Publications

Research Participants' Perspectives on Precision Diagnostics for Alzheimer's Disease.

J Alzheimers Dis
Smith HS, Robinson JO, Levchenko A, Pereira S, Pascual B, Bradbury K, Arbones V, Fong J, Shulman JM, McGuire AL, Masdeu J

The motivation and process for developing a consortium-wide time and motion study to estimate resource implications of innovations in the use of genome sequencing to inform patient care.

Clin Transl Sci
Hoban HG, Yip TA, Chau JC, Bensen JT, Desrosiers LR, Finnila CR, Hindorff LA, Kelly NR, Lynch FL, Rolf BA, Smith HS, Wasserstein MP, Hassmiller Lich K

Parent-Reported Clinical Utility of Pediatric Genomic Sequencing.

Pediatrics
Smith HS, Ferket BS, Gelb BD, Hindorff L, Ferar KD, Norton ME, Sahin-Hodoglugil N, Slavotinek A, Lich KH, Berg JS, Russell HV

Pediatric Genomic Medicine: Value, Implementation, and Access.

Clin Ther
Lavelle TA, Smith HS

Conversations With the Editors: Stewardship in Genomic Medicine-Insights From Health Care Payers at the Forefront of Clinical Innovation and Partnerships.

Clin Ther
Smith HS, Sherman M, Cardeiro D

The Other Side of the Self-Advocacy Coin: How For-Profit Companies Can Divert the Path to Justice in Rare Disease

Clinically Indicated Genomic Sequencing of Children in Foster Care: Legal and Ethical Issues.

J Pediatr
Smith HS, Bonkowski ES, Hickingbotham MR, Pereira S, May T, Guerrini CJ

Framing the Family: A Qualitative Exploration of Factors That Shape Family-Level Experience of Pediatric Genomic Sequencing

Cascade testing after exome sequencing: Retrospective analysis of linked family data at 2 US laboratories.

Genet Med
Stefka J, Streff H, Liu P, Towne M, Smith HS

Lessons learned while starting multi-institutional genetics research in diverse populations: A report from the Clinical Sequencing Evidence-Generating Research (CSER) consortium.

Contemp Clin Trials
Russell H, Smith HS, Bensen JT, Murali P, Ferket BS, Finnlia C, Hindorff LA, Sahin-Hodoglugil N

Access to clinically indicated genetic tests for pediatric patients with Medicaid: Evidence from outpatient genetics clinics in Texas.

Genet Med
Streff H, Uhles CL, Fisher H, Franciskovich R, Littlejohn RO, Gerard A, Hudnall J, Smith HS

Key drivers of family-level utility of pediatric genomic sequencing: a qualitative analysis to support preference research.

Eur J Hum Genet
Smith HS, Bonkowski ES, Deloge RB, Gutierrez AM, Recinos AM, Lavelle TA, Veenstra DL, McGuire AL, Pereira S

Patient and Clinician Perceptions of Precision Cardiology Care: Findings From the HeartCare Study.

Circ Genom Precis Med
Smith HS, Sanchez CE, Maag R, Buentello A, Murdock DR, Metcalf GA, Hadley TD, Riconda DL, Boerwinkle E, Wehrens XHT, Ballantyne CM, Gibbs RA, McGuire AL, Pereira S

A call for an integrated approach to improve efficiency, equity and sustainability in rare disease research in the United States.

Nat Genet
Halley MC, Smith HS, Ashley EA, Goldenberg AJ, Tabor HK

Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study.

Front Genet
Armstrong B, Christensen KD, Genetti CA, Parad RB, Robinson JO, Blout Zawatsky CL, Zettler B, Beggs AH, Holm IA, Green RC, McGuire AL, Smith HS, Pereira S,

Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project: A Randomized Clinical Trial.

JAMA Pediatr
Pereira S, Smith HS, Frankel LA, Christensen KD, Islam R, Robinson JO, Genetti CA, Blout Zawatsky CL, Zettler B, Parad RB, Waisbren SE, Beggs AH, Green RC, Holm IA, McGuire AL,

Family-level impact of genetic testing: integrating health economics and ethical, legal, and social implications.

Per Med
Smith HS, McGuire AL, Wittenberg E, Lavelle TA.