Jonathan E Wickiser

Associate Professor (Nontenured Clinical), Pediatrics
Hematology & Oncology

Emailjonathan.wickiser@utsouthwestern.edu

Source: Scopus
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358 Citations
11 h-Index
17 Article
2 Comment/debate
1 Letter

De novo SDHB gene mutation in a family with extra-adrenal paraganglioma
Mauer, C. B., Reys, B. & Wickiser, J., Jul 1 2020, In: Familial Cancer. 19, 3, p. 269-271 3 p.
Research output: Contribution to journal › Article › peer-review
Summary of COVID-19 clinical practice adjustments across select institutions
Schultz, L., Link, M. P., Rheingold, S., Hawkins, D. S., Dome, J. S., Wickiser, J., Kung, A. L., Henderson, T. O. & Aftandilian, C., Nov 1 2020, In: Pediatric Blood and Cancer. 67, 11, e28411.
Research output: Contribution to journal › Letter › peer-review

Open Access

2 Scopus citations
Addition of vincristine and irinotecan to standard therapy in a patient with refractory high-risk hepatoblastoma achieving long-term relapse-free survival
Powers, J. M., Pacheco, M. M. & Wickiser, J. E., Apr 1 2019, In: Journal of Pediatric Hematology/Oncology. 41, 3, p. E171-E173
Research output: Contribution to journal › Article › peer-review
2 Scopus citations
A large prenatally undiagnosed mass in a preterm infant, what could it be?
Ibrahim, J., Pavageau, L., Miller, J., Timmons, C. F., Wickiser, J. E., Piper, H., Dariya, V. & Brion, L. P., Jul 2018, In: NeoReviews. 19, 7, p. e413-e417
Research output: Contribution to journal › Article › peer-review

1 Scopus citations
Erratum: Publisher Correction: Somatic mutations in DROSHA and DICER1 impair microRNA biogenesis through distinct mechanisms in Wilms tumours
Rakheja, D., Chen, K. S., Liu, Y., Shukla, A. A., Schmid, V., Chang, T. C., Khokhar, S., Wickiser, J. E., Karandikar, N. J., Malter, J. S., Mendell, J. T. & Amatruda, J. F., 2017, In: Nature communications. 8, p. 16177 1 p., 16177.
Research output: Contribution to journal › Comment/debate › peer-review

Open Access

De novo SDHB gene mutation in a family with extra-adrenal paraganglioma

Summary of COVID-19 clinical practice adjustments across select institutions

Addition of vincristine and irinotecan to standard therapy in a patient with refractory high-risk hepatoblastoma achieving long-term relapse-free survival

A large prenatally undiagnosed mass in a preterm infant, what could it be?

Erratum: Publisher Correction: Somatic mutations in DROSHA and DICER1 impair microRNA biogenesis through distinct mechanisms in Wilms tumours