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
1 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, , 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 -
Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders
Yang, C., Farias, F. H. G., Ibanez, L., Suhy, A., Sadler, B., Fernandez, M. V., Wang, F., Bradley, J. L., Eiffert, B., Bahena, J. A., Budde, J. P., Li, Z., Dube, U., Sung, Y. J., Mihindukulasuriya, K. A., Morris, J. C., Fagan, A. M., Perrin, R. J., Benitez, B. A., Rhinn, H. & 2 others, , Sep 2021, In: Nature neuroscience. 24, 9, p. 1302-1312 11 p.Research output: Contribution to journal › Article › peer-review
2 Scopus citations -
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
1 Scopus citations