Maher A. Noureddine, Ph.D.

University of North Carolina, Chapel Hill, Chapel Hill, NC 
Cell cycle
"Maher Noureddine"
Mean distance: 19.14 (cluster 32)


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Robert J. Duronio grad student 2002 UNC Chapel Hill
 (Genetic and molecular characterization of the melanogaster RING -H2 gene dRoc1a.)
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Noureddine MA, Menendez D, Campbell MR, et al. (2009) Probing the functional impact of sequence variation on p53-DNA interactions using a novel microsphere assay for protein-DNA binding with human cell extracts. Plos Genetics. 5: e1000462
Chorley BN, Wang X, Campbell MR, et al. (2008) Discovery and verification of functional single nucleotide polymorphisms in regulatory genomic regions: current and developing technologies. Mutation Research. 659: 147-57
Oliveira SA, Li YJ, Noureddine MA, et al. (2005) Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease. American Journal of Human Genetics. 77: 252-64
Noureddine MA, Li YJ, van der Walt JM, et al. (2005) Genomic convergence to identify candidate genes for Parkinson disease: SAGE analysis of the substantia nigra. Movement Disorders : Official Journal of the Movement Disorder Society. 20: 1299-309
Hauser MA, Li YJ, Xu H, et al. (2005) Expression profiling of substantia nigra in Parkinson disease, progressive supranuclear palsy, and frontotemporal dementia with parkinsonism. Archives of Neurology. 62: 917-21
Noureddine MA, Qin XJ, Oliveira SA, et al. (2005) Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson disease. Human Genetics. 117: 27-33
Haines JL, Hauser MA, Schmidt S, et al. (2005) Complement factor H variant increases the risk of age-related macular degeneration. Science (New York, N.Y.). 308: 419-21
Züchner S, Noureddine M, Kennerson M, et al. (2005) Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease. Nature Genetics. 37: 289-94
Donaldson TD, Noureddine MA, Reynolds PJ, et al. (2004) Targeted disruption of Drosophila Roc1b reveals functional differences in the Roc subunit of Cullin-dependent E3 ubiquitin ligases. Molecular Biology of the Cell. 15: 4892-903
van der Walt JM, Noureddine MA, Kittappa R, et al. (2004) Fibroblast growth factor 20 polymorphisms and haplotypes strongly influence risk of Parkinson disease. American Journal of Human Genetics. 74: 1121-7
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