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Christensen KD, Vassy JL, Phillips KA, Blout CL, Azzariti DR, Lu CY, Robinson JO, Lee K, Douglas MP, Yeh JM, Machini K, Stout NK, Rehm HL, McGuire AL, Green RC, Dukhovny D. (2018) Short-term costs of integrating whole-genome sequencing into primary care and cardiology settings: a pilot randomized trial. Genet Med. EPub ahead of print.
Amendola LM, Robinson JO, Hart R, Biswas S, Lee K, Bernhardt BA, East K, Gilmore MJ, Kauffman TL, Lewis KL, Roche M, Scollon S, Wynn J, Blout C. Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium (2018) J Genet Couns. EPub ahead of print.
Vassy JL, Christensen KD, Schonman EF, Blout CL, Robinson JO, Krier JB, Diamond PM, Lebo M, Machini K, Azzariti DR, Dukhovny D, Bates DW, MacRae CA, Murray MF, McGuire AL, Green RC, for the MedSeq Project. (2017) The Impact of Whole Genome Sequencing on Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial. Annals Intern Med. EPub ahead of print.
Bergner A, Bollinger J, Raraigh K, Tichnell C, Murray B, Blout C, Telegrafi A, James C. (2014) Informed consent for exome sequencing research in families with genetic disease: The emerging issue of incidental findings. (2014) American Journal of Medical Genetics. 164(11):2745-52.
Blout, C. Walsh Vockley, A Gaviglio, M. Fox, L Williamson Dean, The Newborn screening task for on behalf of the NSGC Public Policy Committee. (2013) Newborn Screening: Education Consent, and the Residual Blood Spot. The Position of the National Society of Genetic Counselors. (2013) C. The Journal of Genetic Counseling. 23(1):16-19.