Gabriel Haddad
Affiliations: | Neurosciences | University of California, San Diego, La Jolla, CA |
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Children
Sign in to add trainee| Merril J. Gersten | grad student | 2011 | UCSD |
| DeeAnn W. Visk | grad student | 2011 | UCSD |
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Publications
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| Stobdan T, Sahoo D, Haddad GG. (2022) A Boolean approach for novel hypoxia-related gene discovery. Plos One. 17: e0273524 |
| Zhou D, Stobdan T, Visk D, et al. (2021) Genetic interactions regulate hypoxia tolerance conferred by activating Notch in excitatory amino acid transporter 1-positive glial cells in Drosophila melanogaster. G3 (Bethesda, Md.) |
| Azad P, Villafuerte FC, Bermudez D, et al. (2021) Protective role of estrogen against excessive erythrocytosis in Monge's disease. Experimental & Molecular Medicine |
| Ghosh SG, Becker K, Huang H, et al. (2018) Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome. American Journal of Human Genetics |
| Stobdan T, Akbari A, Azad P, et al. (2017) New insights into the genetic basis of Monge's disease and adaptation to high-altitude. Molecular Biology and Evolution |
| Gan Z, Powell FL, Zambon AC, et al. (2017) Transcriptomic analysis identifies a role of PI3K/Akt signalling in the responses of skeletal muscle to acute hypoxia in vivo. The Journal of Physiology |
| Jha AR, Zhou D, Brown CD, et al. (2015) Shared genetic signals of hypoxia adaptation in Drosophila and in high-altitude human populations. Molecular Biology and Evolution |
| Stobdan T, Zhou D, Ao-Ieong E, et al. (2015) Endothelin receptor B, a candidate gene from human studies at high altitude, improves cardiac tolerance to hypoxia in genetically engineered heterozygote mice. Proceedings of the National Academy of Sciences of the United States of America. 112: 10425-30 |
| Manchenkov T, Pasillas MP, Haddad GG, et al. (2015) Novel Genes Critical for Hypoxic Preconditioning in Zebrafish Are Regulators of Insulin and Glucose Metabolism. G3 (Bethesda, Md.). 5: 1107-16 |
| Griesi-Oliveira K, Acab A, Gupta AR, et al. (2014) Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons. Molecular Psychiatry |