Sunday M. Francis, Ph.D.

Affiliations: 
2009 University of Chicago, Chicago, IL 
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"Sunday Francis"
Mean distance: 15.11 (cluster 17)
 
SNBCP

Parents

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Nicholas G. Hatsopoulos grad student 2009 Chicago
 (Sensorimotor learning versus motor skill acquisition: Effects on a cortical network.)
Suma Jacob post-doc University of Illinois at Chicago (UIC); University of Minnesota

Collaborators

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Angela Tseng collaborator UMN (PsychTree)
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Publications

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Francis SM, Kim SJ, Kistner-Griffin E, et al. (2016) ASD and Genetic Associations with Receptors for Oxytocin and Vasopressin-AVPR1A, AVPR1B, and OXTR. Frontiers in Neuroscience. 10: 516
Francis SM, Kirkpatrick MG, de Wit H, et al. (2016) Urinary and plasma oxytocin changes in response to MDMA or intranasal oxytocin administration. Psychoneuroendocrinology. 74: 92-100
Francis SM, Kistner-Griffin E, Yan Z, et al. (2016) Variants in Adjacent Oxytocin/Vasopressin Gene Region and Associations with ASD Diagnosis and Other Autism Related Endophenotypes. Frontiers in Neuroscience. 10: 195
Levin-Decanini T, Francis SM, Sagar A, et al. (2015) Oxytocin and vasopressin in autism and genetic syndromes The Molecular Basis of Autism. 275-306
Kirkpatrick MG, Francis SM, Lee R, et al. (2014) Plasma oxytocin concentrations following MDMA or intranasal oxytocin in humans. Psychoneuroendocrinology. 46: 23-31
Ceroni F, Sagar A, Simpson NH, et al. (2014) A deletion involving CD38 and BST1 results in a fusion transcript in a patient with autism and asthma. Autism Research : Official Journal of the International Society For Autism Research. 7: 254-63
Francis SM, Sagar A, Levin-Decanini T, et al. (2014) Oxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders. Brain Research. 1580: 199-218
Levin-Decanini T, Maltman N, Francis SM, et al. (2013) Parental broader autism subphenotypes in ASD affected families: relationship to gender, child's symptoms, SSRI treatment, and platelet serotonin. Autism Research : Official Journal of the International Society For Autism Research. 6: 621-30
Davis LK, Maltman N, Mosconi MW, et al. (2012) Rare inherited A2BP1 deletion in a proband with autism and developmental hemiparesis. American Journal of Medical Genetics. Part A. 158: 1654-61
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