| CoREST: a functional corepressor required for regulation of neural-specific gene expression ME Andrés, C Burger, MJ Peral-Rubio, E Battaglioli, ME Anderson, ... Proceedings of the National Academy of Sciences 96 (17), 9873-9878, 1999 | 607 | 1999 |
| Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder AJ Abrams, RB Hufnagel, A Rebelo, C Zanna, N Patel, MA Gonzalez, ... Nature genetics 47 (8), 926-932, 2015 | 221 | 2015 |
| Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa S Züchner, J Dallman, R Wen, G Beecham, A Naj, A Farooq, MA Kohli, ... The American Journal of Human Genetics 88 (2), 201-206, 2011 | 193 | 2011 |
| Crossing the blood–brain–barrier with transferrin conjugated carbon dots: A zebrafish model study S Li, Z Peng, J Dallman, J Baker, AM Othman, PL Blackwelder, ... Colloids and Surfaces B: Biointerfaces 145, 251-256, 2016 | 152 | 2016 |
| Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes A Cortese, Y Zhu, AP Rebelo, S Negri, S Courel, L Abreu, CJ Bacon, ... Nature genetics 52 (5), 473-481, 2020 | 140 | 2020 |
| Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss KO Yariz, D Duman, CZ Seco, J Dallman, M Huang, TA Peters, A Sirmaci, ... The American Journal of Human Genetics 91 (5), 872-882, 2012 | 131 | 2012 |
| Function over form: modeling groups of inherited neurological conditions in zebrafish RA Kozol, AJ Abrams, DM James, E Buglo, Q Yan, JE Dallman Frontiers in molecular neuroscience 9, 55, 2016 | 123 | 2016 |
| Translocation of CaM kinase II to synaptic sites in vivo MR Gleason, S Higashijima, J Dallman, K Liu, G Mandel, JR Fetcho Nature neuroscience 6 (3), 217-218, 2003 | 112 | 2003 |
| Tryptophan carbon dots and their ability to cross the blood-brain barrier KJ Mintz, G Mercado, Y Zhou, Y Ji, SD Hettiarachchi, PY Liyanage, ... Colloids and Surfaces B: Biointerfaces 176, 488-493, 2019 | 106 | 2019 |
| Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of … RA Kozol, HN Cukier, B Zou, V Mayo, S De Rubeis, G Cai, AJ Griswold, ... Human molecular genetics 24 (14), 4006-4023, 2015 | 89 | 2015 |
| A conserved role but different partners for the transcriptional corepressor CoREST in fly and mammalian nervous system formation JE Dallman, J Allopenna, A Bassett, A Travers, G Mandel Journal of Neuroscience 24 (32), 7186-7193, 2004 | 75 | 2004 |
| Intestinal dysmotility in a zebrafish (Danio rerio) shank3a;shank3b mutant model of autism DM James, RA Kozol, Y Kajiwara, AL Wahl, EC Storrs, JD Buxbaum, ... Molecular autism 10, 1-15, 2019 | 71 | 2019 |
| Cryptic amyloidogenic elements in the 3′ UTRs of neurofilament genes trigger axonal neuropathy AP Rebelo, AJ Abrams, E Cottenie, A Horga, M Gonzalez, DM Bis, ... The American Journal of Human Genetics 98 (4), 597-614, 2016 | 63 | 2016 |
| Genetic compensation in a stable slc25a46 mutant zebrafish: A case for using F0 CRISPR mutagenesis to study phenotypes caused by inherited disease E Buglo, E Sarmiento, NB Martuscelli, DW Sant, MC Danzi, AJ Abrams, ... PloS one 15 (3), e0230566, 2020 | 59 | 2020 |
| “Dark” carbon dots specifically “light-up” calcified zebrafish bones S Li, I Skromne, Z Peng, J Dallman, AO Al-Youbi, AS Bashammakh, ... Journal of Materials Chemistry B 4 (46), 7398-7405, 2016 | 58 | 2016 |
| Mutations in RIT1 cause Noonan syndrome – additional functional evidence and expanding the clinical phenotype M Koenighofer, CY Hung, JL McCauley, J Dallman, EJ Back, I Mihalek, ... Clinical genetics 89 (3), 359-366, 2016 | 54 | 2016 |
| Zebrafish calls for reinterpretation for the roles of P/Q calcium channels in neuromuscular transmission H Wen, MW Linhoff, JM Hubbard, NR Nelson, D Stensland, J Dallman, ... Journal of Neuroscience 33 (17), 7384-7392, 2013 | 40 | 2013 |
| Synaptic homeostasis in a zebrafish glial glycine transporter mutant R Mongeon, MR Gleason, MA Masino, JR Fetcho, G Mandel, P Brehm, ... Journal of neurophysiology 100 (4), 1716-1723, 2008 | 37 | 2008 |
| Spontaneous activity regulates calcium‐dependent K+ current expression in developing ascidian muscle JE Dallman, AK Davis, WJ Moody The Journal of physiology 511 (3), 683-693, 1998 | 37 | 1998 |
| Persistent Electrical Coupling and Locomotory Dysfunction in the Zebrafish Mutant shocked VM Luna, M Wang, F Ono, MR Gleason, JE Dallman, G Mandel, P Brehm Journal of neurophysiology 92 (4), 2003-2009, 2004 | 26 | 2004 |