| Drosophila Acyl-CoA synthetase long-chain family member 4 regulates axonal transport of synaptic vesicles and is required for synaptic development and transmission Z Liu, Y Huang, Y Zhang, D Chen, YQ Zhang Journal of Neuroscience 31 (6), 2052-2063, 2011 | 66 | 2011 |
| dAcsl, the Drosophila ortholog of acyl-CoA synthetase long-chain family member 3 and 4, inhibits synapse growth by attenuating bone morphogenetic protein signaling via … Z Liu, Y Huang, W Hu, S Huang, Q Wang, J Han, YQ Zhang Journal of Neuroscience 34 (8), 2785-2796, 2014 | 40 | 2014 |
| The glycosphingolipid MacCer promotes synaptic bouton formation in Drosophila by interacting with Wnt Y Huang, S Huang, C Di Scala, Q Wang, HH Wandall, J Fantini, ... Elife 7, e38183, 2018 | 26 | 2018 |
| Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures S Lu, R Hernan, PC Marcogliese, Y Huang, TS Gertler, M Akcaboy, S Liu, ... The American Journal of Human Genetics 109 (4), 571-586, 2022 | 25 | 2022 |
| Acsl, the Drosophila ortholog of intellectual-disability-related ACSL4, inhibits synaptic growth by altered lipids Y Huang, S Huang, SM Lam, Z Liu, G Shui, YQ Zhang Journal of cell science 129 (21), 4034-4045, 2016 | 24 | 2016 |
| Variants in CAPZA2, a member of an F-actin capping complex, cause intellectual disability and developmental delay Y Huang, X Mao, RH van Jaarsveld, L Shu, PA Terhal, Z Jia, H Xi, Y Peng, ... Human molecular genetics 29 (9), 1537-1546, 2020 | 22 | 2020 |
| The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability Y Huang, G Lemire, LC Briere, F Liu, MW Wessels, X Wang, M Osmond, ... Am J Hum Genet, https://doi.org/10.1016/j.ajhg.2022.08.011, 2022 | 18 | 2022 |
| Novel dominant and recessive variants in human ROBO1 cause distinct neurodevelopmental defects through different mechanisms Y Huang, M Ma, X Mao, D Pehlivan, O Kanca, F Un-Candan, L Shu, ... Human Molecular Genetics, https://doi.org/10.1093/hmg/ddac070 31 (16), 2751-2765, 2022 | 7 | 2022 |
| A comprehensive Drosophila resource to identify key functional interactions between SARS-CoV-2 factors and host proteins A Guichard, S Lu, O Kanca, D Bressan, Y Huang, M Ma, SS Juste, ... Cell reports 42 (8), 2023 | 5 | 2023 |
| Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies Z Nil, AR Deshwar, Y Huang, S Barish, X Zhang, S Choufani, PLQ Stabej, ... The American Journal of Human Genetics 110 (11), 1919-1937, 2023 | 1 | 2023 |
