Julia E. Dallman
Affiliations: | University of Miami, Coral Gables, FL |
Area:
Developmental neuroscienceGoogle:
"Julia Dallman"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| William Moody | grad student | 1991-1998 | University of Washington - Seattle/ NIH |
| Paul Brehm | post-doc | Oregon State University - OHSU | |
| Gail Mandel | post-doc | 1998-2004 | Oregon State University - OHSU |
Children
Sign in to add trainee| Alex J. Abrams | grad student | University of Miami | |
| Elena Buglo | grad student | University of Miami | |
| Qing Yan | grad student | 2008-2016 | University of Miami |
| Robert A Kozol | grad student | 2013-2018 | University of Miami |
| David M. James | grad student | 2014-2021 | University of Miami |
| Elizabeth A. Davidson | grad student | 2018-2023 | University of Miami |
| Lisa R. Ganser | post-doc | 2009-2011 | University of Miami |
Collaborators
Sign in to add collaborator| Calliope Hoilgue | collaborator | Kennedy Krieger Institute | |
| Baharak Moshiree | collaborator | Atrium Health Wake Forest Baptist | |
| Stephan Zuchner | collaborator |
BETA: Related publications
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Publications
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| Kozol RA, James DM, Varela I, et al. (2021) Restoring Shank3 in the rostral brainstem of shank3ab-/- zebrafish autism models rescues sensory deficits. Communications Biology. 4: 1411 |
| James DM, Davidson EA, Yanes J, et al. (2021) The Gut-Brain-Microbiome Axis and Its Link to Autism: Emerging Insights and the Potential of Zebrafish Models. Frontiers in Cell and Developmental Biology. 9: 662916 |
| Venincasa MJ, Randlett O, Sumathipala SH, et al. (2021) Elevated preoptic brain activity in zebrafish glial glycine transporter mutants is linked to lethargy-like behaviors and delayed emergence from anesthesia. Scientific Reports. 11: 3148 |
| Cortese A, Zhu Y, Rebelo AP, et al. (2020) Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes. Nature Genetics |
| Cortese A, Zhu Y, Rebelo AP, et al. (2020) Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes. Nature Genetics |
| Buglo E, Sarmiento E, Martuscelli NB, et al. (2020) Genetic compensation in a stable slc25a46 mutant zebrafish: A case for using F0 CRISPR mutagenesis to study phenotypes caused by inherited disease. Plos One. 15: e0230566 |
| James DM, Kozol RA, Kajiwara Y, et al. (2019) Intestinal dysmotility in a zebrafish () mutant model of autism. Molecular Autism. 10: 3 |
| Bedell V, Buglo E, Marcato D, et al. (2018) Zebrafish: A Pharmacogenetic Model for Anesthesia. Methods in Enzymology. 602: 189-209 |
| Hung CY, Volkmar B, Baker JD, et al. (2017) A defect in the inner kinetochore protein CENPT causes a new syndrome of severe growth failure. Plos One. 12: e0189324 |
| Yan Q, Zhai L, Zhang B, et al. (2016) Spatial patterning of excitatory and inhibitory neuropil territories during spinal circuit development. The Journal of Comparative Neurology |