ZFIN Person: Dallman, Julia

ZFIN ID: ZDB-PERS-091217-1

Dallman, Julia

Email:	j.dallman@miami.edu
URL:	https://dallmanlab.weebly.com/
Affiliation:	Julia Dallman Lab
Address:	Dallman Lab UM/G-Biology Dept X000153 1301 Memorial Drive, Rm 215 Miami, FL 33146
Country:	United States
Phone:	(305) 284 3954
Fax:	(305) 284 3039
ORCID ID:	0000-0002-5839-807X

BIOGRAPHY AND RESEARCH INTERESTS

PUBLICATIONS

Kozol, R.A., Dallman, J.E. (2023) Drugs prescribed for Phelan-McDermid syndrome differentially impact sensory behaviors in shank3 zebrafish models. F1000Research. 12:8484

Davidson, E.A., Holingue, C., Jimenez-Gomez, A., Dallman, J.E., Moshiree, B. (2023) Gastrointestinal Dysfunction in Genetically Defined Neurodevelopmental Disorders. Seminars in neurology. 43(4):645-660

Zhou, Y., Chen, J., Kirbas Cilingir, E., Zhang, W., Gonzalez, L., Perez, S., Davila, A., Brejcha, N., Gu, J., Shi, W., Domena, J.B., Ferreira, B.C.L.B., Zhang, F., Vallejo, F.A., Toledo, D., Liyanage, P.Y., Graham, R.M., Dallman, J., Peng, Z., Agatemor, C., Catenazzi, A., Leblanc, R.M. (2022) An insight into embryogenesis interruption by carbon nitride dots: can they be nucleobase analogs?. Nanoscale. 14(47):17607-17624

Kozol, R.A., James, D.M., Varela, I., Sumathipala, S.H., Züchner, S., Dallman, J.E. (2021) Restoring Shank3 in the rostral brainstem of shank3ab-/- zebrafish autism models rescues sensory deficits. Communications biology. 4:1411

James, D.M., Davidson, E.A., Yanes, J., Moshiree, B., Dallman, J.E. (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, M.J., Randlett, O., Sumathipala, S.H., Bindernagel, R., Stark, M.J., Yan, Q., Sloan, S.A., Buglo, E., Meng, Q.C., Engert, F., Züchner, S., Kelz, M.B., Syed, S., Dallman, J.E. (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

Buglo, E., Sarmiento, E., Martuscelli, N.B., Sant, D.W., Danzi, M.C., Abrams, A.J., Dallman, J.E., Züchner, S. (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, D.M., Kozol, R.A., Kajiwara, Y., Wahl, A.L., Storrs, E.C., Buxbaum, J.D., Klein, M., Moshiree, B., Dallman, J.E. (2019) Intestinal dysmotility in a zebrafish (Danio rerio) shank3a;shank3b mutant model of autism. Molecular autism. 10:3

Mintz, K.J., Mercado, G., Zhou, Y., Ji, Y., Hettiarachchi, S.D., Liyanage, P.Y., Pandey, R.R., Chusuei, C.C., Dallman, J., Leblanc, R.M. (2019) Tryptophan carbon dots and their ability to cross the blood-brain barrier. Colloids and surfaces. B, Biointerfaces. 176:488-493

Bedell, V., Buglo, E., Marcato, D., Pylatiuk, C., Mikut, R., Stegmaier, J., Scudder, W., Wray, M., Züchner, S., Strähle, U., Peravali, R., Dallman, J.E. (2018) Zebrafish: A Pharmacogenetic Model for Anesthesia. Methods in enzymology. 602:189-209

Hung, C.Y., Volkmar, B., Baker, J.D., Bauer, J.W., Gussoni, E., Hainzl, S., Klausegger, A., Lorenzo, J., Mihalek, I., Rittinger, O., Tekin, M., Dallman, J.E., Bodamer, O.A. (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., Dallman, J.E. (2017) Spatial patterning of excitatory and inhibitory neuropil territories during spinal circuit development. The Journal of comparative neurology. 525(7):1649-1667

Li, S., Peng, Z., Dallman, J., Baker, J., Othman, A.M., Blackwelder, P.L., Leblanc, R.M. (2016) Crossing the blood-brain-barrier with transferrin conjugated carbon dots: A zebrafish model study. Colloids and surfaces. B, Biointerfaces. 145:251-256

Kozol, R.A., Abrams, A.J., James, D.M., Buglo, E., Yan, Q., Dallman, J.E. (2016) Function Over Form: Modeling Groups of Inherited Neurological Conditions in Zebrafish. Frontiers in molecular neuroscience. 9:55

