, S., Horemuzova, E., Lindstrand, A., Weis, M. A., et al. (2019) · Nature Medicine

MicroRNA in disease regulationConnective tissue disorders research

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The Genomic History of the Bronze Age Southern Levant

Agranat-Tamir, L., Waldman, S., Martin, M. A. S., Gokhman, D., Mishol, N., Eshel, T., Cheronet, O., Rohland, N., Mallick, S., Adamski, N., et al. (2020) · Cell

Forensic and Genetic ResearchGenetic diversity and population structure

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A de novo GABRA2 missense mutation in severe early-onset epileptic encephalopathy with a choreiform movement disorder

Orenstein, N., Goldberg-Stern, H., Straussberg, R., Bazak, L., Weisz Hubshman, M., Kropach, N., Gilad, O., Scheuerman, O., Dory, Y., Kraus, D., et al. (2018) · European Journal of Paediatric Neurology

Epilepsy research and treatmentGenomics and Rare Diseases

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