Paolo Moretti

Affiliations: 
Baylor College of Medicine, Houston, TX 
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"Paolo Moretti"
Mean distance: 16.34 (cluster 11)
 
SNBCP
Cross-listing: BCM Tree

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Publications

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Murdock DR, Dai H, Burrage LC, et al. (2020) Transcriptome-directed analysis for Mendelian disease diagnosis overcomes limitations of conventional genomic testing. The Journal of Clinical Investigation
Wang X, Posey JE, Rosenfeld JA, et al. (2018) Phenotypic expansion in - a common cause of intellectual disability in females. Annals of Clinical and Translational Neurology. 5: 1277-1285
Boone PM, Yuan B, Campbell IM, et al. (2014) The Alu-rich genomic architecture of SPAST predisposes to diverse and functionally distinct disease-associated CNV alleles. American Journal of Human Genetics. 95: 143-61
Fyffe SL, Neul JL, Samaco RC, et al. (2008) Deletion of Mecp2 in Sim1-expressing neurons reveals a critical role for MeCP2 in feeding behavior, aggression, and the response to stress. Neuron. 59: 947-58
Moretti P, Peters SU, Del Gaudio D, et al. (2008) Brief report: autistic symptoms, developmental regression, mental retardation, epilepsy, and dyskinesias in CNS folate deficiency. Journal of Autism and Developmental Disorders. 38: 1170-7
Moretti P, Zoghbi HY. (2006) MeCP2 dysfunction in Rett syndrome and related disorders. Current Opinion in Genetics & Development. 16: 276-81
Moretti P, Levenson JM, Battaglia F, et al. (2006) Learning and memory and synaptic plasticity are impaired in a mouse model of Rett syndrome. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 319-27
Moretti P, Sahoo T, Hyland K, et al. (2005) Cerebral folate deficiency with developmental delay, autism, and response to folinic acid. Neurology. 64: 1088-90
Moretti P, Bouwknecht JA, Teague R, et al. (2005) Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome. Human Molecular Genetics. 14: 205-20
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