Rebelo, A.P., Abrams, A.J., Cottenie, E., Horga, A., Gonzalez, M., Bis, D.M., Sanchez-Mejias, A., Pinto, M., Buglo, E., Markel, K., Prince, J., Laura, M., Houlden, H., Blake, J., Woodward, C., Sweeney, M.G., Holton, J.L., Hanna, M., Dallman, J.E., Auer-Grumbach, M., Reilly, M.M., Zuchner, S. (2016) Cryptic Amyloidogenic Elements in the 3' UTRs of Neurofilament Genes Trigger Axonal Neuropathy. American journal of human genetics. 98(4):597-614

Koenighofer, M., Hung, C.Y., McCauley, J.L., Dallman, J., Back, E.J., Mihalek, I., Gripp, K.W., Sol-Church, K., Rusconi, P., Zhang, Z., Shi, G.X., Andres, D.A., Bodamer, O.A. (2016) Mutations in RIT1 cause Noonan syndrome - additional functional evidence and expanding the clinical phenotype. Clinical genetics. 89(3):359-66

Abrams, A.J., Hufnagel, R.B., Rebelo, A., Zanna, C., Patel, N., Gonzalez, M.A., Campeanu, I.J., Griffin, L.B., Groenewald, S., Strickland, A.V., Tao, F., Speziani, F., Abreu, L., Schüle, R., Caporali, L., La Morgia, C., Maresca, A., Liguori, R., Lodi, R., Ahmed, Z.M., Sund, K.L., Wang, X., Krueger, L.A., Peng, Y., Prada, C.E., Prows, C.A., Schorry, E.K., Antonellis, A., Zimmerman, H.H., Abdul-Rahman, O.A., Yang, Y., Downes, S.M., Prince, J., Fontanesi, F., Barrientos, A., Németh, A.H., Carelli, V., Huang, T., Zuchner, S., Dallman, J.E. (2015) Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder. Nature Genetics. 47(8):926-32

Kozol, R.A., Cukier, H.N., Zou, B., Mayo, V., De Rubeis, S., Cai, G., Griswold, A.J., Whitehead, P.L., Haines, J.L., Gilbert, J.R., Cuccaro, M.L., Martin, E.R., Baker, J.D., Buxbaum, J.D., Pericak-Vance, M.A., Dallman, J.E. (2015) Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis. Human molecular genetics. 24(14):4006-23

Wen, R., Dallman, J.E., Li, Y., Züchner, S.L., Vance, J.M., Peričak-Vance, M.A., Lam, B.L. (2014) Knock-Down DHDDS Expression Induces Photoreceptor Degeneration in Zebrafish. Advances in experimental medicine and biology. 801:543-50

Ganser, L.R., Yan, Q., James, V.M., Kozol, R., Topf, M., Harvey, R.J., and Dallman, J.E. (2013) Distinct phenotypes in zebrafish models of human startle disease. Neurobiology of disease. 60:139-51

Wen, H., Linhoff, M.W., Hubbard, J.M., Nelson, N.R., Stensland, D., Dallman, J., Mandel, G., and Brehm, P. (2013) Zebrafish calls for reinterpretation for the roles of p/q calcium channels in neuromuscular transmission. The Journal of neuroscience : the official journal of the Society for Neuroscience. 33(17):7384-7392

Yariz, K.O., Duman, D., Seco, C.Z., Dallman, J., Huang, M., Peters, T.A., Sirmaci, A., Lu, N., Schraders, M., Skromne, I., Oostrik, J., Diaz-Horta, O., Young, J.I., Tokgoz-Yilmaz, S., Konukseven, O., Shahin, H., Hetterschijt, L., Kanaan, M., Oonk, A.M., Edwards, Y.J., Li, H., Atalay, S., Blanton, S., Desmidt, A.A., Liu, X.Z., Pennings, R.J., Lu, Z., Chen, Z.Y., Kremer, H., and Tekin, M. (2012) Mutations in OTOGL, Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss. American journal of human genetics. 91(5):872-882

Zuchner, S., Dallman, J., Wen, R., Beecham, G., Naj, A., Farooq, A., Kohli, M.A., Whitehead, P.L., Hulme, W., Konidari, I., Edwards, Y.J., Cai, G., Peter, I., Seo, D., Buxbaum, J.D., Haines, J.L., Blanton, S., Young, J., Alfonso, E., Vance, J.M., Lam, B.L., and Periak-Vance, M.A. (2011) Whole-Exome Sequencing Links a Variant in DHDDS to Retinitis Pigmentosa. American journal of human genetics. 88(2):201-206

Ganser, L.R., and Dallman, J.E. (2009) Glycinergic synapse development, plasticity, and homeostasis in zebrafish. Frontiers in molecular neuroscience. 2:30

Luna, V.M., Wang, M., Ono, F., Gleason, M.R., Dallman, J.E., Mandel, G., and Brehm, P. (2004) Persistent electrical coupling and locomotory dysfunction in the zebrafish mutant shocked. Journal of neurophysiology. 92(4):2003-2009

NON-ZEBRAFISH PUBLICATIONS