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.
Available to Mentor:
- PhD/MSTP Students
Fingerprint
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.
- 1 Similar Profiles
Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
-
Streamlined identification of clinically and functionally relevant genetic regulators of lower-tract urogenital development
Haller, M., Yin, Y., Haller, G., Li, T., Li, Q., Lamb, L. E. & Ma, L., 2024, In: Proceedings of the National Academy of Sciences of the United States of America. 121, 6Research output: Contribution to journal › Article › peer-review
Open Access -
A Refined, Controlled 16S rRNA Gene Sequencing Approach Reveals Limited Detection of Cerebrospinal Fluid Microbiota in Children with Bacterial Meningitis
the Cerebrospinal FLuId MicroBiota in Shunts (CLIMB) Study Group, Pope, C. E., Whitlock, K. B., Hodor, P., Limbrick, D. D., McDonald, P. J., Hauptman, J., Hoffman, L. R., Simon, T. D., Morales, D., Haller, G., Cheong, A., Sedano, S., Vega, J., Berger, D., Bond, W., Botteron, H., Dethlefs, C., Foster, J. & Gabir, M. & 7 others, , May 2023, In: Microbiology spectrum. 11, 3Research output: Contribution to journal › Article › peer-review
Open Access3 Scopus citations -
Characterization of copy-number variants in a large cohort of patients with von Willebrand disease reveals a relationship between disrupted regions and disease type
Zimmerman Program Investigators, Sadler, B., Christopherson, P. A., Perry, C. L., Bellissimo, D. B., Haberichter, S. L., Haller, G., Antunes, L., Flood, V. H., Di Paola, J. & Montgomery, R. R., Oct 2023, In: Research and Practice in Thrombosis and Haemostasis. 7, 7, 102232.Research output: Contribution to journal › Article › peer-review
Open Access -
Comprehensive functional characterization of SGCB coding variants predicts pathogenicity in limb-girdle muscular dystrophy type R4/2E
Li, C., Wilborn, J., Pittman, S., Daw, J., Alonso-Pérez, J., Díaz-Manera, J., Weihl, C. C. & Haller, G., Jun 15 2023, In: Journal of Clinical Investigation. 133, 12, e168156.Research output: Contribution to journal › Article › peer-review
Open Access6 Scopus citations -
Elucidating the Genetic Basis of Chiari I Malformation
Haller, G. & Sadler, B., Jan 2023, In: Neurosurgery clinics of North America. 34, 1, p. 55-60 6 p.Research output: Contribution to journal › Review article › peer-review
2 Scopus citations