Jennifer R. Holle

Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center’s Experience

F. Zou, J. Harley, R. Hopkin, 2015, Front. Pediatr..

Jeffrey’s insights: Jeffrey Modell Foundation’s global genetic sequencing pilot program to identify specific primary immunodeficiency defects to optimize disease management and treatment

J. Orange, R. Truty, S. Aradhya, 2020, Immunologic research.

Expanded Gene Panel Use for Women With Breast Cancer: Identification and Intervention Beyond Breast Cancer Risk

Shan Yang, E. O'Leary, Jennifer R. Holle, 2017, Annals of Surgical Oncology.

Next generation sequencing for clinical diagnostics: Five year experience of an academic laboratory

K. Beckman, P. Mróz, K. Silverstein, 2019, Molecular genetics and metabolism reports.

Pediatric Whole Exome Sequencing: an Assessment of Parents’ Perceived and Actual Understanding.

M. Myers, C. A. Valencia, Jennifer R. Holle, 2017, Journal of Genetic Counseling.

Prevalence of mutations in inherited retinal diseases: A comparison between the United States and India

Arkasubhra Ghosh, L. Schimmenti, S. Murugan, 2019, Molecular genetics & genomic medicine.

Hemophagocytic lymphohistiocytosis in a female patient due to a heterozygous XIAP mutation and skewed X chromosome inactivation

S. Davies, Kejian Zhang, Jennifer R. Holle, 2015, Pediatric blood & cancer.