Year |
Citation |
Score |
2015 |
Choi EY, Patel K, Haddad MR, Yi L, Holmes C, Goldstein DS, Dutra A, Pak E, Kaler SG. Tandem Duplication of Exons 1-7 Neither Impairs ATP7A Expression Nor Causes a Menkes Disease Phenotype. Jimd Reports. 20: 57-63. PMID 25638460 DOI: 10.1007/8904_2014_391 |
0.433 |
|
2015 |
El Waly B, Buhler E, Haddad MR, Villard L. Nhej1 Deficiency Causes Abnormal Development of the Cerebral Cortex. Molecular Neurobiology. 52: 771-82. PMID 25288157 DOI: 10.1007/S12035-014-8919-Y |
0.517 |
|
2014 |
Haddad MR, Patel KD, Sullivan PH, Goldstein DS, Murphy KM, Centeno JA, Kaler SG. Molecular and biochemical characterization of Mottled-dappled, an embryonic lethal Menkes disease mouse model. Molecular Genetics and Metabolism. 113: 294-300. PMID 25456742 DOI: 10.1016/j.ymgme.2014.10.001 |
0.328 |
|
2014 |
Wada T, Haddad MR, Yi L, Murakami T, Sasaki A, Shimbo H, Kodama H, Osaka H, Kaler SG. A novel two-nucleotide deletion in the ATP7A gene associated with delayed infantile onset of Menkes disease. Pediatric Neurology. 50: 417-20. PMID 24630286 DOI: 10.1016/j.pediatrneurol.2014.01.005 |
0.351 |
|
2013 |
Haddad MR, Donsante A, Zerfas P, Kaler SG. Fetal Brain-directed AAV Gene Therapy Results in Rapid, Robust, and Persistent Transduction of Mouse Choroid Plexus Epithelia. Molecular Therapy. Nucleic Acids. 2: e101. PMID 23799375 DOI: 10.1038/Mtna.2013.27 |
0.309 |
|
2009 |
Cantagrel V, Haddad MR, Ciofi P, Andrieu D, Lossi AM, Maldergem Lv, Roux JC, Villard L. Spatiotemporal expression in mouse brain of Kiaa2022, a gene disrupted in two patients with severe mental retardation. Gene Expression Patterns : Gep. 9: 423-9. PMID 19524067 DOI: 10.1016/J.Gep.2009.06.001 |
0.661 |
|
2009 |
Haddad MR, Mignon-Ravix C, Cacciagli P, Mégarbané A, Villard L. Characterization of a de novo balanced translocation in a patient with moderate mental retardation and dysmorphic features. European Journal of Medical Genetics. 52: 211-7. PMID 19379847 DOI: 10.1016/J.Ejmg.2009.04.002 |
0.69 |
|
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