Year | Citation | Score | |||
---|---|---|---|---|---|
2021 | Kozol RA, James DM, Varela I, Sumathipala SH, Züchner S, Dallman JE. Restoring Shank3 in the rostral brainstem of shank3ab-/- zebrafish autism models rescues sensory deficits. Communications Biology. 4: 1411. PMID 34921227 DOI: 10.1038/s42003-021-02920-6 | 0.6 | |||
2019 | James DM, Kozol RA, Kajiwara Y, Wahl AL, Storrs EC, Buxbaum JD, Klein M, Moshiree B, Dallman JE. Intestinal dysmotility in a zebrafish () mutant model of autism. Molecular Autism. 10: 3. PMID 30733854 DOI: 10.1186/S13229-018-0250-4 | 0.624 | |||
2016 | Kozol RA, Abrams AJ, James DM, Buglo E, Yan Q, Dallman JE. Function Over Form: Modeling Groups of Inherited Neurological Conditions in Zebrafish. Frontiers in Molecular Neuroscience. 9: 55. PMID 27458342 DOI: 10.3389/Fnmol.2016.00055 | 0.621 | |||
2015 | Kozol RA, Cukier HN, Zou B, Mayo V, De Rubeis S, Cai G, Griswold AJ, Whitehead PL, Haines JL, Gilbert JR, Cuccaro ML, Martin ER, Baker JD, Buxbaum JD, Pericak-Vance MA, et al. 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: 4006-23. PMID 25882707 DOI: 10.1093/Hmg/Ddv138 | 0.64 | |||
2013 | Ganser LR, Yan Q, James VM, Kozol R, Topf M, Harvey RJ, Dallman JE. Distinct phenotypes in zebrafish models of human startle disease. Neurobiology of Disease. 60: 139-51. PMID 24029548 DOI: 10.1016/J.Nbd.2013.09.002 | 0.613 | |||
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