Research output per year
Research output per year
Personal profile
Research interests
Genetic basis of connective tissue diseases and neurological diseases, primarily in pediatric populations.
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Dive into the research topics where Brooke Sadler is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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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
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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 Access -
Rare and de novo coding variants in chromodomain genes in Chiari I malformation
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., Burnetti-Pierri, N., Tartaglia, M., Niceta, M., Leoni, C., Zampino, G., Ashley-Koch, A., Urbizu, A., Garrett, M. E. & 11 others, , Jan 7 2021, In: American journal of human genetics. 108, 1, p. 100-114 15 p.Research output: Contribution to journal › Article › peer-review
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von Willebrand factor antigen levels are associated with burden of rare nonsynonymous variants in the VWF gene
Zimmerman Program Investigators, Jun 10 2021, In: Blood. 137, 23, p. 3277-3283 7 p.Research output: Contribution to journal › Article › peer-review
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Obex position is associated with syringomyelia and use of posterior fossa decompression among patients with Chiari I malformation
Haller, G., Sadler, B., Kuensting, T., Lakshman, N., Greenberg, J. K., Strahle, J. M., Park, T. S., Dobbs, M. B., Gurnett, C. A. & Limbrick, D. D., Jul 2020, In: Journal of Neurosurgery: Pediatrics. 26, 1, p. 45-52 8 p.Research output: Contribution to journal › Article › peer-review