Noureddine M - Search Results

1

Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage.

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. Hauser MA, et al. Among authors: noureddine m. Hum Mol Genet. 2003 Mar 15;12(6):671-7. Hum Mol Genet. 2003. PMID: 12620972

2

Fibroblast growth factor 20 polymorphisms and haplotypes strongly influence risk of Parkinson disease.

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. van der Walt JM, et al. Among authors: noureddine ma. Am J Hum Genet. 2004 Jun;74(6):1121-7. doi: 10.1086/421052. Epub 2004 Apr 30. Am J Hum Genet. 2004. PMID: 15122513 Free PMC article.

3

Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson disease.

Noureddine MA, Qin XJ, Oliveira SA, Skelly TJ, van der Walt J, Hauser MA, Pericak-Vance MA, Vance JM, Li YJ. Noureddine MA, et al. Hum Genet. 2005 Jun;117(1):27-33. doi: 10.1007/s00439-005-1259-2. Epub 2005 Apr 13. Hum Genet. 2005. PMID: 15827745

4

Expression profiling of substantia nigra in Parkinson disease, progressive supranuclear palsy, and frontotemporal dementia with parkinsonism.

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, Vance JM. Hauser MA, et al. Among authors: noureddine ma. Arch Neurol. 2005 Jun;62(6):917-21. doi: 10.1001/archneur.62.6.917. Arch Neurol. 2005. PMID: 15956162

5

Genomic convergence to identify candidate genes for Parkinson disease: SAGE analysis of the substantia nigra.

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. Noureddine MA, et al. Mov Disord. 2005 Oct;20(10):1299-309. doi: 10.1002/mds.20573. Mov Disord. 2005. PMID: 15966006

6

Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.

Oliveira SA, Li YJ, Noureddine MA, Zuchner S, Qin X, Pericak-Vance MA, Vance JM. Oliveira SA, et al. Among authors: noureddine ma. Am J Hum Genet. 2005 Aug;77(2):252-64. doi: 10.1086/432588. Epub 2005 Jun 28. Am J Hum Genet. 2005. PMID: 15986317 Free PMC article.

7

Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease.

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, Vance JM. Züchner S, et al. Among authors: noureddine m. Nat Genet. 2005 Mar;37(3):289-94. doi: 10.1038/ng1514. Epub 2005 Jan 30. Nat Genet. 2005. PMID: 15731758

8

Complement factor H variant increases the risk of age-related macular degeneration.

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. Haines JL, et al. Among authors: noureddine m. Science. 2005 Apr 15;308(5720):419-21. doi: 10.1126/science.1110359. Epub 2005 Mar 10. Science. 2005. PMID: 15761120

9

Noncanonical DNA motifs as transactivation targets by wild type and mutant p53.

Jordan JJ, Menendez D, Inga A, Noureddine M, Bell DA, Resnick MA. Jordan JJ, et al. Among authors: noureddine m. PLoS Genet. 2008 Jun 27;4(6):e1000104. doi: 10.1371/journal.pgen.1000104. PLoS Genet. 2008. PMID: 18714371 Free PMC article.

10

Probing the functional impact of sequence variation on p53-DNA interactions using a novel microsphere assay for protein-DNA binding with human cell extracts.

Noureddine MA, Menendez D, Campbell MR, Bandele OJ, Horvath MM, Wang X, Pittman GS, Chorley BN, Resnick MA, Bell DA. Noureddine MA, et al. PLoS Genet. 2009 May;5(5):e1000462. doi: 10.1371/journal.pgen.1000462. Epub 2009 May 8. PLoS Genet. 2009. PMID: 19424414 Free PMC article.

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