Greenberg, Cheryl R.
University of Manitoba
6 papers on CoChatORCID 0000-0002-4741-8442
Most cited papers
- Verified
Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm
Telenius, H., Kremer, B., Goldberg, Y. P., Theilmann, J., Andrew, S. E., Zeisler, J., Adam, S., Greenberg, C., Ives, E. J., Clarke, L. A., et al. (1994) · Nature Genetics
Genetic Neurodegenerative DiseasesGenetic factors in colorectal cancer
Cited by 439
- Verified
Limb-Girdle Muscular Dystrophy Type 2H Associated with Mutation in TRIM32, a Putative E3-Ubiquitin–Ligase Gene
Frosk, P., Weiler, T., Nylen, E., Sudha, T., Greenberg, C. R., Morgan, K., Fujiwara, T. M., & Wrogemann, K. (2002) · The American Journal of Human Genetics
Muscle Physiology and DisordersGenomics and Rare Diseases
Cited by 261
- Verified
TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone.
Huang, L., Szymanska, K., Jensen, V. L., Janecke, A. R., Innes, A. M., Davis, E. E., Frosk, P., Li, C., Willer, J. R., Chodirker, B. N., et al. (2011) · The American Journal of Human Genetics
Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances
Cited by 194
- Verified
A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus
Weiler, T., Greenberg, C. R., Zelinski, T., Nylen, E., Coghlan, G., Crumley, M. J., Fujiwara, T. M., Morgan, K., & Wrogemann, K. (1998) · The American Journal of Human Genetics
Muscle Physiology and DisordersGenomics and Rare Diseases
Cited by 115
- Verified
Clinical genetics and the Hutterite population: a review of Mendelian disorders.
Boycott, K. M., Parboosingh, J. S., Chodirker, B. N., Lowry, R. B., McLeod, D. R., Morris, J., Greenberg, C. R., Chudley, A. E., Bernier, F. P., Midgley, J., et al. (2008) · American Journal of Medical Genetics Part A
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 50
- Verified
Elevated neonatal 3-OH isovalerylcarnitine due to breast milk sources in maternal 3-MCC deficiency
Eichhorst, J., Alcorn, J., LePage, J., Etter, M., Antonishyn, N. A., Fitterer, B., Birch, D. A., Agopsowicz, K. L., Ruthnum, L., Greenberg, C. R., et al. (2010) · Molecular Genetics and Metabolism
Metabolism and Genetic DisordersLysosomal Storage Disorders Research
Cited by 8
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