Dr Yemima Berman

Clinical Associate Lecturer
Genetic Medicine, Children's Hospital, Westmead

C29 - Children's Hospital Westmead
The University of Sydney
NSW 2006 Australia

Publications

Chang, F., Berman, Y., Buckland, M., Mackinlay, N., McGlade, A., Collins, S., Ng, K. (2011), Genetic prion disease-associated myelodysplasia and SIADH in siblings. European Journal of Neurology. , e149-50. [Abstract]
Yang, N., Schindeler, A., McDonald, M., Seto, J., Houweling, P., Lek, M., Hogarth, M., Morse, A., Raftery, J., Balasuriya, D., Macarthur, D., Berman, Y., Quinlan, K., Eisman, J., Nguyen, T., Center, J., Prince, R., Wilson, S., Zhu, K., Little, D., North, K. (2011), α-Actinin-3 deficiency is associated with reduced bone mass in human and mouse. Bone. 49(4), 790-798. [Abstract]
Seto, J., Chan, S., Turner, N., Macarthur, D., Raftery, J., Berman, Y., Quinlan, K., Cooney, G., Head, S., Yang, N., North, K. (2011), The effect of α-actinin-3 deficiency on muscle aging. Experimental gerontology. 46(4), 292-302. [Abstract]

Berman, Y., North, K. (2010), A Gene for Speed: The Emerging Role of {alpha}-Actinin-3 in Muscle Metabolism. Physiology. 25(4), 250-259. [Abstract]

Macarthur, D., Seto, J., Raftery, J., Quinlan, K., Huttley, G., Hook, J., Lemckert, F., Kee, A., Edwards, M., Berman, Y., Hardeman, E., Gunning, P., Easteal, S., Yang, N., North, K. (2007), Loss of ACTN3 gene function alters mouse muscle metabolism and shows evidence of positive selection in humans. Nature genetics. 39(10), 1261-5. [Abstract]
Uyanik, G., Morris-Rosendahl, D., Stiegler, J., Klapecki, J., Gross, C., Berman, Y., Martin, P., Dey, L., Spranger, S., Korenke, G., Schreyer, I., Hertzberg, C., Neumann, T., Burkart, P., Spaich, C., Meng, M., Holthausen, H., Adès, L., Seidel, J., Mangold, E., Buyse, G., Meinecke, P., Schara, U., Zeschnigk, C., Muller, D., Helland, G., Schulze, B., Wright, M., Kortge-Jung, S., Hehr, A., Bogdahn, U., Schuierer, G., Kohlhase, J., Aigner, L., Wolff, G., Hehr, U., Winkler, J. (2007), Location and type of mutation in the LIS1 gene do not predict phenotypic severity. Neurology. 69(5), 442-447. [Abstract]
Tay, T., Smith, J., Berman, Y., Adès, L., Missotte, I., Saglibène, H., Martin, F., Mitchell, P., Taylor, D. (2007), Nanophthalmos in a Melanesian population. Clinical & experimental ophthalmology. 35(4), 348-354. [Abstract]