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Maher Noureddine

Research Profile

Disorders

Parkinson's Disease

Genes & Molecular Sequences

Physiology

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Genetic Techniques

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Publications

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Maher A Noureddine; Daniel Menendez; Michelle R Campbell; Omari J Bandele; Monica M Horvath; Xuting Wang; Gary S Pittman; Brian N Chorley; Michael A Resnick; Douglas A Bell
Probing the functional impact of sequence variation on p53-DNA interactions using a novel microsphere assay for protein-DNA binding with human cell extracts.
Brian N Chorley; Xuting Wang; Michelle R Campbell; Gary S Pittman; Maher A Noureddine; Douglas A Bell
Discovery and verification of functional single nucleotide polymorphisms in regulatory genomic regions: current and developing technologies.
Maher A Noureddine; Yi-Ju Li; Joelle M van der Walt; Robert Walters; Rita M Jewett; Hong Xu; Tianyuan Wang; Jeffrey W Walter; Burton L Scott; Christine M Hulette; Donald E Schmechel; Judith E Stenger; Fred S Dietrich; Jeffery Vance; Michael A Hauser
Genomic convergence to identify candidate genes for Parkinson disease: SAGE analysis of the substantia nigra.

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All Publications

2009: Maher A Noureddine; Daniel Menendez; Michelle R Campbell; Omari J Bandele; Monica M Horvath; Xuting Wang; Gary S Pittman; Brian N Chorley; Michael A Resnick; Douglas A Bell
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 2009;5(5):e1000462.
2008: Brian N Chorley; Xuting Wang; Michelle R Campbell; Gary S Pittman; Maher A Noureddine; Douglas A Bell
Discovery and verification of functional single nucleotide polymorphisms in regulatory genomic regions: current and developing technologies.
Mutation research 2008;659(1-2):147-57.
2005: Maher A Noureddine; Yi-Ju Li; Joelle M van der Walt; Robert Walters; Rita M Jewett; Hong Xu; Tianyuan Wang; Jeffrey W Walter; Burton L Scott; Christine M Hulette; Donald E Schmechel; Judith E Stenger; Fred S Dietrich; Jeffery Vance; Michael A Hauser
Genomic convergence to identify candidate genes for Parkinson disease: SAGE analysis of the substantia nigra.
Movement disorders : official journal of the Movement Disorder Society 2005;20(10):1299-309.
2005: Sofia A Oliveira; Yi-Ju Li; Maher A Noureddine; Stephan Zuchner; Xuejun Qin; Margaret Pericak-Vance; Jeffery Vance
Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.
American journal of human genetics 2005;77(2):252-64.
2005: Michael A Hauser; Yi-Ju Li; Hong Xu; Maher A Noureddine; Yujun S Shao; Steven R Gullans; Clemens R Scherzer; Roderick V Jensen; Adam C McLaurin; Jason R Gibson; Burton L Scott; Rita M Jewett; Judith E Stenger; Donald E Schmechel; Christine M Hulette; Jeffery Vance
Expression profiling of substantia nigra in Parkinson disease, progressive supranuclear palsy, and frontotemporal dementia with parkinsonism.
Archives of neurology 2005;62(6):917-21.
2005: Maher A Noureddine; Xue-Jun Qin; Sofia A Oliveira; Tara J Skelly; Joelle M van der Walt; Michael A Hauser; Margaret Pericak-Vance; Jeffery Vance; Yi-Ju Li
Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson disease.
Human genetics 2005;117(1):27-33.
2005: Jonathan L Haines; Michael A Hauser; Silke Schmidt; William Scott; Lana M Olson; Paul Gallins; Kylee L Spencer; Shu Ying Kwan; Maher A Noureddine; John Gilbert; Nathalie Schnetz-Boutaud; Anita Agarwal; Eric A Postel; Margaret Pericak-Vance
Complement factor H variant increases the risk of age-related macular degeneration.
Science (New York, N.Y.) 2005;308(5720):419-21.
2005: Stephan Zuchner; Maher A Noureddine; Marina L Kennerson; Kristien Verhoeven; Kristl G Claeys; Peter De Jonghe; John Merory; Sofia A Oliveira; Marcy C Speer; Judith E Stenger; Gina Walizada; Danqing Zhu; Margaret Pericak-Vance; Garth Nicholson; Vincent Timmerman; Jeffery Vance
Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease.
Nature genetics 2005;37(3):289-94.
2004: Timothy D Donaldson; Maher A Noureddine; Patrick J Reynolds; William Bradford; Robert J Duronio
Targeted disruption of Drosophila Roc1b reveals functional differences in the Roc subunit of Cullin-dependent E3 ubiquitin ligases.
Molecular biology of the cell 2004;15(11):4892-903.
2004: Joelle M van der Walt; Maher A Noureddine; Raja Kittappa; Michael A Hauser; William Scott; Ron McKay; Fengyu Zhang; Jeffrey M Stajich; Kenichiro Fujiwara; Burton L Scott; Margaret Pericak-Vance; Jeffery Vance; Eden R Martin
Fibroblast growth factor 20 polymorphisms and haplotypes strongly influence risk of Parkinson disease.
American journal of human genetics 2004;74(6):1121-7.
2003: Michael A Hauser; Yi-Ju Li; Satoshi Takeuchi; Robert Walters; Maher A Noureddine; Melinda Maready; Tiffany Darden; Christine M Hulette; Eden R Martin; Elizabeth R Hauser; Hong Xu; Donald E Schmechel; Judith E Stenger; Fred S Dietrich; Jeffery Vance
Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage.
Human molecular genetics 2003;12(6):671-7.
2002: Maher A Noureddine; Timothy D Donaldson; Stephen A Thacker; Robert J Duronio
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 2002;2(6):757-70.
2000: Vincent C Henrich; M E Vogtli; Christophe Antoniewski; Margarethe Spindler-Barth; Sabina Przibilla; Maher A Noureddine; Markus Lezzi
Developmental effects of a chimeric ultraspiracle gene derived from Drosophila and Chironomus.
Genesis (New York, N.Y. : 2000) 2000;28(3-4):125-33.