Publications

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Hanson et al. (April 2007) “The Use of Complementary and Alternative Medicine by Parents for a Child with an Autism Spectrum Disorder,” The Journal of Autism and Developmental Disorders, 37, 4: 628-636.

Ching M, Nasir R, Shen Y, Tan W, Jeste S, Morrow E, Chen X, Mukaddess NM, Yoo S, Hanson E, et al.(2010). Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B:4: 937-947.

Ching M, Nasir R, Shen Y, Tan W, Jeste S, Morrow E, Chen X, Mukaddess NM, Yoo S, Hanson E, et al.(2010). Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B:4: 937-947.

Shen Y., Dies K.A., Holm I.A., Bridgemohan C., Sobeih M.M., Caronna E.B., Miller K.J., Frazier J.A., Silverstein I., Picker J., Weissman L., Raffalli P., Jeste S., Demmer L.A., Peters H.K., Brewster S.J., Kowalczyk S.J., Rosen-Sheidley B., McGowan C., Duda A.W. 3rd, Lincoln S.A., Lowe K.R., Schonwald A., Robbins M., Hisama F., Wolff R., Becker R., Nasir R, Urion DK, Milunsky JM, Rappaport L, Gusella JF, Walsh CA, Wu BL, Miller D.T.; Autism Consortium Clinical Genetics/DNA Diagnostics Collaboration. (April 2010). Clinical Genetic Testing for Patients with Autism Spectrum Disorders. Pediatrics 125(4).

Hanson, E., Nasir, R.H, Fong, A., Lian, A., Hundley, R., Shen, Y., Wu, B.L., Holm, I.A., Miller, D.T.  (October 2010)  Cognitive and Behavioral Characterization of 16p11.2 Deletion Syndrome. Journal of Developmental and Behavioral Pediatrics. 2010 Oct; 31:8: 649-657

Price CS; Thompson WW; Goodson B; Weintraub ES; Croen LA; Hinrichsen VL; Marcy M; Robertson A; Eriksen E; Lewis E; Bernal P; Shay D; Davis RL; DeStefano F. (October 2010). Prenatal and Infant Exposure to Thimerosal from Vaccines and Immunoglobulin’s and Risk of Autism.  Pediatrics 126 (4): 656-64. (*Acknowledged)

Davit, C., Hundley, R, Bacic, J, Hanson, E. (2011) Improving venipuncture compliance in children and adolescents with Autism Spectrum Disorders (ASD). Journal of Developmental and Behavior Pediatrics 32(7).

The Simons VIP Consortium. (2012) Simons Variation in Individuals Project (Simons VIP): A Genetics-First Approach to Studying Autism Spectrum and Related Neurodevelopmental Disorders. Neuron 73(6). (*member of the investigative team cited in the appendix of the manuscript)

Kong, S.W.; Kohane, I.; Hanson, E., (2012) Characteristics and Predictive Value of Blood Transcriptome signature in Autism Spectrum Disorders.  Science Translational Medicine. PLOS One

Hanson, E.; Cerban, B.M.; Slater, C.M.; Caccamo, L.M. Bacic, J.; Chan, E. (2012) Prevalence of Attention Deficit/Hyperactivity Disorder among Individuals with an Autism Spectrum Disorder. The Journal of Autism and Developmental Disorders.

The Simons VIP Consortium (Submitted) A 600 kb Deletion Syndrome at 16p11.2 Leads to Energy Imbalance and Neuropsychiatric Disorders. The New England Journal of Medicine. (*member of the investigative team cited in the appendix of the manuscript)

Moreno-De-Luca, A.; Myers, S.M; Challman, T.D.; Evans, D.W.; Goin-Kochel, R.P.; Hanson, E.; Bernier, R.; Green-Snyder, L.; Spiro, J.; Chung, W.K.; Ledbetter, D. H., (In Review) Cognitive and behavioral impact of deletion 16p11.2 when viewed as continuous traits rather than dichotomous traits. 

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