Research output per year
Research output per year
Personal profile
Research interests
My goal is to identify genetic variants associated with nicotine dependence in human populations.
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Dive into the research topics where Gabriel Haller 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, , 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 -
Occipital-Cervical Fusion and Ventral Decompression in the Surgical Management of Chiari-1 Malformation and Syringomyelia: Analysis of Data from the Park-Reeves Syringomyelia Research Consortium
Crevecoeur, T. S., Yahanda, A. T., Maher, C. O., Johnson, G. W., Ackerman, L. L., David Adelson, P. D., Ahmed, R., Albert, G. W., Aldana, P. R., Alden, T. D., Anderson, R. C. E., Baird, L., Bauer, D. F., Bierbrauer, K. S., Brockmeyer, D. L., Chern, J. J., Couture, D. E., Daniels, D. J., Dauser, R. C., Durham, S. R. & 48 others, , Feb 1 2021, In: Neurosurgery. 88, 2, p. 332-341 10 p.Research output: Contribution to journal › Article › peer-review
Open Access1 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