David Hessl

Fragile X-associated tremor/ataxia syndrome: influence of the FMR1 gene on motor fiber tracts in males with normal and premutation alleles.

Andrea Schneider, Flora Tassone, Jun Yi Wang, 2013, JAMA neurology.

Psychophysiological Responses to Emotional Stimuli in Children and Adolescents with Autism and Fragile X Syndrome

Katherine E. Masyn, A. Mastergeorge, D. Hessl, 2015, Journal of clinical child and adolescent psychology : the official journal for the Society of Clinical Child and Adolescent Psychology, American Psychological Association, Division 53.

Reliability of Eye Tracking and Pupillometry Measures in Individuals with Fragile X Syndrome

Faraz Farzin, F. Farzin, D. Hessl, 2011, Journal of autism and developmental disorders.

The neuroanatomy and neuroendocrinology of fragile X syndrome.

Allan L Reiss, S. Rivera, A. Reiss, 2004, Mental retardation and developmental disabilities research reviews.

Genetic and environmental influences on the cognitive outcomes of children with fragile X syndrome.

Allan L Reiss, A. Reiss, D. Hessl, 2002, Journal of the American Academy of Child and Adolescent Psychiatry.

Abnormal trajectories in cerebellum and brainstem volumes in carriers of the fragile X premutation

Tony J. Simon, Emilio Ferrer, Flora Tassone, 2017, Neurobiology of Aging.

Decreased Fragile X Mental Retardation Protein Expression Underlies Amygdala Dysfunction in Carriers of the Fragile X Premutation

Andrea Schneider, Kami Koldewyn, Flora Tassone, 2011, Biological Psychiatry.

Drug development for neurodevelopmental disorders: lessons learned from fragile X syndrome

Mark F. Bear, Eva Loth, Jacqueline N. Crawley, 2017, Nature Reviews Drug Discovery.

Psychometric Study of the Aberrant Behavior Checklist in Fragile X Syndrome and Implications for Targeted Treatment

Allan L. Reiss, Scott S. Hall, Keith F. Widaman, 2012, Journal of autism and developmental disorders.

Advances in the Treatment of Fragile X Syndrome

Randi J. Hagerman, Jonathan Picker, Walter E. Kaufmann, 2009, Pediatrics.

Autoimmune disease in mothers with the FMR1 premutation is associated with seizures in their children with fragile X syndrome

Danh V. Nguyen, Andrea Schneider, Flora Tassone, 2010, Human Genetics.