Dr. Smith's Publications

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• Smith, T.F., Schmidt-Kastner, R., McGeary, J.E, Kaczorowski, J.A., & Knopik, V.S.  (2016). Prenatal ischemia-hypoxia, the ischemia-hypoxia response pathway, and ADHD risk: A multi-omic perspective. Behavior Genetics. Advance online publication. doi:10.1007/s10519-016-9784-4

• Marceau, K. Palmer, R.H.C., Neiderhiser, J.M., Smith, T.F., McGeary, J.E., & Knopik, V.S. (2016). Passive rGE or developmental gene-environment cascade? An investigation of the role of xenobiotic genes in the association between smoking during pregnancy and child birthweight. Behavior Genetics. Advance online publication. doi:10.1007/s10519-016-9778-2

• Knopik, V.S., Marceau, K., Bidwell, L.C., Palmer, R.H.C, Smith, T.F., Todorov, A., Evans, A.S., Heath, A.C. (2016). Smoking during pregnancy and ADHD risk: A genetically-informed, multiple-rater approach. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. Advance online publication. doi: 10.1002/ajmg.b.32421

• Marceau, K., Minni, M.T.B., Smith, T.F., Daams, J.G., van Beijsterveldt, C.E.M., McMaster, M.C., Boomsma, D.I., Knopik, V.S (2016). The Prenatal Environment in Twin Studies: A Review on Chorionicity. Behavior Genetics. Advance online publication. doi:10.1007/s10519-016-9782-6

• Knopik, V.S., Marceau, K. Palmer, R.H.C., Smith, T.F., Heath, A.C. (2015). Maternal smoking during pregnancy and offspring birth weight:  A genetically-informed approach incorporating multiple raters. Behavior Genetics. Advance online publication. doi:10.1007/s10519-015-9750-6

• Smith T.F., Anastopoulos, A.D., Garrett, M.E., Arias-Vasquez, A., Franke, B., Oades, R.D., Sonuga-Barke, E., Asherson, P., Gill, M., Buitelaar, J.K., Sergeant, J.A., Kollins, S.H., Faraone, S.V., the IMAGE Consortium, & Ashley-Koch, A (2014). Angiogenic, Neurotrophic, and Inflammatory System SNPs Moderate the Association between Birth Weight and ADHD Symptom Severity. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 165(8), 691-704. doi: 10.1002/ajmg.b.32275

• Smith, T.F., Maccani, M.A., & Knopik, V.S. (2013). Maternal smoking during pregnancy and offspring health outcomes: The role of epigenetic research in informing legal policy and practice. Hastings Law Journal, 64(6), 1591-1618.

• Smith, T.F., Russell, H.F., Kelly, E.H, Mulcahey, M.J., Betz, R.R., & Vogel, L.C. (2013). Examination and measurement of coping among adolescents with spinal cord injury. Spinal Cord, 51, 710-714. doi:10.1038/sc.2013.65

• Kaczorowski, J.A., Williams, A.S., Smith, T.F., Fallah, N., Mendez, J., & Nelson-Gray, R. (2011). Adapting clinical services to accommodate needs of refugee populations. Professional Psychology: Research and Practice, 42(5), 361-367. doi: 10.1037/a0025022

• Anastopoulos, A. D., Smith, T. F., Garrett, M. E., Morrissey-Kane, E., Schatz, N. K., Sommer, J.L., Kollins, S. H., & Ashley-Koch, A. (2010). Self-Regulation of emotion, functional impairment, and comorbidity among children with attention-deficit/hyperactivity disorder.  Journal of Attention Disorders, 15(7), 583-592. doi:10.1177/1087054710370567

• Smith, T.F. (2010). Meta-analysis of the heterogeneity in association of DRD4 7-repeat allele and ADHD: Stronger association with ADHD combined type. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 153B, 1189-1199. doi: 10.1002/ajmg.b.31090

 

Dr. Kaczorowski's Publications

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• Smith, T.F., Schmidt-Kastner, R., McGeary, J.E, Kaczorowski, J.A., & Knopik, V.S.  (2016). Prenatal ischemia-hypoxia, the ischemia-hypoxia response pathway, and ADHD risk: A multi-omic perspective. Behavior Genetics. Advance online publication. doi:10.1007/s10519-016-9784-4

• Kaczorowski, J.A., Williams, A.S., Smith, T.F., Fallah, N., Mendez, J., & Nelson-Gray, R. (2011). Adapting clinical services to accommodate needs of refugee populations. Professional Psychology: Research and Practice, 42(5), 361-367. doi: 10.1037/a0025022

• Shashi, V., Keshavan, M., Kaczorowski, J.A., Schoch, K., Lewandowski, K.E., McConkie-Rosell, A., Hooper, S.R., Kwapil, T.R. (2010). Socioeconomic status and psychological function in children with chromosome 22q11.2 deletion syndrome: implications for genetic counseling. Journal of Genetic Counseling, 19(5), 535-544. doi: 10.1007/s10897-010-9309-x.

• Shashi, V. Howard, T.D., Keshavan, M.S., Kaczorowski, J.A., Berry, M.N., Schoch, K., Spence, E.J., Kwapil, T.R. (2010). COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome. Psychiatry Research, 178(2), 433 – 436. doi: 10.1016/j.psychres.2010.04.048

• Shashi, V., Kwapil, T.R., Kaczorowski, J.A., Berry, M.N., Santos, C.S., Howard, T.D., Goradia, D., Prasad, K., Vaibhav, D., Rajarethinam, R., Spence, E., & Keshavan, M.S. (2010). Evidence of neuronal reduction and dysfunction in chromosome 22q11.2 deletion syndrome. Psychiatry Research: Neuroimaging, 181, 1 - 8. doi: 10.1016/j.pscychresns.2009.07.003

• Kaczorowski, J.A., Barrantes-Vidal, N., & Kwapil, T.R. (2009). Neurological soft signs in psychometrically identified schizotypy. Schizophrenia Research, 115, 293-302. doi: 10.1016/j.schres.2009.06.018