M. Noureddine

发表

Complement Factor H Variant Increases the Risk of Age-Related Macular Degeneration

J. Gilbert, J. Haines, M. Pericak-Vance, 2005, Science.

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

M. Pericak-Vance, Yi-Ju Li, J. Vance, 2005, Human Genetics.

Probing the Functional Impact of Sequence Variation on p53-DNA Interactions Using a Novel Microsphere Assay for Protein-DNA Binding with Human Cell Extracts

Douglas A. Bell, Brian N. Chorley, Michelle R. Campbell, 2009, PLoS genetics.

Discovery and verification of functional single nucleotide polymorphisms in regulatory genomic regions: current and developing technologies.

Michelle R. Campbell, Brian N Chorley, M. Noureddine, 2008, Mutation research.

Developmental effects of a chimeric ultraspiracle gene derived from Drosophila and Chironomus.

M. Noureddine, C. Antoniewski, M. Spindler-Barth, 2000, Genesis.

Developmental effects of a chimeric ultraspiracle gene derived from Drosophila and Chironomus

M. Noureddine, C. Antoniewski, M. Spindler-Barth, 2000 .

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

Danqing Zhu, Stephan Züchner, M. Pericak-Vance, 2005, Nature Genetics.

Conserved roles of Osiris genes in insect development, polymorphism and protection

M. Noureddine, C. Smith, C. Morandin, 2018, Journal of evolutionary biology.

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

R. Jensen, Yi-Ju Li, J. Vance, 2005, Archives of neurology.

Drosophila Roc1a encodes a RING-H2 protein with a unique function in processing the Hh signal transducer Ci by the SCF E3 ubiquitin ligase.

M. Noureddine, R. Duronio, T. Donaldson, 2002, Developmental cell.

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

F. Dietrich, J. M. van der Walt, Yi-Ju Li, 2005, Movement disorders : official journal of the Movement Disorder Society.

ANALYSIS OF COURTSHIP SUCCESS IN THE FUNNEL-WEB SPIDER AGELENOPSIS APERTA

M. Noureddine, S. Riechert, Anthony W. Morris, 2000 .

Targeted disruption of Drosophila Roc1b reveals functional differences in the Roc subunit of Cullin-dependent E3 ubiquitin ligases.

M. Noureddine, R. Duronio, T. Donaldson, 2004, Molecular biology of the cell.

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

M. Pericak-Vance, Yi-Ju Li, J. Vance, 2005, American journal of human genetics.

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

Eden R Martin, Kenichiro Fujiwara, Fengyu Zhang, 2004, American journal of human genetics.

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

Eden Martin, F. Dietrich, E. Hauser, 2003, Human molecular genetics.