Matthew F. Pescosolido

2013- Neuroscience Brown University, Providence, RI 
"Matthew Pescosolido"
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Lizarraga SB, Ma L, Maguire AM, et al. (2021) Human neurons from Christianson syndrome iPSCs reveal mutation-specific responses to rescue strategies. Science Translational Medicine. 13
Pescosolido MF, Kavanaugh BC, Pochet N, et al. (2019) Complex Neurological Phenotype in Female Carriers of Mutations. Molecular Neuropsychiatry. 5: 98-108
Xu M, Ouyang Q, Gong J, et al. (2017) Mixed Neurodevelopmental and Neurodegenerative Pathology in Nhe6-Null Mouse Model of Christianson Syndrome. Eneuro. 4
Gamsiz ED, Sciarra LN, Maguire AM, et al. (2015) Discovery of Rare Mutations in Autism: Elucidating Neurodevelopmental Mechanisms. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. 12: 553-71
Pescosolido MF, Schwede M, Johnson Harrison A, et al. (2014) Expansion of the clinical phenotype associated with mutations in activity-dependent neuroprotective protein. Journal of Medical Genetics. 51: 587-9
Pescosolido MF, Stein DM, Schmidt M, et al. (2014) Genetic and phenotypic diversity of NHE6 mutations in Christianson syndrome. Annals of Neurology. 76: 581-93
Viscidi EW, Triche EW, Pescosolido MF, et al. (2013) Clinical characteristics of children with autism spectrum disorder and co-occurring epilepsy. Plos One. 8: e67797
Young ME, Galvan T, Reidy BL, et al. (2013) Family functioning deficits in bipolar disorder and ADHD in youth. Journal of Affective Disorders. 150: 1096-102
Seymour KE, Pescosolido MF, Reidy BL, et al. (2013) Emotional face identification in youths with primary bipolar disorder or primary attention-deficit/hyperactivity disorder. Journal of the American Academy of Child and Adolescent Psychiatry. 52: 537-546.e3
Pescosolido MF, Gamsiz ED, Nagpal S, et al. (2013) Distribution of disease-associated copy number variants across distinct disorders of cognitive development. Journal of the American Academy of Child and Adolescent Psychiatry. 52: 414-430.e14
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