Research output per year
Research output per year
Personal profile
Research interests
Cerebrospinal fluid flow and related disorders, hydrocephalus, neurodevelopment, ependymal biology, cilia, germinal matrix hemorrhage, intraventricular hemorrhage, CSF-tumor microenvironment
Areas of Clinical Interest
Pediatric Neurosurgery
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Dive into the research topics where Jennifer Strahle is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Case report of mesenteric strangulation secondary to longstanding ventriculoperitoneal shunt catheter
Grant, M. T., Wilson, N. A., Keller, M. S., Huguenard, A. L., Strahle, J. M. & Vrecenak, J. D., Aug 2021, In: Child's Nervous System. 37, 8, p. 2719-2722 4 p.Research output: Contribution to journal › Article › peer-review
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Dural augmentation approaches and complication rates after posterior fossa decompression for Chiari I malformation and syringomyelia: A Park-Reeves Syringomyelia Research Consortium study
Yahanda, A. T., David Adelson, P., Hassan, S., Albert, G. W., Aldana, P. R., Alden, T. D., Anderson, R. C. E., Bauer, D. F., Bethel-Anderson, T., Brockmeyer, D. L., Chern, J. J., Couture, D. E., Daniels, D. J., Dlouhy, B. J., Durham, S. R., Ellenbogen, R. G., Eskandari, R., George, T. M., Grant, G. A., Graupman, P. C. & 36 others, , Apr 2021, In: Journal of Neurosurgery: Pediatrics. 27, 4, p. 459-468 10 p.Research output: Contribution to journal › Article › peer-review
1 Scopus citations -
Erratum: Use of fast-sequence spine MRI in pediatric patients (J Neurosurg Pediatr (2020) 26:6 (676-681) DOI: 10.3171/2020.5.PEDS20137)
Gewirtz, J. I. & Strahle, J. M., Jul 2021, In: Journal of Neurosurgery: Pediatrics. 28, 1, p. 113 1 p.Research output: Contribution to journal › Comment/debate
Open Access -
Erratum: Rare and de novo coding variants in chromodomain genes in Chiari I malformation (The American Journal of Human Genetics (2021) 108(1) (100–114), (S0002929720304377), (10.1016/j.ajhg.2020.12.001))
Sadler, B., Wilborn, J., Antunes, L., Kuensting, T., Hale, A. T., Gannon, S. R., McCall, K., Cruchaga, C., Harms, M., Voisin, N., Reymond, A., Cappuccio, G., Brunetti-Pierri, N., Tartaglia, M., Niceta, M., Leoni, C., Zampino, G., Ashley-Koch, A., Urbizu, A., Garrett, M. E. & 11 others, , Mar 4 2021, In: American journal of human genetics. 108, 3, p. 530-531 2 p.Research output: Contribution to journal › Comment/debate
Open Access1 Scopus citations -
Erratum: Rare and de novo coding variants in chromodomain genes in Chiari I malformation (The American Journal of Human Genetics (2021) 108(1) (100–114), (S0002929720304377), (10.1016/j.ajhg.2020.12.001))
Sadler, B., Wilborn, J., Antunes, L., Kuensting, T., Hale, A. T., Gannon, S. R., McCall, K., Cruchaga, C., Harms, M., Voisin, N., Reymond, A., Cappuccio, G., Brunetti-Pierri, N., Tartaglia, M., Niceta, M., Leoni, C., Zampino, G., Ashley-Koch, A., Urbizu, A., Garrett, M. E. & 11 others, , Feb 4 2021, In: American journal of human genetics. 108, 2, p. 368 1 p.Research output: Contribution to journal › Comment/debate
1 Scopus citations