Maher Noureddine

University of North Carolina at Chapel Hill — United States

Neuroscience · Life Sciences

16h-index3.8kcitations25works0.02yr avg
OpenAlex↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Neurobiology and Insect Physiology Research(5), Parkinson's Disease Mechanisms and Treatments(4), Cancer-related Molecular Pathways(4), Ubiquitin and proteasome pathways(4), Genetic Neurodegenerative Diseases(3)

Publications25 total

Drosophila Roc1a Encodes a RING-H2 Protein with a Unique Function in Processing the Hh Signal Transducer Ci by the SCF E3 Ubiquitin Ligase
UNC Libraries·2021· 1 citedOpen Access
Correction: Noncanonical DNA Motifs as Transactivation Targets by Wild Type and Mutant p53
UNC Libraries·2021Open Access
Targeted Disruption of Drosophila Roc1b Reveals Functional Differences in the Roc Subunit of Cullin-dependent E3 Ubiquitin Ligases
UNC Libraries·2020· 4 citedOpen Access
Conserved roles of Osiris genes in insect development, polymorphism and protection
Journal of Evolutionary Biology·2018· 57 citedOpen Access
Abstract 4744: Sequence-specific p53-DNA binding to gene regulatory elements is altered by single-nucleotide polymorphisms
Cancer Research·2010
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· 43 citedOpen Access
Correction: Motility Screen Identifies Drosophila IGF-II mRNA-Binding Protein, a Zipcode-Binding Protein Acting in Oogenesis and Synaptogenesis
PLoS Genetics·2008Open Access
Correction: Noncanonical DNA Motifs as Transactivation Targets by Wild Type and Mutant p53
PLoS Genetics·2008· 6 citedOpen Access
Discovery and verification of functional single nucleotide polymorphisms in regulatory genomic regions: Current and developing technologies
Mutation Research/Reviews in Mutation Research·2008· 179 citedOpen Access
Evolutionary divergence of human p53 binding sites: use of high throughput DNA binding assays to characterize functional variation in cell cycle and apoptosis pathways
Cancer Research·2007
Identification of Risk and Age-at-Onset Genes on Chromosome 1p in Parkinson Disease
The American Journal of Human Genetics·2005· 79 citedOpen Access
Genomic convergence to identify candidate genes for Parkinson disease: SAGE analysis of the substantia nigra
Movement Disorders·2005· 51 cited
Expression Profiling of Substantia Nigra in Parkinson Disease, Progressive Supranuclear Palsy, and Frontotemporal Dementia With Parkinsonism
Archives of Neurology·2005· 158 cited
Mutations in the Pleckstrin Homology Domain of Dynamin 2 Cause Dominant Intermediate Charcot-Marie-Tooth Disease
Neurology·2005· 4 cited
Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson disease
Human Genetics·2005· 76 cited
Complement Factor H Variant Increases the Risk of Age-Related Macular Degeneration
Science·2005· 2.4k cited
Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease
Nature Genetics·2005· 356 cited
Targeted Disruption of<i>Drosophila</i>Roc1b Reveals Functional Differences in the Roc Subunit of Cullin-dependent E3 Ubiquitin Ligases
Molecular Biology of the Cell·2004· 31 citedOpen Access
Growth Factor 20 Polymorphisms and Haplotypes Strongly Influence Risk of Parkinson Disease
2004
Fibroblast Growth Factor 20 Polymorphisms and Haplotypes Strongly Influence Risk of Parkinson Disease
The American Journal of Human Genetics·2004· 135 citedOpen Access
page 1 of 2Next →

Frequent Co-authors

Jeffery M. Vance(9), Douglas A. Bell(7), Michael A. Hauser(6), Judith E. Stenger(5), Yi‐Ju Li(5), Sofia A. Oliveira(4), Robert J. Duronio(4), Daniel Menéndez(4), Michael A. Resnick(4), Margaret A. Pericak‐Vance(3), Stephan Züchner(3), Margaret A. Pericak‐Vance(3), Xuting Wang(3), Gary S. Pittman(3), B.L. Scott(3), Eden R. Martin(3), Timothy D. Donaldson(3), Jennifer Jordan(3), Alberto Inga(3), William K. Scott(2)