Samantha Paterson

University of Glasgow, Glasgow, Scotland, United Kingdom 
Physics, MRI, pre-clinical MRI, Sleeping Sickness
"Samantha Paterson"
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Newschaffer CJ, Schriver E, Berrigan L, et al. (2016) Development and validation of a streamlined autism case confirmation approach for use in epidemiologic risk factor research in prospective cohorts. Autism Research : Official Journal of the International Society For Autism Research
St John T, Estes AM, Dager SR, et al. (2016) Emerging Executive Functioning and Motor Development in Infants at High and Low Risk for Autism Spectrum Disorder. Frontiers in Psychology. 7: 1016
Ha TT, Sadleir LG, Mandelstam SA, et al. (2016) A mutation in COL4A2 causes autosomal dominant porencephaly with cataracts. American Journal of Medical Genetics. Part A. 170: 1059-63
Swanson MR, Wolff JJ, Elison JT, et al. (2015) Splenium development and early spoken language in human infants. Developmental Science
Estes A, Zwaigenbaum L, Gu H, et al. (2015) Behavioral, cognitive, and adaptive development in infants with autism spectrum disorder in the first 2 years of life. Journal of Neurodevelopmental Disorders. 7: 24
Sadleir LG, Paterson S, Smith KR, et al. (2015) Myoclonic occipital photosensitive epilepsy with dystonia (MOPED): A familial epilepsy syndrome. Epilepsy Research. 114: 98-105
Pruett JR, Kandala S, Hoertel S, et al. (2015) Accurate age classification of 6 and 12 month-old infants based on resting-state functional connectivity magnetic resonance imaging data. Developmental Cognitive Neuroscience. 12: 123-33
Elison JT, Wolff JJ, Reznick JS, et al. (2014) Repetitive behavior in 12-month-olds later classified with autism spectrum disorder. Journal of the American Academy of Child and Adolescent Psychiatry. 53: 1216-24
Wolff JJ, Botteron KN, Dager SR, et al. (2014) Longitudinal patterns of repetitive behavior in toddlers with autism. Journal of Child Psychology and Psychiatry, and Allied Disciplines. 55: 945-53
Sadleir LG, Agher D, Chabrol E, et al. (2013) Seizure semiology in autosomal dominant epilepsy with auditory features, due to novel LGI1 mutations. Epilepsy Research. 107: 311-7
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