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M. Haddad · SciRah

Researcher profile · Semantic Scholar

M. Haddad

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M. Haddad — researcher profile on SciRah

h-index: 7
Works: 14
Citations: 251

Most-cited papers

Disruption of the ATP8A2 gene in a patient with a t(10;13) de novo balanced translocation and a severe neurological phenotype
Pierre Cacciagli, M. Haddad, C. Mignon‐Ravix, Bilal El-Waly +4 more
2010European Journal of Human Genetics75 citations Open access
Semantic Scholar
Genetic Studies on the Tripartite Glutamate Synapse in the Pathophysiology and Therapeutics of Mood Disorders
R. T. de Sousa, A. Loch, A. Carvalho, A. Brunoni +4 more
2017Neuropsychopharmacology45 citations Open access
Semantic Scholar
Fetal Brain-directed AAV Gene Therapy Results in Rapid, Robust, and Persistent Transduction of Mouse Choroid Plexus Epithelia
M. Haddad, Anthony Donsante, P. Zerfas, S. Kaler
2013Molecular Therapy: Nucleic Acids40 citations Open access
Semantic Scholar
Cerebrospinal Fluid-Directed rAAV9-rsATP7A Plus Subcutaneous Copper Histidinate Advance Survival and Outcomes in a Menkes Disease Mouse Model
M. Haddad, E. Choi, P. Zerfas, Ling Yi +7 more
2018Molecular Therapy: Methods & Clinical Development24 citations Open access
Semantic Scholar
Spatiotemporal expression in mouse brain of Kiaa2022, a gene disrupted in two patients with severe mental retardation.
Vincent Cantagrel, M. Haddad, P. Ciofi, David Andrieu +4 more
2009Gene Expression Patterns24 citations
Semantic Scholar
In utero copper treatment for Menkes disease associated with a severe ATP7A mutation
M. Haddad, C. Macri, C. Holmes, D. Goldstein +5 more
2012Molecular Genetics and Metabolism20 citations Open access
Semantic Scholar
Nhej1 Deficiency Causes Abnormal Development of the Cerebral Cortex
B. El Waly, E. Buhler, M. Haddad, L. Villard
2015Molecular Neurobiology11 citations
Semantic Scholar
Molecular and biochemical characterization of Mottled-dappled, an embryonic lethal Menkes disease mouse model.
M. Haddad, K. Patel, Patricia Sullivan, D. Goldstein +3 more
2014Molecular Genetics and Metabolism6 citations Open access
Semantic Scholar
Characterization of a de novo balanced translocation in a patient with moderate mental retardation and dysmorphic features.
M. Haddad, C. Mignon‐Ravix, Pierre Cacciagli, A. Mégarbané +1 more
2009European Journal of Medical Genetics3 citations
Semantic Scholar
A novel two-nucleotide deletion in the ATP7A gene associated with delayed infantile onset of Menkes disease
T. Wada, M. Haddad, Ling Yi, T. Murakami +5 more
2014Pediatric Neurology2 citations Open access
Semantic Scholar
Tandem Duplication of Exons 1-7 Neither Impairs ATP7A Expression Nor Causes a Menkes Disease Phenotype.
E. Choi, K. Patel, M. Haddad, Ling Yi +5 more
2015JIMD Reports1 citations Open access
Semantic Scholar
Nhej1 Deficiency Causes Abnormal Development of the Cerebral Cortex
B. El Waly, E. Buhler, M. Haddad, L. Villard
2014Molecular Neurobiology1 citations
Semantic Scholar
356. High-Resolution X-Ray Fluorescence Microscopy (XFM) Indicates Enhanced Brain Copper Delivery in AAV9-Treated Menkes Disease Mice
M. Haddad, M. Ralle, D. Vine, P. Zerfas +1 more
20160 citations Open access
Semantic Scholar
197. Survival, Growth, and Neurobehavioral Outcomes in a Mouse Model of Menkes Disease With CSF-Directed AAV9 and Subcutaneous Copper Histidine
M. Haddad, D. Martinelli, E. Choi, P. Zerfas +5 more
20150 citations Open access
Semantic Scholar

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