Dr Yemima Berman

Clinical Associate Lecturer
Genetic Medicine, Northern Clinical School

Telephone +61 2 94631727
Fax +61 2 9845 3204

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Selected publications

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Journals

  • 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, 18(12), e149-e150. [More Information]
  • Seto, J., Chan, S., Turner, N., MacArthur, D., Raftery, J., Berman, Y., Quinlan (nee Edwards), 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. [More Information]
  • Yang, N., Schindeler, A., McDonald, M., Seto, J., Houweling, P., Lek, M., Hogarth, M., Morse, A., Raftery, J., Balasuriya, D., Berman, Y., Quinlan (nee Edwards), K., Little, D., North, K., et al (2011). α-Actinin-3 deficiency is associated with reduced bone mass in human and mouse. Bone, 49(4), 790-798. [More Information]
  • Berman, Y., North, K. (2010). A Gene for Speed: The Emerging Role of {alpha}-Actinin-3 in Muscle Metabolism. Physiology, 25(4), 250-259. [More Information]
  • Uyanik, G., Morris-Rosendahl, D., Stiegler, J., Klapecki, J., Gross, C., Berman, Y., Martin, P., Dey, L., Spranger, S., Korenke, G., Ades, L., et al (2007). Location and type of mutation in the LIS1 gene do not predict phenotypic severity. Neurology, 69(5), 442-447. [More Information]
  • MacArthur, D., Seto, J., Raftery, J., Quinlan (nee Edwards), K., Huttley, G., Hook, J., Lemckert, F., Kee, A., Edwards, M., Berman, Y., Hardeman, E., Gunning, P., Yang, N., North, K., et al (2007). Loss of ACTN3 gene function alters mouse muscle metabolism and shows evidence of positive selection in humans. Nature Genetics, 39(10), 1261-1265. [More Information]
  • Fletcher, J., Hu, M., Berman, Y., Collins, F., Grigg, J., McIver, M., Juppner, H., Alexander, S. (2005). Multicystic dysplastic kidney and variable phenotype in a family with a novel deletion mutation of PAX2. Journal of the American Society of Nephrology, 16(9), 2754-2761. [More Information]

2011

  • 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, 18(12), e149-e150. [More Information]
  • Seto, J., Chan, S., Turner, N., MacArthur, D., Raftery, J., Berman, Y., Quinlan (nee Edwards), 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. [More Information]
  • Yang, N., Schindeler, A., McDonald, M., Seto, J., Houweling, P., Lek, M., Hogarth, M., Morse, A., Raftery, J., Balasuriya, D., Berman, Y., Quinlan (nee Edwards), K., Little, D., North, K., et al (2011). α-Actinin-3 deficiency is associated with reduced bone mass in human and mouse. Bone, 49(4), 790-798. [More Information]

2010

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

2007

  • Uyanik, G., Morris-Rosendahl, D., Stiegler, J., Klapecki, J., Gross, C., Berman, Y., Martin, P., Dey, L., Spranger, S., Korenke, G., Ades, L., et al (2007). Location and type of mutation in the LIS1 gene do not predict phenotypic severity. Neurology, 69(5), 442-447. [More Information]
  • MacArthur, D., Seto, J., Raftery, J., Quinlan (nee Edwards), K., Huttley, G., Hook, J., Lemckert, F., Kee, A., Edwards, M., Berman, Y., Hardeman, E., Gunning, P., Yang, N., North, K., et al (2007). Loss of ACTN3 gene function alters mouse muscle metabolism and shows evidence of positive selection in humans. Nature Genetics, 39(10), 1261-1265. [More Information]

2005

  • Fletcher, J., Hu, M., Berman, Y., Collins, F., Grigg, J., McIver, M., Juppner, H., Alexander, S. (2005). Multicystic dysplastic kidney and variable phenotype in a family with a novel deletion mutation of PAX2. Journal of the American Society of Nephrology, 16(9), 2754-2761. [More Information]

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