Publications

Division/Center

Trends and Disparities in Newer GLP1 Receptor Agonist Initiation among Real-World Adult Patients Eligible for Obesity Treatment.

medRxiv
Radwan RM, Lee YA, Kotecha P, Wright DR, Hernandez I, Ramon R, Donahoo WT, Chen Y, Allen JM, Bian J, Guo J.

Approaches to Incorporation of Preferences into Health Economic Models of Genomic Medicine: A Critical Interpretive Synthesis and Conceptual Framework.

Appl Health Econ Health Policy
Smith HS, Regier DA, Goranitis I, Bourke M, IJzerman MJ, Degeling K, Montgomery T, Phillips KA, Wordsworth S, Buchanan J, Marshall DA

Genome-Wide and Rare Variant Association Studies of Amblyopia in the All of Us Research Program.

Ophthalmology
Lee KAV, Aboobakar IF, Jain A, Tesdahl CD, Jin K, Oke I, Whitman MC.

Genetic Test Utilization and Cost among Families of Children Evaluated for Genetic Conditions: An Analysis of USA Commercial Claims Data.

Appl Health Econ Health Policy
Smith HS, Lakoma M, Hickingbotham MR, Cardeiro D, Callahan KP, Wojcik MH, Wu AC, Lu CY

Cost Effectiveness Analysis of Digital Therapeutics for Amblyopia.

Ophthalmology
Koc I, Bagheri S, Chau RK, Hoyek S, Abou Shousha N, Mahmoudinezhad G, Falcone MM, Oke I, Hunter DG, Patel NA

Pediatric Triage Accuracy in Pediatric and General Emergency Departments.

Hosp Pediatr
Geanacopoulos AT, Peltz A, Melton K, Neuman MI, Gutman CK, Walsh KE, Samuels-Kalow ME, Michelson KA.

Association Between Area Deprivation Index and Retinopathy of Prematurity.

Ophthalmol Retina
Jordan JA, Turner C, Oke I, Oatts JT

Family Genetic Risk Communication and Reverse Cascade Testing in the BabySeq Project.

Genet Med
Uveges MK, Smith HS, Pereira S, Genetti C, McGuire AL, Beggs AH, Green RC, Holm IA,

Where the Genetic Code Meets the Zip Code: Advancing Equity in Rare Disease Genomics.

Hastings Cent Rep
Wojcik MH, Smith HS, Fraiman YS

Common variable immunodeficiency clinical manifestations are shaped by presence and type of heterozygous NFKB1 variants.

J Allergy Clin Immunol Pract
Yin J, Hayes KM, Ong MS, Mizgerd JP, Cunningham-Rundles C, Dominguez I, Barmettler S, Farmer JR, Maglione PJ

Disparities in Genetic Testing for Inborn Errors of Immunity.

J Allergy Clin Immunol Pract
Gilbert KM, McLaughlin HM, Farmer JR, Ong MS

Using machine learning to identify pediatric ophthalmologists.

J AAPOS
Oke I, Elze T, Miller JW, Lorch AC, Ong MS, Wu AC, Hunter DG,

Payer Perspectives on Genomic Testing in the United States: A systematic literature review.

Genet Med
Wiedower J, Smith HS, Farrell CL, Parker V, Rebek L, Davis SC

Modern Family: An Ethical Justification for System-Led Contact of Relatives Eligible for Cascade Screening in the United States.

Public Health Genomics
Bonini KE, Smith HS, Bonkowski ES, Berkman BE, Jamal L

Multidimensional and Longitudinal Impact of a Genetic Diagnosis for Critically Ill Infants.

Pediatrics
Wojcik MH, Del Rosario MC, Feldman HA, Smith HS, Holm IA

Association of CD19+-Targeted Chimeric Antigen Receptor (CAR) T-cell Therapy with Hypogammaglobulinemia, Infection and Mortality.

J Allergy Clin Immunol
Sutherland NM, Zhou B, Zhang L, Ong MS, Hong JS, Pak A, Liu KJ, Frigault MJ, Maus MV, Hill JA, Reynolds K, Walter JE, Camargo CA, Barmettler S

Experiences with diagnostic delay among underserved racial and ethnic patients: a systematic review of the qualitative literature.

BMJ Qual Saf
Faugno E, Galbraith AA, Walsh K, Maglione PJ, Farmer JR, Ong MS

Distribution of port wine birthmarks and glaucoma outcomes in Sturge-Weber Syndrome.

Ophthalmol Glaucoma
Vu DM, Gjerde H, Elhusseiny AM, Oke I, VanderVeen DK

Early Intervention services in the era of genomic medicine: setting a research agenda.

Pediatr Res
MacDuffie KE, Cohn B, Appelbaum P, Brothers KB, Doherty D, Goldenberg AJ, Reynolds E, Smith HS, Wheeler A, Yu JH

Communicating Risk in Imaging: A Scoping Review of Risk Presentation in Patient Decision Aids.

J Am Coll Radiol
Baird TA, Previtera M, Brady S, Wright DR, Trout AT, Hayatghaibi SE