Maher A. Noureddine, Ph.D. - Publications

Affiliations: 
University of North Carolina, Chapel Hill, Chapel Hill, NC 
Area:
Cell cycle

12 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2009 Noureddine MA, Menendez D, Campbell MR, Bandele OJ, Horvath MM, Wang X, Pittman GS, Chorley BN, Resnick MA, Bell DA. 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. PMID 19424414 DOI: 10.1371/Journal.Pgen.1000462  0.88
2008 Chorley BN, Wang X, Campbell MR, Pittman GS, Noureddine MA, Bell DA. Discovery and verification of functional single nucleotide polymorphisms in regulatory genomic regions: current and developing technologies. Mutation Research. 659: 147-57. PMID 18565787 DOI: 10.1016/j.mrrev.2008.05.001  0.88
2005 Oliveira SA, Li YJ, Noureddine MA, Zuchner S, Qin X, Pericak-Vance MA, Vance JM. Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease. American Journal of Human Genetics. 77: 252-64. PMID 15986317 DOI: 10.1086/432588  0.88
2005 Noureddine MA, Li YJ, van der Walt JM, Walters R, Jewett RM, Xu H, Wang T, Walter JW, Scott BL, Hulette C, Schmechel D, Stenger JE, Dietrich F, Vance JM, Hauser MA. 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. PMID 15966006 DOI: 10.1002/Mds.20573  0.88
2005 Hauser MA, Li YJ, Xu H, Noureddine MA, Shao YS, Gullans SR, Scherzer CR, Jensen RV, McLaurin AC, Gibson JR, Scott BL, Jewett RM, Stenger JE, Schmechel DE, Hulette CM, et al. Expression profiling of substantia nigra in Parkinson disease, progressive supranuclear palsy, and frontotemporal dementia with parkinsonism. Archives of Neurology. 62: 917-21. PMID 15956162 DOI: 10.1001/Archneur.62.6.917  0.88
2005 Noureddine MA, Qin XJ, Oliveira SA, Skelly TJ, van der Walt J, Hauser MA, Pericak-Vance MA, Vance JM, Li YJ. Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson disease. Human Genetics. 117: 27-33. PMID 15827745 DOI: 10.1007/S00439-005-1259-2  0.88
2005 Haines JL, Hauser MA, Schmidt S, Scott WK, Olson LM, Gallins P, Spencer KL, Kwan SY, Noureddine M, Gilbert JR, Schnetz-Boutaud N, Agarwal A, Postel EA, Pericak-Vance MA. Complement factor H variant increases the risk of age-related macular degeneration. Science (New York, N.Y.). 308: 419-21. PMID 15761120 DOI: 10.1126/Science.1110359  0.88
2005 Züchner S, Noureddine M, Kennerson M, Verhoeven K, Claeys K, De Jonghe P, Merory J, Oliveira SA, Speer MC, Stenger JE, Walizada G, Zhu D, Pericak-Vance MA, Nicholson G, Timmerman V, et al. Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease. Nature Genetics. 37: 289-94. PMID 15731758 DOI: 10.1038/Ng1514  0.88
2004 Donaldson TD, Noureddine MA, Reynolds PJ, Bradford W, Duronio RJ. 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. PMID 15331761 DOI: 10.1091/Mbc.E04-03-0180  0.88
2004 van der Walt JM, Noureddine MA, Kittappa R, Hauser MA, Scott WK, McKay R, Zhang F, Stajich JM, Fujiwara K, Scott BL, Pericak-Vance MA, Vance JM, Martin ER. Fibroblast growth factor 20 polymorphisms and haplotypes strongly influence risk of Parkinson disease. American Journal of Human Genetics. 74: 1121-7. PMID 15122513 DOI: 10.1086/421052  0.88
2003 Hauser MA, Li YJ, Takeuchi S, Walters R, Noureddine M, Maready M, Darden T, Hulette C, Martin E, Hauser E, Xu H, Schmechel D, Stenger JE, Dietrich F, Vance J. Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage. Human Molecular Genetics. 12: 671-7. PMID 12620972 DOI: 10.1093/Hmg/Ddg070  0.88
2002 Noureddine MA, Donaldson TD, Thacker SA, Duronio RJ. Drosophila Roc1a encodes a RING-H2 protein with a unique function in processing the Hh signal transducer Ci by the SCF E3 ubiquitin ligase. Developmental Cell. 2: 757-70. PMID 12062088 DOI: 10.1016/S1534-5807(02)00164-8  0.88
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