| Suppression of astrocytic autophagy by αB-crystallin contributes to α-synuclein inclusion formation S Lu, Y Guo, P Liang, S Zhang, S Yin, Y Yin, X Wang, F Ding, X Gu, ... Translational neurodegeneration 8, 1-14, 2019 | 42 | 2019 |
| Extracellular αB-crystallin modulates the inflammatory responses Y Guo, P Liang, S Lu, R Chen, Y Yin, J Zhou Biochemical and biophysical research communications 508 (1), 282-288, 2019 | 41 | 2019 |
| TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila LD Goodman, H Cope, Z Nil, TA Ravenscroft, WL Charng, S Lu, AC Tien, ... The American Journal of Human Genetics 108 (9), 1669-1691, 2021 | 23 | 2021 |
| 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 | 20 | 2022 |
| 'Fly-ing'from rare to common neurodegenerative disease mechanisms M Ma, MJ Moulton, S Lu, HJ Bellen Trends in Genetics 38 (9), 972-984, 2022 | 18 | 2022 |
| Very Long-Chain Fatty Acids Induce Glial-Derived Sphingosine-1-Phosphate Synthesis, Secretion, and Neuroinflammation H Chung, Q Ye, YJ Park, Z Zuo, O Kanca, JW Mok, SG Tattikota, S Lu, ... Cell Metabolism 35 (5), 855-874, 2023 | 17 | 2023 |
| De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movement S Lu, M Ma, X Mao, CA Bacino, J Jankovic, VR Sutton, JA Bartley, X Wang, ... The American Journal of Human Genetics 109 (10), 1932-1943, 2022 | 16 | 2022 |
| Sphingolipids in neurodegenerative diseases X Pan, D Dutta, S Lu, HJ Bellen Frontiers in Neuroscience 17, 1137893, 2023 | 13 | 2023 |
| 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, ... The American Journal of Human Genetics 109 (10), 1923-1931, 2022 | 11 | 2022 |
| Inhibition of astrocytic DRD2 suppresses CNS inflammation in an animal model of multiple sclerosis S Lu, Y Wu, Y Guo, P Liang, S Yin, Y Yin, X Zhang, YF Liu, H Wang, ... Journal of Experimental Medicine 219 (9), e20210998, 2022 | 9 | 2022 |
| Finding the ‘Guilty’ Gene Variant of Sporadic Parkinson’s Disease Via CRISPR/Cas9 S Lu, J Zhou Neuroscience bulletin 33, 115-117, 2017 | 7 | 2017 |
| Loss of neuron navigator 2 impairs brain and cerebellar development A Accogli, S Lu, I Musante, P Scudieri, JA Rosenfeld, M Severino, ... The Cerebellum 22 (2), 206-222, 2023 | 6 | 2023 |
| The fly homolog of SUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survival M Ma, X Zhang, Y Zheng, S Lu, X Pan, X Mao, H Pan, H Chung, H Wang, ... Human Molecular Genetics 32 (6), 984-997, 2023 | 5 | 2023 |
| 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 31 (16), 2751-2765, 2022 | 5 | 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 | 3 | 2023 |
| Isolation and identification of a strain of deltamethrin degrading bacteria and its degradation characteristics LY Xiang, HY Zhao, MF Huang, SZ Lu, JY Fan, YC Geng, K Tao, TP Hou Journal of Sichuan University: Natural Science Edition 49 (4), 914-918, 2012 | 3 | 2012 |
| Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays X Pan, AN Alvarez, M Ma, S Lu, MW Crawford, LC Briere, O Kanca, ... Elife 12, RP89891, 2023 | 2 | 2023 |
| De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features X Pan, AM Tao, S Lu, M Ma, SB Hannan, R Slaugh, SD Williams, ... The American Journal of Human Genetics 111 (4), 742-760, 2024 | | 2024 |
| Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for … M Ma, M Ganapathi, Y Zheng, KL Tan, O Kanca, KE Bove, N Quintanilla, ... Genetics in Medicine, 101125, 2024 | | 2024 |
| De novo variants in PLCG1 are associated with hearing impairment, ocular pathology, and cardiac defects M Ma, Y Zheng, S Lu, X Pan, KC Worley, LC Burrage, LS Blieden, ... medRxiv, 2024 | | 2024 |
